Daniele Merico

Cited by

	All	Since 2016
Citations	12009	9051
h-index	44	39
i10-index	68	64

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200920102011201220132014201520162017201820192020202141 124 290 366 397 623 925 1231 1518 1855 2010 2322 75

Co-authors

Scherer, Stephen W.The Hospital for Sick Children, Peter Gilgan Centre for Research and Learning (PGCRL), 686 Bay StVerified email at sickkids.ca
Christian MarshallThe Hospital for Sick ChildrenVerified email at sickkids.ca
Ruth IsserlinDonnelly Centre, University of TorontoVerified email at utoronto.ca
Ryan K.C. YuenScientist, Hospital for Sick ChildrenVerified email at sickkids.ca
Gary BaderProfessor of Molecular Genetics and Computer Science, The Donnelly Centre, University of TorontoVerified email at utoronto.ca
Brendan FreyFounder & CEO, Deep Genomics; Co-Founder, Vector Institute; Professor, University of TorontoVerified email at psi.toronto.edu
Anath C. LionelDepartment of Medicine, University of TorontoVerified email at mail.utoronto.ca
Andrew EmiliBoston University (formerly University of Toronto)Verified email at bu.edu
Babak AlipanahiGoogle AI, GenomicsVerified email at google.com
Benjamin J. BlencoweProfessor, University of TorontoVerified email at utoronto.ca
Roberto MantovaniDipartimento di Bioscienze, Università degli Studi di MilanoVerified email at unimi.it
Hui Yuan XiongRenaissance TechnologiesVerified email at psi.toronto.edu
Sergio PereiraThe Hospital for Sick ChildrenVerified email at utoronto.ca
Jeffrey Robert MacDonaldThe Hospital for Sick ChildrenVerified email at sickkids.ca
Pingzhao HuAssistant Professor, Univ. of Manitoba; Assistant Professor (Status), Univ. of TorontoVerified email at umanitoba.ca
Marco AntoniottiAssociate Professor of Computer Science, Università degli Studi di Milano-BicoccaVerified email at unimib.it
Quaid MorrisComputational and Systems Biology Program, Memorial Sloan Kettering Cancer CenterVerified email at mskcc.org
Timothy R. HughesUniversity of TorontoVerified email at utoronto.ca
Hannes BretschneiderDonnelly Centre and Department of Molecular Genetics, University of TorontoVerified email at utoronto.ca
Leo J. LeeSenior Research Scientist, University of TorontoVerified email at psi.toronto.edu

Daniele Merico

Deep Genomics Inc.

Verified email at deepgenomics.com

human genetics genomics systems biology rare disorders oligonucleotide therapeutics


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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	1917	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	1288	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), 2015	896	2015
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	725	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	568	2015
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	470	2016
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	429	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	418	2017
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	400	2013
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder RKC Yuen, D Merico, M Bookman, JL Howe, B Thiruvahindrapuram, ... Nature neuroscience 20 (4), 602-611, 2017	392	2017
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	246	2015
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	243	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	238	2019
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	211	2016
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	199	2018
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	176	2015
Deep learning in biomedicine M Wainberg, D Merico, A Delong, BJ Frey Nature biotechnology 36 (9), 829-838, 2018	158	2018
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	150	2012
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	149	2016
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, ... PLoS genetics 8 (8), e1002843, 2012	147	2012

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