Allele Frequency Matching Between SNPs Reveals an Excess of Linkage Disequilibrium in Genic Regions of the Human Genome

Por Eberle, Michael A, Rieder, Mark J, Kruglyak, Leonid, Nickerson, Deborah A
Publicado em 2006

Sequence Variation and Linkage Disequilibrium in the Human T-Cell Receptor β (TCRB) Locus

Por Subrahmanyan, Lakshman, Eberle, Michael A., Clark, Andrew G., Kruglyak, Leonid, Nickerson, Deborah A.
Publicado em 2001

Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium

Por Carlson, Christopher S., Eberle, Michael A., Rieder, Mark J., Yi, Qian, Kruglyak, Leonid, Nickerson, Deborah A.
Publicado em 2004

Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes

Por Akey, Joshua M, Eberle, Michael A, Rieder, Mark J, Carlson, Christopher S, Shriver, Mark D, Nickerson, Deborah A, Kruglyak, Leonid
Publicado em 2004

Lower-Than-Expected Linkage Disequilibrium between Tightly Linked Markers in Humans Suggests a Role for Gene Conversion

Por Ardlie, Kristin, Liu-Cordero, Shau Neen, Eberle, Michael A., Daly, Mark, Barrett, Jeff, Winchester, Ellen, Lander, Eric S., Kruglyak, Leonid
Publicado em 2001

Extensive and breed-specific linkage disequilibrium in Canis familiaris

Por Sutter, Nathan B., Eberle, Michael A., Parker, Heidi G., Pullar, Barbara J., Kirkness, Ewen F., Kruglyak, Leonid, Ostrander, Elaine A.
Publicado em 2004

Genomic regions exhibiting positive selection identified from dense genotype data

Por Carlson, Christopher S., Thomas, Daryl J., Eberle, Michael A., Swanson, Johanna E., Livingston, Robert J., Rieder, Mark J., Nickerson, Deborah A.
Publicado em 2005

Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations

Por Crawford, Dana C., Carlson, Christopher S., Rieder, Mark J., Carrington, Dana P., Yi, Qian, Smith, Joshua D., Eberle, Michael A., Kruglyak, Leonid, Nickerson, Deborah A.
Publicado em 2004

Whole-genome haplotyping by dilution, amplification, and sequencing

Por Kaper, Fiona, Swamy, Sajani, Klotzle, Brandy, Munchel, Sarah, Cottrell, Joseph, Bibikova, Marina, Chuang, Han-Yu, Kruglyak, Semyon, Ronaghi, Mostafa, Eberle, Michael A., Fan, Jian-Bing
Publicado em 2013

A New Susceptibility Locus for Autosomal Dominant Pancreatic Cancer Maps to Chromosome 4q32-34

Por Eberle, Michael A., Pfützer, Roland, Pogue-Geile, Kay L., Bronner, Mary P., Crispin, David, Kimmey, Michael B., Duerr, Richard H., Kruglyak, Leonid, Whitcomb, David C., Brentnall, Teresa A.
Publicado em 2002

Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels

Por Eberle, Michael A, Ng, Pauline C, Kuhn, Kenneth, Zhou, Lixin, Peiffer, Daniel A, Galver, Luana, Viaud-Martinez, Karine A, Lawley, Cynthia Taylor, Gunderson, Kevin L, Shen, Richard, Murray, Sarah S
Publicado em 2007

A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree

Por Eberle, Michael A., Fritzilas, Epameinondas, Krusche, Peter, Källberg, Morten, Moore, Benjamin L., Bekritsky, Mitchell A., Iqbal, Zamin, Chuang, Han-Yu, Humphray, Sean J., Halpern, Aaron L., Kruglyak, Semyon, Margulies, Elliott H., McVean, Gil, Bentley, David R.
Publicado no Genome Res (2017)

Improved Imputation of Common and Uncommon Single Nucleotide Polymorphisms (SNPs) with a New Reference Set

Por Wang, Zhaoming, Jacobs, Kevin B., Yeager, Meredith, Hutchinson, Amy, Sampson, Joshua, Chatterjee, Nilanjan, Albanes, Demetrius, Berndt, Sonja I., Chung, Charles C., Diver, W. Ryan, Gapstur, Susan M., Teras, Lauren R., Haiman, Christopher A., Henderson, Brian E., Stram, Daniel, Deng, Xiang, Hsing, Ann W., Virtamo, Jarmo, Eberle, Michael A., Stone, Jennifer L., Purdue, Mark P., Taylor, Phil, Tucker, Margaret, Chanock, Stephen J.
Publicado em 2011