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Showing results (771-780 of 915) with videos related to

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American Journal of Human Genetics|February 4, 2018
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion SyndromeMohammed Uddin, Brianna K Unda, Vickie Kwan, et al.
Biological Psychiatry|April 12, 2015
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive DisorderJames J H Rucker, Katherine E Tansey, Margarita Rivera, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Clinical Genetics|October 19, 2021
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genesClaudia Ismania Samogy Costa, Eduarda Morgana da Silva Montenegro, Mehdi Zarrei, et al.
BMC Medical Genomics|July 11, 2019
New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndromeEric Chater-Diehl, Resham Ejaz, Cheryl Cytrynbaum, et al.
BMC Genomics|November 14, 2019
Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populationsLian Deng, Haiyi Lou, Xiaoxi Zhang, et al.
NPJ Genomic Medicine|December 17, 2019
Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panelsSupanun Lauhasurayotin, Geoff D Cuvelier, Robert J Klaassen, et al.
Cancer Cell|December 8, 2009
Frequent amplification of a chr19q13.41 microRNA polycistron in aggressive primitive neuroectodermal brain tumorsMeihua Li, Kyle F Lee, Yuntao Lu, et al.
Frontiers in Genetics|October 28, 2020
Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome SequencesRoozbeh Manshaei, Daniele Merico, Miriam S Reuter, et al.
Human Genetics|November 30, 2014
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genesMarc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, et al.
Pageof 92

Showing results (771-780 of 915) with videos related to

Sort By:
Pageof 92
American Journal of Human Genetics|February 4, 2018
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion SyndromeMohammed Uddin, Brianna K Unda, Vickie Kwan, et al.
Biological Psychiatry|April 12, 2015
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive DisorderJames J H Rucker, Katherine E Tansey, Margarita Rivera, et al.
American Journal of Human Genetics|June 7, 2014
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery projectChandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, et al.
Clinical Genetics|October 19, 2021
Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genesClaudia Ismania Samogy Costa, Eduarda Morgana da Silva Montenegro, Mehdi Zarrei, et al.
BMC Medical Genomics|July 11, 2019
New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndromeEric Chater-Diehl, Resham Ejaz, Cheryl Cytrynbaum, et al.
BMC Genomics|November 14, 2019
Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populationsLian Deng, Haiyi Lou, Xiaoxi Zhang, et al.
NPJ Genomic Medicine|December 17, 2019
Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panelsSupanun Lauhasurayotin, Geoff D Cuvelier, Robert J Klaassen, et al.
Cancer Cell|December 8, 2009
Frequent amplification of a chr19q13.41 microRNA polycistron in aggressive primitive neuroectodermal brain tumorsMeihua Li, Kyle F Lee, Yuntao Lu, et al.
Frontiers in Genetics|October 28, 2020
Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome SequencesRoozbeh Manshaei, Daniele Merico, Miriam S Reuter, et al.
Human Genetics|November 30, 2014
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genesMarc Woodbury-Smith, Andrew D Paterson, Bhooma Thiruvahindrapduram, et al.
Pageof 92