Showing results (81-90 of 88) with videos related to
Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2016
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causalityJulia N Bailey, Christopher Patterson, Laurence de Nijs, et al.Translational Psychiatry|December 6, 2020
Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorderHidekazu Kato, Itaru Kushima, Daisuke Mori, et al.Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.The New England Journal of Medicine|March 15, 2018
Variant Intestinal-Cell Kinase in Juvenile Myoclonic EpilepsyJulia N Bailey, Laurence de Nijs, Dongsheng Bai, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2022
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformationsKerith-Rae Dias, Colleen M Carlston, Laura E R Blok, et al.Cell Reports|September 13, 2018
Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological InsightsItaru Kushima, Branko Aleksic, Masahiro Nakatochi, et al.Biological Psychiatry|June 6, 2022
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum DisorderItaru Kushima, Masahiro Nakatochi, Branko Aleksic, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.Pageof 9