Daniele Merico
Daniele Merico
Deep Genomics Inc.
Verified email at deepgenomics.com
TitleCited byYear
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
16502010
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
8692010
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
5752015
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
5102014
A copy number variation map of the human genome
M Zarrei, JR MacDonald, D Merico, SW Scherer
Nature reviews genetics 16 (3), 172, 2015
3752015
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
3152013
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
3112015
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
2982016
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
1852015
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
1812017
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
1572017
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
1552015
New p63 targets in keratinocytes identified by a genome‐wide approach
MA Vigan˛, J Lamartine, B Testoni, D Merico, D Alotto, C Castagnoli, ...
The EMBO journal 25 (21), 5105-5116, 2006
1372006
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
1242012
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
1222016
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
1212012
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
1162015
The histone-like NF-Y is a bifunctional transcription factor
M Ceribelli, D Dolfini, D Merico, R Gatta, AM Vigano, G Pavesi, ...
Molecular and cellular biology 28 (6), 2047-2058, 2008
1162008
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
1072014
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
992013
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