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
John VincentCentre for Addiction & Mental Health, Toronto, CanadaVerified email at camh.ca
Dalila PintoAssistant Professor, Icahn School of Medicine at Mount Sinai, NYVerified email at mssm.edu
Ryan K.C. YuenScientist, Hospital for Sick ChildrenVerified email at sickkids.ca
Bridget FernandezProfessor of Clinical Pediatrics, Keck School of Medicine, University of Southern CaliforniaVerified email at chla.usc.edu
Daniele MericoDeep Genomics Inc.Verified email at deepgenomics.com
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
Aparna PrasadProgenityVerified email at progenity.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
Brett TrostPostdoctoral fellow at The Centre for Applied Genomics, Hospital for Sick ChildrenVerified email at sickkids.ca
Andy Wing Chun PangPhDVerified email at bionanogenomics.com
Kohji OkamuraNational Research Institute 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
Shin-ichi Horike金沢大学　学際科学実験センターVerified email at staff.kanazawa-u.ac.jp

Scherer, Stephen W.

The Hospital for Sick Children, Peter Gilgan Centre for Research and Learning (PGCRL), 686 Bay St

Verified email at sickkids.ca - Homepage

www.researcherid.com/rid/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	4799	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	3318	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	2347	2010
Structural variation in the human genome L Feuk, AR Carson, SW Scherer Nature Reviews Genetics 7 (2), 85-97, 2006	2285	2006
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	2031	2007
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	1981	1999
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	1957	2010
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	1952	2010
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	1855	2007
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, 2015	1831	2015
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	1806	2008
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. CDG the Psychiatric Genomics Nature Genetics 45 (9), 984-94, 2013	1787	2013
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	1779	2014
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	1687	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	1459	2007
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	1199	1993
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	1196	1996
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	1021	1996
Copy number variation: new insights in genome diversity JL Freeman, GH Perry, L Feuk, R Redon, SA McCarroll, DM Altshuler, ... Genome Research 16 (8), 949-961, 2006	959	2006
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	940	2015

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