Stefan Johansson
Stefan Johansson
Department of Clinical Science, University of Bergen, Bergen Norwary
Verified email at
Cited by
Cited by
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
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
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, 2017
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, 2012
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, 2014
Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction
H Rĉder, S Johansson, PI Holm, IS Haldorsen, E Mas, V Sbarra, ...
Nature genetics 38 (1), 54, 2006
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, 2010
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, 2010
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ĝ Helgeland, ...
Nature Genetics, 1, 2019
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, 2018
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
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
NF Magitta, ASB Wolff, S Johansson, B Skinningsrud, BA Lie, KM Myhr, ...
Genes and immunity 10 (2), 120, 2009
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
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
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, 2015
FTO, type 2 diabetes, and weight gain throughout adult life: a meta-analysis of 41,504 subjects from the Scandinavian HUNT, MDC, and MPP studies
JK Hertel, S Johansson, E Sonestedt, A Jonsson, RT Lie, CGP Platou, ...
Diabetes 60 (5), 1637-1644, 2011
Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcification
SH Rafaelsen, H Rĉder, AK Fagerheim, P Knappskog, TO Carpenter, ...
Journal of Bone and Mineral Research 28 (6), 1378-1385, 2013
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
J Flannick, NL Beer, AG Bick, V Agarwala, J Molnes, N Gupta, NP Burtt, ...
Nature genetics 45 (11), 1380, 2013
Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based …
JK Hertel, S Johansson, H Raeder, K Midthjell, V Lyssenko, L Groop, ...
Diabetologia 51 (6), 971, 2008
Exome sequencing and genetic testing for MODY
S Johansson, H Irgens, KK Chudasama, J Molnes, J Aerts, FS Roque, ...
PloS one 7 (5), e38050, 2012
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