Andreas Dufke

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Anita Rauch, Dagmar Wieczorek, Elisabeth Graf et al. · The Lancet · 2012 · 1.1K citations · Full text

Genetic Mutations, Mendelian Disorder, Genetic Disorder +7

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 · 299 citations · Full text

Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability

Juliane Hoyer, Arif B. Ekici, Sabine Endele et al. · The American Journal of Human Genetics · 2012 · 257 citations · Full text

Chromatin, Developmental Biology, Chromatin Structure +11

Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation

Thomas Liehr, Kristin Mrasek, Anja Weise et al. · Cytogenetic and Genome Research · 2005 · 205 citations

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification

Heike Starke, Angela Nietzel, Anja Weise et al. · Human Genetics · 2003 · 162 citations

Cytogenetics, Genetics, Statistical Genetics +4