Stephan J. Sanders

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Bernie DevlinUniversity of Pittsburgh School of MedicineGeverifieerd e-mailadres voor upmc.edu
Matthew StateucsfGeverifieerd e-mailadres voor ucsf.edu
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteGeverifieerd e-mailadres voor atgu.mgh.harvard.edu
Kathryn RoederProfessor of Statistics, Carnegie Mellon UniversityGeverifieerd e-mailadres voor andrew.cmu.edu
Joseph D BuxbaumIcahn School of Medicine at Mount Sinai, New York, NYGeverifieerd e-mailadres voor mssm.edu
Elise RobinsonAssistant Professor of Psychiatry, Massachusetts General Hospital and Harvard Medical SchoolGeverifieerd e-mailadres voor broadinstitute.org
Somer BishopUniversity of California San FranciscoGeverifieerd e-mailadres voor ucsf.edu
Dan GeschwindDistinguished Professor of Neurology, Psychiatry and Human Genetics, UCLAGeverifieerd e-mailadres voor mednet.ucla.edu
Nenad SestanYale UniversityGeverifieerd e-mailadres voor yale.edu
Kevin J. BenderCenter for Integrative Neuroscience, Dept. of Neurology, UCSFGeverifieerd e-mailadres voor ucsf.edu
Daniel Moreno De Luca, MD MScCASA Research Chair, Associate Professor, University of AlbertaGeverifieerd e-mailadres voor ualberta.ca
Jack A. KosmickiRegeneron Genetics CenterGeverifieerd e-mailadres voor fas.harvard.edu
Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalGeverifieerd e-mailadres voor geisinger.edu
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité - Universitätsmedizin BerlinGeverifieerd e-mailadres voor charite.de
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical SchoolGeverifieerd e-mailadres voor broadinstitute.org
John ConstantinoChildren's Healthcare of AtlantaGeverifieerd e-mailadres voor choa.org
James S SutcliffeAssociate Professor, Vanderbilt UniversityGeverifieerd e-mailadres voor vanderbilt.edu
Kaitlin E. SamochaMassachusetts General HospitalGeverifieerd e-mailadres voor partners.org
Sven SandinBiostatistician. Epidemiology. Dpt Medical Epidemiology and Biostatistics, Karolinska InstitutetGeverifieerd e-mailadres voor ki.se
Timothy W. YuHarvard Medical School and Boston Children's HospitalGeverifieerd e-mailadres voor childrens.harvard.edu

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Stephan J. Sanders

Professor, Oxford and UCSF

Geverifieerd e-mailadres voor ucsf.edu - Homepage

Genetics Genomics Exome/WGS mutations autism


Titel Sorteren op citaties Sorteren op jaar Sorteren op titel	Geciteerd door Geciteerd door	Jaar
Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ... Nature 515 (7526), 209-215, 2014	2971	2014
The contribution of de novo coding mutations to autism spectrum disorder I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ... Nature 515 (7526), 216-221, 2014	2761	2014
De novo mutations revealed by whole-exome sequencing are strongly associated with autism SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ... Nature 485 (7397), 237-241, 2012	2449	2012
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	2421	2013
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ... Cell 180 (3), 568-584. e23, 2020	2023	2020
Predicting splicing from primary sequence with deep learning K Jaganathan, SK Panagiotopoulou, JF McRae, SF Darbandi, D Knowles, ... Cell 176 (3), 535-548. e24, 2019	2015	2019
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
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ... Neuron 70 (5), 863-885, 2011	1535	2011
Most genetic risk for autism resides with common variation T Gaugler, L Klei, SJ Sanders, CA Bodea, AP Goldberg, AB Lee, ... Nature genetics 46 (8), 881-885, 2014	1446	2014
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ... Cell 179 (7), 1469-1482. e11, 2019	1195	2019
A framework for the interpretation of de novo mutation in human disease KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ... Nature genetics 46 (9), 944-950, 2014	1141	2014
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism AJ Willsey, SJ Sanders, M Li, S Dong, AT Tebbenkamp, RA Muhle, ... Cell 155 (5), 997-1007, 2013	1021	2013
De novo mutations in histone-modifying genes in congenital heart disease S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ... Nature 498 (7453), 220-223, 2013	1008	2013
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ... Science 350 (6265), 1262-1266, 2015	842	2015
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ... Nature genetics 49 (11), 1593-1601, 2017	822	2017
Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority AK Halladay, S Bishop, JN Constantino, AM Daniels, K Koenig, K Palmer, ... Molecular autism 6, 1-5, 2015	758	2015
Integrative functional genomic analysis of human brain development and neuropsychiatric risks M Li, G Santpere, Y Imamura Kawasawa, OV Evgrafov, FO Gulden, ... Science 362 (6420), eaat7615, 2018	726	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	625	2015
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations K Bilgüvar, AK Öztürk, A Louvi, KY Kwan, M Choi, B Tatlı, D Yalnızoğlu, ... Nature 467 (7312), 207-210, 2010	619	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	542	2017

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