Obserwuj
Francisco M. De La Vega
Francisco M. De La Vega
Stanford University School of Medicine
Zweryfikowany adres z stanford.edu - Strona główna
Tytuł
Cytowane przez
Cytowane przez
Rok
A global reference for human genetic variation
TGP Consortium
Nature 526, 68-74, 2015
16631*2015
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
89912010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
86092012
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
J Hampe, A Franke, P Rosenstiel, A Till, M Teuber, K Huse, M Albrecht, ...
Nature genetics 39 (2), 207-211, 2007
23912007
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
2081*2020
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
13212011
Organoid modeling of the tumor immune microenvironment
JT Neal, X Li, J Zhu, V Giangarra, CL Grzeskowiak, J Ju, IH Liu, SH Chiou, ...
Cell 175 (7), 1972-1988. e16, 2018
12772018
An Aboriginal Australian genome reveals separate human dispersals into Asia
M Rasmussen, X Guo, Y Wang, KE Lohmueller, S Rasmussen, ...
Science 334 (6052), 94-98, 2011
9112011
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
KJ McKernan, HE Peckham, GL Costa, SF McLaughlin, Y Fu, EF Tsung, ...
Genome research 19 (9), 1527-1541, 2009
8272009
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
8262010
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
7402011
Variation in genome-wide mutation rates within and between human families
Nature genetics 43 (7), 712-714, 2011
7032011
Neratinib after trastuzumab-based adjuvant therapy in HER2-positive breast cancer (ExteNET): 5-year analysis of a randomised, double-blind, placebo-controlled, phase 3 trial
M Martin, FA Holmes, B Ejlertsen, S Delaloge, B Moy, H Iwata, ...
The lancet oncology 18 (12), 1688-1700, 2017
7012017
Development of personalized tumor biomarkers using massively parallel sequencing
RJ Leary, I Kinde, F Diehl, K Schmidt, C Clouser, C Duncan, A Antipova, ...
Science translational medicine 2 (20), 20ra14-20ra14, 2010
6912010
Genomics for the world
CD Bustamante, FM De La Vega, EG Burchard
Nature 475 (7355), 163-165, 2011
6732011
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America
R Kosoy, R Nassir, C Tian, PA White, LM Butler, G Silva, R Kittles, ...
Human mutation 30 (1), 69-78, 2009
6142009
A high-density admixture map for disease gene discovery in African Americans
MW Smith, N Patterson, JA Lautenberger, AL Truelove, GJ McDonald, ...
The American Journal of Human Genetics 74 (5), 1001-1013, 2004
4862004
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
4692014
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
4272013
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
SM Waszak, PA Northcott, I Buchhalter, GW Robinson, C Sutter, ...
The Lancet Oncology 19 (6), 785-798, 2018
3972018
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