Ksenya Cohen‐Katsenelson

Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation

Ofer Sarig, Sagi Nahum, Debora Rapaport et al. · The American Journal of Human Genetics · 2012 · 67 citations · Full text

Down Syndrome, Developmental Anomaly, Facial Dysmorphism +7

Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3‐Methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and leigh‐Like Syndrome) caused by novel mutations in <i>SERAC1</i>

Ofer Sarig, Dorit Goldsher, Janna Nousbeck et al. · American Journal of Medical Genetics Part A · 2013 · 45 citations

Pleckstrin homology domain leucine-rich repeat protein phosphatases set the amplitude of receptor tyrosine kinase output

Gloria Reyes, Matt Niederst, Ksenya Cohen‐Katsenelson et al. · Proceedings of the National Academy of Sciences · 2014 · 39 citations · Full text

Docking interactions of the JNK scaffold protein WDR62

Ksenya Cohen‐Katsenelson, Tanya Wasserman, Samer Khateb et al. · Biochemical Journal · 2011 · 34 citations · Full text

Signal Transduction, Signaling Pathway, Medicine +11

Identification and Analysis of a Novel Dimerization Domain Shared by Various Members of c-Jun N-terminal Kinase (JNK) Scaffold Proteins

Ksenya Cohen‐Katsenelson, Tanya Wasserman, Ilona Darlyuk‐Saadon et al. · Journal of Biological Chemistry · 2013 · 21 citations · Full text

Various Members, Molecular Biology, Synaptic Signaling +23