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Tom Walsh

Showing results (111-120 of 193) with videos related to

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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.
Molecular Biology and Evolution|June 28, 2024
Rapid Adaptation and Interspecific Introgression in the North American Crop Pest Helicoverpa zeaHenry L North, Zhen Fu, Richard Metz, 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.
Neurology|October 31, 2014
Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic featuresHiroyuki Morino, Sarah B Pierce, Yukiko Matsuda, 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.
The Lancet. HIV|September 8, 2024
Optimising HIV spending in 12 eastern European and central Asian countries: a modelling studyDebra C Ten Brink, Anna L Bowring, Rowan Martin-Hughes, et al.
Human Mutation|February 4, 2016
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 IsoformM'hamed Grati, Denise Yan, Manmeet H Raval, et al.
Genome Research|December 9, 2024
Resolving the chromatin impact of mosaic variants with targeted Fiber-seqStephanie C Bohaczuk, Zachary J Amador, Chang Li, et al.
Biorxiv : the Preprint Server for Biology|July 19, 2024
Resolving the chromatin impact of mosaic variants with targeted Fiber-seqStephanie C Bohaczuk, Zachary J Amador, Chang Li, et al.
Pageof 20

Showing results (111-120 of 193) with videos related to

Sort By:
Pageof 20
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.
Molecular Biology and Evolution|June 28, 2024
Rapid Adaptation and Interspecific Introgression in the North American Crop Pest Helicoverpa zeaHenry L North, Zhen Fu, Richard Metz, 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.
Neurology|October 31, 2014
Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic featuresHiroyuki Morino, Sarah B Pierce, Yukiko Matsuda, 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.
The Lancet. HIV|September 8, 2024
Optimising HIV spending in 12 eastern European and central Asian countries: a modelling studyDebra C Ten Brink, Anna L Bowring, Rowan Martin-Hughes, et al.
Human Mutation|February 4, 2016
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 IsoformM'hamed Grati, Denise Yan, Manmeet H Raval, et al.
Genome Research|December 9, 2024
Resolving the chromatin impact of mosaic variants with targeted Fiber-seqStephanie C Bohaczuk, Zachary J Amador, Chang Li, et al.
Biorxiv : the Preprint Server for Biology|July 19, 2024
Resolving the chromatin impact of mosaic variants with targeted Fiber-seqStephanie C Bohaczuk, Zachary J Amador, Chang Li, et al.
Pageof 20