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Juha Kere

Professor/senior physician

Visiting address : Novum, Hälsovägen 7 (By Car), Blickagången 6 (By Train) 141 57 Huddinge, Sweden
Postal address : Department of Biosciences and Nutrition (BioNut), H2, Department of Biosciences and Nutrition (BioNut), H2, Novum 141 83 Huddinge, Sweden
Delivery address : Novum, Hälsovägen 7-9, Hiss D, Plan 7 141 57 Huddinge, Sweden

About me

Juha Kere (born 1958) is professor of molecular genetics at KI since 2001. He graduated with MD (1984), PhD in molecular genetics (1989) and specialist physician degree in clinical genetics (1994) from University of Helsinki. He was postdoctoral associate at Washington University in St.Louis, Missouri 1990-93 and became acting professor and chief physician of medical genetics at University of Helsinki and Helsinki University Central Hospital 1994. He was then founding director of the Finnish Genome Center 1998-2001, after which he moved to KI. He has published over 400 scientific original and review articles and supervised 35 completed doctoral thesis in Finland and Sweden.

Links

Publications

DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis
Joubert Br, Felix Jf, Yousefi P, Bakulski Km, Just Ac, Breton C, et al
American journal of human genetics 2016;98(4):680-96

Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1
Massinen S, Wang J, Laivuori K, Bieder A, Tapia Paez I, Jiao H, et al
Journal of neurodevelopmental disorders 2016;8():4-

Increased YKL-40 and Chitotriosidase in Asthma and Chronic Obstructive Pulmonary Disease
James Aj, Reinius Le, Verhoek M, Gomes A, Kupczyk M, Hammar U, et al
American journal of respiratory and critical care medicine 2016;193(2):131-42

NOD-like receptor signaling and inflammasome-related pathways are highlighted in psoriatic epidermis
Tervaniemi Mh, Katayama S, Skoog T, Siitonen Ha, Vuola J, Nuutila K, et al
Scientific reports 2016;6():22745-

Single-cell transcriptome analysis of endometrial tissue
Krjutškov K, Katayama S, Saare M, Vera-rodriguez M, Lubenets D, Samuel K, et al
Human reproduction (Oxford, England) 2016;31(4):844-53

Aberrant splicing of genes involved in haemoglobin synthesis and impaired terminal erythroid maturation in SF3B1 mutated refractory anaemia with ring sideroblasts
Conte S, Katayama S, Vesterlund L, Karimi M, Dimitriou M, Jansson M, et al
British journal of haematology 2015;171(4):478-90

Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytes
Acevedo N, Reinius Le, Vitezic M, Fortino V, Söderhäll C, Honkanen H, et al
Clinical epigenetics 2015;7():34-

A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease
Kyöstilä K, Syrjä P, Jagannathan V, Chandrasekar G, Jokinen Ts, Seppälä Eh, et al
PLoS genetics 2015;11(4):e1005169-

Associations between the 17q21 region and allergic rhinitis in 5 birth cohorts
Fuertes E, Söderhäll C, Acevedo N, Becker A, Brauer M, Chan-yeung M, et al
The Journal of allergy and clinical immunology 2015;135(2):573-6

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3
Haapaniemi Em, Kaustio M, Rajala Hl, Van Adrichem Aj, Kainulainen L, Glumoff V, et al
Blood 2015;125(4):639-48

Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis
Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Åkesson K, et al
The spine journal : official journal of the North American Spine Society 2015;15(10):2239-46

CTNND2-a candidate gene for reading problems and mild intellectual disability
Hofmeister W, Nilsson D, Topa A, Anderlid Bm, Darki F, Matsson H, et al
Journal of medical genetics 2015;52(2):111-22

DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling
Schueler M, Braun Da, Chandrasekar G, Gee Hy, Klasson Td, Halbritter J, et al
American journal of human genetics 2015;96(1):81-92

Evidence of streptococcal origin of acute non-necrotising cellulitis: a serological study
Karppelin M, Siljander T, Haapala Am, Aittoniemi J, Huttunen R, Kere J, et al
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES 2015;34(4):669-72

Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity
Jiao H, Arner P, Gerdhem P, Strawbridge Rj, Näslund E, Thorell A, et al
European journal of human genetics : EJHG 2015;23(9):1216-22

Gene expression analysis of skin grafts and cultured keratinocytes using synthetic RNA normalization reveals insights into differentiation and growth control
Katayama S, Skoog T, Jouhilahti Em, Siitonen Ha, Nuutila K, Tervaniemi Mh, et al
BMC genomics 2015;16():476-

Gene expression profiling of pre-eclamptic placentae by RNA sequencing
Finnpec Core Invest Grp, Kaartokallio T, Cervera A, Kyllonen A, Laivuori K, Kere J, et al
SCIENTIFIC REPORTS 2015;:14107-

Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus
Kunz M, König Ir, Schillert A, Kruppa J, Ziegler A, Grallert H, et al
Experimental dermatology 2015;24(7):510-5

GIMAP GTPase family genes: potential modifiers in autoimmune diabetes, asthma, and allergy
Heinonen Mt, Laine Ap, Söderhäll C, Gruzieva O, Rautio S, Melén E, et al
Journal of immunology (Baltimore, Md. : 1950) 2015;194(12):5885-94

Helsinki alert of biodiversity and health
Von Hertzen L, Beutler B, Bienenstock J, Blaser M, Cani Pd, Eriksson J, et al
ANNALS OF MEDICINE 2015;47(3):218-25

High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia
Karimi M, Nilsson C, Dimitriou M, Jansson M, Matsson H, Unneberg P, et al
Haematologica 2015;100(6):e223-5

Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family
Einarsdottir E, Svensson I, Darki F, Peyrard-janvid M, Lindvall Jm, Ameur A, et al
Human genetics 2015;134(11-12):1239-48

Novel PRD-like homeodomain transcription factors and retrotransposon elements in early human development
Töhönen V, Katayama S, Vesterlund L, Jouhilahti Em, Sheikhi M, Madissoon E, et al
Nature communications 2015;6():8207-

Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-hemmi J, et al
Journal of human genetics 2015;60(7):399-401

Predictors of recurrent cellulitis in five years. Clinical risk factors and the role of PTX3 and CRP
Karppelin M, Siljander T, Aittoniemi J, Hurme M, Huttunen R, Huhtala H, et al
The Journal of infection 2015;70(5):467-73

Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus
Hafrén L, Einarsdottir E, Kentala E, Hammarén-malmi S, Bhutta Mf, Macarthur Cj, et al
PloS one 2015;10(7):e0132551-

Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
Acevedo N, Reinius Le, Greco D, Gref A, Orsmark-pietras C, Persson H, et al
Human molecular genetics 2015;24(3):875-90

Transcriptome analysis of controlled and therapy-resistant childhood asthma reveals distinct gene expression profiles
Persson H, Kwon At, Ramilowski Ja, Silberberg G, Söderhäll C, Orsmark-pietras C, et al
The Journal of allergy and clinical immunology 2015;136(3):638-48

Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma
Huang J, Löhr Jm, Nilsson M, Segersvärd R, Matsson H, Verbeke C, et al
Clinical chemistry 2015;61(11):1408-16

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease
Flanagan Se, Haapaniemi E, Russell Ma, Caswell R, Lango Allen H, De Franco E, et al
Nature genetics 2014;46(8):812-4

A promoter-level mammalian expression atlas
Riken Pmi Clst Dgt, Fantom Consortium, Forrest Arr, Kawaji H, Rehli M, Baillie Jk, et al
NATURE 2014;507(7493):462-70

Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate
Pegelow M, Koillinen H, Magnusson M, Fransson I, Unneberg P, Kere J, et al
CLEFT PALATE-CRANIOFACIAL JOURNAL 2014;51(1):49-55

Azacitidine induces profound genome-wide hypomethylation in primary myelodysplastic bone marrow cultures but may also reduce histone acetylation
Grövdal M, Karimi M, Tobiasson M, Reinius L, Jansson M, Ekwall K, et al
Leukemia 2014;28(2):411-3

Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment
Rodin S, Antonsson L, Niaudet C, Simonson Oe, Salmela E, Hansson Em, et al
Nature communications 2014;5():3195-

DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development
Darki F, Peyrard-janvid M, Matsson H, Kere J, Klingberg T
The Journal of neuroscience : the official journal of the Society for Neuroscience 2014;34(43):14455-62

Differences in gene expression between mouse and human for dynamically regulated genes in early embryo
Madissoon E, Töhönen V, Vesterlund L, Katayama S, Unneberg P, Inzunza J, et al
PloS one 2014;9(8):e102949-

Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7
Hannula-jouppi K, Muurinen M, Lipsanen-nyman M, Reinius Le, Ezer S, Greco D, et al
Epigenetics 2014;9(3):351-65

Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development
Peyrard-janvid M, Leslie Ej, Kousa Ya, Smith Tl, Dunnwald M, Magnusson M, et al
American journal of human genetics 2014;94(1):23-32

Enhanced expression of neuropeptide S (NPS) receptor in eosinophils from severe asthmatics and subjects with total IgE above 100 IU/ml
Ilmarinen P, James A, Moilanen E, Pulkkinen V, Daham K, Saarelainen S, et al
PEPTIDES 2014;:100-9

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Becker J, Czamara D, Scerri Ts, Ramus F, Csépe V, Talcott Jb, et al
European journal of human genetics : EJHG 2014;22(5):675-80

Microsatellite polymorphism in the heme oxygenase-1 promoter is associated with nonsevere and late-onset preeclampsia
Kaartokallio T, Klemetti Mm, Timonen A, Uotila J, Heinonen S, Kajantie E, et al
Hypertension (Dallas, Tex. : 1979) 2014;64(1):172-7

Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors
Pulkkinen V, Ezer S, Sundman L, Hagstrom J, Remes S, Soderhall C, et al
VIRCHOWS ARCHIV 2014;465(2):173-83

Neuropeptide S receptor 1 (NPSR1) activates cancer-related pathways and is widely expressed in neuroendocrine tumors (vol 465, pg 173, 2014)
Pulkkinen V, Ezer S, Sundman L, Hagstrom J, Remes S, Soderhall C, et al
VIRCHOWS ARCHIV 2014;465(2):251-251

NPSR1 polymorphisms influence recurrent abdominal pain in children: a population-based study
Henström M, Zucchelli M, Söderhäll C, Bergström A, Kere J, Melén E, et al
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2014;26(10):1417-25

Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents
Söderqvist S, Matsson H, Peyrard-janvid M, Kere J, Klingberg T
Journal of cognitive neuroscience 2014;26(1):54-62

Sequencing of breast cancer stem cell populations indicates a dynamic conversion between differentiation states in vivo
Klevebring D, Rosin G, Ma R, Lindberg J, Czene K, Kere J, et al
BREAST CANCER RESEARCH 2014;16(4):R72-

The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype
Kere J
Biochemical and biophysical research communications 2014;452(2):236-43

The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
Bölte S, Willfors C, Berggren S, Norberg J, Poltrago L, Mevel K, et al
Twin research and human genetics : the official journal of the International Society for Twin Studies 2014;17(3):164-76

