Kelly A. Frazer
Kelly A. Frazer
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A haplotype map of the human genome
International HapMap Consortium
Nature 437 (7063), 1299, 2005
A second generation human haplotype map of over 3.1 million SNVs
KA Frazer, DG Ballinger, DR Cox, DA Hinds
Nature 449 (7164), 851-61, 2007
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
VISTA: computational tools for comparative genomics
KA Frazer, L Pachter, A Poliakov, EM Rubin, I Dubchak
Nucleic acids research 32 (suppl_2), W273-W279, 2004
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
N Patil, AJ Berno, DA Hinds, WA Barrett, JM Doshi, CR Hacker, ...
Science 294 (5547), 1719-1723, 2001
Whole-genome patterns of common DNA variation in three human populations
DA Hinds, LL Stuve, GB Nilsen, E Halperin, E Eskin, DG Ballinger, ...
Science 307 (5712), 1072-1079, 2005
PipMaker—a web server for aligning two genomic DNA sequences
S Schwartz, Z Zhang, KA Frazer, A Smit, C Riemer, J Bouck, R Gibbs, ...
Genome research 10 (4), 577-586, 2000
Human genetic variation and its contribution to complex traits
KA Frazer, SS Murray, NJ Schork, EJ Topol
Nature Reviews Genetics 10 (4), 241-251, 2009
VISTA: visualizing global DNA sequence alignments of arbitrary length
C Mayor, M Brudno, JR Schwartz, A Poliakov, EM Rubin, KA Frazer, ...
Bioinformatics 16 (11), 1046-1047, 2000
Identification of a coordinate regulator of interleukins 4, 13, and 5 by cross-species sequence comparisons
GG Loots, RM Locksley, CM Blankespoor, ZE Wang, W Miller, EM Rubin, ...
Science 288 (5463), 136-140, 2000
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana
RM Clark, G Schweikert, C Toomajian, S Ossowski, G Zeller, P Shinn, ...
science 317 (5836), 338-342, 2007
Common vs. rare allele hypotheses for complex diseases
NJ Schork, SS Murray, KA Frazer, EJ Topol
Current opinion in genetics & development 19 (3), 212-219, 2009
Evaluation of next generation sequencing platforms for population targeted sequencing studies
O Harismendy, PC Ng, RL Strausberg, X Wang, TB Stockwell, KY Beeson, ...
Genome biology 10 (3), R32, 2009
9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response
O Harismendy, D Notani, X Song, NG Rahim, B Tanasa, N Heintzman, ...
Nature 470 (7333), 264-268, 2011
Genomewide SNP variation reveals relationships among landraces and modern varieties of rice
KL McNally, KL Childs, R Bohnert, RM Davidson, K Zhao, VJ Ulat, ...
Proceedings of the National Academy of Sciences 106 (30), 12273-12278, 2009
High-resolution whole-genome association study of Parkinson disease
DM Maraganore, M De Andrade, TG Lesnick, KJ Strain, MJ Farrer, ...
The American Journal of Human Genetics 77 (5), 685-693, 2005
Microdroplet-based PCR enrichment for large-scale targeted sequencing
R Tewhey, JB Warner, M Nakano, B Libby, M Medkova, PH David, ...
Nature biotechnology 27 (11), 1025-1031, 2009
A sequence-based variation map of 8.27 million SNPs in inbred mouse strains
KA Frazer, E Eskin, HM Kang, MA Bogue, DA Hinds, EJ Beilharz, ...
Nature 448 (7157), 1050-1053, 2007
Implementing genomic medicine in the clinic: the future is here
TA Manolio, RL Chisholm, B Ozenberger, DM Roden, MS Williams, ...
Genetics in Medicine 15 (4), 258-267, 2013
Common deletions and SNPs are in linkage disequilibrium in the human genome
DA Hinds, AP Kloek, M Jen, X Chen, KA Frazer
Nature genetics 38 (1), 82-85, 2006
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