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Stefan Johansson
Stefan Johansson
Department of Clinical Science, University of Bergen, Bergen Norwary
Verified email at biomed.uib.no
Title
Cited by
Cited by
Year
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
16652018
Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children
TO Kilpeläinen, L Qi, S Brage, SJ Sharp, E Sonestedt, E Demerath, ...
PLoS medicine 8 (11), e1001116, 2011
7862011
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium
Science (New York, NY) 360 (6395), eaap8757, 2018
7852018
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
7312017
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ø Helgeland, ...
Nature genetics 51 (5), 804-814, 2019
6072019
The genetics of attention deficit/hyperactivity disorder in adults, a review
B Franke, SV Faraone, P Asherson, J Buitelaar, CHD Bau, ...
Molecular psychiatry 17 (10), 960-987, 2012
6052012
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
J Flannick, G Thorleifsson, NL Beer, SBR Jacobs, N Grarup, NP Burtt, ...
Nature genetics 46 (4), 357-363, 2014
6022014
Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction
H Ræder, S Johansson, PI Holm, IS Haldorsen, E Mas, V Sbarra, ...
Nature genetics 38 (1), 54-62, 2006
4822006
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
4382018
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
M Arcos-Burgos, M Jain, MT Acosta, S Shively, H Stanescu, D Wallis, ...
Molecular psychiatry 15 (11), 1053-1066, 2010
3822010
Dominant mutations in the autoimmune regulator AIRE are associated with common organ-specific autoimmune diseases
BE Oftedal, A Hellesen, MM Erichsen, E Bratland, A Vardi, J Perheentupa, ...
Immunity 42 (6), 1185-1196, 2015
3032015
Mutations in ABHD12 cause the neurodegenerative disease PHARC: an inborn error of endocannabinoid metabolism
T Fiskerstrand, DHB Brahim, S Johansson, A M'zahem, BI Haukanes, ...
The American Journal of Human Genetics 87 (3), 410-417, 2010
2702010
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD
B Franke, AA Vasquez, S Johansson, M Hoogman, J Romanos, ...
Neuropsychopharmacology 35 (3), 656-664, 2010
2432010
Familial Diarrhea Syndrome Caused by an Activating GUCY2C Mutation
T Fiskerstrand, N Arshad, BI Haukanes, RR Tronstad, KDC Pham, ...
New England Journal of Medicine 366 (17), 1586-1595, 2012
2402012
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
NF Magitta, AS Bøe Wolff, S Johansson, B Skinningsrud, BA Lie, KM Myhr, ...
Genes & Immunity 10 (2), 120-124, 2009
2282009
A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis
K Fjeld, FU Weiss, D Lasher, J Rosendahl, JM Chen, BB Johansson, ...
Nature genetics 47 (5), 518-522, 2015
2252015
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ...
Biological psychiatry 83 (12), 1044-1053, 2018
2242018
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits
S Vogelezang, JP Bradfield, TS Ahluwalia, JA Curtin, TA Lakka, N Grarup, ...
PLoS genetics 16 (10), e1008718, 2020
2062020
Trends in congenital heart defects in infants with Down syndrome
S Bergström, H Carr, G Petersson, O Stephansson, AKE Bonamy, ...
Pediatrics 138 (1), e20160123, 2016
2022016
Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes
J Flannick, S Johansson, PR Njølstad
Nature Reviews Endocrinology 12 (7), 394-406, 2016
2022016
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Articles 1–20