A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18
Majander Kk, Villa Pm, Kivinen K, Kere J, Laivuori H
EUROPEAN JOURNAL OF HUMAN GENETICS 2013;21(9):1024-6

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis
Weidinger S, Willis-owen Sag, Kamatani Y, Baurecht H, Morar N, Liang Lm, et al
HUMAN MOLECULAR GENETICS 2013;22(23):4841-56

Altered Methylation of IGF2 Locus 20 Years after Preterm Birth at Very Low Birth Weight
Wehkalampi K, Muurinen M, Wirta Sb, Hannula-jouppi K, Hovi P, Jarvenpaa Al, et al
PLOS ONE 2013;8(6):-

DNA methylation in the Neuropeptide S Receptor 1 (NPSR1) promoter in relation to asthma and environmental factors
Reinius Le, Gref A, Sääf A, Acevedo N, Joerink M, Kupczyk M, et al
PloS one 2013;8(1):e53877-

Drug repositioning: a machine-learning approach through data integration
Napolitano F, Zhao Y, Moreira Vm, Tagliaferri R, Kere J, D'amato M, et al
JOURNAL OF CHEMINFORMATICS 2013;:30-

Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis
Liu Y, Aryee Mj, Padyukov L, Fallin Md, Hesselberg E, Runarsson A, et al
NATURE BIOTECHNOLOGY 2013;31(2):142-7

Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations
Wang C, Ahlford A, Järvinen Tm, Nordmark G, Eloranta Ml, Gunnarsson I, et al
European journal of human genetics : EJHG 2013;21(9):994-9

Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease
Finnpec Study Grp, Johnson Mp, Brennecke Sp, East Ce, Dyer Td, Roten Lt, et al
MOLECULAR HUMAN REPRODUCTION 2013;19(7):423-37

Genetic Susceptibility to Non-Necrotizing Erysipelas/Cellulitis
Hannula-jouppi K, Massinen S, Siljander T, Makela S, Kivinen K, Leinonen R, et al
PLOS ONE 2013;8(2):e56225-

Interaction between retinoid acid receptor-related orphan receptor alpha (RORA) and neuropeptide S receptor 1 (NPSR1) in asthma
Acevedo N, Sääf A, Söderhäll C, Melén E, Mandelin J, Pietras Co, et al
PloS one 2013;8(4):e60111-

Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort
Nwaru Bi, Takkinen Hm, Niemela O, Kaila M, Erkkola M, Ahonen S, et al
ALLERGY 2013;68(4):507-16

Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins
Tammimies K, Vitezic M, Matsson H, Le Guyader S, Bürglin Tr, Ohman T, et al
Biological psychiatry 2013;73(6):583-90

Recurrent cellulitis with benzathine penicillin prophylaxis is associated with diabetes and psoriasis
Karppelin M, Siljander T, Huhtala H, Aromaa A, Vuopio J, Hannula-jouppi K, et al
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES 2013;32(3):369-72

Rule-based models of the interplay between genetic and environmental factors in childhood allergy
Bornelöv S, Sääf A, Melén E, Bergström A, Torabi Moghadam B, Pulkkinen V, et al
PloS one 2013;8(11):e80080-

SAMstrt: statistical test for differential expression in single-cell transcriptome with spike-in normalization
Katayama S, Töhönen V, Linnarsson S, Kere J
Bioinformatics (Oxford, England) 2013;29(22):2943-5

The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function
Chandrasekar G, Vesterlund L, Hultenby K, Tapia-páez I, Kere J
PloS one 2013;8(5):e63123-

Timing of infant feeding in relation to childhood asthma and allergic diseases
Nwaru Bi, Takkinen Hm, Niemela O, Kaila M, Erkkola M, Ahonen S, et al
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 2013;131(1):78-86

Transcriptome analysis reveals upregulation of bitter taste receptors in severe asthmatics
Orsmark-pietras C, James A, Konradsen Jr, Nordlund B, Söderhäll C, Pulkkinen V, et al
The European respiratory journal 2013;42(1):65-78

Ultra-Rare Mutation in Long-Range Enhancer Predisposes to Thyroid Carcinoma with High Penetrance
He Hl, Li W, Wu Dy, Nagy R, Liyanarachchi S, Akagi K, et al
PLOS ONE 2013;8(5):e61920-

Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1
Hackman P, Sarparanta J, Lehtinen S, Vihola A, Evila A, Jonson Ph, et al
ANNALS OF NEUROLOGY 2013;73(4):500-9

Acquisition of Complement Factor H Is Important for Pathogenesis of Streptococcus pyogenes Infections: Evidence from Bacterial In Vitro Survival and Human Genetic Association
Haapasalo K, Vuopio J, Syrjanen J, Suvilehto J, Massinen S, Karppelin M, et al
JOURNAL OF IMMUNOLOGY 2012;188(1):426-35

A novel screening method detects herpesviral DNA in the idiopathic pulmonary fibrosis lung
Pulkkinen V, Salmenkivi K, Kinnula Vl, Sutinen E, Halme M, Hodgson U, et al
ANNALS OF MEDICINE 2012;44(2):178-86

Centrosomal Localization of the Psoriasis Candidate Gene Product, CCHCR1, Supports a Role in Cytoskeletal Organization
Tervaniemi Mh, Siitonen Ha, Soderhall C, Minhas G, Vuola J, Tiala I, et al
PLOS ONE 2012;7(11):e49920-

Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis
I-chip Psoriasis Consortium, Genetic Anal Psoriasis Consortium, Wellcome Trust Case Control, Knight J, Spain Sl, Capon F, et al
HUMAN MOLECULAR GENETICS 2012;21(23):5185-92

Current Knowledge of the Genetics of Otitis Media
Hafren L, Kentala E, Einarsdottir E, Kere J, Mattila Ps
CURRENT ALLERGY AND ASTHMA REPORTS 2012;12(6):582-9

Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility
Reinius Le, Acevedo N, Joerink M, Pershagen G, Dahlén Se, Greco D, et al
PloS one 2012;7(7):e41361-

DNA methylation levels within the CD14 promoter region are lower in placentas of mothers living on a farm
Slaats Ggg, Reinius Le, Alm J, Kere J, Scheynius A, Joerink M
ALLERGY 2012;67(7):895-903

Dopamine, Working Memory, and Training Induced Plasticity: Implications for Developmental Research
Soderqvist S, Nutley Sb, Peyrard-janvid M, Matsson H, Humphreys K, Kere J, et al
DEVELOPMENTAL PSYCHOLOGY 2012;48(3):836-43

Genetic background and the risk of otitis media
Hafren L, Kentala E, Jarvinen Tm, Leinonen E, Onkamo P, Kere J, et al
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY 2012;76(1):41-4

Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene
Finnpec Study Grp, Johnson Mp, Brennecke Sp, East Ce, Goring Hhh, Kent Jw, et al
PLOS ONE 2012;7(3):e33666-

Genome-wide linkage analysis of human auditory cortical activation suggests distinct loci on chromosomes 2, 3, and 8
Renvall H, Salmela E, Vihla M, Illman M, Leinonen E, Kere J, et al
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012;32(42):14511-8

Human ROBO1 Regulates Interaural Interaction in Auditory Pathways
Lamminmaki S, Massinen S, Nopola-hemmi J, Kere J, Hari R
JOURNAL OF NEUROSCIENCE 2012;32(3):966-71

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Wellcome Trust Case Control Consor, Psoriasis Assoc Genetics Extension, Genetic Anal Psoriasis Consortium, Collaborative Assoc Study Psoriasi, Tsoi Lc, Spain Sl, et al
NATURE GENETICS 2012;44(12):1341-8

In vivo differentiated human embryonic stem cells can acquire chromosomal aberrations more frequently than in vitro during the same period
Zucchelli M, Ström S, Holm F, Malmgren H, Sahlén S, Religa P, et al
Stem cells and development 2012;21(18):3363-71

PP009. A follow-up study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18
Laivuori Hm, Majander Kk, Villa P, Kivinen K, Kere J
Pregnancy hypertension 2012;2(3):244-5

Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population
Jarvinen Tm, Hellquist A, Zucchelli M, Koskenmies S, Panelius J, Hasan T, et al
RHEUMATOLOGY 2012;51(1):87-92

Research Resource: Interactome of Human Embryo Implantation: Identification of Gene Expression Pathways, Regulation, and Integrated Regulatory Networks
Altmae S, Reimand J, Hovatta O, Zhang P, Kere J, Laisk T, et al
MOLECULAR ENDOCRINOLOGY 2012;26(1):203-17

The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language
Anthoni H, Sucheston Le, Lewis Ba, Tapia-paez I, Fan Xt, Zucchelli M, et al
BEHAVIOR GENETICS 2012;42(4):509-27

The dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer
Rosin G, Hannelius U, Lindstrom L, Hall P, Bergh J, Hartman J, et al
BMC CANCER 2012;:79-

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure
Scerri Ts, Darki F, Newbury Df, Whitehouse Ajo, Peyrard-janvid M, Matsson H, et al
PLOS ONE 2012;7(11):e50321-

The rs3743205 SNP Is Important for the Regulation of the Dyslexia Candidate Gene DYX1C1 by Estrogen Receptor beta and DNA Methylation
Tammimies K, Tapia-paez I, Ruegg J, Rosin G, Kere J, Gustafsson Ja, et al
MOLECULAR ENDOCRINOLOGY 2012;26(4):619-29

Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure
Darki F, Peyrard-janvid M, Matsson H, Kere J, Klingberg T
Biological psychiatry 2012;72(8):671-6

Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development
Ziermans T, Dumontheil I, Roggeman C, Peyrard-janvid M, Matsson H, Kere J, et al
Translational psychiatry 2012;2():e85-

A comprehensive analysis of the COL29A1 gene does not support a role in eczema
Naumann A, Soderhall C, Folster-holst R, Baurecht H, Harde V, Muller-wehling K, et al
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 2011;127(5):1187-94.e7

Co-localization of neural cell adhesion molecule and fibroblast growth factor receptor 2 in early embryo development
Vesterlund L, Tohonen V, Hovatta O, Kere J
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY 2011;55(3):313-9

Factor V Leiden as a risk factor for preterm birth - a population-based nested case-control study
Hiltunen Lm, Laivuori H, Rautanen A, Kaaja R, Kere J, Krusius T, et al
JOURNAL OF THROMBOSIS AND HAEMOSTASIS 2011;9(1):71-8

FV Leiden as risk factor for preterm birth - a population-based nested case-control study
Hiltunen L, Laivuori H, Rautanen A, Kaaj R, Kere J, Krusius T, et al
THROMBOSIS RESEARCH 2011;:S140-S140

Genetic Association and Gene Expression Analysis Identify FGFR1 as a New Susceptibility Gene for Human Obesity
Jiao H, Arner P, Dickson Sl, Vidal H, Mejhert N, Henegar C, et al
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 2011;96(6):E962-6

Genome-wide analysis of extended pedigrees confirms IL2-IL21 linkage and shows additional regions of interest potentially influencing coeliac disease risk
Einarsdottir E, Koskinen Lle, De Kauwe Al, Dukes E, Mustalahti K, Balogh M, et al
TISSUE ANTIGENS 2011;78(6):428-37

