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Suleyman Gulsuner

Showing results (21-30 of 63) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2021
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum DisorderRyan J Carlson, Alicia Quesnel, Dawson Wells, et al.
Cold Spring Harbor Molecular Case Studies|August 24, 2016
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive diseaseSarah B Pierce, Suleyman Gulsuner, Gail A Stapleton, et al.
Journal of Medical Genetics|April 16, 2015
Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failureYardena Tenenbaum-Rakover, Ariella Weinberg-Shukron, Paul Renbaum, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2026
Loss of function of the chromatin remodeling gene <i>INO80D</i> leads to neurogenic features of schizophreniaAnna B Sunshine, Suleyman Gulsuner, C Andrew Williams, et al.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Blood|April 24, 2019
Reprogramming identifies functionally distinct stages of clonal evolution in myelodysplastic syndromesJasper Hsu, Andreea Reilly, Brian J Hayes, et al.
European Journal of Human Genetics : EJHG|August 25, 2018
Genetics of hearing loss in the Arab population of Northern IsraelNada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, et al.
JAMA Otolaryngology-- Head & Neck Surgery|January 12, 2023
Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant OutcomesRyan J Carlson, Tom Walsh, Jessica B Mandell, et al.
American Journal of Human Genetics|October 8, 2013
Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophreniaCaitlin Rippey, Tom Walsh, Suleyman Gulsuner, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2019
Characterization of splice-altering mutations in inherited predisposition to cancerSilvia Casadei, Suleyman Gulsuner, Brian H Shirts, et al.
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2021
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum DisorderRyan J Carlson, Alicia Quesnel, Dawson Wells, et al.
Cold Spring Harbor Molecular Case Studies|August 24, 2016
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive diseaseSarah B Pierce, Suleyman Gulsuner, Gail A Stapleton, et al.
Journal of Medical Genetics|April 16, 2015
Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failureYardena Tenenbaum-Rakover, Ariella Weinberg-Shukron, Paul Renbaum, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 2026
Loss of function of the chromatin remodeling gene <i>INO80D</i> leads to neurogenic features of schizophreniaAnna B Sunshine, Suleyman Gulsuner, C Andrew Williams, et al.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Blood|April 24, 2019
Reprogramming identifies functionally distinct stages of clonal evolution in myelodysplastic syndromesJasper Hsu, Andreea Reilly, Brian J Hayes, et al.
European Journal of Human Genetics : EJHG|August 25, 2018
Genetics of hearing loss in the Arab population of Northern IsraelNada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, et al.
JAMA Otolaryngology-- Head & Neck Surgery|January 12, 2023
Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant OutcomesRyan J Carlson, Tom Walsh, Jessica B Mandell, et al.
American Journal of Human Genetics|October 8, 2013
Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophreniaCaitlin Rippey, Tom Walsh, Suleyman Gulsuner, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2019
Characterization of splice-altering mutations in inherited predisposition to cancerSilvia Casadei, Suleyman Gulsuner, Brian H Shirts, et al.
Pageof 7