Gholson Lyon

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Kai WangChildren's Hospital of PhiladelphiaEmail verificata su email.chop.edu
Yiyang Wu M.D., Ph.D.Vanderbilt University Medical CenterEmail verificata su vumc.org
Tom W. MuirPrinceton UniversityEmail verificata su princeton.edu
Carol Anne MathewsUniversity of FloridaEmail verificata su ufl.edu
Jeremiah M. ScharfCenter for Genomic Medicine, Departments of Neurology & Psychiatry, MGHEmail verificata su broadinstitute.org
Han FangGenAI, MetaEmail verificata su fb.com
Marco GradosProfessor of Psychiatry & Behavioral Sciences, Johns Hopkins University School of MedicineEmail verificata su jhmi.edu
Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNEmail verificata su email.chop.edu
Matthew E. Hirschtritt, M.D., M.P.H.Clinical Fellow, Forensic Psychiatry; University of California, San FranciscoEmail verificata su ucsf.edu
Laura T Jiménez-BarrónCold Spring Harbor Laboratory, National Autonomous University of Mexico, Max Planck Institute ofEmail verificata su cshl.edu
Michael C. SchatzBloomberg Distinguished Professor, Johns Hopkins UniversityEmail verificata su cs.jhu.edu
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board ChairEmail verificata su utahresearch.org
Giuseppe NarzisiAssociate Director, Computational Biology, New York Genome CenterEmail verificata su nygenome.org
Barbara J. Coffey, MDProfessor of Psychiatry (Clinical), University of Miami Miller School of MedicineEmail verificata su miami.edu
Zhi WeiProf of Comp Sci and Statistics, NJIT; Adjunct Prof. at UPenn.Email verificata su njit.edu
Lifeng TianThe Children's Hospital of PhiladelphiaEmail verificata su email.chop.edu
Michael Wiglercold spring harbor laboratoryEmail verificata su cshl.edu
W. Evan JohnsonProfessor of MedicineEmail verificata su rutgers.edu
Paul BodilyAssistant Professor of Computer Science, Idaho State UniversityEmail verificata su isu.edu
Thomas ArnesenProfessor, Department of Biomedicine, University of BergenEmail verificata su uib.no

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Gholson Lyon

Institute for Basic Research in Developmental Disabilities

Email verificata su opwdd.ny.gov - Home page

Genomics Genetics Proteomics Neuropsychiatric illness amino-terminal acetylation


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1545	2018
Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome ME Hirschtritt, PC Lee, DL Pauls, Y Dion, MA Grados, C Illmann, RA King, ... JAMA psychiatry 72 (4), 325-333, 2015	729	2015
The human phenotype ontology in 2017 S Köhler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Aymé, ... Nucleic acids research 45 (D1), D865-D876, 2017	646	2017
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing J O'Rawe, T Jiang, G Sun, Y Wu, W Wang, J Hu, P Bodily, L Tian, ... Genome medicine 5, 1-18, 2013	560	2013
Peptide signaling in Staphylococcus aureus and other Gram-positive bacteria GJ Lyon, RP Novick Peptides 25 (9), 1389-1403, 2004	489	2004
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder J Elia, JT Glessner, K Wang, N Takahashi, CJ Shtir, D Hadley, ... Nature Genetics, 2011	430	2011
Exfoliatin-Producing Strains Define a Fourthagr Specificity Group in Staphylococcus aureus S Jarraud, GJ Lyon, AMS Figueiredo, L Gérard, F Vandenesch, J Etienne, ... Journal of bacteriology 182 (22), 6517-6522, 2000	374	2000
The human phenotype ontology in 2017 S Kohler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Ayme, ...	372	2017
Rational design of a global inhibitor of the virulence response in Staphylococcus aureus, based in part on localization of the site of inhibition to the receptor … GJ Lyon, P Mayville, TW Muir, RP Novick Proceedings of the National Academy of Sciences 97 (24), 13330-13335, 2000	362	2000
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ... American Journal of Psychiatry 176 (3), 217-227, 2019	338	2019
SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data Z Wei, W Wang, P Hu, GJ Lyon, H Hakonarson Nucleic acids research 39 (19), e132-e132, 2011	328	2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency AF Rope, K Wang, R Evjenth, J Xing, JJ Johnston, JJ Swensen, B Moore, ... The American Journal of Human Genetics, 2011	302	2011
Long-read sequencing and de novo assembly of a Chinese genome L Shi, Y Guo, C Dong, J Huddleston, H Yang, X Han, A Fu, Q Li, N Li, ... Nature communications 7 (1), 12065, 2016	292	2016
Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age‐onset cataract formation and disruption of the lens DT Gilmour, GJ Lyon, MBL Carlton, JR Sanes, JM Cunningham, ... The EMBO journal, 1998	292	1998
Key determinants of receptor activation in the agr autoinducing peptides of Staphylococcus aureus GJ Lyon, JS Wright, TW Muir, RP Novick Biochemistry 41 (31), 10095-10104, 2002	268	2002
Accurate de novo and transmitted indel detection in exome-capture data using microassembly G Narzisi, JA O'rawe, I Iossifov, H Fang, Y Lee, Z Wang, Y Wu, GJ Lyon, ... Nature methods 11 (10), 1033-1036, 2014	242	2014
Genome-wide association study of Tourette's syndrome JM Scharf, D Yu, CA Mathews, BM Neale, SE Stewart, JA Fagerness, ... Molecular psychiatry 18 (6), 721-728, 2013	234	2013
Reducing INDEL calling errors in whole genome and exome sequencing data H Fang, Y Wu, G Narzisi, JA ORawe, LTJ Barrón, J Rosenbaum, ... Genome medicine 6, 1-17, 2014	206	2014
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ... Neuron 94 (6), 1101-1111. e7, 2017	197	2017
De novo coding variants are strongly associated with Tourette disorder AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ... Neuron 94 (3), 486-499. e9, 2017	189	2017

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