Daniele Merico

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Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoAdresse e-mail validée de sickkids.ca
Christian R. MarshallThe Hospital for Sick ChildrenAdresse e-mail validée de sickkids.ca
Ryan K.C. YuenSenior Scientist, Hospital for Sick ChildrenAdresse e-mail validée de sickkids.ca
Gary BaderProfessor of Molecular Genetics and Computer Science, The Donnelly Centre, University of TorontoAdresse e-mail validée de utoronto.ca
Ruth IsserlinDonnelly Centre, University of TorontoAdresse e-mail validée de utoronto.ca
Brendan FreyFounder & CEO, Deep Genomics; Co-Founder, Vector Institute; Professor, University of TorontoAdresse e-mail validée de psi.toronto.edu
Chaim M Roifmanprofessor of Pediatrics and Immunology ,University of TorontoAdresse e-mail validée de sickkids.ca
Anath C. LionelDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer CenterAdresse e-mail validée de medportal.ca
Andrew EmiliKnight Cancer Institute - OHSUAdresse e-mail validée de ohsu.edu
Babak AlipanahiExai BioAdresse e-mail validée de exai.bio
Gregory CostainPhysician-Scientist, The Hospital for Sick Children & University of TorontoAdresse e-mail validée de sickkids.ca
Benjamin J. BlencoweProfessor, University of TorontoAdresse e-mail validée de utoronto.ca
Sergio PereiraThe Hospital for Sick ChildrenAdresse e-mail validée de utoronto.ca
Mona MeyerHospital for Sick Children, Toronto, CanadaAdresse e-mail validée de sickkids.ca
Michael KuceraUniversity of TorontoAdresse e-mail validée de utoronto.ca
Hui Yuan XiongRenaissance TechnologiesAdresse e-mail validée de psi.toronto.edu
Andrew DelongAssistant Professor (former), Concordia UniversityAdresse e-mail validée de concordia.ca
Jeffrey Robert MacDonaldThe Hospital for Sick ChildrenAdresse e-mail validée de sickkids.ca
Roberto MantovaniDipartimento di Bioscienze, Università degli Studi di MilanoAdresse e-mail validée de unimi.it
Michael WainbergProsserman Centre for Population Health Research, Lunenfeld-Tanenbaum Research Institute, TorontoAdresse e-mail validée de stanford.edu

Suivre

Daniele Merico

Vevo Tx / TCAG (SickKids)

Adresse e-mail validée de vevo.ai

human genetics genomics systems biology rare diseases drug discovery


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
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	2386	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	2323	2010
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	1674	2019
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	1491	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	1138	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	1010	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	1004	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	895	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	839	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	617	2015
Deep learning in biomedicine M Wainberg, D Merico, A Delong, BJ Frey Nature biotechnology 36 (9), 829-838, 2018	615	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	585	2018
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	559	2013
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	457	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	400	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	398	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), 1015-1022, 2015	314	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	246	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	223	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	201	2012

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