Maria Kaffe

Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

Juliane Winkelmann, Darina Czamara, Barbara Schormair et al. · PLoS Genetics · 2011 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Restless Legs Syndrome-associated intronic common variant in <i>Meis1</i> alters enhancer function in the developing telencephalon

Derek Spieler, Maria Kaffe, José Bessa et al. · Genome Research · 2014 · 114 citations · Full text

Life Sciences, Genetics, Neuroscience +16

Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

Dagmar Wieczorek, William G. Newman, Thomas Wieland et al. · The American Journal of Human Genetics · 2014 · 65 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

<i>MEIS1</i> and <i>BTBD9</i>: genetic association with restless leg syndrome in end stage renal disease

Barbara Schormair, Jens Plag, Maria Kaffe et al. · Journal of Medical Genetics · 2011 · 65 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

Michael Zech, Angela Jochim, Florian Castrop et al. · Movement Disorders · 2013 · 56 citations

Life Sciences, Genetics, Molecular Genetics +13