Genome wide association study identifies KCNMA1 contributing to human obesity
Jiao H, Arner P, Hoffstedt J, Brodin D, Dubern B, Czernichow S, et al
BMC MEDICAL GENOMICS 2011;:51-

Genomic Strategy Identifies a Missense Mutation in WD-Repeat Domain 65 (WDR65) in an Individual With Van der Woude Syndrome
Rorick Nk, Kinoshita A, Weirather Jl, Peyrard-janvid M, De Lima Rllf, Dunnwald M, et al
AMERICAN JOURNAL OF MEDICAL GENETICS PART A 2011;155A(6):1314-21

Glucocorticoid receptor gene haplotype predicts increased risk of hospital admission for depressive disorders in the Helsinki birth cohort study
Lahti J, Raikkonen K, Bruce S, Heinonen K, Pesonen Ak, Rautanen A, et al
JOURNAL OF PSYCHIATRIC RESEARCH 2011;45(9):1160-4

Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons
Massinen S, Hokkanen Me, Matsson H, Tammimies K, Tapia-paez I, Dahlstrom-heuser V, et al
PLOS ONE 2011;6(6):e20580-

Influence of the COMT Genotype on Working Memory and Brain Activity Changes During Development
Dumontheil I, Roggeman C, Ziermans T, Peyrard-janvid M, Matsson H, Kere J, et al
BIOLOGICAL PSYCHIATRY 2011;70(3):222-9

LifeGene-a large prospective population-based study of global relevance
Almqvist C, Adami Ho, Franks Pw, Groop L, Ingelsson E, Kere J, et al
EUROPEAN JOURNAL OF EPIDEMIOLOGY 2011;26(1):67-77

Meta-Analysis Confirms the LCE3C_LCE3B Deletion as a Risk Factor for Psoriasis in Several Ethnic Groups and Finds Interaction with HLA-Cw6
Riveira-munoz E, He Sm, Escaramis G, Stuart Pe, Huffmeier U, Lee C, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2011;131(5):1105-9

Methylation of H19 and its imprinted control region (H19 ICR1) in Mullerian aplasia
Sandbacka M, Bruce S, Halttunen M, Puhakka M, Lahermo P, Hannula-jouppi K, et al
FERTILITY AND STERILITY 2011;95(8):2703-6

Molecular genetics and molecular biology of dyslexia
Kere J
WILEY INTERDISCIPLINARY REVIEWS-COGNITIVE SCIENCE 2011;2(4):441-8

Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations
Einarsdottir E, Bevova Mr, Zhernakova A, Monsuur A, Koskinen Lle, Van't Slot R, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2011;19(6):682-6

Multiple Polymorphisms Affect Expression and Function of the Neuropeptide S Receptor (NPSR1)
Anedda F, Zucchelli M, Schepis D, Hellquist A, Corrado L, D'alfonso S, et al
PLOS ONE 2011;6(12):e29523-

SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations
Matsson H, Tammimies K, Zucchelli M, Anthoni H, Onkamo P, Nopola-hemmi J, et al
BEHAVIOR GENETICS 2011;41(1):134-40

Study of Estrogen Receptor-alpha and Receptor-beta Gene Polymorphisms on Alzheimer's Disease
Goumidi L, Dahlman-wright K, Tapia-paez I, Matsson H, Pasquier F, Amouyel P, et al
JOURNAL OF ALZHEIMERS DISEASE 2011;26(3):431-9

Swedish Population Substructure Revealed by Genome-Wide Single Nucleotide Polymorphism Data
Salmela E, Lappalainen T, Liu Jj, Sistonen P, Andersen Pm, Schreiber S, et al
PLOS ONE 2011;6(2):e16747-

The asthma candidate gene NPSR1 mediates isoform specific downstream signalling
Pietras Co, Vendelin J, Anedda F, Bruce S, Adner M, Sundman L, et al
BMC pulmonary medicine 2011;11():39-

The zebrafish transcriptome during early development
Vesterlund L, Jiao H, Unneberg P, Hovatta O, Kere J
BMC DEVELOPMENTAL BIOLOGY 2011;:30-

Update on SLC26A3 Mutations in Congenital Chloride Diarrhea
Wedenoja S, Pekansaari E, Hoglund P, Makela S, Holmberg C, Kere J
HUMAN MUTATION 2011;32(7):715-22

A genome-wide association scan on estrogen receptor-negative breast cancer
Li Jm, Humphreys K, Darabi H, Rosin G, Hannelius U, Heikkinen T, et al
BREAST CANCER RESEARCH 2010;12(6):R93-

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
Genetic Anal Psoriasis Consortium, Wellcome Trust Case Control, Strange A, Capon F, Spencer Cca, Knight J, et al
NATURE GENETICS 2010;42(11):985-90

Analysis of Neuropeptide S Receptor Gene (NPSR1) Polymorphism in Rheumatoid Arthritis
D'amato M, Zucchelli M, Seddighzadeh M, Anedda F, Lindblad S, Kere J, et al
PLOS ONE 2010;5(2):e9315-

Assessment of the Neuropeptide S System in Anxiety Disorders
Donner J, Haapakoski R, Ezer S, Melen E, Pirkola S, Gratacos M, et al
BIOLOGICAL PSYCHIATRY 2010;68(5):474-83

A Teratocarcinoma-Like Human Embryonic Stem Cell (hESC) Line and Four hESC Lines Reveal Potentially Oncogenic Genomic Changes
Hovatta O, Jaconi M, Tohonen V, Bena F, Gimelli S, Bosman A, et al
PLOS ONE 2010;5(4):e10263-

ELMOD2, a candidate gene for idiopathic pulmonary fibrosis, regulates antiviral responses
Pulkkinen V, Bruce S, Rintahaka J, Hodgson U, Laitinen T, Alenius H, et al
FASEB JOURNAL 2010;24(4):1167-77

Factors predisposing to acute and recurrent bacterial non-necrotizing cellulitis in hospitalized patients: a prospective case-control study
Karppelin M, Siljander T, Vuopio-varkila J, Kere J, Huhtala H, Vuento R, et al
CLINICAL MICROBIOLOGY AND INFECTION 2010;16(6):729-34

Factor V Leiden as risk factor for unexplained stillbirth - a population-based nested case-control study
Hiltunen Lm, Laivuori H, Rautanen A, Kaaja R, Kere J, Krusius T, et al
THROMBOSIS RESEARCH 2010;125(6):505-10

Genetic evidence of multiple loci in dystocia - difficult labour
Algovik M, Kivinen K, Peterson H, Westgren M, Kere J
BMC MEDICAL GENETICS 2010;:105-

Genetics of complex disorders
Kere J
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 2010;396(1):143-6

[Genetics of multifactorial diseases]
Kere J, Ripatti S, Perola M
Duodecim; laaketieteellinen aikakauskirja 2010;126(19):2305-10

Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease
Kangas-kontio T, Kakko S, Tamminen M, Von Rohr P, Hoeschele I, Juvonen T, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2010;18(5):604-13

Genomic landscape of positive natural selection in Northern European populations
Lappalainen T, Salmela E, Andersen Pm, Dahlman-wright K, Sistonen P, Savontaus Ml, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2010;18(4):471-8

Interaction between early maternal smoking and variants in TNF and GSTP1 in childhood wheezing
Panasevich S, Lindgren C, Kere J, Wickman M, Pershagen G, Nyberg F, et al
CLINICAL AND EXPERIMENTAL ALLERGY 2010;40(3):458-67

Lack of Interaction Between Systemic Lupus Erythematosus-associated Polymorphisms in TYK2 and IRF5 Reply
Hellquist A, Jarvinen Tm, Koskenmies S, Zucchelli M, Orsmark-pietras C, Berglind L, et al
JOURNAL OF RHEUMATOLOGY 2010;37(3):678-678

Localization of psoriasis candidate gene product CCHCR1 at centrosomes
Tervaniemi M, Soderhall C, Siitonen A, Samuelsson L, Suomela S, Saarialho-kere U, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2010;:S81-S81

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy
Bouzigon E, Forabosco P, Koppelman Gh, Cookson Wocm, Dizier Mh, Duffy Dl, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2010;18(6):700-6

MMP-9,-10, and-26, and TIMP-1 expression in relation to filaggrin mutations in atopic dermatitis
Widen-karlsson V, Virolainen S, Soderhall C, Skoog T, Kero M, Kere J, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2010;:S19-S19

Molecular genetic and epigenetic analysis of NCX2/SLC8A2 at 19q13.3 in human gliomas
Qu M, Jiao H, Zhao J, Ren Zp, Smits A, Kere J, et al
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY 2010;36(3):198-210

Neuropeptide S receptor 1 expression in the intestine and skin - putative role in peptide hormone secretion
Sundman L, Saarialho-kere U, Vendelin J, Lindfors K, Assadi G, Kaukinen K, et al
NEUROGASTROENTEROLOGY AND MOTILITY 2010;22(1):79-87

Polymorphisms of the ITGAM Gene Confer Higher Risk of Discoid Cutaneous Than of Systemic Lupus Erythematosus
Jarvinen Tm, Hellquist A, Koskenmies S, Einarsdottir E, Panelius J, Hasan T, et al
PLOS ONE 2010;5(12):e14212-

Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients
Bruce S, Hannula-jouppi K, Puoskari M, Fransson I, Simola Koj, Lipsanen-nyman M, et al
JOURNAL OF MEDICAL GENETICS 2010;47(12):816-22

The SNAP25 Gene Is Linked to Working Memory Capacity and Maturation of the Posterior Cingulate Cortex During Childhood
Soderqvist S, Mcnab F, Peyrard-janvid M, Matsson H, Humphreys K, Kere J, et al
BIOLOGICAL PSYCHIATRY 2010;68(12):1120-5

Tyrosine kinase 2 and interferon regulatory factor 5 polymorphisms are associated with discoid and subacute cutaneous lupus erythematosus
Jarvinen Tm, Hellquist A, Koskenmies S, Einarsdottir E, Koskinen Lle, Jeskanen L, et al
EXPERIMENTAL DERMATOLOGY 2010;19(2):123-31

Variation in STAT4 is associated with systemic lupus erythematosus in a Finnish family cohort
Hellquist A, Sandling Jk, Zucchelli M, Koskenmies S, Julkunen H, D'amato M, et al
ANNALS OF THE RHEUMATIC DISEASES 2010;69(5):883-6

Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families
Kainu K, Kivinen K, Zucchelli M, Suomela S, Kere J, Inerot A, et al
EXPERIMENTAL DERMATOLOGY 2009;18(2):109-15

Association study of the IL18RAP locus in three European populations with coeliac disease
Koskinen Lle, Einarsdottir E, Dukes E, Heap Gar, Dubois P, Korponay-szabo Ir, et al
HUMAN MOLECULAR GENETICS 2009;18(6):1148-55

A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24
He Hl, Nagy R, Liyanarachchi S, Jiao H, Li W, Suster S, et al
CANCER RESEARCH 2009;69(2):625-31

