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J-S Chan

Showing results (101-110 of 114) with videos related to

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Psychiatry Research|December 1, 1985
Pro-opiomelanocortin-related peptides in cerebrospinal fluid: a study of manic-depressive disorderW H Berrettini, J I Nurnberger, J S Chan, et al.
QJM : Monthly Journal of the Association of Physicians|January 3, 2022
COVID-19 vaccine-induced encephalitis and status epilepticusH-T Fan, Y-Y Lin, W-F Chiang, et al.
NPJ Genomic Medicine|May 3, 2019
Expanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variantsAda J S Chan, Cheryl Cytrynbaum, Ny Hoang, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 13, 2016
Anti-LG3 Antibodies Aggravate Renal Ischemia-Reperfusion Injury and Long-Term Renal Allograft DysfunctionB Yang, M Dieudé, K Hamelin, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Autism Research : Official Journal of the International Society for Autism Research|November 8, 2019
Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian CohortEduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, et al.
Human Genetics|November 15, 2022
SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencingQiliang Ding, Cherith Somerville, Roozbeh Manshaei, et al.
European Journal of Human Genetics : EJHG|June 6, 2023
Three generation families: Analysis of de novo variants in autismClaudia I Samogy Costa, Gabriele da Silva Campos, Eduarda Morgana da Silva Montenegro, et al.
Frontiers in Pharmacology|April 24, 2025
Interpreting the clinical significance of multiple large-scale mitochondrial DNA deletions (MLSMD) in skeletal muscle tissue in the diagnostic evaluation of primary mitochondrial diseaseJing Wang, James T Peterson, Joaquim Diego D Santos, et al.
Nature Communications|October 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorderAda J S Chan, Worrawat Engchuan, Miriam S Reuter, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Psychiatry Research|December 1, 1985
Pro-opiomelanocortin-related peptides in cerebrospinal fluid: a study of manic-depressive disorderW H Berrettini, J I Nurnberger, J S Chan, et al.
QJM : Monthly Journal of the Association of Physicians|January 3, 2022
COVID-19 vaccine-induced encephalitis and status epilepticusH-T Fan, Y-Y Lin, W-F Chiang, et al.
NPJ Genomic Medicine|May 3, 2019
Expanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variantsAda J S Chan, Cheryl Cytrynbaum, Ny Hoang, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 13, 2016
Anti-LG3 Antibodies Aggravate Renal Ischemia-Reperfusion Injury and Long-Term Renal Allograft DysfunctionB Yang, M Dieudé, K Hamelin, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Autism Research : Official Journal of the International Society for Autism Research|November 8, 2019
Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian CohortEduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, et al.
Human Genetics|November 15, 2022
SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencingQiliang Ding, Cherith Somerville, Roozbeh Manshaei, et al.
European Journal of Human Genetics : EJHG|June 6, 2023
Three generation families: Analysis of de novo variants in autismClaudia I Samogy Costa, Gabriele da Silva Campos, Eduarda Morgana da Silva Montenegro, et al.
Frontiers in Pharmacology|April 24, 2025
Interpreting the clinical significance of multiple large-scale mitochondrial DNA deletions (MLSMD) in skeletal muscle tissue in the diagnostic evaluation of primary mitochondrial diseaseJing Wang, James T Peterson, Joaquim Diego D Santos, et al.
Nature Communications|October 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorderAda J S Chan, Worrawat Engchuan, Miriam S Reuter, et al.
Pageof 12