Barbara Schormair

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

Juliane Winkelmann, Barbara Schormair, Peter Lichtner et al. · Nature Genetics · 2007 · 690 citations

Genome-wide Association Study, Genetic Disorder, Genetics +5

Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy

Paulina Navon Elkan, Sarah B. Pierce, Reeval Segel et al. · New England Journal of Medicine · 2014 · 690 citations

Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits

Anke R. Hammerschlag, Sven Stringer, Christiaan de Leeuw et al. · Nature Genetics · 2017 · 302 citations · Full text

Genome-wide Association Study, Sleep, Metabolic Traits +9

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

Barbara Schormair, David Kemlink, Darina Roeske et al. · Nature Genetics · 2008 · 273 citations · Full text

Clinical Disorders, Signal Transduction, Physiology +6

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

Juliane Winkelmann, Ling Lin, Barbara Schormair et al. · Human Molecular Genetics · 2012 · 259 citations · Full text

Systems Biology, Mendelian Disorder, Genetic Disorder +13