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Frontiers in Psychiatry|November 2, 2023
A whole exome sequencing study to identify rare variants in multiplex families with alcohol use disorderShirley Y Hill, Joseph HostykNature Reviews. Genetics|October 13, 2019
Rare-variant collapsing analyses for complex traits: guidelines and applicationsGundula Povysil, Slavé Petrovski, Joseph Hostyk, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2022
Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome SequencingRahul K Sharma, Madeleine Drusin, Joseph Hostyk, et al.JAMA Network Open|October 28, 2022
Risk Variants in the Exomes of Children With Critical IllnessJoshua E Motelow, Natalie C Lippa, Joseph Hostyk, et al.Bone|November 7, 2021
Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosisAdi Cohen, Joseph Hostyk, Evan H Baugh, et al.American Journal of Medical Genetics. Part A|September 27, 2021
Genomic analysis of "microphenotypes" in epilepsyKate Stanley, Joseph Hostyk, Linh Tran, et al.The New England Journal of Medicine|August 14, 2020
Causal Genetic Variants in StillbirthKate E Stanley, Jessica Giordano, Vanessa Thorsten, et al.Nature Medicine|September 25, 2019
A framework for the investigation of rare genetic disorders in neuropsychiatryStephan J Sanders, Mustafa Sahin, Joseph Hostyk, et al.Pageof 1