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Ryan E. Mills
Ryan E. Mills
Associate Professor, University of Michigan Medical School
Verified email at umich.edu - Homepage
Title
Cited by
Cited by
Year
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
150432015
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87782010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82902012
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
23992015
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
14532007
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
13812012
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
12882011
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
8562006
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
7682019
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
7172011
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
6742010
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
5762007
CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome
PK Todd, SY Oh, A Krans, F He, C Sellier, M Frazer, AJ Renoux, K Chen, ...
Neuron 78 (3), 440-455, 2013
5072013
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
D Pinto, K Darvishi, X Shi, D Rajan, D Rigler, T Fitzgerald, AC Lionel, ...
Nature biotechnology 29 (6), 512-520, 2011
4822011
Small insertions and deletions (INDELs) in human genomes
JM Mullaney, RE Mills, WS Pittard, SE Devine
Human molecular genetics 19 (R2), R131-R136, 2010
4782010
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
4742022
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
4692021
Structural variation in the sequencing era
SS Ho, AE Urban, RE Mills
Nature Reviews Genetics 21 (3), 171-189, 2020
4492020
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
4452014
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
4202013
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