บทความที่มีข้อกำหนดการเข้าถึงสาธารณะ - Daniele Mericoดูข้อมูลเพิ่มเติม
ไม่มีให้ใช้งานในทุกที่: 7
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
ข้อกำหนด: Canadian Institutes of Health Research, Genome Canada, Swedish Research …
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
ข้อกำหนด: Canadian Institutes of Health Research, Cancer Research UK, Wellcome Trust
The effects of RelB deficiency on lymphocyte development and function
N Sharfe, D Merico, A Karanxha, C Macdonald, H Dadi, B Ngan, ...
Journal of autoimmunity 65, 90-100, 2015
ข้อกำหนด: US National Institutes of Health, Genome Canada
Visualizing gene-set enrichment results using the Cytoscape plug-in enrichment map
D Merico, R Isserlin, GD Bader
Network Biology: Methods and Applications, 257-277, 2011
ข้อกำหนด: US National Institutes of Health
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes
M Woodbury-Smith, AD Paterson, B Thiruvahindrapduram, AC Lionel, ...
Human genetics 134, 191-201, 2015
ข้อกำหนด: US National Institutes of Health, Canadian Institutes of Health Research …
Preferential expression of IGHV and IGHD encoding antibodies with exceptionally long CDR3H and a rapid global shift in transcriptome characterizes development of bovine …
Y Pasman, D Merico, AK Kaushik
Developmental & Comparative Immunology 67, 495-507, 2017
ข้อกำหนด: Natural Sciences and Engineering Research Council of Canada
A regional burden of sequence-level variation in the 22q11. 2 region influences schizophrenia risk and educational attainment
EJ Breetvelt, KC Smit, J van Setten, D Merico, X Wang, I Vaartjes, ...
Biological Psychiatry 91 (8), 718-726, 2022
ข้อกำหนด: US National Institutes of Health
มีให้ใช้งานในบางที่: 71
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
ข้อกำหนด: US National Institutes of Health, Canadian Institutes of Health Research …
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
ข้อกำหนด: US National Institutes of Health, Genome Canada, Heart and Stroke Foundation …
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
ข้อกำหนด: US National Institutes of Health, Natural Sciences and Engineering Research …
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
ข้อกำหนด: US National Institutes of Health, Canadian Institutes of Health Research …
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
ข้อกำหนด: US National Institutes of Health, Canadian Institutes of Health Research …
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
ข้อกำหนด: US National Institutes of Health, UK Medical Research Council, National …
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
ข้อกำหนด: Canadian Institutes of Health Research, Genome Canada
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
ข้อกำหนด: Canadian Institutes of Health Research
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
ข้อกำหนด: US National Institutes of Health, Canadian Institutes of Health Research …
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
ข้อกำหนด: Canadian Institutes of Health Research, Genome Canada
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
ข้อกำหนด: US National Institutes of Health, Canadian Institutes of Health Research …
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
ข้อกำหนด: Canadian Institutes of Health Research, Genome Canada, Swedish Research …
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
ข้อกำหนด: Canadian Institutes of Health Research, Genome Canada
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