List of works - Richard F Wintle

A genotype resource for postmortem brain samples from the Autism Tissue Program

scientific article

A high-resolution copy-number variation resource for clinical and population genetics

scientific article published on 11 December 2014

A large data resource of genomic copy number variation across neurodevelopmental disorders

scientific article published on 07 October 2019

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

scientific article

Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015

scientific article

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations

scientific article published in July 2005

Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting

scientific article

Clinically relevant copy number variations detected in cerebral palsy

scientific article

DLG5 variants contribute to Crohn disease risk in a Canadian population

article

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy

scientific article

Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans.

scientific article

FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project

scientific article

Functional variants of OCTN cation transporter genes are associated with Crohn disease

scientific article

Genetic Polymorphism and Recombination in the Subtelomeric Region of Chromosome 14q

scientific article published on 01 March 1997

Mapping of Human Immunoglobulin Heavy Chain Variable Gene Segments outside the Major IGH Locus

article

Molecular analysis redefines three human chromosome 14 deletions

article

SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population

article

Structural variants: changing the landscape of chromosomes and design of disease studies

scientific article

Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome

scientific article

List of works by Richard F Wintle

A genotype resource for postmortem brain samples from the Autism Tissue Program

A high-resolution copy-number variation resource for clinical and population genetics

A large data resource of genomic copy number variation across neurodevelopmental disorders

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations

Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting

Clinically relevant copy number variations detected in cerebral palsy

DLG5 variants contribute to Crohn disease risk in a Canadian population

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy

Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans.

FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project

Functional variants of OCTN cation transporter genes are associated with Crohn disease

Genetic Polymorphism and Recombination in the Subtelomeric Region of Chromosome 14q

Mapping of Human Immunoglobulin Heavy Chain Variable Gene Segments outside the Major IGH Locus

Molecular analysis redefines three human chromosome 14 deletions

SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population

Structural variants: changing the landscape of chromosomes and design of disease studies

Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome