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A GWAS meta-analysis suggests roles for xenobiotic metabolism and ion channel activity in the biology of stool frequency
Jankipersadsing Sa, Hadizadeh F, Bonder Mj, Tigchelaar Ef, Deelen P, Fu J, et al
Gut 2017;66(4):756-758

A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population
Bonfiglio F, Hysi Pg, Ek W, Karhunen V, Rivera Nv, Männikkö M, et al
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2017;29(2):-

Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis
Westerlind H, Mellander Mr, Bresso F, Munch A, Bonfiglio F, Assadi G, et al
Gut 2017;66(3):421-428

Dynamics of the human gut microbiome in inflammatory bowel disease
Halfvarson J, Brislawn Cj, Lamendella R, Vázquez-baeza Y, Walters Wa, Bramer Lm, et al
Nature microbiology 2017;2():17004-

Faecal microbiota composition associates with abdominal pain in the general population
Hadizadeh F, Bonfiglio F, Belheouane M, Vallier M, Sauer S, Bang C, et al
Gut 2017;():-

Fine-mapping inflammatory bowel disease loci to single-variant resolution
Huang H, Fang M, Jostins L, Umićević Mirkov M, Boucher G, Anderson Ca, et al
Nature 2017;547(7662):173-178

Identification of a Genetic Variation in ERAP1 Aminopeptidase that Prevents Human Cytomegalovirus miR-UL112-5p-Mediated Immunoevasion
Romania P, Cifaldi L, Pignoloni B, Starc N, D'alicandro V, Melaiu O, et al
Cell reports 2017;20(4):846-853

Increased Expression of Toll-Like Receptors 4, 5, and 9 in Small Bowel Mucosa from Patients with Irritable Bowel Syndrome
Dlugosz A, Zakikhany K, Acevedo N, D'amato M, Lindberg G
BioMed research international 2017;2017():9624702-

miR-16 and miR-103 impact 5-HT receptor signalling and correlate with symptom profile in irritable bowel syndrome
Wohlfarth C, Schmitteckert S, Härtle Jd, Houghton La, Dweep H, Fortea M, et al
Scientific reports 2017;7(1):14680-

Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma
Acevedo N, Ezer S, Kebede Merid S, Gaertner Vd, Söderhäll C, D'amato M, et al
PloS one 2017;12(5):e0176568-

polymorphisms associated with increased risk of IBS-C and IBS-M
Henström M, Hadizadeh F, Beyder A, Bonfiglio F, Zheng T, Assadi G, et al
Gut 2017;66(9):1725-1727

Relevance of DNA repair gene polymorphisms to gastric cancer risk and phenotype
Carrera-lasfuentes P, Lanas A, Bujanda L, Strunk M, Quintero E, Santolaria S, et al
Oncotarget 2017;8(22):35848-35862

SOX17 regulates cholangiocyte differentiation and acts as a tumor suppressor in cholangiocarcinoma
Merino-azpitarte M, Lozano E, Perugorria Mj, Esparza-baquer A, Erice O, Santos-laso Á, et al
Journal of hepatology 2017;67(1):72-83

Stool frequency is associated with gut microbiota composition
Hadizadeh F, Walter S, Belheouane M, Bonfiglio F, Heinsen Fa, Andreasson A, et al
Gut 2017;66(3):559-560

Subphenotypes of inflammatory bowel disease are characterized by specific serum protein profiles
Andersson E, Bergemalm D, Kruse R, Neumann G, D'amato M, Repsilber D, et al
PloS one 2017;12(10):e0186142-

Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci
Ellinghaus D, Jostins L, Spain Sl, Cortes A, Bethune J, Han B, et al
Nature genetics 2016;48(5):510-8

A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition
Li D, Achkar Jp, Haritunians T, Jacobs Jp, Hui Ky, D'amato M, et al
Gastroenterology 2016;151(4):724-32

A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Rivas Ma, Graham D, Sulem P, Stevens C, Desch An, Goyette P, et al
Nature communications 2016;7():12342-

C13orf31 (FAMIN) is a central regulator of immunometabolic function
Cader Mz, Boroviak K, Zhang Q, Assadi G, Kempster Sl, Sewell Gw, et al
NATURE IMMUNOLOGY 2016;17(9):1046-56

