Devine Scott E.
Devine Scott E.
University of Maryland School of Medicine
Overená e-mailová adresa na:
Citované v
Citované v
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
Classical nuclear localization signals: definition, function, and interaction with importin α
A Lange, RE Mills, CJ Lange, M Stewart, SE Devine, AH Corbett
Journal of Biological Chemistry 282 (8), 5101-5105, 2007
An initial map of insertion and deletion (INDEL) variation in the human genome
RE Mills, CT Luttig, CE Larkins, A Beauchamp, C Tsui, WS Pittard, ...
Genome research 16 (9), 1182-1190, 2006
The SIR2 gene family, conserved from bacteria to humans, functions in silencing, cell cycle progression, and chromosome stability.
CB Brachmann, JM Sherman, SE Devine, EE Cameron, L Pillus, ...
Genes & development 9 (23), 2888-2902, 1995
Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1784, 2019
Natural mutagenesis of human genomes by endogenous retrotransposons
RC Iskow, MT McCabe, RE Mills, S Torene, WS Pittard, AF Neuwald, ...
Cell 141 (7), 1253-1261, 2010
Which transposable elements are active in the human genome?
RE Mills, EA Bennett, RC Iskow, SE Devine
Trends in genetics 23 (4), 183-191, 2007
Small insertions and deletions (INDELs) in human genomes
JM Mullaney, RE Mills, WS Pittard, SE Devine
Human molecular genetics 19 (R2), R131-R136, 2010
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
M Byrska-Bishop, US Evani, X Zhao, AO Basile, HJ Abel, AA Regier, ...
Cell 185 (18), 3426-3440. e19, 2022
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
P Ebert, PA Audano, Q Zhu, B Rodriguez-Martin, D Porubsky, MJ Bonder, ...
Science 372 (6537), eabf7117, 2021
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
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
Brain feminization requires active repression of masculinization via DNA methylation
BM Nugent, CL Wright, AC Shetty, GE Hodes, KM Lenz, A Mahurkar, ...
Nature neuroscience 18 (5), 690-697, 2015
The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology
EJ Gardner, VK Lam, DN Harris, NT Chuang, EC Scott, WS Pittard, ...
Genome research 27 (11), 1916-1929, 2017
Active Alu retrotransposons in the human genome
EA Bennett, H Keller, RE Mills, S Schmidt, JV Moran, O Weichenrieder, ...
Genome research 18 (12), 1875-1883, 2008
Natural genetic variation caused by small insertions and deletions in the human genome
RE Mills, WS Pittard, JM Mullaney, U Farooq, TH Creasy, AA Mahurkar, ...
Genome research 21 (6), 830-839, 2011
A hot L1 retrotransposon evades somatic repression and initiates human colorectal cancer
EC Scott, EJ Gardner, A Masood, NT Chuang, PM Vertino, SE Devine
Genome research 26 (6), 745-755, 2016
Integration of the yeast retrotransposon Ty1 is targeted to regions upstream of genes transcribed by RNA polymerase III.
SE Devine, JD Boeke
Genes & development 10 (5), 620-633, 1996
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Články 1–20