Blood group AB and factor V Leiden as risk factors for pre-eclampsia: A population-based nested case-control study
Hiltunen Lm, Laivuori H, Rautanen A, Kaaja R, Kere J, Krusius T, et al
THROMBOSIS RESEARCH 2009;124(2):167-73

CCHCR1 Is Up-Regulated in Skin Cancer and Associated with EGFR Expression
Suomela S, Elomaa O, Skoog T, Ala-aho R, Jeskanen L, Parssinen J, et al
PLOS ONE 2009;4(6):e6030-

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree of H19 Hypomethylation Associates with Phenotype Severity and Genital and Skeletal Anomalies
Bruce S, Hannula-jouppi K, Peltonen J, Kere J, Lipsanen-nyman M
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 2009;94(2):579-87

Evidence for Genetic Association and Interaction Between the TYK2 and IRF5 Genes in Systemic Lupus Erythematosus
Hellquist A, Jarvinen Tm, Koskenmies S, Zucchelli M, Orsmark-pietras C, Berglind L, et al
JOURNAL OF RHEUMATOLOGY 2009;36(8):1631-8

Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations
Koskinen Lle, Einarsdottir E, Korponay-szabo Ir, Kurppa K, Kaukinen K, Sistonen P, et al
TISSUE ANTIGENS 2009;74(5):408-16

Finnish patients with systemic lupus erythematosus share predisposing genetic risk factors with other populations
Jarvinen Tm, Zucchelli M, Hellquist A, Berglind L, Koskenmies S, Panelius J, et al
ARCHIVES OF DERMATOLOGICAL RESEARCH 2009;301(1):48-48

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia
Massinen S, Tammimies K, Tapia-paez I, Matsson H, Hokkanen Me, Soderberg O, et al
HUMAN MOLECULAR GENETICS 2009;18(15):2802-12

Further evidence for DYX1C1 as a susceptibility factor for dyslexia
Dahdouh F, Anthoni H, Tapia-paez I, Peyrard-janvid M, Schulte-korne G, Warnke A, et al
PSYCHIATRIC GENETICS 2009;19(2):59-63

Identification of MAMDC1 as a Candidate Susceptibility Gene for Systemic Lupus Erythematosus (SLE)
Hellquist A, Zucchelli M, Lindgren Cm, Saarialho-kere U, Jarvinen Tm, Koskenmies S, et al
PLOS ONE 2009;4(12):e8037-

IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease
Einarsdottir E, Koskinen Lle, Dukes E, Kainu K, Suomela S, Lappalainen M, et al
BMC MEDICAL GENETICS 2009;:8-

Lack of Association between Neuropeptide S Receptor 1 Gene (NPSR1) and Eczema in Five European Populations
Ekelund E, Bradley M, Weidinger S, Jovanovic Dl, Johansson C, Lindgren Cm, et al
ACTA DERMATO-VENEREOLOGICA 2009;89(2):115-21

MMP12, Lung Function, and COPD in High-Risk Populations
Hunninghake Gm, Cho Mh, Tesfaigzi Y, Soto-quiros Me, Avila L, Lasky-su J, et al
NEW ENGLAND JOURNAL OF MEDICINE 2009;361(27):2599-608

No Association Between the Eczema Genes COL29Al and IL3l and Inflammatory Bowel Disease
Zucchelli M, Torkvist L, Bresso F, Halfvarson J, Soderhall C, Lee Ya, et al
INFLAMMATORY BOWEL DISEASES 2009;15(7):961-2

PepT1 Oligopeptide Transporter (SLC15A1) Gene Polymorphism in Inflammatory Bowel Disease
Zucchelli M, Torkvist L, Bresso F, Halfvarson J, Hellquist A, Anedda F, et al
INFLAMMATORY BOWEL DISEASES 2009;15(10):1562-9

Population Structure in Contemporary Sweden-A Y-Chromosomal and Mitochondrial DNA Analysis
Lappalainen T, Hannelius U, Salmela E, Von Dobeln U, Lindgren Cm, Huoponen K, et al
ANNALS OF HUMAN GENETICS 2009;:61-73

ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population
Peterson H, Laivuori H, Kerkela E, Jiao H, Hiltunen L, Heino S, et al
MOLECULAR HUMAN REPRODUCTION 2009;15(7):443-9

The protective effect of farm animal exposure on childhood allergy is modified by NPSR1 polymorphisms
Bruce S, Nyberg F, Melen E, James A, Pulkkinen V, Orsmark-pietras C, et al
JOURNAL OF MEDICAL GENETICS 2009;46(3):159-67

Transcriptome Profiling of Human Pre-Implantation Development
Zhang P, Zucchelli M, Bruce S, Hambiliki F, Stavreus-evers A, Levkov L, et al
PLOS ONE 2009;4(11):e7844-

Acute bacterial, nonnecrotizing cellulitis in Finland: Microbiological findings
Siljander T, Karppelin M, Vahakuopus S, Syrjanen J, Toropainen M, Kere J, et al
CLINICAL INFECTIOUS DISEASES 2008;46(6):855-61

Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis
Jiao H, Kaaman M, Dungner E, Kere J, Arner P, Dahlman I
INTERNATIONAL JOURNAL OF OBESITY 2008;32(5):816-25

Biological and genetic interaction between Tenascin C and Neuropeptide S receptor 1 in allergic diseases
Parsifal Genet Study Grp, Orsmark-pietras C, Melen E, Vendelin J, Bruce S, Laitinen A, et al
HUMAN MOLECULAR GENETICS 2008;17(11):1673-82

Expression Analysis of the NLRP Gene Family Suggests a Role in Human Preimplantation Development
Zhang P, Dixon M, Zucchelli M, Hambiliki F, Levkov L, Hovatta O, et al
PLOS ONE 2008;3(7):e2755-

Familial non-syndromic cleft lip and palate - analysis of the IRF6 gene and clinical phenotypes
Pegelow M, Peyrard-janvid M, Zucchelli M, Fransson I, Larson O, Kere J, et al
EUROPEAN JOURNAL OF ORTHODONTICS 2008;30(2):169-75

Finnish patients with systemic lupus erythematosus share predisposing genetic risk factors with other populations
Jarvinen Tm, Zucchelli M, Hellquist A, Berglind L, Koskenmies S, Panelius I, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2008;:S113-S113

Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe
Salmela E, Lappalainen T, Fransson I, Andersen Pm, Dahlman-wright K, Fiebig A, et al
PLOS ONE 2008;3(10):e3519-

Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease
Melen E, Nyberg F, Lindgren Cm, Berglind N, Zucchelli M, Nordling E, et al
ENVIRONMENTAL HEALTH PERSPECTIVES 2008;116(8):1077-84

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
Ludwig Ku, Schumacher J, Schulte-korne G, Konig Ir, Warnke A, Plume E, et al
PSYCHIATRIC GENETICS 2008;18(6):310-2

Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association
Koskinen Lle, Korponay-szabo Ir, Viiri K, Juuti-uusitalo K, Kaukinen K, Lindfors K, et al
JOURNAL OF MEDICAL GENETICS 2008;45(4):222-7

Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients 2 from different ethnic groups
Erdos Me, Jiao H, Toth B, Erdos M, Fransson I, Rakoczi E, et al
CLINICAL AND EXPERIMENTAL IMMUNOLOGY 2008;:66-66

Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups
Jiao H, Toth B, Erdos M, Fransson I, Rakoczi E, Balogh I, et al
MOLECULAR IMMUNOLOGY 2008;46(1):202-6

Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs
Hannelius U, Salmela E, Lappalainen T, Guillot G, Lindgren Cm, Von Dobeln U, et al
BMC GENETICS 2008;:54-

Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR
Bruce S, Hannula-jouppi K, Lindgren Cm, Lipsanen-nyman M, Kere J
CLINICAL CHEMISTRY 2008;54(3):491-9

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia
Tapia-paez I, Tammimies K, Massinen S, Roy Al, Kere J
FASEB JOURNAL 2008;22(8):3001-9

The impact of sodium chloride and volume depletion in the chronic kidney disease of congenital chloride diarrhea
Wedenoja S, Ormala T, Berg Ub, Halling Sfe, Jalanko H, Karikoski R, et al
KIDNEY INTERNATIONAL 2008;74(8):1085-93

The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice
Tiala I, Wakkinen J, Suomela S, Puolakkainen P, Tammi R, Forsberg S, et al
HUMAN MOLECULAR GENETICS 2008;17(7):1043-51

A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis
Dahlman I, Dicker A, Jiao H, Kere J, Blomqvist L, Van Harmelen V, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2007;80(6):1115-24

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
Anthoni H, Zucchelli M, Matsson H, Muller-myhsok B, Fransson I, Schumacher J, et al
HUMAN MOLECULAR GENETICS 2007;16(6):667-77

An unfavorable combination of factor V Leiden with age, weight, and blood group causes high risk of pregnancy-associated venous thrombosis - a population-based nested case-control study
Hiltunen L, Rautanen A, Rasi V, Kaaja R, Kere J, Krusius T, et al
THROMBOSIS RESEARCH 2007;119(4):423-32

A recurrent mutation in PALB2 in Finnish cancer families
Erkko H, Xia B, Nikkilae J, Schleutker J, Syrjaekoski K, Mannermaa A, et al
NATURE 2007;446(7133):316-9

Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma
Malerba G, Lindgren Cm, Xumerle L, Kiviluoma P, Trabetti E, Laitinen T, et al
CLINICAL AND EXPERIMENTAL ALLERGY 2007;37(1):83-9

Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis
Suomela S, Kainu K, Onkamo P, Tiala I, Himberg J, Koskinen L, et al
ACTA DERMATO-VENEREOLOGICA 2007;87(2):127-34

Distinct sets of developmentally regulated genes that are expressed by human oocytes and human embryonic stem cells
Zhang P, Kerkela E, Skottman H, Levkov L, Kivinen K, Lahesmaa R, et al
FERTILITY AND STERILITY 2007;87(3):677-90

Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample
Kivinen K, Peterson H, Hiltunen L, Laivuori H, Heino S, Tiala I, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2007;15(4):494-7

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer
Pylkas K, Tommiska J, Syrjakoski K, Kere J, Gatei M, Waddell N, et al
CARCINOGENESIS 2007;28(5):1040-5

Exclusion of coding-region mutations in luteinizing hormone and follicle-stimulating hormone receptor genes as the cause of ovarian hyperstimulation syndrome
Kerkela E, Skottman H, Friden B, Bjuresten K, Kere J, Hovatta O
FERTILITY AND STERILITY 2007;87(3):603-6

Expression of allograft inflammatory factor-1 in inflammatory skin disorders
Orsmark C, Skoog T, Jeskanen L, Kere J, Saarialho-kere U
ACTA DERMATO-VENEREOLOGICA 2007;87(3):223-7

Expression of ion transport-associated proteins in human efferent and epididymal ducts
Kujala M, Hihnala S, Tienari J, Kaunisto K, Hastbacka J, Holmberg C, et al
REPRODUCTION 2007;133(4):775-84

