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Lista de obras de Richard F Wintle

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2019

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

artículo científico publicado en 2005

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

artículo científico publicado en 2016

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

artículo científico publicado en 2005

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

artículo científico publicado en 2008

Clinically relevant copy number variations detected in cerebral palsy

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans.

artículo científico publicado en 2004

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

artículo científico publicado en 2014

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

artículo científico publicado en 2004

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

artículo científico publicado en 2006

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

artículo científico publicado en 2015

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