Daniele Merico

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Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoPotvrđena adresa e-pošte na sickkids.ca
Christian R. MarshallThe Hospital for Sick ChildrenPotvrđena adresa e-pošte na sickkids.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenPotvrđena adresa e-pošte na sickkids.ca
Ruth IsserlinDonnelly Centre, University of TorontoPotvrđena adresa e-pošte na utoronto.ca
Gary BaderProfessor of Molecular Genetics and Computer Science, The Donnelly Centre, University of TorontoPotvrđena adresa e-pošte na utoronto.ca
Brendan FreyFounder & CEO, Deep Genomics; Co-Founder, Vector Institute; Professor, University of TorontoPotvrđena adresa e-pošte na psi.toronto.edu
Anath C. LionelDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer CenterPotvrđena adresa e-pošte na medportal.ca
Chaim M Roifmanprofessor of Pediatrics and Immunology ,University of TorontoPotvrđena adresa e-pošte na sickkids.ca
Andrew EmiliBoston University (formerly University of Toronto)Potvrđena adresa e-pošte na bu.edu
Babak AlipanahiExai BioPotvrđena adresa e-pošte na exai.bio
Gregory CostainPhysician-Scientist, The Hospital for Sick Children & University of TorontoPotvrđena adresa e-pošte na sickkids.ca
Benjamin J. BlencoweProfessor, University of TorontoPotvrđena adresa e-pošte na utoronto.ca
Sergio PereiraThe Hospital for Sick ChildrenPotvrđena adresa e-pošte na utoronto.ca
Hui Yuan XiongRenaissance TechnologiesPotvrđena adresa e-pošte na psi.toronto.edu
Mona MeyerHospital for Sick Children, Toronto, CanadaPotvrđena adresa e-pošte na sickkids.ca
Michael KuceraUniversity of TorontoPotvrđena adresa e-pošte na utoronto.ca
Jeffrey Robert MacDonaldThe Hospital for Sick ChildrenPotvrđena adresa e-pošte na sickkids.ca
Andrew DelongAssistant Professor (former), Concordia UniversityPotvrđena adresa e-pošte na concordia.ca
maria alessandra viganouniversity of BaselPotvrđena adresa e-pošte na unibas.ch
john weiThe Hospital for Sick ChildrenPotvrđena adresa e-pošte na sickkids.ca

Prati

Daniele Merico

Vevo Tx / TCAG (SickKids)

Potvrđena adresa e-pošte na vevo.ai

human genetics genomics systems biology rare disorders drug discovery


Naslov Poredaj po navodima Poredaj po godini Poredaj po naslovu	Citirano Citirano	Godina
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	2255	2010
Enrichment map: a network-based method for gene-set enrichment visualization and interpretation D Merico, R Isserlin, O Stueker, A Emili, GD Bader PloS one 5 (11), e13984, 2010	2081	2010
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
Pathway enrichment analysis and visualization of omics data using g: Profiler, GSEA, Cytoscape and EnrichmentMap J Reimand, R Isserlin, V Voisin, M Kucera, C Tannus-Lopes, ... Nature protocols 14 (2), 482-517, 2019	1260	2019
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ... The American Journal of Human Genetics 94 (5), 677-694, 2014	1029	2014
A copy number variation map of the human genome M Zarrei, JR MacDonald, D Merico, SW Scherer Nature reviews genetics 16 (3), 172-183, 2015	888	2015
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects JS Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma ... Nature Genetics 49 (1), 27-35, 2017	846	2017
Immune checkpoint inhibition for hypermutant glioblastoma multiforme resulting from germline biallelic mismatch repair deficiency E Bouffet, V Larouche, BB Campbell, D Merico, R De Borja, M Aronson, ... Journal of clinical oncology 34 (19), 2206-2211, 2016	776	2016
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ... Nature neuroscience 20 (4), 602-611, 2017	727	2017
Whole-genome sequencing of quartet families with autism spectrum disorder RKC Yuen, B Thiruvahindrapuram, D Merico, S Walker, K Tammimies, ... Nature medicine 21 (2), 185-191, 2015	560	2015
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing Y Jiang, RKC Yuen, X Jin, M Wang, N Chen, X Wu, J Ju, J Mei, Y Shi, ... The American Journal of Human Genetics 93 (2), 249-263, 2013	519	2013
Deep learning in biomedicine M Wainberg, D Merico, A Delong, BJ Frey Nature biotechnology 36 (9), 829-838, 2018	482	2018
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test AC Lionel, G Costain, N Monfared, S Walker, MS Reuter, SM Hosseini, ... Genetics in Medicine 20 (4), 435-443, 2018	478	2018
Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder K Tammimies, CR Marshall, S Walker, G Kaur, B Thiruvahindrapuram, ... Jama 314 (9), 895-903, 2015	399	2015
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers A Shlien, BB Campbell, R De Borja, LB Alexandrov, D Merico, D Wedge, ... Nature genetics 47 (3), 257-262, 2015	353	2015
Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine DJ Stavropoulos, D Merico, R Jobling, S Bowdin, N Monfared, ... NPJ genomic medicine 1 (1), 1-9, 2016	348	2016
BRAF mutation and CDKN2A deletion define a clinically distinct subgroup of childhood secondary high-grade glioma M Mistry, N Zhukova, D Merico, P Rakopoulos, R Krishnatry, M Shago, ... Journal of clinical oncology 33 (9), 1015, 2015	283	2015
Genome-wide characteristics of de novo mutations in autism RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ... NPJ genomic medicine 1 (1), 1-10, 2016	226	2016
A discovery resource of rare copy number variations in individuals with autism spectrum disorder A Prasad, D Merico, B Thiruvahindrapuram, J Wei, AC Lionel, D Sato, ... G3: Genes\| Genomes\| Genetics 2 (12), 1665-1685, 2012	210	2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways CK Silversides, AC Lionel, G Costain, D Merico, O Migita, B Liu, T Yuen, ... Public Library of Science 8 (8), e1002843, 2012	191	2012

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