Daniele Merico - Google Scholar Citations

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	All	Since 2014
Citations	8864	7491
h-index	37	35
i10-index	61	58

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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
Gary BaderProfessor of Molecular Genetics and Computer Science, The Donnelly Centre, University of TorontoVerified email at utoronto.ca
Ryan K.C. YuenScientist, Hospital for Sick ChildrenVerified email at sickkids.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
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 rentec.com
Pingzhao HuAssistant Professor, Univ. of Manitoba; Assistant Professor (Status), Univ. of TorontoVerified email at umanitoba.ca
Jeffrey Robert MacDonaldThe Hospital for Sick ChildrenVerified email at sickkids.ca
Mohammed UddinAssistant Professor, MBRU, Dubai, UAE; Associate Investigator, TCAG, SickKids, CanadaVerified email at mbru.ac.ae
Marco AntoniottiAssociate Professor of Computer Science, Università degli Studi di Milano-BicoccaVerified email at unimib.it
Kristiina TammimiesCentre of Neurodevelopmental Disorders at Karolinska InstitutetVerified email at ki.se
Giancarlo MauriProfessor of Computer Science - University of Milano-BicoccaVerified email at disco.unimib.it
Quaid MorrisProfessor, Donnelly Centre, University of TorontoVerified email at utoronto.ca
Timothy R. HughesUniversity of TorontoVerified email at utoronto.ca
Hannes BretschneiderDonnelly Centre and Department of Molecular Genetics, University of TorontoVerified email at utoronto.ca

Daniele Merico

Deep Genomics Inc.

Verified email at deepgenomics.com

human genetics genomics systems biology rare disorders oligonucleotide therapeutics


Title	Cited by	Year
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, 2010	1697	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	945	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	656	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	552	2014
A copy number variation map of the human genome M Zarrei, JR MacDonald, D Merico, SW Scherer Nature reviews genetics 16 (3), 172, 2015	423	2015
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, 2015	341	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	333	2013
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	330	2016
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	227	2017
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, 2017	224	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, 2015	199	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	175	2015
New p63 targets in keratinocytes identified by a genome‐wide approach MA Viganò, J Lamartine, B Testoni, D Merico, D Alotto, C Castagnoli, ... The EMBO journal 25 (21), 5105-5116, 2006	138	2006
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, 15012, 2016	136	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	132	2012
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	128	2015
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	126	2012
The histone-like NF-Y is a bifunctional transcription factor M Ceribelli, D Dolfini, D Merico, R Gatta, AM Viganò, G Pavesi, ... Molecular and cellular biology 28 (6), 2047-2058, 2008	119	2008
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder M Uddin, K Tammimies, G Pellecchia, B Alipanahi, P Hu, Z Wang, D Pinto, ... Nature genetics 46 (7), 742, 2014	115	2014
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures AC Lionel, AK Vaags, D Sato, MJ Gazzellone, EB Mitchell, HY Chen, ... Human molecular genetics 22 (10), 2055-2066, 2013	107	2013

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