Theo dõi
Gholson Lyon
Gholson Lyon
Institute for Basic Research in Developmental Disabilities
Email được xác minh tại opwdd.ny.gov - Trang chủ
Tiêu đề
Trích dẫn bởi
Trích dẫn bởi
Năm
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
15572018
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
7372015
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
6512017
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
5602013
Peptide signaling in Staphylococcus aureus and other Gram-positive bacteria
GJ Lyon, RP Novick
Peptides 25 (9), 1389-1403, 2004
4922004
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
4322011
The human phenotype ontology in 2017
S Kohler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Ayme, ...
3752017
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
3742000
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
3632000
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
3422019
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
3302011
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
3022011
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
2931998
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
2922016
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
2692002
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
2422014
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
2372013
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
2072014
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
2002017
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
1922017
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