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Gholson Lyon
Gholson Lyon
Institute for Basic Research in Developmental Disabilities
在 opwdd.ny.gov 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13752018
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
6662015
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
6222017
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
5402013
Peptide signaling in Staphylococcus aureus and other Gram-positive bacteria
GJ Lyon, RP Novick
Peptides 25 (9), 1389-1403, 2004
4692004
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
4222011
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
3732000
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
3552000
The human phenotype ontology in 2017
S Kohler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Ayme, ...
3492017
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
3232011
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
2912011
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
2852016
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
2841998
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
2792019
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
2662002
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
2392014
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
2212013
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
1972014
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
1772017
Chemical signaling among bacteria and its inhibition
GJ Lyon, TW Muir
Chemistry & biology 10 (11), 1007-1021, 2003
1762003
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