Thomas F. Wienker

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hao Hu, Stefan A. Haas, Jamel Chelly et al. · Molecular Psychiatry · 2015 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21

Youngae Lee, U. Wahn, Rainer Kehrt et al. · Nature Genetics · 2000 · 266 citations

Life Sciences, Genetics, Molecular Genetics +14

Genetics of intellectual disability in consanguineous families

Hao Hu, Kimia Kahrizi, Luciana Musante et al. · Molecular Psychiatry · 2018 · 217 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Philipp G. Maass, Friedrich C. Luft, Carolin Schächterle et al. · Nature Genetics · 2015 · 171 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

Matthew N. Bainbridge, Hao Hu, Donna M. Muzny et al. · Genome Medicine · 2013 · 164 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15