Gene-environment interactions of tumor necrosis factor single nucleoticle polymorphisms with passive smoking and development of asthma symptoms in early childhood
Panasevich S, Melen E, Lindgren C, Kere J, Wickman M, Pershagen G, et al
ALLERGY 2007;:58-58

Large-scale zygosity testing using single nucleotide polymorphisms
Hannelius U, Gherman L, Makela Vv, Lindstedt A, Zucchelli M, Lagerberg C, et al
TWIN RESEARCH AND HUMAN GENETICS 2007;10(4):604-25

Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach
Ollikainen M, Hannelius U, Lindgren Cm, Abdel-rahman Wm, Kere J, Peltomaki P
ONCOGENE 2007;26(31):4541-9

Mutations in the gene encoding the 3 '-5 ' DNA exonuclease TREX1 are associated with systemic lupus erythematosus
Lee-kirsch Ma, Gong M, Chowdhury D, Senenko L, Engel K, Lee Ya, et al
NATURE GENETICS 2007;39(9):1065-7

Neuropeptide S receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease
D'amato M, Bruce S, Bresso F, Zucchelli M, Ezer S, Pulkkinen V, et al
GASTROENTEROLOGY 2007;133(3):808-17

[Not Available]
Kere J
Duodecim; laaketieteellinen aikakauskirja 2007;123(8):864-6

Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells
Otonkoski T, Jiao H, Kaminen-ahola N, Tapia-paez I, Ullah Ms, Parton Le, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2007;81(3):467-74

Regulation of the basolateral chloride/base exchangers AE1 and SLC26A7 in the kidney collecting duct in potassium depletion
Barone S, Amlal H, Kujala M, Xu J, Karet F, Blanchard A, et al
NEPHROLOGY DIALYSIS TRANSPLANTATION 2007;22(12):3462-70

The CCHCR1 (HCR) gene is relevant for skin steroidogenesis and downregulated in cultured psoriatic keratinocytes
Tiala I, Suomela S, Huuhtanen J, Wakkinen J, Holtta-vuori M, Kainu K, et al
JOURNAL OF MOLECULAR MEDICINE-JMM 2007;85(6):589-601

The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus
Hellquist A, Zucchelli M, Kivinen K, Saarialho-kere U, Koskenmies S, Widen E, et al
JOURNAL OF MEDICAL GENETICS 2007;44(5):314-21

Two Chinese families with pulverulent congenital cataracts and Delta G91 CRYBA1 mutations
Lu Ss, Zhao C, Jiao H, Kere J, Tang X, Zhao F, et al
MOLECULAR VISION 2007;13(124-26):1154-60

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
Feuk L, Kalervo A, Lipsanen-nyman M, Skaug J, Nakabayashi K, Finucane B, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2006;79(5):965-72

A quality assessment survey of SNP genotyping laboratories
Lahermo P, Liljedahl U, Alnaes G, Axelsson T, Brookes Aj, Ellonen P, et al
HUMAN MUTATION 2006;27(7):711-4

Associations of body size at birth with late-life cortisol concentrations and glucose tolerance are modified by haplotypes of the glucocorticoid receptor gene
Rautanen A, Eriksson Jg, Kere J, Andersson S, Osmond C, Tienari P, et al
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 2006;91(11):4544-51

Characterization of susceptibility locus for preeclampsia on chromosome 2p25.
Peterson H, Kivinen K, Laivuori H, Kerkela E, Jiao H, Makela Vv, et al
HYPERTENSION IN PREGNANCY 2006;:47-47

Downstream target genes of the neuropeptide S-NPSR1 pathway
Vendelin J, Bruce S, Holopainen P, Pulkkinen V, Rytila P, Pirskanen A, et al
HUMAN MOLECULAR GENETICS 2006;15(19):2923-35

DYX1C1 functions in neuronal migration in developing neocortex
Wang Y, Paramasivam M, Thomas A, Bai J, Kaminen-ahola N, Kere J, et al
NEUROSCIENCE 2006;143(2):515-22

Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis
Ekelund E, Saaf A, Tengvall-linder M, Melen E, Link J, Barker J, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2006;78(6):1060-5

ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis
Hodgson U, Pulkkinen V, Dixon M, Peyrard-janvid M, Rehn M, Lahermo P, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2006;79(1):149-54

Expression of SLC26A3, CFTR and NHE3 in the human male reproductive tract: role in male subfertility caused by congenital chloride diarrhoea
Hihnala S, Kujala M, Toppari J, Kere J, Holmberg C, Hoglund P
MOLECULAR HUMAN REPRODUCTION 2006;12(2):107-11

Genome scan on Swedish Alzheimer's disease families
Sillen A, Forsell C, Lilius L, Axwlman K, Bjork Bf, Onkamo P, et al
MOLECULAR PSYCHIATRY 2006;11(2):182-6

G protein-coupled receptor for asthma susceptibility associates with respiratory distress syndrome
Pulkkinen V, Haataja R, Hannelius U, Helve O, Pitkanen Om, Karikoski R, et al
ANNALS OF MEDICINE 2006;38(5):357-66

Heterogeneity-based genome search meta-analysis for preeclampsia
Zintzaras E, Kitsios G, Harrison Ga, Laivuori H, Kivinen K, Kere J, et al
HUMAN GENETICS 2006;120(3):360-70

Interaction between variants in the interleukin-4 receptor alpha and interleukin-9 receptor genes in childhood wheezing: evidence from a birth cohort study
Melen E, Umerkajeff S, Nyberg F, Zucchelli M, Lindstedt A, Gullsten H, et al
CLINICAL AND EXPERIMENTAL ALLERGY 2006;36(11):1391-8

Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity
Dahlman I, Nilsson M, Jiao H, Hoffstedt J, Lindgren Cm, Humphreys K, et al
PHARMACOGENETICS AND GENOMICS 2006;16(12):881-9

Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses
Pulkkinen V, Majuri Ml, Wang Gy, Holopainen P, Obase Y, Vendelin J, et al
HUMAN MOLECULAR GENETICS 2006;15(10):1667-79

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies
Karppinen Sm, Barkardottir Rb, Backenhorn K, Sydenham T, Syrjakoski K, Schleutker J, et al
JOURNAL OF MEDICAL GENETICS 2006;43(11):856-62

Overview of the SLC26 family and associated diseases
Kere J
Novartis Foundation symposium 2006;273():2-11

PSORS1: a comparison of HLA-Cw6 and CCHCR1
Suomela S, Kainu K, Onkamo P, Majuri I, Himberg J, Koskinen L, et al
BRITISH JOURNAL OF DERMATOLOGY 2006;154(1):-

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
Schumacher J, Anthoni H, Dahdouh F, Konig Ir, Hillmer Am, Kluck N, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2006;78(1):52-62

Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes
Salmela E, Taskinen O, Seppanen Jk, Sistonen P, Daly Mj, Lahermo P, et al
JOURNAL OF MEDICAL GENETICS 2006;43(7):590-7

The CCHCR1 gene is relevant for skin steroidogenesis: Possible involvement in psoriasis?
Tiala I, Suomela S, Ikonen E, Kere J, Saarialho-kere U, Elomaa O
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2006;:41-41

The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus
De Jager Pl, Graham R, Farwell L, Sawcer S, Richardson A, Behrens Tw, et al
GENES AND IMMUNITY 2006;7(4):327-34

Variation in DNA repair genes ERCC2, XRCC1, and XRCC3 and risk of follicular lymphoma
Smedby Ke, Lindgren Cm, Hjalgrim H, Humphreys K, Schollkopf C, Chang Et, et al
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION 2006;15(2):258-65

Absence of association between asthma and high serum immunoglobulin E associated GPRA haplotypes and adult atopic dermatitis
Veal Cd, Reynolds Nj, Meggitt Sj, Allen Mh, Lindgren Cm, Kere J, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2005;125(2):399-401

A common beta(2)-adrenoceptor gene haplotype protects against obesity in Swedish women
Jiao H, Dahlman I, Eriksson P, Kere J, Arner P
OBESITY RESEARCH 2005;13(10):1645-50

A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families
Koillinen H, Lahermo P, Rautio J, Hukki J, Peyrard-janvid M, Kere J
JOURNAL OF MEDICAL GENETICS 2005;42(2):177-84

A haplotype association analysis in UK families indicates that variation at the 3 ' end of PDCD1 increases risk of SLE
Mendiratta Ml, Vyse Tj, Lindgren C, Kere J, Hudson Tj, Nashi E, et al
ANNALS OF THE RHEUMATIC DISEASES 2005;:79-79

Association analysis of common variants of STAT6, GATA3, and STAT4 to asthma and high serum IgE phenotypes
Pykalainen M, Kinos R, Valkonen S, Rydman P, Kilpelalainen M, Laitinen La, et al
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 2005;115(1):80-7

Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families - Increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease
Wu H, Cantor Ra, Graham Dsc, Lingren Ca, Farwell L, De Jager Pl, et al
ARTHRITIS AND RHEUMATISM 2005;52(8):2396-402

BMPR2 mutations have short lifetime expectancy in primary pulmonary hypertension
Sankelo M, Flanagan Ja, Machado R, Harrison R, Rudarakanchana N, Morrell N, et al
HUMAN MUTATION 2005;26(2):119-24

Characterization of GPRA, a novel G protein-coupled receptor related to asthma
Vendelin J, Pulkkinen V, Rehn M, Pirskanen A, Raisanen-sokolowski A, Laitinen A, et al
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY 2005;33(3):262-70

Family-based association study of DYX1C1 variants in autism
Ylisaukko-oja T, Peyrard-janvid M, Lindgren Cm, Rehnstrom K, Vanhala R, Peltonen L, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2005;13(1):127-30

Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6
Cluster 17 Collaborat, Abecasis G, Allen M, Barker Jnwn, Burden D, Capon F, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2005;124(5):921-30

Functional comparison of mouse slc26a6 anion exchanger with human SLC26A6 polypeptide variants - Differences in anion selectivity, regulation, and electrogenicity
Chernova Mn, Jiang Lw, Friedman Dj, Darman Rb, Lohi H, Kere J, et al
JOURNAL OF BIOLOGICAL CHEMISTRY 2005;280(9):8564-80

Gene mapping with pooled samples on three genotyping platforms
Rautanen A, Zucchelli M, Makela S, Kere J
MOLECULAR AND CELLULAR PROBES 2005;19(6):408-16

Genetic characterization of familial hypercholesterolemia in Sweden
Lind S, Jiao H, Lindgren Cm, Eriksson M, Eggertsen G, Kere J, et al
CLINICA CHIMICA ACTA 2005;:S92-S92

Global analysis of uniparental disomy using high density genotyping arrays
Bruce S, Leinonen R, Lindgren Cm, Kivinen K, Dahlman-wright K, Lipsanen-nyman M, et al
JOURNAL OF MEDICAL GENETICS 2005;42(11):847-51

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes
Holmkvist J, Almgren P, Parikh H, Zucchelli M, Kere J, Groop L, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2005;13(7):849-55

Haplotypes of G protein-coupled receptor 154 are associated with childhood allergy and asthma
Parsifal Genetics Study Grp, Melen E, Bruce S, Doekes G, Kabesch M, Laitinen T, et al
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE 2005;171(10):1089-95

