Lisa D Brooks
Overview
Explore the profile of Lisa D Brooks including associated specialties, affiliations and a list of published articles.
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15
Citations
24002
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Recent Articles
1.
Auton A, Brooks L, Durbin R, Garrison E, Kang H, Korbel J, et al.
Nature
. 2015 Oct;
526(7571):68-74.
PMID: 26432245
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations. Here...
2.
Rehm H, Berg J, Brooks L, Bustamante C, Evans J, Landrum M, et al.
N Engl J Med
. 2015 May;
372(23):2235-42.
PMID: 26014595
On autopsy, a patient is found to have hypertrophic cardiomyopathy. The patient’s family pursues genetic testing that shows a “likely pathogenic” variant for the condition on the basis of a...
3.
Colonna V, Ayub Q, Chen Y, Pagani L, Luisi P, Pybus M, et al.
Genome Biol
. 2014 Jul;
15(6):R88.
PMID: 24980144
Background: Population differentiation has proved to be effective for identifying loci under geographically localized positive selection, and has the potential to identify loci subject to balancing selection. We have previously...
4.
Ramos E, Din-Lovinescu C, Berg J, Brooks L, Duncanson A, Dunn M, et al.
Am J Med Genet C Semin Med Genet
. 2014 Mar;
166C(1):93-104.
PMID: 24634402
Genome-wide association studies, DNA sequencing studies, and other genomic studies are finding an increasing number of genetic variants associated with clinical phenotypes that may be useful in developing diagnostic, preventive,...
5.
Rodriguez L, Brooks L, Greenberg J, Green E
Science
. 2013 Jan;
339(6117):275-6.
PMID: 23329035
No abstract available.
6.
Abecasis G, Auton A, Brooks L, DePristo M, Durbin R, Handsaker R, et al.
Nature
. 2012 Nov;
491(7422):56-65.
PMID: 23128226
By characterizing the geographic and functional spectrum of human genetic variation, the 1000 Genomes Project aims to build a resource to help to understand the genetic contribution to disease. Here...
7.
Abecasis G, Altshuler D, Auton A, Brooks L, Durbin R, Gibbs R, et al.
Nature
. 2010 Oct;
467(7319):1061-73.
PMID: 20981092
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation as a foundation for investigating the relationship between genotype and phenotype. Here we present results...
8.
Peltonen L, Altshuler D, de Bakker P, Deloukas P, Gabriel S, Gwilliam R, et al.
Nature
. 2010 Sep;
467(7311):52-8.
PMID: 20811451
Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding requires genome-wide studies that fully examine less common alleles in...
9.
Manolio T, Brooks L, Collins F
J Clin Invest
. 2008 May;
118(5):1590-605.
PMID: 18451988
The International HapMap Project was designed to create a genome-wide database of patterns of human genetic variation, with the expectation that these patterns would be useful for genetic association studies...
10.
Sabeti P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, et al.
Nature
. 2007 Oct;
449(7164):913-8.
PMID: 17943131
With the advent of dense maps of human genetic variation, it is now possible to detect positive natural selection across the human genome. Here we report an analysis of over...