Agne Liedén

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

Article: GENETICS IN MEDICINE. 2022;24(11):2296-2307
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability
Lindstrand A; Ek M; Kvarnung M; Anderlid B-M; Bjoerck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjoe A; Helgadottir HT; Hellstroem-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-A; Lieden A; Lindeloef H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A
Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2022;23(14):8001
DNA Methylation Signature for JARID2-Neurodevelopmental Syndrome
Verberne EA; van der Laan L; Haghshenas S; Rooney K; Levy MA; Alders M; Maas SM; Jansen S; Lieden A; Anderlid B-M; Rafael-Croes L; Campeau PM; Chaudhry A; Koolen DA; Pfundt R; Hurst ACE; Tran-Mau-Them F; Bruel A-L; Lambert L; Isidor B; Mannens MMAM; Sadikovic B; Henneman P; van Haelst MM
Article: GENETICS IN MEDICINE. 2021;23(2):374-383
JARID2haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome
Verberne EA; Goh S; England J; van Ginkel M; Rafael-Croes L; Maas S; Polstra A; Zarate YA; Bosanko KA; Pechter KB; Bedoukian E; Izumi K; Chaudhry A; Robin NH; Boothe M; Lippa NC; Aggarwal V; De Vivo DC; Lehman A; Stockler S; Bruel A-L; Isidor B; Lemons J; Rodriguez-Buritica DF; Richmond CM; Stark Z; Agrawal PB; Kooy RF; Meuwissen MEC; Koolen DA; Pfundt R; Lieden A; Anderlid B-M; Glatz D; Mannens MMAM; Bakshi M; Mallette FA; van Haelst MM; Campeau PM
Article: PLOS ONE. 2021;16(2):e0245488
Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients
Wallander K; Eisfeldt J; Lindblad M; Nilsson D; Billiau K; Foroughi H; Nordenskjold M; Lieden A; Tham E
Article: GENOME MEDICINE. 2019;11(1):68
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid B-M; Bjerin O; Gustavsson P; Hammarsjo A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjold M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
Article: FRONTIERS IN GENETICS. 2019;10:896
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
Kvarnung M; Shahsavani M; Taylan F; Moslem M; Breeuwsma N; Laan L; Schuster J; Jin Z; Nilsson D; Lieden A; Anderlid B-M; Nordenskjold M; Lundberg ES; Birnir B; Dahl N; Nordgren A; Lindstrand A; Falk A
Article: PLOS ONE. 2019;14(1):e0210017
Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth
Sahlin E; Green A; Gustavsson P; Lieden A; Nordenskjold M; Papadogiannakis N; Pettersson K; Nilsson D; Jonasson J; Iwarsson E
Article: PLOS GENETICS. 2018;14(11):e1007780
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
Nazaryan-Petersen L; Eisfeldt J; Pettersson M; Lundin J; Nilsson D; Wincent J; Lieden A; Lovmar L; Ottosson J; Gacic J; Makitie O; Nordgren A; Vezzi F; Wirta V; Kaller M; Hjortshoj TD; Jespersgaard C; Houssari R; Pignata L; Bak M; Tommerup N; Lundberg ES; Tumer Z; Lindstrand A
Article: ACTA DERMATO-VENEREOLOGICA. 2018;98(7):630-635
Prognosis of Preschool Eczema and Factors of Importance for Remission
Johansson EK; Bergstrom A; Kull I; Lind T; Soderhall C; Melen E; Asad S; Bradley M; Lieden A; Ballardini N; Wahlgren C-F
Article: NATURE GENETICS. 2016;48(11):1359-1369
TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons
Caubit X; Gubellini P; Andrieux J; Roubertoux PL; Metwaly M; Jacq B; Fatmi A; Had-Aissouni L; Kwan KY; Salin P; Carlier M; Lieden A; Rudd E; Shinawi M; Vincent-Delorme C; Cuisset J-M; Lemaitre M-P; Abderrehamane F; Duban B; Lemaitre J-F; Woolf AS; Bockenhauer D; Severac D; Dubois E; Zhu Y; Sestan N; Garratt AN; Goff LK-L; Fasano L
Article: NATURE COMMUNICATIONS. 2016;7:12175
Deletion of Wiskott-Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells
Baptista MAP; Keszei M; Oliveira M; Sunahara KKS; Andersson J; Dahlberg CIM; Worth AJ; Lieden A; Kuo I-C; Wallin RPA; Snapper SB; Eidsmo L; Scheynius A; Karlsson MCI; Bouma G; Burns SO; Forsell MNE; Thrasher AJ; Nylen S; Westerberg LS
Article: BRITISH JOURNAL OF DERMATOLOGY. 2016;175(1):95-101
Vitamin D levels and atopic eczema in infancy and early childhood in Norway: a cohort study
Berents TL; Carlsen KCL; Mowinckel P; Sandvik L; Skjerven HO; Rolfsjord LB; Kvenshagen B; Hunderi JOG; Bradley M; Lieden A; Carlsen K-H; Thorsby PM; Gjersvik P
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2016;98(2):363-372
Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability
Kasher PR; Schertz KE; Thomas M; Jackson A; Annunziata S; Ballesta-Martinez MJ; Campeau PM; Clayton PE; Eaton JL; Granata T; Guillen-Navarro E; Hernando C; Laverriere CE; Lieden A; Villa-Marcos O; McEntagart M; Nordgren A; Pantaleoni C; Pebrel-Richard C; Sarret C; Sciacca FL; Wright R; Kerr B; Glasgow E; Banka S
Article: ACTA PAEDIATRICA, INTERNATIONAL JOURNAL OF PAEDIATRICS. 2015;104(6):610-618
Rare copy number variants are common in young children with autism spectrum disorder
Eriksson MA; Lieden A; Westerlund J; Bremer A; Wincent J; Sahlin E; Gillberg C; Fernell E; Anderlid B-M
Article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2015;58(3):129-133
No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations
Winberg J; Berggren H; Malm T; Johansson S; Ramgren JJ; Nilsson B; Lieden A; Nordenskjold A; Gustavsson P; Nordgren A
Article: PLOS ONE. 2015;10(6):e0130145
Skin Barrier Function and Staphylococcus aureus Colonization in Vestibulum Nasi and Fauces in Healthy Infants and Infants with Eczema: A Population-Based Cohort Study
Berents TL; Carlsen KCL; Mowinckel P; Skjerven HO; Kvenshagen B; Rolfsjord LB; Bradley M; Lieden A; Carlsen K-H; Gaustad P; Gjersvik P
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART A. 2014;164(12):3083-3087
Intragenic Duplication-A Novel Causative Mechanism for SATB2-Associated Syndrome
Lieden A; Kvarnung M; Nilssson D; Sahlin E; Lundberg ES
Article: PLOS ONE. 2014;9(9):e107712
Characterization of Stem-Like Cells in Mucoepidermoid Tracheal Paediatric Tumor
Lim ML; Ooi BNS; Jungebluth P; Sjoqvist S; Hultman I; Lemon G; Gustafsson Y; Asmundsson J; Baiguera S; Douagi I; Gilevich I; Popova A; Haag JC; Rodriguez AB; Lim J; Lieden A; Nordenskjold M; Alici E; Baker D; Unger C; Luedde T; Vassiliev I; Inzunza J; Ahrlund-Richter L; Macchiarini P
Article: FETAL DIAGNOSIS AND THERAPY. 2014;36(4):326-332
Molecular and Cytogenetic Analysis in Stillbirth: Results from 481 Consecutive Cases
Sahlin E; Gustavsson P; Lieden A; Papadogiannakis N; Bjareborn L; Pettersson K; Nordenskjold M; Iwarsson E
Article: HUMAN MOLECULAR GENETICS. 2013;22(23):4841-4856
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 L; Edser P; Street T; Rodriguez E; O'Regan GM; Beattie P; Foelster-Holst R; Franke A; Novak N; Fahy CM; Winge MCG; Kabesch M; Illig T; Heath S; Soderhall C; Melen E; Pershagen G; Kere J; Bradley M; Lieden A; Nordenskjold M; Harper JI; Mclean WHI; Brown SJ; Cookson WOC; Lathrop GM; Irvine AD; Moffatt MF
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART A. 2013;161A(6):1284-1290
Partial Tetrasomy 14 Associated With Multiple Malformations
Winberg J; Robinson KL; Naess K; Lesko N; Wibom R; Lieden A; Anderlid B-M; Graff C; Nordenskjoeld A; Nordgren A; Gustavsson P
Article: SEXUAL DEVELOPMENT. 2013;7(4):173-179
Association of a Tagging Single Nucleotide Polymorphism in the Androgen Receptor Gene Region with Susceptibility to Severe Hypospadias in a Caucasian Population
Adamovic T; Thai HTT; Lieden A; Nordenskjold A