Functional Analyses of the Crohn's Disease Risk Gene LACC1
Assadi G, Vesterlund L, Bonfiglio F, Mazzurana L, Cordeddu L, Schepis D, et al
PloS one 2016;11(12):e0168276-

Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome
Henström M, Diekmann L, Bonfiglio F, Hadizadeh F, Kuech Em, Von Köckritz-blickwede M, et al
Gut 2016;():-

Genetics of irritable bowel syndrome
Henström M, D'amato M
Molecular and cellular pediatrics 2016;3(1):7-

Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota
Wang J, Thingholm Lb, Skiecevičienė J, Rausch P, Kummen M, Hov Jr, et al
Nature genetics 2016;48(11):1396-1406

HLA Associations Distinguish Collagenous From Lymphocytic Colitis
Westerlind H, Bonfiglio F, Mellander Mr, Hübenthal M, Brynedal B, Björk J, et al
The American journal of gastroenterology 2016;111(8):1211-3

Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
Cleynen I, Boucher G, Jostins L, Schumm Lp, Zeissig S, Ahmad T, et al
Lancet (London, England) 2016;387(10014):156-67

Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease
Ventham Nt, Kennedy Na, Adams At, Kalla R, Heath S, O'leary Kr, et al
Nature communications 2016;7():13507-

LACC1 polymorphisms in inflammatory bowel disease and juvenile idiopathic arthritis
Assadi G, Saleh R, Hadizadeh F, Vesterlund L, Bonfiglio F, Halfvarson J, et al
Genes and immunity 2016;17(4):261-4

Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
Ek We, Reznichenko A, Ripke S, Niesler B, Zucchelli M, Rivera Nv, et al
Gut 2015;64(11):1774-82

High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis
Goyette P, Boucher G, Mallon D, Ellinghaus E, Jostins L, Huang H, et al
Nature genetics 2015;47(2):172-9

Increased serum levels of lipopolysaccharide and antiflagellin antibodies in patients with diarrhea-predominant irritable bowel syndrome
Dlugosz A, Nowak P, D'amato M, Mohammadian Kermani G, Nyström J, Abdurahman S, et al
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2015;27(12):1747-54

Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstruction
Bonora E, Bianco F, Cordeddu L, Bamshad M, Francescatto L, Dowless D, et al
Gastroenterology 2015;148(4):771-782.e11

Severe gastrointestinal dysmotility developed after treatment with gonadotropin-releasing hormone analogs
Cordeddu L, Bergvall M, Sand E, Roth B, Papadaki E, Li L, et al
Scandinavian journal of gastroenterology 2015;50(3):291-9

Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data
Chen Gb, Lee Sh, Brion Mj, Montgomery Gw, Wray Nr, Radford-smith Gl, et al
Human molecular genetics 2014;23(17):4710-20

Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis
Stickel F, Buch S, Zoller H, Hultcrantz R, Gallati S, Österreicher C, et al
Human molecular genetics 2014;23(14):3883-90

Genetic variants in CDC42 and NXPH1 as susceptibility factors for constipation and diarrhoea predominant irritable bowel syndrome
Wouters Mm, Lambrechts D, Knapp M, Cleynen I, Whorwell P, Agréus L, et al
Gut 2014;63(7):1103-11

Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome
Holliday Eg, Attia J, Hancock S, Koloski N, Mcevoy M, Peel R, et al
The American journal of gastroenterology 2014;109(5):770-2

HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Heap Ga, Weedon Mn, Bewshea Cm, Singh A, Chen M, Satchwell Jb, et al
Nature genetics 2014;46(10):1131-4

Human enteroendocrine cell responses to infection with Chlamydia trachomatis: a microarray study
Dlugosz A, Muschiol S, Zakikhany K, Assadi G, D'amato M, Lindberg G
Gut pathogens 2014;6():24-

Loss-of-function of the voltage-gated sodium channel NaV1.5 (channelopathies) in patients with irritable bowel syndrome
Beyder A, Mazzone A, Strege Pr, Tester Dj, Saito Ya, Bernard Ce, et al
Gastroenterology 2014;146(7):1659-1668

