Scherer, Stephen W.

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Christian R. MarshallThe Hospital for Sick ChildrenDirección de correo verificada de sickkids.ca
Lars FeukProfessor, Uppsala UniversityDirección de correo verificada de igp.uu.se
Berge MinassianProfessor, Pediatrics, University of Toronto, Sr. Scientist, Genetics and Genome Biology, Sick KidsDirección de correo verificada de sickkids.ca
Anath C. LionelDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer CenterDirección de correo verificada de medportal.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenDirección de correo verificada de sickkids.ca
John VincentCentre for Addiction & Mental Health, Toronto, CanadaDirección de correo verificada de camh.ca
Dalila PintoAssociate Professor, Icahn School of Medicine at Mount Sinai, NYDirección de correo verificada de mssm.edu
Daniele MericoVevo Tx / TCAG (SickKids)Dirección de correo verificada de vevo.ai
Bridget FernandezProfessor of Clinical Pediatrics, Keck School of Medicine, University of Southern CaliforniaDirección de correo verificada de chla.usc.edu
Kazuhiko NakabayashiNational Research Institute for Child Health and DevelopmentDirección de correo verificada de ncchd.go.jp
Mohammed Uddin (Dafil)Associate Professor, MBRU, Dubai Health, UAE; Founder of GenomeArc Inc, Toronto, CanadaDirección de correo verificada de mbru.ac.ae
Brett TrostScientist, Molecular Medicine, The Hospital for Sick ChildrenDirección de correo verificada de sickkids.ca
Miriam ReuterThe Hospital for Sick ChildrenDirección de correo verificada de sickkids.ca
Brian H.Y. ChungThe University of Hong Kong, Department of Paediatrics & Adolescent MedicineDirección de correo verificada de hku.hk
Aparna PrasadInvitaeDirección de correo verificada de invitae.com
Danielle AndradeProfessor of Neurology, University of TorontoDirección de correo verificada de uhn.ca
Kristiina TammimiesCentre of Neurodevelopmental Disorders at Karolinska InstitutetDirección de correo verificada de ki.se
Worrawat EngchuanThe Centre for Applied Genomics, The Hospital for Sick ChildrenDirección de correo verificada de sickkids.ca
Andy Wing Chun PangPhDDirección de correo verificada de bionano.com
Kohji OkamuraNational Center for Child Health and DevelopmentDirección de correo verificada de ncchd.go.jp

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Scherer, Stephen W.

The Hospital for Sick Children, Genetics and Genome Biology Program, University of Toronto

Dirección de correo verificada de sickkids.ca - Página principal

ORCID: 0000-0002-8326-1999 Web of Science ResearcherID: B-3785-2013


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
Global variation in copy number in the human genome R Redon, S Ishikawa, KR Fitch, L Feuk, GH Perry, TD Andrews, H Fiegler, ... Nature 444 (7118), 444-454, 2006	5530	2006
An atlas of genetic correlations across human diseases and traits B Bulik-Sullivan, HK Finucane, V Anttila, A Gusev, FR Day, PR Loh, ... Nature genetics 47 (11), 1236-1241, 2015	4052	2015
Detection of large-scale variation in the human genome AJ Iafrate, L Feuk, MN Rivera, ML Listewnik, PK Donahoe, Y Qi, ... Nature Genetics 36 (9), 949-951, 2004	3613	2004
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies DT Miller, MP Adam, S Aradhya, LG Biesecker, AR Brothman, NP Carter, ... The American Journal of Human Genetics 86 (5), 749-764, 2010	3280	2010
Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ... Nature 515 (7526), 209-215, 2014	2974	2014
Structural variation in the human genome L Feuk, AR Carson, SW Scherer Nature Reviews Genetics 7 (2), 85-97, 2006	2824	2006
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. CDG the Psychiatric Genomics Nature Genetics 45 (9), 984-94, 2013	2437	2013
Functional impact of global rare copy number variation in autism spectrum disorders D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ... Nature 466 (7304), 368-372, 2010	2419	2010
The diploid genome sequence of an individual human S Levy, G Sutton, PC Ng, L Feuk, AL Halpern, BP Walenz, N Axelrod, ... PLoS Biology 5 (10), e254, 2007	2348	2007
Origins and functional impact of copy number variation in the human genome DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ... Nature 464 (7289), 704-712, 2010	2315	2010
Structural variation of chromosomes in autism spectrum disorder CR Marshall, A Noor, JB Vincent, AC Lionel, L Feuk, J Skaug, M Shago, ... The American Journal of Human Genetics 82 (2), 477-488, 2008	2224	2008
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency A Brooks-Wilson, M Marcil, SM Clee, LH Zhang, K Roomp, M Van Dam, ... Nature Genetics 22 (4), 336-345, 1999	2148	1999
Relative impact of nucleotide and copy number variation on gene expression phenotypes BE Stranger, MS Forrest, M Dunning, CE Ingle, C Beazley, N Thorne, ... Science 315 (5813), 848-853, 2007	2108	2007
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ... Cell, 2020	2063	2020
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal L Schmidt, FM Duhl, F Chen, T Kishidaz, G Glenn, P Choyke, SW Scherer, ... Nature Genetics 16, 68-73, 1997	1918	1997
Mapping autism risk loci using genetic linkage and chromosomal rearrangements P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ... Nature Genetics 39 (3), 319-328, 2007	1646*	2007
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1556	2018
The human splicing code reveals new insights into the genetic determinants of disease HY Xiong, B Alipanahi, LJ Lee, H Bretschneider, D Merico, RKC Yuen, ... Science 347 (6218), 1254806, 2015	1494	2015
The Database of Genomic Variants: a curated collection of structural variation in the human genome JR MacDonald, R Ziman, RKC Yuen, L Feuk, SW Scherer Nucleic acids research 42 (D1), D986-D992, 2014	1472	2014
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, SW Scherer, LC Tsui, ... Nature Genetics 14 (3), 357-360, 1996	1361	1996

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