Scherer, Stephen W.

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Christian R. 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 Lymphoma and Myeloma, The University of Texas MD Anderson Cancer CenterVerified email at medportal.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenVerified email at sickkids.ca
John VincentCentre for Addiction & Mental Health, Toronto, CanadaVerified email at camh.ca
Dalila PintoAssociate Professor, Icahn School of Medicine at Mount Sinai, NYVerified email at mssm.edu
Daniele MericoVevo Tx / TCAG (SickKids)Verified email at vevo.ai
Bridget FernandezProfessor of Clinical Pediatrics, Keck School of Medicine, University of Southern CaliforniaVerified email at chla.usc.edu
Mehdi ZarreiQueens Hospital Center, New YorkVerified email at nychhc.org
Kazuhiko NakabayashiNational Research Institute for Child Health and DevelopmentVerified email at ncchd.go.jp
Mohammed Uddin (Dafil)Associate Professor, MBRU, Dubai Health, UAE; Scientist, GenomeArc Inc, TorontoVerified email at mbru.ac.ae
Brett TrostScientist, Molecular Medicine, The Hospital for Sick ChildrenVerified email at sickkids.ca
Miriam ReuterThe Hospital for Sick ChildrenVerified email at sickkids.ca
Brian H.Y. ChungThe University of Hong Kong, Department of Paediatrics & Adolescent MedicineVerified email at hku.hk
Aparna PrasadInvitaeVerified email at invitae.com
Danielle AndradeProfessor of Neurology, University of TorontoVerified email at uhn.ca
Kristiina TammimiesCentre of Neurodevelopmental Disorders at Karolinska InstitutetVerified email at ki.se
Worrawat EngchuanThe Centre for Applied Genomics, The Hospital for Sick ChildrenVerified email at sickkids.ca
Andy Wing Chun PangPhDVerified email at bionano.com

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	5506	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	3745	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	3615	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	3245	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	2874	2014
Structural variation in the human genome L Feuk, AR Carson, SW Scherer Nature Reviews Genetics 7 (2), 85-97, 2006	2790	2006
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. CDG the Psychiatric Genomics Nature Genetics 45 (9), 984-94, 2013	2403	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	2361	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	2337	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	2296	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	2192	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	2139	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	2094	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	1944	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	1932	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	1669*	2007
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	1470	2015
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1454	2018
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	1442	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	1362	1996

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