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

The history of genetics in inflammatory bowel disease
Ek We, D'amato M, Halfvarson J
Annals of gastroenterology 2014;27(4):294-303

The oxysterol receptor LXRβ protects against DSS- and TNBS-induced colitis in mice
Jakobsson T, Vedin Ll, Hassan T, Venteclef N, Greco D, D'amato M, et al
Mucosal immunology 2014;7(6):1416-28

Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies
Ellinghaus D, Zhang H, Zeissig S, Lipinski S, Till A, Jiang T, et al
GASTROENTEROLOGY 2013;145(2):339-47

Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis
Int Ibd Genetics Consortium, Niddk Ibd Genetics Consortium, Quebec Ibd Genetics Consortium, Beaudoin M, Goyette P, Boucher G, et al
PLOS GENETICS 2013;9(9):e1003723-

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-

Duodenal epithelial transport in functional dyspepsia: Role of serotonin
Witte Ab, D'amato M, Poulsen Ss, Laurent A, Knuhtsen S, Bindslev N, et al
World journal of gastrointestinal pathophysiology 2013;4(2):28-36

Expression and distribution of GnRH, LH, and FSH and their receptors in gastrointestinal tract of man and rat
Sand E, Bergvall M, Ekblad E, D'amato M, Ohlsson B
Regulatory peptides 2013;187():24-8

Genes and functional GI disorders: from casual to causal relationship
D'amato M
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2013;25(8):638-49

Germline genetic contributions to risk for esophageal adenocarcinoma, Barrett's esophagus, and gastroesophageal reflux
Ek We, Levine Dm, D'amato M, Pedersen Nl, Magnusson Pk, Bresso F, et al
Journal of the National Cancer Institute 2013;105(22):1711-8

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-

Polymorphism in the retinoic acid metabolizing enzyme CYP26B1 and the development of Crohn's Disease
Fransén K, Franzén P, Magnuson A, Elmabsout Aa, Nyhlin N, Wickbom A, et al
PloS one 2013;8(8):e72739-

The impact of Crohn's disease genes on healthy human gut microbiota: a pilot study
Quince C, Lundin Ee, Andreasson An, Greco D, Rafter J, Talley Nj, et al
Gut 2013;62(6):952-4

Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients
Parmar As, Lappalainen M, Paavola-sakki P, Halme L, Färkkilä M, Turunen U, et al
Genes and immunity 2012;13(6):474-80

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Int Ibd Genetics Consortium Iibdgc, Jostins L, Ripke S, Weersma Rk, Duerr Rh, Mcgovern Dp, et al
NATURE 2012;491(7422):119-24

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

Association of TNFSF15 polymorphism with irritable bowel syndrome
Zucchelli M, Camilleri M, Andreasson An, Bresso F, Dlugosz A, Halfvarson J, et al
GUT 2011;60(12):1671-1677

CD98 expression modulates intestinal homeostasis, inflammation, and colitis-associated cancer in mice
Hang Ttn, Dalmasso G, Torkvist L, Halfvarson J, Yan Yt, Laroui H, et al
JOURNAL OF CLINICAL INVESTIGATION 2011;121(5):1733-47

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
Int Inflammatory Bowel Dis, United Kingdom Inflammatory Bowel, Natl Inst Diabet Digestive Kidney, Rivas Ma, Beaudoin M, Gardet A, et al
NATURE GENETICS 2011;43(11):1066-73

Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis
Camilleri M, Carlson P, Mckinzie S, Zucchelli M, D'amato M, Busciglio I, et al
NEUROGASTROENTEROLOGY AND MOTILITY 2011;23(10):935-e398

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Anderson Ca, Boucher G, Lees Cw, Franke A, D'amato M, Taylor Kd, et al
NATURE GENETICS 2011;43(3):246-52

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-

Polygenic Risk Score Improves Prostate Cancer Risk Prediction: Results from the Stockholm-1 Cohort Study
Aly M, Wiklund F, Xu Jf, Isaacs Wb, Eklund M, D'amato M, et al
EUROPEAN UROLOGY 2011;60(1):21-8

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
Rossin Ej, Lage K, Raychaudhuri S, Xavier Rj, Tatar D, Benita Y, et al
PLoS genetics 2011;7(1):e1001273-

