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Richard F Wintle

Showing results (11-20 of 33) with videos related to

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G3 (Bethesda, Md.)|June 8, 2022
Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue ProgramRichard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|March 14, 2018
Copy number variation in fetal alcohol spectrum disorderMehdi Zarrei, Geoffrey G Hicks, James N Reynolds, et al.
Nature Genetics|April 27, 2004
Functional variants of OCTN cation transporter genes are associated with Crohn diseaseVanya D Peltekova, Richard F Wintle, Laurence A Rubin, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Clinical actionability of genetic findings in cerebral palsySara A Lewis, Maya Chopra, Julie S Cohen, et al.
Arthritis and Rheumatism|June 30, 2005
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populationsMark van Oene, Richard F Wintle, Xiangdong Liu, et al.
JAMA Pediatrics|December 2, 2024
Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-AnalysisSara A Lewis, Maya Chopra, Julie S Cohen, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
The EMBO Journal|January 24, 2004
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegansSuparna Sanyal, Richard F Wintle, Katie S Kindt, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
G3 (Bethesda, Md.)|June 8, 2022
Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue ProgramRichard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|March 14, 2018
Copy number variation in fetal alcohol spectrum disorderMehdi Zarrei, Geoffrey G Hicks, James N Reynolds, et al.
Nature Genetics|April 27, 2004
Functional variants of OCTN cation transporter genes are associated with Crohn diseaseVanya D Peltekova, Richard F Wintle, Laurence A Rubin, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Clinical actionability of genetic findings in cerebral palsySara A Lewis, Maya Chopra, Julie S Cohen, et al.
Arthritis and Rheumatism|June 30, 2005
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populationsMark van Oene, Richard F Wintle, Xiangdong Liu, et al.
JAMA Pediatrics|December 2, 2024
Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-AnalysisSara A Lewis, Maya Chopra, Julie S Cohen, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
The EMBO Journal|January 24, 2004
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegansSuparna Sanyal, Richard F Wintle, Katie S Kindt, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Pageof 4