University of Toronto
PhD, Molecular and Medical Genetics

University of Toronto
BSc, Molecular Genetics & Molecular Biology

Molecular and clinical characterization of de novo and familial cases with
microduplication 3q29: guidelines for copy number variation case reporting.
Goobie S, Knijnenburg J, Fitzpatrick D, Sharkey F, Lionel A, Marshall C, Azam T, Shago M, Chong K,
Mendoza-Londono R, den Hollander N, Ruivenkamp C, Maher E, Tanke H, Szuhai K, Wintle R, Scherer S
Cytogenetic and genome research
Volume 123 Issue 1-4 pages 65-78 Year 2008

Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting.
Okamura K, Wintle R, Scherer S
Genome biology
Volume 9 Issue 11 pages R160 Year 2008

Structural variants: changing the landscape of chromosomes and design of disease studies.
Feuk L, Marshall C, Wintle R, Scherer S
Human molecular genetics
Volume 15 Spec No 1 pages R57-66 Year 2006

DLG5 variants contribute to Crohn disease risk in a Canadian population.
Newman W, Gu X, Wintle R, Liu X, van Oene M, Amos C, Siminovitch K
Human mutation
Volume 27 Issue 4 pages 353-8 Year 2006

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.
van Oene M, Wintle R, Liu X, Yazdanpanah M, Gu X, Newman B, Kwan A, Johnson B, Owen J, Greer W, Mosher D, Maksymowych W, Keystone E, Rubin L, Amos C, Siminovitch K
Arthritis and rheumatism
Volume 52 Issue 7 pages 1993-8 Year 2005

SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population.
Newman B, Wintle R, van Oene M, Yazdanpanah M, Owen J, Johnson B, Gu X, Amos
C, Keystone E, Rubin L, Siminovitch K
Arthritis and rheumatism
Volume 52 Issue 2 pages 425-9 Year 2005

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease.
Newman B, Gu X, Wintle R, Cescon D, Yazdanpanah M, Liu X, Peltekova V,
Van Oene M, Amos C, Siminovitch K
Gastroenterology
Volume 128 Issue 2 pages 260-9 Year 2005

Functional variants of OCTN cation transporter genes are associated with Crohn disease.
Peltekova V, Wintle R, Rubin L, Amos C, Huang Q, Gu X, Newman B, Van Oene M,
Cescon D, Greenberg G, Griffiths A, St George-Hyslop P, Siminovitch K
Nature genetics
Volume 36 Issue 5 pages 471-5 Year 2004

Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans.
Sanyal S, Wintle R, Kindt K, Nuttley W, Arvan R, Fitzmaurice P, Bigras E,
Merz D, Hébert T, van der Kooy D, Schafer W, Culotti J, Van Tol H
The EMBO journal
Volume 23 Issue 2 pages 473-82 Year 2004

Dopamine signaling in Caenorhabditis elegans-potential for parkinsonism research.
Volume 7 Issue 3 pages 177-183 Year 2001

Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q.
Wintle R, Nygaard T, Herbrick J, Kvaløy K, Cox D
Genomics
Volume 40 Issue 3 pages 409-14 Year 1997

Molecular analysis redefines three human chromosome 14 deletions.
Wintle R, Costa T, Haslam R, Teshima I, Cox D
Human genetics
Volume 95 Issue 5 pages 495-500 Year 1995

Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locus.
Wintle R, Cox D
Genomics
Volume 23 Issue 1 pages 151-7 Year 1994

In situ hybridization to human chromosome 1 of a cDNA probe for the gene encoding
the basement membrane heparan sulfate proteoglycan (HSPG).
Wintle R, Kisilevsky R, Noonan D, Duncan A
Cytogenetics and cell genetics
Volume 54 Issue 1-2 pages 60-1 Year 1990

Postdoctoral Fellowship 1998
MRC Canada (now CIHR) | University of Toronto