Stefan Johansson

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane et al. · Science · 2018 · 2K citations · Full text

Brain Function, Psychiatric Disorders, Genetics +23

Rare and low-frequency coding variants alter human adult height

Eirini Marouli, Mariaelisa Graff, Carolina Medina‐Gómez et al. · Nature · 2017 · 647 citations · Full text

Allelic Variant, Genetics, Statistical Genetics +2

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Jason Flannick, Nicola L. Beer, Suzanne B.R. Jacobs et al. · Nature Genetics · 2014 · 488 citations · Full text

Genetics, Diabetes, Type 2 +4

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Valérie Turcot, Yingchang Lu, Heather M. Highland et al. · Nature Genetics · 2017 · 420 citations · Full text

Obesity, Metabolic Syndrome, Nutrition +10

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

Helge Ræder, Stefan Johansson, Pål I. Holm et al. · Nature Genetics · 2005 · 372 citations

Metabolic Syndrome, Genetic Disorder, Medicine +6