Scherer, Stephen W.

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Christian MarshallThe Hospital for Sick ChildrenVerified email at sickkids.ca
Lars FeukProfessor, Uppsala UniversityVerified email at igp.uu.se
Berge MinassianProfessor, Pediatrics, University of Toronto, Sr. Scientist, Genetics and Genome Biology, Sick KidsVerified email at sickkids.ca
Anath C. LionelDepartment of Medicine, University of TorontoVerified email at mail.utoronto.ca
John VincentCentre for Addiction & Mental Health, Toronto, CanadaVerified email at camh.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenVerified email at sickkids.ca
Dalila PintoAssistant Professor, Icahn School of Medicine at Mount Sinai, NYVerified email at mssm.edu
Daniele MericoDeep Genomics Inc.Verified email at deepgenomics.com
Bridget FernandezProfessor of Clinical Pediatrics, Keck School of Medicine, University of Southern CaliforniaVerified email at chla.usc.edu
Kazuhiko NakabayashiNational Research Institute for Child Health and DevelopmentVerified email at ncchd.go.jp
Mohammed UddinAssociate Professor, MBRU, Dubai, UAE; Scientist, Cellular Intelligent Lab,GenomeArc Inc, TorontoVerified email at mbru.ac.ae
Brett TrostResearch Associate at The Centre for Applied Genomics, Hospital for Sick ChildrenVerified email at sickkids.ca
Aparna PrasadInvitaeVerified email at invitae.com
Brian H.Y. ChungThe University of Hong Kong, Department of Paediatrics & Adolescent MedicineVerified email at hku.hk
Danielle AndradeProfessor of Neurology, University of TorontoVerified email at uhn.ca
Kristiina TammimiesCentre of Neurodevelopmental Disorders at Karolinska InstitutetVerified email at ki.se
Andy Wing Chun PangPhDVerified email at bionanogenomics.com
Kohji OkamuraNational Center for Child Health and DevelopmentVerified email at ncchd.go.jp
Dorota A CrawfordProfessor of Kinesiology and Health Science, York UniversityVerified email at yorku.ca
Robert William DaviesDepartment of Statistics, University of OxfordVerified email at stats.ox.ac.uk

Scherer, Stephen W.

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

Verified email at sickkids.ca - Homepage

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


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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	5098	2006
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	3442	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	2665	2010
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	2500	2015
Structural variation in the human genome L Feuk, AR Carson, SW Scherer Nature Reviews Genetics 7 (2), 85-97, 2006	2490	2006
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	2231	2014
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	2187	2007
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	2137	2010
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. CDG the Psychiatric Genomics Nature Genetics 45 (9), 984-94, 2013	2110	2013
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	2097	2010
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	2045	1999
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	1973	2008
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	1964	2007
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	1815	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	1560*	2007
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	1299	1996
Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene. PA Marsden, HH Heng, SW Scherer, RJ Stewart, AV Hall, XM Shi, LC Tsui, ... Journal of Biological Chemistry 268 (23), 17478-17488, 1993	1252	1993
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	1171	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	1138	2014
MADR2 Maps to 18q21 and Encodes a TGFβ–Regulated MAD–Related Protein That Is Functionally Mutated in Colorectal Carcinoma K Eppert, SW Scherer, H Ozcelik, R Pirone, P Hoodless, H Kim, LC Tsui, ... Cell 86 (4), 543-552, 1996	1097	1996

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