Independent evidence for the VMP/DCDC2/KAAG1 gene locus on chromosomal region 6p22 as susceptibility factor for dyslexia
Schumacher J, Dahdouh F, Hilmer Am, Koenig Ir, Anthoni H, Zucchelli M, et al
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 2005;138B(1):114-114

Mapping and identifying genes for asthma and psoriasis
Kere J
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES 2005;360(1460):1551-61

Mapping genes for asthma and psoriasis
Kere J
Novartis Foundation symposium 2005;267():46-52

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
Swanberg M, Lidman O, Padyukov L, Eriksson P, Akesson E, Jagodic M, et al
NATURE GENETICS 2005;37(5):486-94

Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure
Makela S, Eklund R, Lahdetie J, Mikkola M, Hovatta O, Kere J
MOLECULAR HUMAN REPRODUCTION 2005;11(2):129-32

Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome
Peyrard-janvid M, Pegelow M, Koillinen H, Larsson C, Fransson I, Rautio J, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2005;13(12):1261-7

Phenylketonuria screening registry as a resource for population genetic studies
Hannelius U, Lindgren Cm, Melen E, Malmberg A, Von Dobeln U, Kere J
JOURNAL OF MEDICAL GENETICS 2005;42(10):e60-

Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus
Sigurdsson S, Nordmark G, Goring Hhh, Lindroos K, Wiman Ac, Sturfelt G, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2005;76(3):528-37

SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney
Kujala M, Tienari J, Lohi H, Elomaa O, Sariola H, Lehtonen E, et al
NEPHRON EXPERIMENTAL NEPHROLOGY 2005;101(2):E50-E58

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia
Hannula-jouppi K, Kaminen-ahola N, Taipale M, Eklund R, Nopola-hemmi J, Kaariainen H, et al
PLOS GENETICS 2005;1(4):467-474

The CIDEA gene V115F polymorphism is associated with obesity in Swedish subjects
Dahlman I, Kaaman M, Jiao H, Kere J, Laakso M, Arner P
DIABETES 2005;54(10):3032-4

alpha(2)-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action
Dahlman I, Eriksson P, Kaaman M, Jiao H, Lindgren Cm, Kere J, et al
DIABETOLOGIA 2004;47(11):1974-9

Anti-telomere antibodies in systemic lupus erythematosus (SLE): a comparison with five antinuclear antibody assays in 430 patients with SLE and other rheumatic diseases
Salonen Em, Miettinen A, Walle Tk, Koskenmies S, Kere J, Julkunen H
ANNALS OF THE RHEUMATIC DISEASES 2004;63(10):1250-4

Association study of 15 novel single-nucleotide polymorphisms of the T-bet locus among Finnish asthma families
Ylikoski E, Kinos R, Sirkkanen N, Pykalainen M, Savolainen J, Laitinen La, et al
CLINICAL AND EXPERIMENTAL ALLERGY 2004;34(7):1049-55

Characterization of a common susceptibility locus for asthma-related traits
Laitinen T, Polvi A, Rydman P, Vendelin J, Pulkkinen V, Salmikangas P, et al
SCIENCE 2004;304(5668):300-4

Developmental regulation of Cl-/HCO3- exchangers in the kidney collecting duct
Petrovic S, Ma Ly, Barone S, Kujala M, Kere J, Soleimani M
FASEB JOURNAL 2004;18(4):A318-A318

Differential regulation of basolateral Cl-/HCO3- exchangers SLC26A7 and AE1 in kidney outer medullary collecting duct
Barone S, Amlal H, Xu H, Kujala M, Kere J, Petrovic S, et al
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY 2004;15(8):2002-11

Examination of a possible influence of genetic variation at the DYX1C1 locus in the development of dyslexia
Dahdouh F, Schumacher J, Koenig Ir, Lindgren C, Peyrard-janvid M, Anthoni H, et al
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 2004;130B(1):106-106

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
Peyrard-janvid M, Anthoni H, Onkamo P, Lahermo P, Zucchelli M, Kaminen N, et al
HUMAN GENETICS 2004;114(5):510-6

Haplotype association for preeclampsia on chromosome 2p25.
Laivuori H, Kerkela E, Jiao H, Makela Vv, Kaaja R, Ylikorkala O, et al
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION 2004;11(2):258A-258A

Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus
Koskenmies S, Widen E, Onkamo P, Sevon P, Julkunen H, Kere J
EUROPEAN JOURNAL OF HUMAN GENETICS 2004;12(6):489-94

Influence of male sex and parental allergic disease on childhood wheezing: role of interactions
Melen E, Kere J, Pershagen G, Svartengren M, Wickman M
CLINICAL AND EXPERIMENTAL ALLERGY 2004;34(6):839-44

Investigation of C5a in multiple sclerosis - two different strategies at the DNA level
Modin H, Boos Im, Duvefelt K, Lindgren Cm, Zucchelli M, Kere J, et al
MULTIPLE SCLEROSIS 2004;:S205-S205

Linkage mapping of systemic lupus erythematosus (SLE) in Finnish families multiply affected by SLE
Koskenmies S, Lahermo P, Julkunen H, Ollikainen V, Kere J, Widen E
JOURNAL OF MEDICAL GENETICS 2004;41(1):e2-5

Positionally cloned susceptibility genes in allergy and asthma
Kere J, Laitinen T
CURRENT OPINION IN IMMUNOLOGY 2004;16(6):689-94

Second-generation candidate genes for asthma and allergy
Kere J
TISSUE ANTIGENS 2004;64(4):351-352

Sex specific protective effects of interleukin-9 receptor haplotypes on childhood wheezing and sensitisation
Melen E, Gullsten H, Zucchelli M, Lindstedt A, Nyberg F, Wickman M, et al
JOURNAL OF MEDICAL GENETICS 2004;41(12):e123-

SLC26A7: a basolateral Cl-/HCO3- exchanger specific to intercalated cells of the outer medullary collecting duct
Petrovic S, Barone S, Xu J, Conforti L, Ma Ly, Kujala M, et al
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY 2004;286(1):F161-9

The association of antibodies to cardiolipin, beta 2-glycoprotein I, prothrombin, and oxidized low-density lipoprotein with thrombosis in 292 patients with familial and sporadic systemic lupus erythematosus
Koskenmies S, Vaarala O, Widen E, Kere J, Palosuo T, Julkunen H
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY 2004;33(4):246-52

The effects of the ACE gene insertion/deletion polymorphism on glucose tolerance and insulin secretion in elderly people are modified by birth weight
Kajantie E, Rautanen A, Kere J, Andersson S, Yliharsila H, Osmond C, et al
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 2004;89(11):5738-41

Transgenic mouse models support HCR as an effector gene in the PSORS1 locus
Elomaa O, Majuri I, Suomela S, Asumalahti K, Jiao H, Mirzaei Z, et al
HUMAN MOLECULAR GENETICS 2004;13(15):1551-61

Two functional variants of the superoxide dismutase genes in Finnish families with asthma
Kinnula Vl, Lehtonen S, Koistinen P, Kakko S, Savolainen M, Kere J, et al
THORAX 2004;59(2):116-9

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
Taipale M, Kaminen N, Nopola-hemmi J, Haltia T, Myllyluoma B, Lyytinen H, et al
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2003;100(20):11553-8

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
Kaminen N, Hannula-jouppi K, Kestila M, Lahermo P, Muller K, Kaaranen M, et al
JOURNAL OF MEDICAL GENETICS 2003;40(5):340-5

Anion exchange properties of SLC26A6 polypeptides are species-specific and isoform-specific.
Alper Sl, Jiang Lw, Friedman Dj, Lohi H, Kere J, Vandorpe Dh, et al
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY 2003;:67A-67A

Anion transporters SLC26A6 and SLC26A7 are coexpressed in collecting ducts of human kidney.
Kujala M, Tienari J, Lohi H, Lehtonen E, Kere J
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY 2003;:775A-775A

Approaches to gene mapping and positional cloning in complex diseases
Kere J
JOURNAL OF MEDICAL GENETICS 2003;:S13-S13

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia
Melkoniemi M, Koillinen H, Mannikko M, Warman Ml, Pihlajamaa T, Kaariainen H, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2003;11(3):265-70

Fine mapping of susceptibility loci for preeclampsia on chromosomes 2p25, 4q23 and 9p13-p21.
Kerkela E, Laivuori H, Jiao H, Makela Vv, Kaaja R, Ylikorkala O, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):498-498

Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis
Asumalahti K, Ameen M, Suomela S, Hagforsen E, Michaelsson G, Evans J, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2003;120(4):627-32

Genomics and pediatric research
Boright Ap, Kere J, Scherer Sw
PEDIATRIC RESEARCH 2003;53(1):4-9

Haploblocks, a software tool for visualization and analysis of haplotype blocks in the human genome.
Zucchelli M, Kere J
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):366-366

Haplotype association studies in target regions on chromosomes 6q23-q27 and 14q21-q23 in systemic lupus erythematosus.
Lindgren Cm, Koskenmies S, Widen E, Onkamo P, Sevno P, Mkalaa V, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):532-532

HCR, a candidate gene for psoriasis, is expressed differently in psoriasis and other hyperproliferative skin disorders and is downregulated by interferon-gamma in keratinocytes
Suomela S, Elomaa O, Asumalahti K, Kariniemi Al, Karvonen Sl, Peltonen J, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2003;121(6):1360-4

Human chromosome 7: DNA sequence and biology
Scherer Sw, Cheung J, Macdonald Jr, Osborne Lr, Nakabayashi K, Herbrick Ja, et al
SCIENCE 2003;300(5620):767-72

Identification of a basolateral Cl-/HCO3- exchanger specific to gastric parietal cells
Petrovic S, Ju X, Barone S, Seidler U, Alper Sl, Lohi H, et al
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY 2003;284(6):G1093-103

Identification of a basolateral Cl-/HCO3 exchanger specific to intercalated cells in outer medullary collecting duct: Co-localization with AE1
Petrovic S, Barone S, Xu J, Ma Ly, Conforti L, Kujala M, et al
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY 2003;:68A-68A

Interleukin 9 receptor gene polymorphisms in childhood wheezing end atopy.
Melen E, Gullsten H, Lindstedt A, Zucchelli M, Nyberg F, Pershagen G, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):504-504

Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains
Lohi H, Lamprecht G, Markovich D, Heil A, Kujala M, Seidler U, et al
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY 2003;284(3):C769-79

Linkage and linkage disequilibrium searched for between non-syndromic cleft palate and four candidate loci
Koillinen H, Ollikainen V, Rautio J, Hukki J, Kere J
JOURNAL OF MEDICAL GENETICS 2003;40(6):464-8

Novel alternatively spliced forms found for seven genes in transcriptional profiling of asthma candidate genes in 11 asthma related cell lines and lung tissue.
Polvi A, Ruosaari S, Vendelin J, West A, Saarikko I, Reinikainen A, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):352-352

Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release
Otonkoski T, Kaminen N, Ustinov J, Lapatto R, Meissner T, Mayatepek E, et al
DIABETES 2003;52(1):199-204

