Researcher
Richard F. Wintle
Hospital for Sick Children
Statistics
21 papers found
All papers authored by Richard F. Wintle
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Albert E. Chudley,
Britt Drögemöller,
Abraham Fainsod ,
Stephen W. Scherer,
Ana Hanlon-Dearman,
Geoffrey G. Hicks
Download from doi.org
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Maya Chopra,
Julie S. Cohen,
Jennifer Bain,
Bhooma Aravamuthan,
Jason B. Carmel,
Michael C. Fahey,
Reeval Segel,
Richard F. Wintle ,
Michael Zech,
Halie May,
Nahla Haque,
Darcy Fehlings,
Siddharth Srivastava,
Michael C. Kruer
Clinical actionability of genetic findings in cerebral palsy
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,
Sylvia Lamoureux,
Ghausia Begum,
Nasna Nassir ,
Hosneara Akter ,
Darren D. O’Rielly,
Proton Rahman,
Richard F. Wintle ,
Stephen W. Scherer,
Mohammed Uddin
Mutational Landscape of Autism Spectrum Disorder Brain Tissue
Download from doi.org
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Edward J. Higginbotham ,
Jeffrey R. MacDonald ,
Brett Trost ,
Ada J. S. Chan,
Susan Walker,
Sylvia Lamoureux,
Tracy Heung,
Bahareh A. Mojarad,
Barbara Kellam,
Tara Paton,
Muhammad Faheem
and 45 other authors
A large data resource of genomic copy number variation across neurodevelopmental disorders
Download from www.nature.com
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Christian R. Marshall,
Ronald D. Cohn,
Rosanna Weksberg,
Dimitri J. Stavropoulos,
Darcy Fehlings,
Michael I. Shevell,
Stephen W. Scherer
Clinically relevant copy number variations detected in cerebral palsy
Download from www.nature.com
,
Adel M. Abuzenadah,
Muhammad Abu-Elmagd,
Stephen W. Scherer
Download from link.springer.com
,
Pingzhao Hu,
Sylvia Lamoureux,
John Wei ,
Jeffrey R. MacDonald ,
Giovanna Pellecchia ,
Chao Lu ,
Anath C. Lionel,
Matthew J. Gazzellone,
John R. McLaughlin ,
Catherine Brown,
Irene L. Andrulis
and 7 other authors
A high-resolution copy-number variation resource for clinical and population genetics
Download from www.nature.com
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Mark E. Samuels,
Bridget A. Fernandez,
Francois P. Bernier,
Michael Brudno,
Bartha Knoppers,
Janet Marcadier,
David Dyment,
Shelin Adam ,
Dennis E. Bulman,
Steve J. M. Jones,
Denise Avard,
Minh Thu Nguyen
and 8 other authors
FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project
Download from www.ncbi.nlm.nih.gov
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D. FitzPatrick,
F. H. Sharkey,
A. C. Lionel,
C. R. Marshall,
T. Azam,
M. Shago,
K. Chong,
R. Mendoza-Londono,
N. S. den Hollander,
C. Ruivenkamp,
E. Maher,
H. J. Tanke,
K. Szuhai
and 2 other authors
Download from www.karger.com
,
Mark van Oene,
Mehrdad Yazdanpanah,
Julie Owen,
Ben Johnson,
Xiangjun Gu,
Christopher I. Amos,
Edward Keystone,
Laurence A. Rubin,
Katherine A. Siminovitch,
WG Wintle RF van Oene M Yazdanpanah M Owen J Johnson B Gu X Amos CI Keystone E Rubin LA Siminovitch Ka Newman
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,
Xiangdong Liu,
Mehrdad Yazdanpanah,
Xiangjun Gu,
Bill Newman,
Albert Kwan,
Benjamin Johnson,
Julie Owen,
Wenda Greer,
Dianne Mosher,
Walter Maksymowych,
Ed Keystone,
Laurence A. Rubin
and 2 other authors
Download from www.researchgate.net
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Laurence A. Rubin,
Christopher I. Amos,
Qiqing Huang,
Xiangjun Gu,
Bill Newman,
Mark Van Oene,
David Cescon,
Gordon Greenberg,
Anne M. Griffiths,
Peter H. St George-Hyslop,
Katherine A. Siminovitch
Functional variants of OCTN cation transporter genes are associated with Crohn disease
Download from www.nature.com
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Katie S. Kindt,
William M. Nuttley,
Rokhand Arvan,
Paul Fitzmaurice,
Eve Bigras,
David C. Merz,
Terence E. Hébert,
Derek van der Kooy,
William R. Schafer,
Joseph G. Culotti,
Hubert H. M. Van Tol
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans
Download from emboj.embopress.org
,
Torbjoern G. Nygaard,
Jo-Anne S. Herbrick,
Kirsti Kvaløy,
Diane W. Cox
Genetic Polymorphism and Recombination in the Subtelomeric Region of Chromosome 14q
Download from doi.org
,
Teresa Costa,
RobertH A. Haslam,
IkukoE Teshima,
DianeW Cox
Molecular analysis redefines three human chromosome 14 deletions
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