Multilocus analysis of GAW15 NARAC chromosome 18 case-control data

por Browning, Sharon R, Thomas, Jessica
Publicado 2007

Protocol for detecting introgressed archaic variants with SPrime

por Zhou, Ying, Browning, Sharon R.
Publicado 2021

Biobank-scale inference of multi-individual identity by descent and gene conversion

por Browning, Sharon R., Browning, Brian L.
Publicado 2023

A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

por Madsen, Bo Eskerod, Browning, Sharon R.
Publicado 2009

Detecting Rare Variant Associations by Identity-by-Descent Mapping in Case-Control Studies

por Browning, Sharon R., Thompson, Elizabeth A.
Publicado 2012

Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort

por Browning, Sharon R., Browning, Brian L.
Publicado 2012

Improving the Accuracy and Efficiency of Identity-by-Descent Detection in Population Data

por Browning, Brian L., Browning, Sharon R.
Publicado 2013

Erratum to: Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort

por Browning, Sharon R., Browning, Brian L.
Publicado 2013

Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection

por Browning, Sharon R., Browning, Brian L.
Publicado 2020

Identity-by-descent-based estimation of the X chromosome effective population size with application to sex-specific demographic history

por Cai, Ruoyi, Browning, Brian L, Browning, Sharon R
Publicado 2023

AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos

por Granot-Hershkovitz, Einat, Sun, Quan, Argos, Maria, Zhou, Hufeng, Lin, Xihong, Browning, Sharon R., Sofer, