Richard F. Wintle - Concepedia

Author

Richard F. Wintle

Also Known As

Ibtessam R. Hussein, R.F. Wintle, Richard F Wintle, Richard F. Wintle, Richard Wintle, RichardF. Wintle, Richard F. Wintle, Robert Tomaszewski

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

University of Toronto Hospital for Sick Children SickKids Foundation Mount Sinai Hospital University of Alberta

About

Richard F. Wintle is an author at University of Toronto specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	1.8K
2	Public Health	3	3	107
3	Social Sciences	2	2	286
4	Natural Sciences	1	1	16
5	Biology	1	1	51

Richard F. Wintle

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Functional variants of OCTN cation transporter genes are associated with Crohn disease Vanya Peltekova, Richard F. Wintle, Laurence A. Rubin, Nature Genetics InflammationAutoimmune DiseaseMucosal ImmunologyGastrointestinal PharmacologyCrohn Disease	2004	839
Genomic architecture of autism from comprehensive whole-genome sequence annotation Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, Cell Functional GenomicsSyndromic AutismGeneticsGenomic ArchitectureAutism	2022	258
FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project Chandree L. Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, The American Journal of Human Genetics	2014	249
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans Suparna Sanyal, Richard F. Wintle, Katie S. Kindt, The EMBO Journal Synaptic PlasticityNeural MechanismMechanosensory ResponsesSensory NeuroscienceNeurobiological Mechanism	2004	246
A large data resource of genomic copy number variation across neurodevelopmental disorders Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, npj Genomic Medicine	2019	189
Clinically relevant copy number variations detected in cerebral palsy Maryam Oskoui, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Nature Communications	2015	143
A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn’s disease Xiangjun Gu, Richard F. Wintle, David W. Cescon, Gastroenterology InflammationDisease MechanismCrohn ’GeneticsPathogenesis	2005	139
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations Mark Van Oene, Richard F. Wintle, Xiangdong Liu, Arthritis & Rheumatism	2005	132
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy Mehdi Zarrei, Darcy Fehlings, Karizma Mawjee, Genetics in Medicine Neurological DisorderCopy-number VariationsGeneticsCorticobasal DegenerationGenetic Epidemiology	2017	91
A high-resolution copy-number variation resource for clinical and population genetics Mohammed Uddin, Bhooma Thiruvahindrapuram, Susan Walker, Genetics in Medicine	2014	88

Page 1