Daniel Moreno De Luca, MD MSc
Daniel Moreno De Luca, MD MSc
Department of Psychiatry and Human Behavior - Brown University
brown.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism
SJ Sanders, V Hus, R Luo, MT Murtha, D Moreno-De-Luca, SH Chu, ...
Neuron 70 (5), 863-885, 2011
2649*2011
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
17242013
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ...
Neuron 87 (6), 1215-1233, 2015
8372015
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
5862018
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
EB Kaminsky, V Kaul, J Paschall, DM Church, B Bunke, D Kunig, ...
Genetics in medicine 13 (9), 777-784, 2011
3942011
Common genetic variants, acting additively, are a major source of risk for autism
L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ...
Molecular autism 3 (1), 1-13, 2012
3592012
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
T Network, C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, ...
Nature neuroscience 18 (2), 199-209, 2015
2862015
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
D Moreno-De-Luca, JG Mulle, EB Kaminsky, SJ Sanders, SM Myers, ...
The American Journal of Human Genetics 87 (5), 618-630, 2010
2842010
Autism genetics: opportunities and challenges for clinical translation
JAS Vorstman, JR Parr, D Moreno-De-Luca, RJL Anney, JI Nurnberger Jr, ...
Nature Reviews Genetics 18 (6), 362, 2017
2262017
Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence
A Moreno-De-Luca, SM Myers, TD Challman, D Moreno-De-Luca, ...
The Lancet Neurology 12 (4), 406-414, 2013
2232013
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder
R Maier, G Moser, GB Chen, S Ripke, D Absher, I Agartz, H Akil, F Amin, ...
The American Journal of Human Genetics 96 (2), 283-294, 2015
1442015
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders
C Depienne, D Moreno-De-Luca, D Heron, D Bouteiller, A Gennetier, ...
Biological psychiatry 66 (4), 349-359, 2009
1412009
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
1322017
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
P Chaste, L Klei, SJ Sanders, V Hus, MT Murtha, JK Lowe, AJ Willsey, ...
Biological psychiatry 77 (9), 775-784, 2015
1282015
Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
D Moreno-De-Luca, SJ Sanders, AJ Willsey, JG Mulle, JK Lowe, ...
Molecular psychiatry 18 (10), 1090-1095, 2013
1252013
Loss of δ-catenin function in severe autism
TN Turner, K Sharma, EC Oh, YP Liu, RL Collins, MX Sosa, DR Auer, ...
Nature 520 (7545), 51-56, 2015
1222015
Impacto de las nuevas definiciones en la prevalencia del síndrome metabólico en una población adulta de Bucaramanga, Colombia
JB Pinzón, NC Serrano, LA Díaz, G Mantilla, HM Velasco, LX Martínez, ...
Biomédica 27 (2), 172-179, 2007
96*2007
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11. 2 deletions
A Moreno-De-Luca, DW Evans, KB Boomer, E Hanson, R Bernier, ...
JAMA psychiatry 72 (2), 119-126, 2015
952015
Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency
CW Carr, D Moreno-De-Luca, C Parker, HH Zimmerman, N Ledbetter, ...
European Journal of Human Genetics 18 (11), 1216-1220, 2010
812010
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait
P Chaste, L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ...
Biological psychiatry 74 (8), 576-584, 2013
722013
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20