Daniel Moreno De Luca, MD MSc

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	Wszystkie	Od 2020
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Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalZweryfikowany adres z geisinger.edu
Bernie DevlinUniversity of Pittsburgh School of MedicineZweryfikowany adres z upmc.edu
David H. Ledbetter, PhD, FACMGProfessor, Institute for Pediatric Rare Diseases, Florida State University College of MedicineZweryfikowany adres z med.fsu.edu
Stephan J. SandersProfessor, Oxford and UCSFZweryfikowany adres z ucsf.edu
Dan GeschwindDistinguished Professor of Neurology, Psychiatry and Human Genetics, UCLAZweryfikowany adres z mednet.ucla.edu
Dorothy GriceProfessor of Psychiatry, Icahn School of Medicine at Mount SinaiZweryfikowany adres z mssm.edu
Jordan SmollerMassachusetts General HospitalZweryfikowany adres z broadinstitute.org
Kenneth KendlerProfessor and Eminent Scholar, Virginia Commonwealth UniversityZweryfikowany adres z vcuhealth.org
Pauline ChasteZweryfikowany adres z ch-sainte-anne.fr
Matthew StateucsfZweryfikowany adres z ucsf.edu
John NurnbergerProfessor of Psychiatry, Indiana University School of MedicineZweryfikowany adres z iupui.edu
Naomi WrayUniversity of QueenslandZweryfikowany adres z uq.edu.au
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteZweryfikowany adres z atgu.mgh.harvard.edu
John R KelsoeUniversity of California San DiegoZweryfikowany adres z ucsd.edu
Patrick F SullivanProfessor of Genetics, University of North Carolina; Professor, MEB, Karolinska InstitutetZweryfikowany adres z med.unc.edu
Michael O'DonovanCardiff UniversityZweryfikowany adres z cardiff.ac.uk
A Jeremy WillseyAssociate Director of Data Science, Calico Life SciencesZweryfikowany adres z calicolabs.com
Timothy W. YuHarvard Medical School and Boston Children's HospitalZweryfikowany adres z childrens.harvard.edu
Eric FombonneProfessor of Psychiatry, OHSUZweryfikowany adres z ohsu.edu
Scott M. MyersProfessor, Geisinger Autism & Developmental Medicine Institute, Geisinger College of Health SciencesZweryfikowany adres z geisinger.edu

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Daniel Moreno De Luca, MD MSc

CASA Research Chair, Associate Professor, University of Alberta

Zweryfikowany adres z ualberta.ca - Strona główna

Autism Neurodevelopment Implementation Science Precision Medicine Genomics


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
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	3533*	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	2431	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	1577	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	1489	2018
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), 2018	706	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	549	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	518	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	384	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	379	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	194	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	152	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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