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Stanislav S. Kholmanskikh, Ph.D. - Publications

Affiliations: 
2002 University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Neuroscience Biology, Cell Biology, Human Development
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9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y, Kuentz P, Courcet JB, Carmignac V, Garret P, Bessis D, Boute O, Bron A, Captier G, Carmi E, et al. Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome. Nature Genetics. PMID 31611689 DOI: 10.1038/S41588-019-0527-3  0.325
2019 Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y, Kuentz P, Courcet JB, Carmignac V, Garret P, Bessis D, Boute O, Bron A, Captier G, Carmi E, et al. Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome. Nature Genetics. PMID 31570889 DOI: 10.1038/S41588-019-0498-4  0.348
2018 Vabres P, Sorlin A, Kholmanskikh S, Duffourd Y, Kuentz P, Carmignac V, Bessis D, Dobyns W, Polubothu S, Faravelli F, Kinsler V, Faivre L, Ross M, Rivière J. 794 Postzygotic dominant-negative mutations of RHOA cause a mosaic neuroectodermal syndrome Journal of Investigative Dermatology. 138: S135. DOI: 10.1016/J.Jid.2018.03.804  0.346
2017 Vabres P, Sorlin A, Kholmanskikh S, Demeer B, St-Onge J, Duffourd Y, Kuentz P, Courcet J, carmignac v, Bessis D, Bernard G, Dobyns W, Faivre L, Ross M, Rivière J. 616 Postzygotic mutations of RHOA cause a mosaic neuroectodermal syndrome Journal of Investigative Dermatology. 137: S298. DOI: 10.1016/J.Jid.2017.07.292  0.344
2014 Mirzaa GM, Parry DA, Fry AE, Giamanco KA, Schwartzentruber J, Vanstone M, Logan CV, Roberts N, Johnson CA, Singh S, Kholmanskikh SS, Adams C, Hodge RD, Hevner RF, Bonthron DT, et al. De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. Nature Genetics. 46: 510-5. PMID 24705253 DOI: 10.1038/Ng.2948  0.389
2013 Gray JD, Kholmanskikh S, Castaldo BS, Hansler A, Chung H, Klotz B, Singh S, Brown AM, Ross ME. LRP6 exerts non-canonical effects on Wnt signaling during neural tube closure. Human Molecular Genetics. 22: 4267-81. PMID 23773994 DOI: 10.1093/Hmg/Ddt277  0.308
2012 Rivière JB, van Bon BW, Hoischen A, Kholmanskikh SS, O'Roak BJ, Gilissen C, Gijsen S, Sullivan CT, Christian SL, Abdul-Rahman OA, Atkin JF, Chassaing N, Drouin-Garraud V, Fry AE, Fryns JP, et al. De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome. Nature Genetics. 44: 440-4, S1-2. PMID 22366783 DOI: 10.1038/Ng.1091  0.43
2006 Kholmanskikh SS, Koeller HB, Wynshaw-Boris A, Gomez T, Letourneau PC, Ross ME. Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility. Nature Neuroscience. 9: 50-7. PMID 16369480 DOI: 10.1038/Nn1619  0.464
2003 Kholmanskikh SS, Dobrin JS, Wynshaw-Boris A, Letourneau PC, Ross ME. 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. PMID 14507966 DOI: 10.1523/Jneurosci.23-25-08673.2003  0.589
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