Michael A Eberle
Michael A Eberle
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A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium
CS Carlson, MA Eberle, MJ Rieder, Q Yi, L Kruglyak, DA Nickerson
The American Journal of Human Genetics 74 (1), 106-120, 2004
Mapping complex disease loci in whole-genome association studies
CS Carlson, MA Eberle, L Kruglyak, DA Nickerson
Nature 429 (6990), 446-452, 2004
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
Population history and natural selection shape patterns of genetic variation in 132 genes
JM Akey, MA Eberle, MJ Rieder, CS Carlson, MD Shriver, DA Nickerson, ...
PLoS Biol 2 (10), e286, 2004
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans
CS Carlson, MA Eberle, MJ Rieder, JD Smith, L Kruglyak, DA Nickerson
Nature genetics 33 (4), 518-521, 2003
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 1-9, 2014
Genomic regions exhibiting positive selection identified from dense genotype data
CS Carlson, DJ Thomas, MA Eberle, JE Swanson, RJ Livingston, ...
Genome research 15 (11), 1553-1565, 2005
Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations
DC Crawford, CS Carlson, MJ Rieder, DP Carrington, Q Yi, JD Smith, ...
The American Journal of Human Genetics 74 (4), 610-622, 2004
A new susceptibility locus for autosomal dominant pancreatic cancer maps to chromosome 4q32-34
MA Eberle, R Pfützer, KL Pogue-Geile, MP Bronner, D Crispin, ...
The American Journal of Human Genetics 70 (4), 1044-1048, 2002
Detection of long repeat expansions from PCR-free whole-genome sequence data
E Dolzhenko, JJFA van Vugt, RJ Shaw, MA Bekritsky, M van Blitterswijk, ...
Genome research 27 (11), 1895-1903, 2017
Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion
K Ardlie, SN Liu-Cordero, MA Eberle, M Daly, J Barrett, E Winchester, ...
The American Journal of Human Genetics 69 (3), 582-589, 2001
Power to detect risk alleles using genome-wide tag SNP panels
MA Eberle, PC Ng, K Kuhn, L Zhou, DA Peiffer, L Galver, ...
PLoS Genet 3 (10), e170, 2007
Whole-genome haplotyping by dilution, amplification, and sequencing
F Kaper, S Swamy, B Klotzle, S Munchel, J Cottrell, M Bibikova, ...
Proceedings of the National Academy of Sciences 110 (14), 5552-5557, 2013
Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome
MA Eberle, MJ Rieder, L Kruglyak, DA Nickerson
PLoS Genet 2 (9), e142, 2006
A numerical study of the interaction between the mantle wedge, subducting slab, and overriding plate
MA Eberle, O Grasset, C Sotin
Physics of the Earth and Planetary Interiors 134 (3-4), 191-202, 2002
Sequence variation and linkage disequilibrium in the human T-cell receptor β (TCRB) locus
L Subrahmanyan, MA Eberle, AG Clark, L Kruglyak, DA Nickerson
The American Journal of Human Genetics 69 (2), 381-395, 2001
An analysis of strategies for discovery of single‐nucleotide polymorphisms
MA Eberle, L Kruglyak
Genetic Epidemiology: The Official Publication of the International Genetic …, 2000
Bioinformatics-based identification of expanded repeats: a non-reference intronic pentamer expansion in RFC1 causes CANVAS
H Rafehi, DJ Szmulewicz, MF Bennett, NLM Sobreira, K Pope, KR Smith, ...
The American Journal of Human Genetics 105 (1), 151-165, 2019
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