Matthew State

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Stephan J. SandersProfessor, Oxford and UCSFAdresse e-mail validée de ucsf.edu
Bernie DevlinUniversity of Pittsburgh School of MedicineAdresse e-mail validée de upmc.edu
A Jeremy WillseyAssociate Director of Data Science, Calico Life SciencesAdresse e-mail validée de calicolabs.com
Nenad SestanYale UniversityAdresse e-mail validée de yale.edu
Dan GeschwindDistinguished Professor of Neurology, Psychiatry and Human Genetics, UCLAAdresse e-mail validée de mednet.ucla.edu
Kathryn RoederProfessor of Statistics, Carnegie Mellon UniversityAdresse e-mail validée de andrew.cmu.edu
Christopher MasonWorldQuant Professor of Genomics, Physiology, & Biophysics, Weill Cornell MedicineAdresse e-mail validée de med.cornell.edu
James S SutcliffeAssociate Professor, Vanderbilt UniversityAdresse e-mail validée de vanderbilt.edu
Daniel Moreno De Luca, MD MScCASA Research Chair, Associate Professor, University of AlbertaAdresse e-mail validée de ualberta.ca
Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalAdresse e-mail validée de geisinger.edu
Fred R. VolkmarProfessor, Yale UniversityAdresse e-mail validée de yale.edu
Hongyu ZhaoYale UniversityAdresse e-mail validée de yale.edu
george m andersonYale universityAdresse e-mail validée de yale.edu
Christopher PittengerYale UniversityAdresse e-mail validée de yale.edu
Donald GilbertProfessor of Child Neurology, Cincinnati Children's Hospital Medical CenterAdresse e-mail validée de cchmc.org
Mladen Roko RašinAssociate professor, Rutgers UniversityAdresse e-mail validée de rwjms.rutgers.edu
John KrystalRobert L. McNeil, Jr., Professor of Translational Research, Chair of Psychiatry, Yale UniversityAdresse e-mail validée de yale.edu
Gamze TanrioverAkdeniz universitesi tip fakultesiAdresse e-mail validée de akdeniz.edu.tr
Kenneth Y. KwanMichigan Neuroscience Inst. (MNI) & Dept. of Human Genetics, Univ. of MichiganAdresse e-mail validée de umich.edu
Jia Nee FooLee Kong Chian School of Medicine, Nanyang Technological UniversityAdresse e-mail validée de aya.yale.edu

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Matthew State

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Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
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	2947	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	2762	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	2440	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	2432	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	2030	2020
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1674	2007
Autism spectrum disorder C Lord, TS Brugha, T Charman, J Cusack, G Dumas, T Frazier, EJH Jones, ... Nature reviews Disease primers 6 (1), 1-23, 2020	1672	2020
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
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	1529	2011
Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome JF Abelson, KY Kwan, BJ O'Roak, DY Baek, AA Stillman, TM Morgan, ... Science 310 (5746), 317-320, 2005	1248	2005
Common genetic variants on 5p14. 1 associate with autism spectrum disorders K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ... Nature 459 (7246), 528-533, 2009	1149	2009
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	1017	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	1003	2013
Rare independent mutations in renal salt handling genes contribute to blood pressure variation W Ji, JN Foo, BJ O'Roak, H Zhao, MG Larson, DB Simon, C Newton-Cheh, ... Nature genetics 40 (5), 592-599, 2008	971	2008
Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO VE Clark, EZ Erson-Omay, A Serin, J Yin, J Cotney, K Özduman, T Avşar, ... Science 339 (6123), 1077-1080, 2013	906	2013
Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder F Volkmar, M Siegel, M Woodbury-Smith, B King, J McCracken, M State Journal of the American Academy of Child & Adolescent Psychiatry 53 (2), 237-257, 2014	799	2014
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	724	2018
Functional and evolutionary insights into human brain development through global transcriptome analysis MB Johnson, YI Kawasawa, CE Mason, Ž Krsnik, G Coppola, ... Neuron 62 (4), 494-509, 2009	676	2009
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	629	2010
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders B Bakkaloglu, BJ O'Roak, A Louvi, AR Gupta, JF Abelson, TM Morgan, ... The American Journal of Human Genetics 82 (1), 165-173, 2008	626	2008

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