Elaine Mardis
Elaine Mardis
Verifierad e-postadress på nationwidechildrens.org
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Initial sequencing and analysis of the human genome
ES Lander, LM Linton, B Birren, C Nusbaum, MC Zody, J Baldwin, ...
Macmillan Publishers Ltd., 2001
266502001
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), 1027-1031, 2006
100572006
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
80202009
Initial sequencing and comparative analysis of the mouse genome
RH Waterston, L Pachter
Nature 420 (6915), 520-562, 2002
74392002
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
74252010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
69972012
Structure, function and diversity of the healthy human microbiome
C Huttenhower, D Gevers, R Knight, S Abubucker, JH Badger, ...
nature 486 (7402), 207, 2012
68052012
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
Cancer Genome Atlas Research Network
Nature 455 (7216), 1061, 2008
56412008
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
48942004
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
39942001
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
38142009
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
33782012
The somatic genomic landscape of glioblastoma
CW Brennan, RGW Verhaak, A McKenna, B Campos, H Noushmehr, ...
Cell 155 (2), 462-477, 2013
32832013
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
32291996
Next-generation DNA sequencing methods
ER Mardis
Annu. Rev. Genomics Hum. Genet. 9, 387-402, 2008
28402008
The impact of next-generation sequencing technology on genetics
ER Mardis
Trends in genetics 24 (3), 133-141, 2008
27352008
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
26832008
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
22882009
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
22482003
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
L Ding, TJ Ley, DE Larson, CA Miller, DC Koboldt, JS Welch, JK Ritchey, ...
Nature 481 (7382), 506-510, 2012
20182012
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Artiklar 1–20