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 cystic fibrosis F508del mutation in Crohn's disease
Bresso F, D'amato M
JOURNAL OF CYSTIC FIBROSIS 2011;10(2):132-

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-

Analysis of 39 Crohn's Disease Risk Loci in Swedish Inflammatory Bowel Disease Patients
Torkvist L, Halfvarson J, Ong Rth, Lordal M, Sjoqvist U, Bresso F, et al
INFLAMMATORY BOWEL DISEASES 2010;16(6):907-9

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

Detection of Celiac Disease and Lymphocytic Enteropathy by Parallel Serology and Histopathology in a Population-Based Study
Walker Mm, Murray Ja, Ronkainen J, Aro P, Storskrubb T, D'amato M, et al
GASTROENTEROLOGY 2010;139(1):112-9

Genome-wide association identifies multiple ulcerative colitis susceptibility loci
Niddk Ibd Genetics Consortium, Mcgovern Dpb, Gardet A, Torkvist L, Goyette P, Essers J, et al
NATURE GENETICS 2010;42(4):332-7

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Franke A, Mcgovern Dpb, Barrett Jc, Wang K, Radford-smith Gl, Ahmad T, et al
NATURE GENETICS 2010;42(12):1118-25

Identification of a DMBT1 Polymorphism Associated with Increased Breast Cancer Risk and Decreased Promoter Activity
Tchatchou S, Riedel A, Lyer S, Schmutzhard J, Strobel-freidekind O, Gronert-sum S, et al
HUMAN MUTATION 2010;31(1):60-6

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

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

Neuropeptide S Receptor Induces Neuropeptide Expression and Associates With Intermediate Phenotypes of Functional Gastrointestinal Disorders
Camilleri M, Carlson P, Zinsmeister Ar, Mckinzie S, Busciglio I, Burton D, et al
GASTROENTEROLOGY 2010;138(1):98-107.e4

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-

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

Cornulin, a marker of late epidermal differentiation, is down-regulated in eczema
Lieden A, Ekelund E, Kuo Ic, Kockum I, Huang Ch, Mallbris L, et al
ALLERGY 2009;64(2):304-11

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

Herpes Simplex Virus Infection Downmodulates NKG2D Ligand Expression
Schepis D, D'amato M, Studahl M, Bergstrom T, Karre K, Berg L
SCANDINAVIAN JOURNAL OF IMMUNOLOGY 2009;69(5):429-36

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-

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

WAFL, a new protein involved in regulation of early endocytic transport at the intersection of actin and microtubule dynamics
Viklund Im, Aspenstrom P, Meas-yedid V, Zhang B, Kopec J, Agren D, et al
EXPERIMENTAL CELL RESEARCH 2009;315(6):1040-52

Identification of a new WASP and FKBP-like (WAFL) protein in inflammatory bowel disease: a potential marker gene for ulcerative colitis
Viklund Im, Kuznetsov Nv, Lofberg R, Daperno M, Sostegni R, Astegiano M, et al
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE 2008;23(10):921-30

Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families
Ekelund E, Lieden A, Link J, Lee Sp, D'amato M, Palmer Cna, et al
ACTA DERMATO-VENEREOLOGICA 2008;88(1):15-9

Solute carriers (SLC) in inflammatory bowel disease - A potential target of probiotics?
Kotka M, Lieden A, Pettersson S, Trinchieri V, Masci A, D'amato M
JOURNAL OF CLINICAL GASTROENTEROLOGY 2008;42(8):S133-5

DMBT1 confers mucosal protection in vivo and a deletion variant is associated with Crohn's disease
Renner M, Bergmann G, Krebs I, End C, Lyer S, Hilberg F, et al
GASTROENTEROLOGY 2007;133(5):1499-509

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

Potential role for the common cystic fibrosis AF508 mutation in Crohn's disease
Bresso F, Askling J, Astegiano M, Demarchi B, Sapone N, Rizzetto M, et al
INFLAMMATORY BOWEL DISEASES 2007;13(5):531-6

