Author

Vishal T

National Heart, Lung, and Blood Institute, National Institutes of Health - Cited by 1,986 - Bioinformatics / Computational Biology

Biography

Vishal T is a Member of American Society for Microbiologist, Member of American Chemical Society, Association for the promotion of DNA fingerprinting and other DNA Technologies ADNAT a division of Centre for Cellular and Molecular Biology (CCMB) Hyderabad. Society for Biological Chemist, India â?? IISC, Bangalore. Currently he is working as Assistant Professor, Department of Biotechnology, AMITY University, Noida, UP, India.
Title
Cited by
Year
The MicroArray Quality Control (MAQC)-II study of common practices for the development and validation of microarray-based predictive models
Nature biotechnology 28 (8), 827-838, 2010201
805
2010
Whole genome sequencing defines the genetic heterogeneity of familial pancreatic cancer
NJ Roberts, AL Norris, GM Petersen, ML Bondy, R Brand, S Gallinger, ...Cancer discovery 6 (2), 166-175, 2016201
321
2016
Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology
IW Deveson, B Gong, K Lai, JS LoCoco, TA Richmond, J Schageman, ...Nature biotechnology 39 (9), 1115-1128, 2021202
105
2021
Exome sequencing of familial bipolar disorder
FS Goes, M Pirooznia, JS Parla, M Kramer, E Ghiban, S Mavruk, YC Chen, ...JAMA psychiatry 73 (6), 590-597, 2016201
105
2016
Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa
GAM Povoleri, E Nova-Lamperti, C Scottà, G Fanelli, YC Chen, PD Becker, ...Nature immunology 19 (12), 1403-1414, 2018201
85
2018
Network analysis and transcriptome profiling identify autophagic and mitochondrial dysfunctions in SARS-CoV-2 infection
K Singh, YC Chen, S Hassanzadeh, K Han, JT Judy, F Seifuddin, I Tunc, ...Frontiers in Genetics 12, 599261, 2021202
69
2021
Neuroanatomic, epigenetic and genetic differences in monozygotic twins discordant for attention deficit hyperactivity disorder
YC Chen, G Sudre, W Sharp, F Donovan, SC Chandrasekharappa, ...Molecular psychiatry 23 (3), 683-690, 2018201
56
2018
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing
W Xiao, L Ren, Z Chen, LT Fang, Y Zhao, J Lack, M Guan, B Zhu, ...Nature biotechnology 39 (9), 1141-1150, 2021202
47
2021
High density lipoprotein proteome is associated with cardiovascular risk factors and atherosclerosis burden as evaluated by coronary CT angiography
SM Gordon, JH Chung, MP Playford, AK Dey, D Sviridov, F Seifuddin, ...Atherosclerosis 278, 278-285, 2018201
47
2018
Significant associations between driver gene mutations and DNA methylation alterations across many cancer types
YC Chen, V Gotea, G Margolin, L ElnitskiPLoS computational biology 13 (11), e1005840, 2017201
39
2017
GOBU: toward an integration interface for biological objects
WD Lin, YC Chen, JM Ho, CD HsiaoJournal of information science and engineering 22 (1), 19-29, 2006200
37
2006
lncRNAKB, a knowledgebase of tissue-specific functional annotation and trait association of long noncoding RNA
F Seifuddin, K Singh, A Suresh, JT Judy, YC Chen, V Chaitankar, I Tunc, ...Scientific Data 7 (1), 326, 2020202
34
2020
Profile analysis of expressed sequence tags derived from the ovary of tilapia, Oreochromis mossambicus
SL Chu, CF Weng, CD Hsiao, PP Hwang, YC Chen, JM Ho, SJ LeeAquaculture 251 (2-4), 537-548, 2006200
29
2006
A hybrid likelihood model for sequence-based disease association studies
YC Chen, H Carter, J Parla, M Kramer, FS Goes, M Pirooznia, PP Zandi, ...PLoS genetics 9 (1), e1003224, 2013201
29
2013
A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency
W Jones, B Gong, N Novoradovskaya, D Li, R Kusko, TA Richmond, ...Genome biology 22 (1), 1-38, 212
20
2021
ZooDDD: a cross-species database for digital differential display analysis
YC Chen, CD Hsiao, WD Lin, CM Hu, PP Hwang, JM HoBioinformatics 22 (17), 2180-2182, 2006200
19
2006
Exonic DNA Sequencing of ERBB4 in Bipolar Disorder
FS Goes, M Rongione, YC Chen, R Karchin, E Elhaik, ...PLoS One 6 (5), e20242, 2011201
17
2011
Aberrant DNA methylation defines isoform usage in cancer, with functional implications
YC Chen, L ElnitskiPLoS Computational Biology (7), e1007095, 2019201
15
2019
A probabilistic model to predict clinical phenotypic traits from genome sequencing
YC Chen, C Douville, C Wang, N Niknafs, G Yeo, V Beleva-Guthrie, ...PLoS computational biology 10 (9), e1003825, 202
14
2014
Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions
B Gong, D Li, R Kusko, N Novoradovskaya, Y Zhang, S Wang, ...Genome biology 22, 1-23, 2021202
14
2021

Referred From: https://scholar.google.com/citations?user=gvFTMLUAAAAJ&hl=zh-TW

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Citations 1986
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