Stanislav S. Kholmanskikh, Ph.D.

Affiliations: 
2002 University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Neuroscience Biology, Cell Biology, Human Development
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"Stanislav Kholmanskikh"
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Paul C. Letourneau grad student 2002 Cornell Medical Center
 (Study of neuronal migration and cytoskeleton defects in a mouse model of lissencephaly.)
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Publications

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Vabres P, Sorlin A, Kholmanskikh SS, et al. (2019) Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome. Nature Genetics
Vabres P, Sorlin A, Kholmanskikh SS, et al. (2019) Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome. Nature Genetics
Vabres P, Sorlin A, Kholmanskikh S, et al. (2018) 794 Postzygotic dominant-negative mutations of RHOA cause a mosaic neuroectodermal syndrome Journal of Investigative Dermatology. 138: S135
Vabres P, Sorlin A, Kholmanskikh S, et al. (2017) 616 Postzygotic mutations of RHOA cause a mosaic neuroectodermal syndrome Journal of Investigative Dermatology. 137: S298
Mirzaa GM, Parry DA, Fry AE, et al. (2014) De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. Nature Genetics. 46: 510-5
Gray JD, Kholmanskikh S, Castaldo BS, et al. (2013) LRP6 exerts non-canonical effects on Wnt signaling during neural tube closure. Human Molecular Genetics. 22: 4267-81
Rivière JB, van Bon BW, Hoischen A, et al. (2012) De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome. Nature Genetics. 44: 440-4, S1-2
Kholmanskikh SS, Koeller HB, Wynshaw-Boris A, et al. (2006) Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility. Nature Neuroscience. 9: 50-7
Kholmanskikh SS, Dobrin JS, Wynshaw-Boris A, et al. (2003) Disregulated RhoGTPases and actin cytoskeleton contribute to the migration defect in Lis1-deficient neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 8673-81
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