Semliki forest virus nonstructural protein 2 is involved in suppression of the type I interferon response
Breakwell L, Dosenovic P, Hedestam Gbk, D'amato M, Liljestrom P, Fazakerley J, et al
JOURNAL OF VIROLOGY 2007;81(16):8677-84

CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins
Halfvarson J, Bresso F, D'amato M, Jarnerot G, Pettersson S, Tysk C
DIGESTIVE AND LIVER DISEASE 2005;37(10):768-72

Functional interaction of CARD15/NOD2 and Crohn's disease-associated TNF alpha polymorphisms
Linderson Y, Bresso F, Buentke E, Pettersson S, D'amato M
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE 2005;20(4):305-11

Molecular basis for keratoconus: Lack of TrkA expression and its transcriptional repression by Sp3
Lambiase A, Merlo D, Mollinari C, Bonini P, Rinaldi Am, D'amato M, et al
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2005;102(46):16795-800

AN RNAi KNOCK-OUT AND GENETIC RECONSTITUTION SYSTEM TO RESTORE wt p53 FUNCTION IN CANCER
D'amato M, Greicius G, Malin S, Pettersson S
ANTICANCER RESEARCH 2004;24(5D):3462-3462

Improved allelic differentiation using sequence-specific oligonucleotide hybridization incorporating an additional base-analogue mismatch
Burgner D, D'amato M, Kwiatkowski Dp, Loakes D
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS 2004;23(5):755-65

Malassezia enhances natural killer cell-induced dendritic cell maturation
Buentke E, D'amato M, Scheynius A
SCANDINAVIAN JOURNAL OF IMMUNOLOGY 2004;59(5):511-6

Malassezia sympodialis stimulation differently affects gene expression in dendritic cells from atopic dermatitis patients and healthy individuals
Gabrielsson S, Buentke E, Lieden A, Schmidt M, D'amato M, Tengvall-linder M, et al
ACTA DERMATO-VENEREOLOGICA 2004;84(5):339-45

Genetic analysis of variegate porphyria (VP) in Italy: identification of six novel mutations in the protoporphyrinogen oxidase (PPOX) gene
D'amato M, Bonuglia M, Barile S, Griso D, Macri A, Biolcati G
Human mutation 2003;21(4):448-

LD mapping of maternally and non-maternally derived alleles and atopy in Fc epsilon RI-beta
Traherne Ja, Hill Mr, D'amato M, Broxholme J, Mott R, Moffatt Mf, et al
HUMAN MOLECULAR GENETICS 2003;12(20):2577-85

The Crohn's associated NOD2 3020InsC frameshift mutation does not confer susceptibility to ankylosing spondylitis
D'amato M, Sorrentino R, Pettersson S
JOURNAL OF RHEUMATOLOGY 2002;29(11):2470-1

The heterogeneity of allergic phenotypes: genetic and environmental interactions
Bonini S, Rasi G, Torre A, D'amato M, Matricardi Pm
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY 2001;87(6):48-51

Genetic variability at the promoter region of beta(2) adrenoceptor gene (ADRB2) and bronchial hyperresponsiveness (BHR): A population study
D'amato M, Vitiani Lr, Bonini S, Matricardi P
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 2000;105(1):S370-S371

Association of persistent BHR with beta 2-adrenoceptor (ADRB2) haplotypes: A population study.
Matricardi Pm, Ricci-vitiani L, Petrelli G, Ferrigno L, Di Pietro M, D'amato M
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 1999;103(1):S244-S244

Atopic and vernal keratoconjunctivitis: a model for studying atopic disease
Bonini S, Lambiase A, Matricardi P, Rasi G, D'amato M, Bonini S
Current problems in dermatology 1999;28():88-94

HLA-DRB1*and allergy to Parietaria: Linkage and association analyses
D'amato M, Picardi A, Menna T, Di Somma C, Ariano R, Di Pietro A, et al
HUMAN IMMUNOLOGY 1999;60(12):1250-8

Mapping and sequencing of the murine 'tissue' Transglutaminase (Tgm2) gene: absence of mutations in MRLlpr/lpr mice
D'amato M, Iannicola C, Monteriu G, Piacentini M
CELL DEATH AND DIFFERENTIATION 1999;6(3):216-7