Article: JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY. 2013;27(1):e124-e127
Lack of association between filaggrin gene mutations and onset of psoriasis in childhood
Winge MCG; Suneson J; Lysell J; Nikamo P; Lieden A; Nordenskjold M; Wahlgren CF; Bradley M; Stahle M
Article: PLOS ONE. 2012;7(11):e49694
Genetic Variation in the Epidermal Transglutaminase Genes Is Not Associated with Atopic Dermatitis
Lieden A; Winge MCG; Saaf A; Kockum I; Ekelund E; Rodriguez E; Foelster-Holst R; Franke A; Illig T; Tengvall-Linder M; Baurecht H; Weidinger S; Wahlgren C-F; Nordenskjold M; Bradley M
Article: BRITISH JOURNAL OF DERMATOLOGY. 2011;165(5):1074-1080
Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis
Winge MCG; Bilcha KD; Lieden A; Shibeshi D; Sandilands A; Wahlgren C-F; McLean WHI; Nordenskjold M; Bradley M
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2011;19(10):1032-1037
Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions
Vergult S; Krgovic D; Loeys B; Lyonnet S; Lieden A; Anderlid B-M; Sharkey F; Joss S; Mortier G; Menten B
Article: ALLERGY. EUROPEAN JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 2009;64(2):304-311
Cornulin, a marker of late epidermal differentiation, is down-regulated in eczema
Lieden A; Ekelund E; Kuo I-C; Kockum I; Huang C-H; Mallbris L; Lee SP; Seng LK; Chin GY; Wahlgren C-F; Palmer CNA; Bjoerksten B; Stahle M; Nordenskoeld M; Bradley M; Chua KY; D'Amato M
Article: ACTA DERMATO-VENEREOLOGICA. 2008;88(1):15-19
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; Kochum I; Bradley M
Article: ACTA DERMATO-VENEREOLOGICA. 2004;84(5):339-345
Malassezia sympodialis stimulation differently affects gene expression in dendritic cells from atopic dermatitis patients and healthy individuals
Gabrielsson S; Buentke E; Liedén A; Schmidt M; D'Amato M; Tengvall-Linder M; Scheynius A
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Review: JOURNAL OF INTERNAL MEDICINE. 2019;286(2):118-136
Cell-free tumour DNA testing for early detection of cancer - a potential future tool
Barbany G; Arthur C; Lieden A; Nordenskjold M; Rosenquist R; Tesi B; Wallander K; Tham E
Letter: JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 2015;136(2):507-9.e19
Whole-exome sequencing of Ethiopian patients with ichthyosis vulgaris and atopic dermatitis
Taylan F; Nilsson D; Asad S; Lieden A; Wahlgren C-F; Winge MCG; Bilcha KD; Nordenskjold M; Bradley M
Letter: JOURNAL OF INVESTIGATIVE DERMATOLOGY. 2013;133(10):2486-2489
Genetic Variation in the Inflammasome and Atopic Dermatitis Susceptibility
Bivik C; Verma D; Winge MC; Lieden A; Bradley M; Rosdahl I; Soderkvist P
Letter: EUROPEAN JOURNAL OF HUMAN GENETICS. 2012;20(4):367
Nasal speech in patients with 12q15 microdeletions
Vergult S; Krgovic D; Loeys B; Lyonnet S; Lieden A; Anderlid B-M; Sharkey F; Joss S; Mortier G; Menten B
Letter: JOURNAL OF DERMATOLOGICAL SCIENCE. 2011;63(1):62-64
Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis
Winge MCG; Hoppe T; Lieden A; Nordenskjold M; Vahlquist A; Wahlgren C-F; Torma H; Bradley M; Berne B
Published conference paper: JOURNAL OF CLINICAL GASTROENTEROLOGY. 2008;42(8):S133-S135
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
Thesis / dissertation: 2007
Gene expression and genetic association studies in eczema
Liedén, Agne

Anställningar

Anknuten till Forskning, Molekylär medicin och kirurgi, Karolinska Institutet, 2022-2025

Examina och utbildning

MEDICINE DOKTORSEXAMEN, Institutionen för molekylär medicin och kirurgi, Karolinska Institutet, 2008
Medicine Magisterexamen, Karolinska Institutet, 2003

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