Thomas Schwarzbraun

An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1

Christian Windpassinger, Benedikt Schoser, Volker Straub et al. · The American Journal of Human Genetics · 2008 · 156 citations · Full text

Mitochondrial Myopathy, Mechanobiology, Muscle Pathology +10

Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenation

Lily Wang, Thomas Schwarzbraun, Michael R. Speicher et al. · Chromosoma · 2007 · 118 citations · Full text

Genetics, Molecular Biology, Human Anaphase Cells +21

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families

Gerald Egger, Katharina M. Roetzer, Abdul Noor et al. · Neurogenetics · 2014 · 113 citations

Syndromic Autism, Genetics, Risk Genes +8

Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the <i>myelin transcription factor 1</i> gene (<i>MYT1</i>)

T Kroepfl, Erwin Petek, Thomas Schwarzbraun et al. · Clinical Genetics · 2008 · 59 citations

Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome

Erwin Petek, Thomas Schwarzbraun, Abdul Noor et al. · Molecular Genetics and Genomics · 2006 · 57 citations

Syndromic Autism, Genetic Disorder, Genetics +9