Are His63Asp or Cys282Tyr HFE mutations associated with porphyria cutanea tarda? Data of patients from central and southern Italy
D'amato M, Macri' A, Griso D, Biolcati G, Ameglio F
JOURNAL OF INVESTIGATIVE DERMATOLOGY 1998;111(6):1241-2

Association of persistent bronchial hyperresponsiveness with beta(2)-adrenoceptor (ADRB2) haplotypes - A population study
D'amato M, Vitiani Lr, Petrelli G, Ferrigno L, Di Pietro A, Trezza R, et al
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE 1998;158(6):1968-73

MICA exon 5 microsatellite typing by DNA heteroduplex analysis: a new polymorphism in the transmembrane region
Vitiani Lr, Potolicchio I, D'amato M, Baricordi Or, Sorrentino R
TISSUE ANTIGENS 1998;51(3):309-11

Predominant T-Helper 1 cytokine profile of hepatitis B virus nucleocapsid-specific T cells in acute self-limited hepatitis B
Penna A, Delprete G, Cavalli A, Bertoletti A, Delios Mm, Sorrentino R, et al
HEPATOLOGY 1997;25(4):1022-7

Susceptibility to ankylosing spondylitis correlates with the C-terminal residue of peptides presented by various HLA-B27 subtypes
Fiorillo Mt, Meadows L, Damato M, Shabanowitz J, Appella E, Sorrentino R
EUROPEAN JOURNAL OF IMMUNOLOGY 1997;27(2):368-73

Association of responsiveness to the major pollen allergen of Parietaria officinalis with HLA-DRB1* alleles - A multicenter study
Damato M, Dabusco As, Maggi E, Menna T, Sacerdoti G, Maurizio Sm, et al
HUMAN IMMUNOLOGY 1996;46(2):100-6

HLA-DRB1* alleles as genetic risk factors in allergy to Parietaria. A multicenter linkage study
Damato M, Picardi A, Dipietro A, Matricardi P, Testa B, Ariano R, et al
HUMAN IMMUNOLOGY 1996;47(1-2):O861-O861

New strategies to improve the resolution of DNA heteroduplex analysis of HLA class II genes.
Sorrentino R, Potolicchio I, Damato M
HUMAN IMMUNOLOGY 1996;47(1-2):P250-P250

Responsiveness to the major pollen allergen of Parietaria officinalis is associated with defined HLA-DRB1* alleles in Italian and Spanish allergic patients
Ruffilli A, D'amato M, Menna T, Maggi E, Sacerdoti G, Laho C
Advances in experimental medicine and biology 1996;409():75-9

Frequency of the new HLA-B*2709 allele in ankylosing spondylitis patients and healthy individuals
D'amato M, Fiorillo Mt, Galeazzi M, Martinetti M, Amoroso A, Sorrentino R
Disease markers 1995;12(3):215-7

FREQUENCY OF THE NEW HLA-B ASTERISK-2709 ALLELE IN ANKYLOSING-SPONDYLITIS PATIENTS AND HEALTHY-INDIVIDUALS
Damato M, Fiorillo Mt, Galeazzi M, Martinetti M, Amoroso A, Sorrentino R
DISEASE MARKERS 1995;12(3):215-217

Relevance of residue 116 of HLA-B27 in determining susceptibility to ankylosing spondylitis
D'amato M, Fiorillo Mt, Carcassi C, Mathieu A, Zuccarelli A, Bitti Pp, et al
European journal of immunology 1995;25(11):3199-201

RELEVANCE OF RESIDUE-116 OF HLA-B27 IN DETERMINING SUSCEPTIBILITY TO ANKYLOSING-SPONDYLITIS
Damato M, Fiorillo Mt, Carcassi C, Mathieu A, Zuccarelli A, Bitti Pp, et al
EUROPEAN JOURNAL OF IMMUNOLOGY 1995;25(11):3199-3201

SHORT INSERTIONS IN THE PARTNER STRANDS GREATLY ENHANCE THE DISCRIMINATING POWER OF DNA HETERODUPLEX ANALYSIS - RESOLUTION OF HLA-DQB1 POLYMORPHISMS
Damato M, Sorrentino R
NUCLEIC ACIDS RESEARCH 1995;23(11):2078-9

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