Katherina Walz

Ankrd11 Is a Chromatin Regulator Involved in Autism that Is Essential for Neural Development

Denis Gallagher, Anastassia Voronova, Mark Zander et al. · Developmental Cell · 2014 · 165 citations · Full text

Neurodevelopmental Disorders, Chromatin, Molecular Neuroscience +15

Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models

Guénola Ricard, Jéssica Molina, Jacqueline Chrast et al. · PLoS Biology · 2010 · 146 citations · Full text

Podocyte-Specific Overexpression of Wild Type or Mutant Trpc6 in Mice Is Sufficient to Cause Glomerular Disease

Paola Krall, César P. Canales, Pamela Kairath et al. · PLoS ONE · 2010 · 129 citations · Full text

Glomerular Disease, Immunology, Pathology +23

Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse

Weimin Bi, Jiong Yan, Paweł Stankiewicz et al. · Genome Research · 2002 · 113 citations · Full text

Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome

Weimin Bi, Gulam Mustafa Saifi, Christine J. Shaw et al. · Human Genetics · 2004 · 111 citations

Phd-containing Protein, Disease Mechanism, Mendelian Disorder +11