Daniel Moreno De Luca, MD MSc

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Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalAdresse e-mail validée de geisinger.edu
Bernie DevlinUniversity of Pittsburgh School of MedicineAdresse e-mail validée de upmc.edu
David H. Ledbetter, PhD, FACMGProfessor, Institute for Pediatric Rare Diseases, Florida State University College of MedicineAdresse e-mail validée de med.fsu.edu
Stephan J. SandersProfessor, Oxford and UCSFAdresse e-mail validée de ucsf.edu
Dan GeschwindDistinguished Professor of Neurology, Psychiatry and Human Genetics, UCLAAdresse e-mail validée de mednet.ucla.edu
Dorothy GriceProfessor of Psychiatry, Icahn School of Medicine at Mount SinaiAdresse e-mail validée de mssm.edu
Jordan SmollerMassachusetts General HospitalAdresse e-mail validée de broadinstitute.org
Kenneth KendlerProfessor and Eminent Scholar, Virginia Commonwealth UniversityAdresse e-mail validée de vcuhealth.org
Pauline ChasteAdresse e-mail validée de ch-sainte-anne.fr
Matthew StateucsfAdresse e-mail validée de ucsf.edu
John NurnbergerProfessor of Psychiatry, Indiana University School of MedicineAdresse e-mail validée de iupui.edu
Naomi WrayUniversity of QueenslandAdresse e-mail validée de uq.edu.au
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteAdresse e-mail validée de atgu.mgh.harvard.edu
John R KelsoeUniversity of California San DiegoAdresse e-mail validée de ucsd.edu
Patrick F SullivanProfessor of Genetics, University of North Carolina; Professor, MEB, Karolinska InstitutetAdresse e-mail validée de med.unc.edu
Michael O'DonovanCardiff UniversityAdresse e-mail validée de cardiff.ac.uk
A Jeremy WillseyAssociate Director of Data Science, Calico Life SciencesAdresse e-mail validée de calicolabs.com
Timothy W. YuHarvard Medical School and Boston Children's HospitalAdresse e-mail validée de childrens.harvard.edu
Eric FombonneProfessor of Psychiatry, OHSUAdresse e-mail validée de ohsu.edu
Scott M. MyersProfessor, Geisinger Autism & Developmental Medicine Institute, Geisinger College of Health SciencesAdresse e-mail validée de geisinger.edu

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Daniel Moreno De Luca, MD MSc

CASA Research Chair, Associate Professor, University of Alberta

Adresse e-mail validée de ualberta.ca - Page d'accueil

Autism Neurodevelopment Implementation Science Precision Medicine Genomics


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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	3530*	2011
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013	2432	2013
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	1578	2015
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1485	2018
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), 2018	702	2018
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature neuroscience 18 (2), 199-209, 2015	547	2015
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), 362-376, 2017	522	2017
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	517	2011
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, 1-13, 2012	481	2012
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	383	2013
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	378	2010
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	361	2017
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	231	2015
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	193	2009
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	188	2013
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	181	2015
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	161	2015
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	151	2015
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	110	2010
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	108*	2007

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