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
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
10482018
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
5952011
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
4472017
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
4422012
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
4202014
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
3692006
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
2642010
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
2022010
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
1942019
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
1902018
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
1892010
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
1862009
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
1722012
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
1692015
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
1512015
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
1402011
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
1342013
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
1242013
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
1202008
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
1132012
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