Scherer, Stephen W.

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Christian R. MarshallThe Hospital for Sick ChildrenPotvrđena adresa e-pošte na sickkids.ca
Lars FeukProfessor, Uppsala UniversityPotvrđena adresa e-pošte na igp.uu.se
Berge MinassianProfessor, Pediatrics, University of Toronto, Sr. Scientist, Genetics and Genome Biology, Sick KidsPotvrđena adresa e-pošte na sickkids.ca
Anath C. LionelDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer CenterPotvrđena adresa e-pošte na medportal.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenPotvrđena adresa e-pošte na sickkids.ca
John VincentCentre for Addiction & Mental Health, Toronto, CanadaPotvrđena adresa e-pošte na camh.ca
Dalila PintoAssistant Professor, Icahn School of Medicine at Mount Sinai, NYPotvrđena adresa e-pošte na mssm.edu
Daniele MericoVevo Tx / TCAG (SickKids)Potvrđena adresa e-pošte na vevo.ai
Bridget FernandezProfessor of Clinical Pediatrics, Keck School of Medicine, University of Southern CaliforniaPotvrđena adresa e-pošte na chla.usc.edu
Kazuhiko NakabayashiNational Research Institute for Child Health and DevelopmentPotvrđena adresa e-pošte na ncchd.go.jp
Brian H.Y. ChungThe University of Hong Kong, Department of Paediatrics & Adolescent MedicinePotvrđena adresa e-pošte na hku.hk
Aparna PrasadInvitaePotvrđena adresa e-pošte na invitae.com
Danielle AndradeProfessor of Neurology, University of TorontoPotvrđena adresa e-pošte na uhn.ca
Kristiina TammimiesCentre of Neurodevelopmental Disorders at Karolinska InstitutetPotvrđena adresa e-pošte na ki.se
Andy Wing Chun PangPhDPotvrđena adresa e-pošte na bionanogenomics.com
Kohji OkamuraNational Center for Child Health and DevelopmentPotvrđena adresa e-pošte na ncchd.go.jp
Dorota A CrawfordProfessor of Kinesiology and Health Science, York UniversityPotvrđena adresa e-pošte na yorku.ca
Robert William DaviesDepartment of Statistics, University of OxfordPotvrđena adresa e-pošte na stats.ox.ac.uk
Shin-ichi Horike金沢大学　疾患モデル総合研究センターPotvrđena adresa e-pošte na staff.kanazawa-u.ac.jp
daisuke satoHokkaido UniversityPotvrđena adresa e-pošte na huhp.hokudai.ac.jp

Prati

Scherer, Stephen W.

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

Potvrđena adresa e-pošte na sickkids.ca - Početna stranica

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


Naslov Poredaj po navodima Poredaj po godini Poredaj po naslovu	Citirano Citirano	Godina
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	5315	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	3525	2004
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	3140	2015
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	2987	2010
Structural variation in the human genome L Feuk, AR Carson, SW Scherer Nature Reviews Genetics 7 (2), 85-97, 2006	2634	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	2592	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	2263	2007
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. CDG the Psychiatric Genomics Nature Genetics 45 (9), 984-94, 2013	2258	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	2252	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	2200	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	2094	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	2071	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	2024	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	1852	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	1615*	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	1515	2020
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	1334	2015
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	1323	1996
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	1300	2014
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	1292	1993

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