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Ekta Khurana
Ekta Khurana
Weill Cornell Medical College, Yale University, University of Pennsylvania, Indian Institute of
Geverifieerd e-mailadres voor med.cornell.edu
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An Integrated Encyclopedia of DNA Elements in the Human Genome
J Khatun
Nature, 2012
13862*2012
A map of human genome variation from population scale sequencing
DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ...
Nature 467 (7319), 1061-1073, 2010
8733*2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82472012
The molecular taxonomy of primary prostate cancer
A Abeshouse, J Ahn, R Akbani, A Ally, S Amin, CD Andry, M Annala, ...
Cell 163 (4), 1011-1025, 2015
25882015
Comprehensive characterization of cancer driver genes and mutations
MH Bailey, C Tokheim, E Porta-Pardo, S Sengupta, D Bertrand, ...
Cell 173 (2), 371-385. e18, 2018
21462018
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
1671*2020
Architecture of the human regulatory network derived from ENCODE data
MB Gerstein, A Kundaje, M Hariharan, SG Landt, KK Yan, C Cheng, ...
Nature 489 (7414), 91-100, 2012
16442012
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
13622012
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
12742011
Integrative Analysis of the Caenorhabditis elegans Genome by the modENCODE Project
MB Gerstein, ZJ Lu, EL Van Nostrand, C Cheng, BI Arshinoff, T Liu, ...
Science 330 (6012), 1775-1787, 2010
10952010
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
7072011
Patterns of somatic structural variation in human cancer genomes
Y Li, ND Roberts, JA Wala, O Shapira, SE Schumacher, K Kumar, ...
Nature 578 (7793), 112-121, 2020
6962020
Role of non-coding sequence variants in cancer
E Khurana, Y Fu, D Chakravarty, F Demichelis, MA Rubin, M Gerstein
Nature Reviews Genetics 17 (2), 93-108, 2016
5192016
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
E Rheinbay, MM Nielsen, F Abascal, JA Wala, O Shapira, G Tiao, ...
Nature 578 (7793), 102-111, 2020
5032020
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
4582010
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
4352014
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
4232013
FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer
Y Fu, Z Liu, S Lou, J Bedford, XJ Mu, KY Yip, E Khurana, M Gerstein
Genome biology 15, 1-15, 2014
3622014
Computational analysis of membrane proteins: the largest class of drug targets
Y Arinaminpathy, E Khurana, DM Engelman, MB Gerstein
Drug discovery today 14 (23-24), 1130-1135, 2009
3162009
Interpretation of Genomic Variants Using a Unified Biological Network Approach
E Khurana, Y Fu, J Chen, M Gerstein
PLOS Computational Biology 9 (3), e1002886, 2013
1932013
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Artikelen 1–20