Positional cloning of candidate genes for developmental dyslexia=.
Kere J, Taipale M, Kaminen N, Nopola-hemmi J, Anthoni H, Haltia T, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):184-184

Psoriasis susceptibility locus on 18p revealed by genome scan in Finnish families not associated with PSORS1
Asumalahti K, Laitinen T, Lahermo P, Suomela S, Itkonen-vatjus R, Jansen C, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2003;121(4):735-40

Refined mapping of the DYX3 dyslexia susceptibility region
Anthoni H, Peyrard-janvid M, Onkamo P, Kaminen N, Hannula K, Nopola-hemmi J, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;73(5):530-530

Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families
Laivuori H, Lahermo P, Ollikainen V, Widen E, Haiva-mallinen L, Sundstrom H, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2003;72(1):168-77

A new locus for coeliac disease mapped to chromosome 15 in a population isolate
Woolley N, Holopainen P, Ollikainen V, Mustalahti K, Maki M, Kere J, et al
HUMAN GENETICS 2002;111(1):40-5

Anion exchangers SLC26A6 and SLC26A7 are expressed in collecting ducts of human kidney
Kujala Mm, Tienari J, Lohi H, Lehtonen E, Kere J
MOLECULAR BIOLOGY OF THE CELL 2002;:269A-269A

A novel low-penetrance locus for familial glioma at 15q23-q26.3
Paunu N, Lahermo P, Onkamo P, Ollikainen V, Rantala I, Helen P, et al
CANCER RESEARCH 2002;62(13):3798-802

Association analysis for quantitative traits by data mining: QHPM
Onkamo P, Ollikainen V, Sevon P, Toivonen Htt, Mannila H, Kere J
ANNALS OF HUMAN GENETICS 2002;:419-29

Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus
Psoriasis Consortium, Asumalahti K, Veal C, Laitinen T, Suomela S, Allen M, et al
HUMAN MOLECULAR GENETICS 2002;11(5):589-97

Down-regulated in adenoma mediates apical Cl-/HCO3- exchange in rabbit, rat, and human duodenum
Jacob P, Rossmann H, Lamprecht G, Kretz A, Neff C, Lin-wu E, et al
GASTROENTEROLOGY 2002;122(3):709-24

Familial dyslexia: neurocognitive and genetic correlation in a large Finnish family
Nopola-hemmi J, Myllyluoma B, Voutilainen A, Leinonen S, Kere J, Ahonen T
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 2002;44(9):580-6

Functional characterization of three novel tissue-specific anion exchangers SLC26A7,-A8, and-A9
Lohi H, Kujala M, Makela S, Lehtonen E, Kestila M, Saarialho-kere U, et al
JOURNAL OF BIOLOGICAL CHEMISTRY 2002;277(16):14246-54

Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause
Hannula K, Lipsanen-nyman M, Kristo P, Kaitila I, Simola Koj, Lenko Hl, et al
PEDIATRICS 2002;109(3):441-8

Genome segmentation using piecewise constant intensity models and reversible jump MCMC
Salmenkivi M, Kere J, Mannila H
BIOINFORMATICS 2002;:S211-8

Healing a natural knockout of epithelial organogenesis
Kere J, Elomaa O
TRENDS IN MOLECULAR MEDICINE 2002;8(5):197-200

Investigatory and analytical approaches to differential gene expression profiling in mantle cell lymphoma
Zhu Y, Hollmen J, Raty R, Aalto Y, Nagy B, Elonen E, et al
BRITISH JOURNAL OF HAEMATOLOGY 2002;119(4):905-15

Long-range control of expression in yeast
Mannila H, Patrikainen A, Seppanen Jk, Kere J
BIOINFORMATICS 2002;18(3):482-3

Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancer
Ahokas K, Lohi J, Lohi H, Elomaa O, Karjalainen-lindsberg Ml, Kere J, et al
GENE 2002;301(1-2):31-41

Physical map of an asthma susceptibility locus in 7p15-p14 and an association study of TCRG
Polvi A, Polvi T, Sevon P, Petays T, Haahtela T, Laitinen La, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2002;10(10):658-65

Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma
Lemeta S, Aalto Y, Niemela M, Jaaskelainen J, Sainio M, Kere J, et al
CANCER GENETICS AND CYTOGENETICS 2002;133(2):174-8

SLC26A3 mutations in congenital chloride diarrhea
Makela S, Kere J, Holmberg C, Hoglund P
HUMAN MUTATION 2002;20(6):425-38

Upregulation of CFTR expression but not SLC26A3 and SLC9A3 in ulcerative colitis
Lohi H, Makela S, Pulkkinen K, Hoglund P, Karjalainen-lindsberg Ml, Puolakkainen P, et al
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY 2002;283(3):G567-75

A dominant gene for developmental dyslexia on chromosome 3
Nopola-hemmi J, Myllyluoma B, Haltia T, Taipale M, Ollikainen V, Ahonen T, et al
JOURNAL OF MEDICAL GENETICS 2001;38(10):658-64

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region
Hannula K, Lipsanen-nyman M, Kontiokari T, Kere J
AMERICAN JOURNAL OF HUMAN GENETICS 2001;68(1):247-53

Anion absorption in the intestine: Anion transporters, short-chain fatty acids, and role of the DRA gene product
Montrose Mh, Kere J
GASTROINTESTINAL TRANSPORT 2001;:301-+

A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population
Laitinen T, Daly Mj, Rioux Jd, Kauppi P, Laprise C, Petays T, et al
NATURE GENETICS 2001;28(1):87-91

Autosomal dominant midfrequency hearing impairment
Kaksonen R, Widen E, Cormand B, Toppila E, Starck J, Pyykko I, et al
SCANDINAVIAN AUDIOLOGY 2001;:85-7

Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans
Kiuru-kuhlefelt S, El-rifai W, Fanburg-smith J, Kere J, Miettinen M, Knuutila S
CYTOGENETICS AND CELL GENETICS 2001;92(3-4):192-5

Cystic fibrosis gene mutations Delta f508 and 394delTT in patients with chronic sinusitis in Finland
Hytonen M, Patjas M, Vento Si, Kauppi P, Malmberg H, Ylikoski J, et al
ACTA OTO-LARYNGOLOGICA 2001;121(8):945-7

Distinct outcomes of chloride diarrhoea in two siblings with identical genetic background of the disease: implications for early diagnosis and treatment
Hoglund P, Holmberg C, Sherman P, Kere J
GUT 2001;48(5):724-7

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?
Hannula K, Kere J, Pirinen S, Holmberg C, Lipsanen-nyman M
JOURNAL OF MEDICAL GENETICS 2001;38(4):273-8

Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein
Elomaa O, Pulkkinen K, Hannelius U, Mikkola M, Saarialho-kere U, Kere J
HUMAN MOLECULAR GENETICS 2001;10(9):953-62

Familial systemic lupus erythematosus in Finland
Koskenmies S, Widen E, Kere J, Julkunen H
JOURNAL OF RHEUMATOLOGY 2001;28(4):758-60

Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families
Barkardottir Rb, Sarantaus L, Arason A, Vehmanen P, Bendahl Po, Kainu T, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2001;9(10):773-9

Human population genetics: Lessons from Finland
Kere J
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS 2001;:103-28

Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea
Hoglund P, Sormaala M, Haila S, Socha J, Rajaram U, Scheurlen W, et al
HUMAN MUTATION 2001;18(3):233-42

Involvement of BRCA1 and BRCA2 in breast cancer in a Western Finnish sub-population
Paakkonen K, Sauramo S, Sarantaus L, Vahteristo P, Hartikainen A, Vehmanen P, et al
GENETIC EPIDEMIOLOGY 2001;20(2):239-46

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34
Koillinen H, Wong Fk, Rautio J, Ollikainen V, Karsten A, Larson O, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2001;9(10):747-52

Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA
Hannula K, Lipsanen-nyman M, Scherer Sw, Holmberg C, Hoglund P, Kere J
GENOMICS 2001;73(1):1-9

Mining associations between genetic markers, phenotypes, and covariates
Sevon P, Ollikainen V, Onkamo P, Toivonen Htt, Mannila H, Kere J
GENETIC EPIDEMIOLOGY 2001;:S588-93

PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas
Zhu Y, Loukola A, Monni O, Kuokkanen K, Franssila K, Elonen E, et al
LEUKEMIA & LYMPHOMA 2001;41(1-2):177-83

Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma
Kauppi P, Lindblad-toh K, Sevon P, Toivonen Htt, Rioux Jd, Villapakkam A, et al
GENOMICS 2001;77(1-2):35-42

SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types
Haila S, Hastbacka J, Bohling T, Karjalainen-lindsberg Ml, Kere J, Saarialho-kere U
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY 2001;49(8):973-82

Ultrastructural features resembling those of harlequin ichthyosis in patients with severe congenital ichthyosiform erythroderma
Virolainen E, Niemi Km, Ganem A, Kere J, Vahlquist A, Saarialho-kere U
BRITISH JOURNAL OF DERMATOLOGY 2001;145(3):480-3

A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele
Asumalahti K, Laitinen T, Itkonen-vatjus R, Lokki Ml, Suomela S, Snellman E, et al
HUMAN MOLECULAR GENETICS 2000;9(10):1533-42

Assignment of a novel locus for autosomal recessive congenital ichthyosis chromosome 19p13.1-p13.2
Virolainen E, Wessman M, Hovatta I, Niemi Km, Ignatius J, Kere J, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2000;66(3):1132-7

Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders
Laitinen T, Ollikainen V, Lazaro C, Kauppi P, De Cid R, Anto Jm, et al
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE 2000;161(3):700-6

Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia
Cambiaghi S, Restano L, Paakkonen K, Caputo R, Kere J
ARCHIVES OF DERMATOLOGY 2000;136(2):217-24

Data mining applied to linkage disequilibrium mapping
Toivonen Htt, Onkamo P, Vasko K, Ollikainen V, Sevon P, Mannila H, et al
AMERICAN JOURNAL OF HUMAN GENETICS 2000;67(1):133-45

Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1
Huopio H, Reimann F, Ashfield R, Komulainen J, Lenko Hl, Rahier J, et al
JOURNAL OF CLINICAL INVESTIGATION 2000;106(7):897-906

Gene mapping in isolated populations: New roles for old friends?
Jorde Lb, Watkins Ws, Kere J, Nyman D, Eriksson Aw
HUMAN HEREDITY 2000;50(1):57-65

Hemangioblastomas of the retina: impact of von Hippel-Lindau disease
Niemela M, Lemeta S, Sainio M, Rauma S, Pukkala E, Kere J, et al
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 2000;41(7):1909-15

Hereditary hearing loss - the role of environmental factors
Kaksonen R, Pyykko I, Kere J, Starck J, Toppila E
ACTA OTO-LARYNGOLOGICA 2000;:70-72

Hereditary hearing loss--the role of environmental factors
Kaksonen R, Pyykkö I, Kere J, Starck J, Toppila E
Acta oto-laryngologica. Supplementum 2000;543():70-2

Inherited disorders of ion transport in the intestine
Kere J, Hoglund P
CURRENT OPINION IN GENETICS & DEVELOPMENT 2000;10(3):306-9

