Daniel Moreno De Luca, MD MSc

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Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalVerified email at geisinger.edu
David H. Ledbetter, PhD, FACMGProfessor, University of Florida College of Medicine-JacksonvilleVerified email at jax.ufl.edu
Stephan J. SandersProfessor, Oxford and UCSFVerified email at ucsf.edu
Bernie DevlinUniversity of Pittsburgh School of MedicineVerified email at upmc.edu
Dan GeschwindDistinguished Professor of Neurology, Psychiatry and Human Genetics, UCLAVerified email at mednet.ucla.edu
Dorothy GriceProfessor of Psychiatry, Icahn School of Medicine at Mount SinaiVerified email at mssm.edu
Pauline ChasteVerified email at ch-sainte-anne.fr
Matthew StateucsfVerified email at ucsf.edu
A Jeremy WillseyAssociate Director of Data Science, Calico Life SciencesVerified email at calicolabs.com
Jordan SmollerMassachusetts General HospitalVerified email at broadinstitute.org
John NurnbergerProfessor of Psychiatry, Indiana University School of MedicineVerified email at iupui.edu
Timothy W. YuHarvard Medical School and Boston Children's HospitalVerified email at childrens.harvard.edu
Eric FombonneProfessor of Psychiatry, Oregon Health & Science UniversityVerified email at ohsu.edu
Scott M. MyersNeurodevelopmental Pediatrician, Geisinger Autism & Developmental Medicine InstituteVerified email at geisinger.edu
Andres Moreno-De-Luca, MD, MBA, D...Neuroradiologist, Assistant Professor, Kingston Health Sciences Centre, Queen’s UniversityVerified email at queensu.ca
Naomi WrayUniversity of QueenslandVerified email at uq.edu.au
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteVerified email at atgu.mgh.harvard.edu
John R KelsoeUniversity of California San DiegoVerified email at ucsd.edu
Patrick F SullivanProfessor of Genetics, University of North Carolina; Professor, MEB, Karolinska InstitutetVerified email at med.unc.edu
Christopher A WalshBoston Children's HospitalVerified email at childrens.harvard.edu

Daniel Moreno De Luca, MD MSc

CASA Research Chair, Associate Professor, University of Alberta

Verified email at ualberta.ca - Homepage

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	3368*	2011
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	1453	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	1360	2018
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	759	2013
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	527	2015
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	502	2011
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	469	2017
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	466	2012
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	356	2010
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	347	2013
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	329	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	221	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	182	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	179	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	166	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	159	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	136	2015
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	105*	2007
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	102	2010
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	82	2013

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