Elaine Mardis
Elaine Mardis
Verified email at nationwidechildrens.org
Title
Cited by
Cited by
Year
Initial sequencing and analysis of the human genome
ES Lander, LM Linton, B Birren, C Nusbaum, MC Zody, J Baldwin, ...
Macmillan Publishers Ltd., 2001
197392001
An obesity-associated gut microbiome with increased capacity for energy harvest
PJ Turnbaugh, RE Ley, MA Mahowald, V Magrini, ER Mardis, JI Gordon
nature 444 (7122), 1027, 2006
90792006
Finding the missing heritability of complex diseases
TA Manolio, FS Collins, NJ Cox, DB Goldstein, LA Hindorff, DJ Hunter, ...
Nature 461 (7265), 747-753, 2009
75532009
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
71462010
Initial sequencing and comparative analysis of the mouse genome
RH Waterston, K Lindblad-Toh, E Birney, J Rogers, JF Abril, P Agarwal, ...
Nature 420 (6915), 520-562, 2002
71462002
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
66232012
Structure, function and diversity of the healthy human microbiome
C Huttenhower, D Gevers, R Knight, S Abubucker, JH Badger, ...
nature 486 (7402), 207, 2012
59762012
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium
Nature 409, 860-921, 2001
57232001
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
Cancer Genome Atlas Research Network
Nature 455 (7216), 1061, 2008
52752008
EGF receptor gene mutations are common in lung cancers from “never smokers” and are associated with sensitivity of tumors to gefitinib and erlotinib
W Pao, V Miller, M Zakowski, J Doherty, K Politi, I Sarkaria, B Singh, ...
Proceedings of the National Academy of Sciences 101 (36), 13306-13311, 2004
47812004
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
R Sachidanandam, D Weissman, SC Schmidt, JM Kakol, LD Stein, ...
Nature 409 (6822), 928-934, 2001
38592001
Supervised risk predictor of breast cancer based on intrinsic subtypes
JS Parker, M Mullins, MCU Cheang, S Leung, D Voduc, T Vickery, ...
Journal of clinical oncology 27 (8), 1160, 2009
34282009
Serine phosphorylation of death agonist BAD in response to survival factor results in binding to 14-3-3 not BCL-XL
J Zha, H Harada, E Yang, J Jockel, SJ Korsmeyer
Cell 87 (4), 619-628, 1996
30401996
VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing
DC Koboldt, Q Zhang, DE Larson, D Shen, MD McLellan, L Lin, CA Miller, ...
Genome research 22 (3), 568-576, 2012
29092012
The somatic genomic landscape of glioblastoma
CW Brennan, RGW Verhaak, A McKenna, B Campos, H Noushmehr, ...
Cell 155 (2), 462-477, 2013
27972013
Next-generation DNA sequencing methods
ER Mardis
Annu. Rev. Genomics Hum. Genet. 9, 387-402, 2008
26942008
The impact of next-generation sequencing technology on genetics
ER Mardis
Trends in genetics 24 (3), 133-141, 2008
25802008
Somatic mutations affect key pathways in lung adenocarcinoma
L Ding, G Getz, DA Wheeler, ER Mardis, MD McLellan, K Cibulskis, ...
Nature 455 (7216), 1069-1075, 2008
25362008
Recurring mutations found by sequencing an acute myeloid leukemia genome
ER Mardis, L Ding, DJ Dooling, DE Larson, MD McLellan, K Chen, ...
New England Journal of Medicine 361 (11), 1058-1066, 2009
21692009
The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes
H Skaletsky, T Kuroda-Kawaguchi, PJ Minx, HS Cordum, LD Hillier, ...
Nature 423 (6942), 825-837, 2003
21652003
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Articles 1–20