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Richard F Wintle

Showing results (1-10 of 33) with videos related to

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Developmental Medicine and Child Neurology|May 29, 2026
Contributing to genomic knowledge in cerebral palsy: Genetic testing and findings from Korean childrenRichard F Wintle
Genome Biology|November 19, 2008
Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprintingKohji Okamura, Richard F Wintle, Stephen W Scherer
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Human Mutation|February 2, 2006
DLG5 variants contribute to Crohn disease risk in a Canadian populationWilliam G Newman, Xiangjun Gu, Richard F Wintle, et al.
Developmental Medicine and Child Neurology|January 17, 2018
Cerebral palsy and genomics: an international consortiumAlastair H MacLennan, Michael C Kruer, Gareth Baynam, et al.
Genes|February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain TissueMarc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.
Scientific Reports|September 16, 2024
Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.
Arthritis and Rheumatism|February 5, 2005
SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian populationBill Newman, Richard F Wintle, Mark van Oene, et al.
Biomolecules|May 24, 2024
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD OutcomesLeo McKay, Berardino Petrelli, Molly Pind, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Developmental Medicine and Child Neurology|May 29, 2026
Contributing to genomic knowledge in cerebral palsy: Genetic testing and findings from Korean childrenRichard F Wintle
Genome Biology|November 19, 2008
Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprintingKohji Okamura, Richard F Wintle, Stephen W Scherer
Human Molecular Genetics|May 3, 2006
Structural variants: changing the landscape of chromosomes and design of disease studiesLars Feuk, Christian R Marshall, Richard F Wintle, et al.
Bioinformatics (Oxford, England)|October 4, 2019
VikNGS: a C++ variant integration kit for next generation sequencing association analysisZeynep Baskurt, Scott Mastromatteo, Jiafen Gong, et al.
Human Mutation|February 2, 2006
DLG5 variants contribute to Crohn disease risk in a Canadian populationWilliam G Newman, Xiangjun Gu, Richard F Wintle, et al.
Developmental Medicine and Child Neurology|January 17, 2018
Cerebral palsy and genomics: an international consortiumAlastair H MacLennan, Michael C Kruer, Gareth Baynam, et al.
Genes|February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain TissueMarc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.
Scientific Reports|September 16, 2024
Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.
Arthritis and Rheumatism|February 5, 2005
SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian populationBill Newman, Richard F Wintle, Mark van Oene, et al.
Biomolecules|May 24, 2024
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD OutcomesLeo McKay, Berardino Petrelli, Molly Pind, et al.
Pageof 4