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28
Taillon-miller P, Bauer-sardina I, Saccone Nl, Putzel J, Laitinen T, Cao A, et al
NATURE GENETICS 2000;25(3):324-8

Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger
Lohi H, Kujala M, Kerkela E, Saarialho-kere U, Kestila M, Kere J
GENOMICS 2000;70(1):102-12

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland
Sarantaus L, Huusko P, Eerola H, Launonen V, Vehmanen P, Rapakko K, et al
EUROPEAN JOURNAL OF HUMAN GENETICS 2000;8(10):757-63

Stromelysin-2 is upregulated during normal wound repair and is induced by cytokines
Rechardt O, Elomaa O, Vaalamo M, Paakkonen K, Jahkola T, Hook-nikanne J, et al
JOURNAL OF INVESTIGATIVE DERMATOLOGY 2000;115(5):778-87

The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells
Haila S, Saarialho-kere U, Karjalainen-lindsberg Ml, Lohi H, Airola K, Holmberg C, et al
HISTOCHEMISTRY AND CELL BIOLOGY 2000;113(4):279-86

The IL9R region contribution in asthma is supported by genetic association in an isolated population
Kauppi P, Laitinen T, Ollikainen V, Mannila H, Laitinen La, Kere J
EUROPEAN JOURNAL OF HUMAN GENETICS 2000;8(10):788-92

Two translocations of chromosome 15q associated with dyslexia
Nopola-hemmi J, Taipale M, Haltia T, Lehesjoki Ae, Voutilainen A, Kere J
JOURNAL OF MEDICAL GENETICS 2000;37(10):771-5

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland
Otonkoski T, Ammala C, Huopio H, Cote Gj, Chapman J, Cosgrove K, et al
DIABETES 1999;48(2):408-15

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
Swan H, Piippo K, Viitasalo M, Heikkila P, Paavonen T, Kainulainen K, et al
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY 1999;34(7):2035-42

Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis
Laiho E, Niemi Km, Ignatius J, Kere J, Palotie A, Saarialho-kere U
EUROPEAN JOURNAL OF HUMAN GENETICS 1999;7(6):625-32

Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF
Pispa J, Jung Hs, Jernvall J, Kettunen P, Mustonen T, Tabata Mj, et al
DEVELOPMENTAL BIOLOGY 1999;216(2):521-34

Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis
Bjorkqvist Am, Wolf M, Nordling S, Tammilehto L, Knuuttila A, Kere J, et al
BRITISH JOURNAL OF CANCER 1999;81(7):1111-5

Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea
Moseley Rh, Hoglund P, Wu Gd, Silberg Dg, Haila S, De La Chapelle A, et al
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY 1999;276(1):G185-92

Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion
Mikkola Ml, Pispa J, Pekkanen M, Paulin L, Nieminen P, Kere J, et al
MECHANISMS OF DEVELOPMENT 1999;88(2):133-46

Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells
Ezer S, Bayes M, Elomaa O, Schlessinger D, Kere J
HUMAN MOLECULAR GENETICS 1999;8(11):2079-86

Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state
Watowich Ss, Xie Xl, Klingmuller U, Kere J, Lindlof M, Berglund S, et al
BLOOD 1999;94(7):2530-2

Functional characterization of the promoter of the X-linked ectodermal dysplasia gene
Pengue G, Srivastava Ak, Kere J, Schlessinger D, Durmowicz Mc
JOURNAL OF BIOLOGICAL CHEMISTRY 1999;274(37):26477-84

Genetic disorders of membrane transport - III. Congenital chloride diarrhea
Kere J, Lohi H, Hoglund P
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY 1999;276(1):G7-G13

Kidney kinetics and chloride ion pumps
Kere J
NATURE GENETICS 1999;21(1):67-8

Long-term prognosis of haemangioblastoma of the CNS: Impact of von Hippel-Lindau disease
Niemela M, Lemeta S, Summanen P, Bohling T, Sainio M, Kere J, et al
ACTA NEUROCHIRURGICA 1999;141(11):1147-56

Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy
Salmikangas P, Mykkanen Om, Gronholm M, Heiska L, Kere J, Carpen O
HUMAN MOLECULAR GENETICS 1999;8(7):1329-36

22-Mb integrated physical and genetic map based on YAC/STS content spanning the interval DXS1125-DXS95 in human Xq12-q21.31
Mumm S, Jermak C, Waeltz P, Schmatz M, Terrell J, Mccauley B, et al
GENE 1998;208(2):147-56

Clustering of private mutations in the congenital chloride diarrhea down-regulated in adenoma gene
Hoglund P, Haila S, Gustavson Kh, Taipale M, Hannula K, Popinska K, et al
HUMAN MUTATION 1998;11(4):321-7

Distinct expression profiles of stromelysin-2 (MMP-10), collagenase-3 (MMP-13), macrophage metalloelastase (MMP-12), and tissue inhibitor of metalloproteinases-3 (TIMP-3) in intestinal ulcerations
Vaalamo M, Karjalainen-lindsberg Ml, Puolakkainen P, Kere J, Saarialho-kere U
AMERICAN JOURNAL OF PATHOLOGY 1998;152(4):1005-14

Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin
Montonen O, Ezer S, Laurikkala J, Karjalainen-lindsberg Ml, Thesleff I, Kere J, et al
EXPERIMENTAL DERMATOLOGY 1998;7(4):168-74

Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait
Hoglund P, Auranen M, Socha J, Popinska K, Nazer H, Rajaram U, et al
AMERICAN JOURNAL OF HUMAN GENETICS 1998;63(3):760-8

Genomic structure of the human congenital chloride diarrhea (CLD) gene
Haila S, Hoglund P, Scherer Sw, Lee Jr, Kristo P, Coyle B, et al
GENE 1998;214(1-2):87-93

Genomic structure of the human ezrin gene
Majander-nordenswan P, Sainio M, Turunen O, Jaaskelainen J, Carpen O, Kere J, et al
HUMAN GENETICS 1998;103(6):662-5

Human TIMP-3 is expressed during fetal development, hair growth cycle, and cancer progression
Airola K, Ahonen M, Johansson N, Heikkila P, Kere J, Kahari Vm, et al
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY 1998;46(4):437-47

Phenotyping asthma patients for a gene mapping study in Finland
Kauppi P, Laitinen La, Laitinen H, Kere J, Laitinen T
CLINICAL AND EXPERIMENTAL ALLERGY 1998;:40-2

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats
Bayes M, Hartung Aj, Ezer S, Pispa J, Thesleff I, Srivastava Ak, et al
HUMAN MOLECULAR GENETICS 1998;7(11):1661-9

The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone
Montonen O, Ezer S, Saarialho-kere Uk, Herva R, Karjalainen-lindsberg Ml, Kaitila I, et al
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY 1998;46(3):281-9

Verification of self-reported asthma and allergy in subjects and their family members volunteering for gene mapping studies
Kauppi P, Laitinen La, Laitinen H, Kere J, Laitinen T
RESPIRATORY MEDICINE 1998;92(11):1281-8

Anhidrotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding
Ezer S, Schlessinger D, Srivastava A, Kere J
HUMAN MOLECULAR GENETICS 1997;6(9):1581-7

Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm
Kiuru-kuhlefelt S, Kristo P, Ruutu T, Knuutila S, Kere J
LEUKEMIA 1997;11(12):2097-104

Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population
Laitinen T, Kauppi P, Ignatius J, Ruotsalainen T, Daly Mj, Kaariainen H, et al
HUMAN MOLECULAR GENETICS 1997;6(12):2069-76

Geographic distribution and regional origin of 272 cystic fibrosis in European populations
Estivill X, Bancells C, Ramos C, Piazza A, Carbonara A, Mastella G, et al
HUMAN MUTATION 1997;10(2):135-54

Microsatellite diversity and the demographic history of modern humans
Jorde Lb, Rogers Ar, Bamshad M, Watkins Ws, Krakowiak P, Sung S, et al
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 1997;94(7):3100-3

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses
Riesewijk Am, Hu L, Schulz U, Tariverdian G, Hoglund P, Kere J, et al
GENOMICS 1997;42(2):236-44

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
Srivastava Ak, Pispa J, Hartung Aj, Du Yz, Ezer S, Jenks T, et al
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 1997;94(24):13069-74

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: Private and recurrent mutations in an isolated population
Laiho E, Ignatius J, Mikkola H, Yee Vc, Teller Dc, Niemi Km, et al
AMERICAN JOURNAL OF HUMAN GENETICS 1997;61(3):529-38

X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content
Nagaraja R, Macmillan S, Kere J, Jones C, Griffin S, Schmatz M, et al
GENOME RESEARCH 1997;7(3):210-22

Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1
Vandermaarel Sm, Scholten Ihjm, Huber I, Philippe C, Suijkerbuijk Rf, Gilgenkrantz S, et al
HUMAN MOLECULAR GENETICS 1996;5(7):887-97

Cloning of candidate genes for X-linked mental retardation by use of chromosome aberrations.
Vandermaarel S, Scholten I, Weghuis Do, Huber I, Rohme D, Gilgenkrantz S, et al
AMERICAN JOURNAL OF MEDICAL GENETICS 1996;64(1):21-21

Fine mapping of the EDA gene: A translocation breakpoint is associated with a CpG island that is transcribed
Srivastava Ak, Montonen O, Saarialhokere U, Chen E, Baybayan P, Pispa J, et al
AMERICAN JOURNAL OF HUMAN GENETICS 1996;58(1):126-32

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea
Hoglund P, Haila S, Socha J, Tomaszewski L, Saarialhokere U, Karjalainenlindsberg Ml, et al
NATURE GENETICS 1996;14(3):316-9

Patterns of matrix metalloproteinase and TIMP-1 expression in chronic and normally healing human cutaneous wounds
Vaalamo M, Weckroth M, Puolakkainen P, Kere J, Saarinen P, Lauharanta J, et al
BRITISH JOURNAL OF DERMATOLOGY 1996;135(1):52-9

Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31
Hoglund P, Haila S, Scherer Sw, Tsui Lc, Green Ed, Weissenbach J, et al
GENOME RESEARCH 1996;6(3):202-10

Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3
Ignatius J, Knuutila S, Scherer Sw, Trask B, Kere J
JOURNAL OF MEDICAL GENETICS 1996;33(6):507-10

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
Kere J, Srivastava Ak, Montonen O, Zonana J, Thomas N, Ferguson B, et al
NATURE GENETICS 1996;13(4):409-16

A 6-MB YAC CONTIG IN XP22.1-P22.2 SPANNING THE DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, AND PHKA2 GENES
Alitalo T, Francis F, Kere J, Lehrach H, Schlessinger D, Willard Hf
GENOMICS 1995;25(3):691-700

FINE MAPPING OF THE CONGENITAL CHLORIDE DIARRHEA GENE BY LINKAGE DISEQUILIBRIUM
Hoglund P, Sistonen P, Norio R, Holmberg C, Dimberg A, Gustavson Kh, et al
AMERICAN JOURNAL OF HUMAN GENETICS 1995;57(1):95-102

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