Stanislav S. Kholmanskikh

De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome

Jean‐Baptiste Rivière, Bregje W.M. van Bon, Alexander Hoischen et al. · Nature Genetics · 2012 · 304 citations · Full text

Baraitser-winter Syndrome, Genetic Disorder, Genetics +6

Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility

Stanislav S. Kholmanskikh, Hajira B. Koeller, Anthony Wynshaw‐Boris et al. · Nature Neuroscience · 2005 · 165 citations

Signal Transduction, Molecular Physiology, Molecular Neuroscience +11

De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

Ghayda Mirzaa, David Parry, Andrew E. Fry et al. · Nature Genetics · 2014 · 148 citations · Full text

Disease Mechanism, Genetic Disorder, Pathogenesis +5

Disregulated RhoGTPases and Actin Cytoskeleton Contribute to the Migration Defect in Lis1-Deficient Neurons

Stanislav S. Kholmanskikh, Joseph S. Dobrin, Anthony Wynshaw‐Boris et al. · Journal of Neuroscience · 2003 · 118 citations · Full text

Severe Brain Malformation, Cytoskeleton, Rho Gtpase Activity +18

LRP6 exerts non-canonical effects on Wnt signaling during neural tube closure

Jason D. Gray, Stanislav S. Kholmanskikh, Bozena S. Castaldo et al. · Human Molecular Genetics · 2013 · 54 citations · Full text