Katherina Walz
University of Miami(US)Austral University(AR)Dr. John T. Macdonald Foundation(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Hearing, Cochlea, Tinnitus, Genetics, Congenital heart defects research, Genetics and Neurodevelopmental Disorders, Genomics and Chromatin Dynamics
Most-Cited Works
- → Ankrd11 Is a Chromatin Regulator Involved in Autism that Is Essential for Neural Development(2014)167 cited
- → Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models(2010)146 cited
- → Podocyte-Specific Overexpression of Wild Type or Mutant Trpc6 in Mice Is Sufficient to Cause Glomerular Disease(2010)129 cited
- → Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse(2002)113 cited
- → Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome(2004)111 cited
- → COP9 Signalosome Subunit 3 Is Essential for Maintenance of Cell Proliferation in the Mouse Embryonic Epiblast(2003)107 cited