Daniele Merico

Alıntı yapanlar

	Hepsi	2020 yılından bugüne
Alıntılar	22498	12432
h-endeksi	56	42
i10-endeksi	90	76

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Genel erişim

Tümünü görüntüle

71 makale

7 makale

genel erişime açık olanlar

genel erişime açık olmayanlar

Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of Torontosickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Christian R. MarshallThe Hospital for Sick Childrensickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Ryan K.C. YuenSenior Scientist, Hospital for Sick Childrensickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Ruth IsserlinDonnelly Centre, University of Torontoutoronto.ca üzerinde doğrulanmış e-posta adresine sahip
Gary BaderProfessor of Molecular Genetics and Computer Science, The Donnelly Centre, University of Torontoutoronto.ca üzerinde doğrulanmış e-posta adresine sahip
Brendan FreyFounder & CEO, Deep Genomics; Co-Founder, Vector Institute; Professor, University of Torontopsi.toronto.edu üzerinde doğrulanmış e-posta adresine sahip
Chaim M Roifmanprofessor of Pediatrics and Immunology ,University of Torontosickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Anath C. LionelDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Centermedportal.ca üzerinde doğrulanmış e-posta adresine sahip
Andrew EmiliKnight Cancer Institute - OHSUohsu.edu üzerinde doğrulanmış e-posta adresine sahip
Babak AlipanahiExai Bioexai.bio üzerinde doğrulanmış e-posta adresine sahip
Gregory CostainPhysician-Scientist, The Hospital for Sick Children & University of Torontosickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Benjamin J. BlencoweProfessor, University of Torontoutoronto.ca üzerinde doğrulanmış e-posta adresine sahip
Mona MeyerHospital for Sick Children, Toronto, Canadasickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Michael KuceraUniversity of Torontoutoronto.ca üzerinde doğrulanmış e-posta adresine sahip
Hui Yuan XiongRenaissance Technologiespsi.toronto.edu üzerinde doğrulanmış e-posta adresine sahip
Andrew DelongAssistant Professor (former), Concordia Universityconcordia.ca üzerinde doğrulanmış e-posta adresine sahip
Jeffrey Robert MacDonaldThe Hospital for Sick Childrensickkids.ca üzerinde doğrulanmış e-posta adresine sahip
Sergio PereiraThe Hospital for Sick Childrenutoronto.ca üzerinde doğrulanmış e-posta adresine sahip
Roberto MantovaniDipartimento di Bioscienze, Università degli Studi di Milanounimi.it üzerinde doğrulanmış e-posta adresine sahip
Michael WainbergProsserman Centre for Population Health Research, Lunenfeld-Tanenbaum Research Institute, Torontostanford.edu üzerinde doğrulanmış e-posta adresine sahip

Takip et

Daniele Merico

Vevo Tx / TCAG (SickKids)

vevo.ai üzerinde doğrulanmış e-posta adresine sahip

human genetics genomics systems biology rare diseases drug discovery


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
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	2406	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	2340	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	1695	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	1485	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	1129	2014
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	1079	2017
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	1014	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	893	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	623	2015
Deep learning in biomedicine M Wainberg, D Merico, A Delong, BJ Frey Nature biotechnology 36 (9), 829-838, 2018	621	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	593	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	552	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	460	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	401	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	317	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	253	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
WordCloud: a Cytoscape plugin to create a visual semantic summary of networks L Oesper, D Merico, R Isserlin, GD Bader Source code for biology and medicine 6, 1-4, 2011	207	2011

Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.

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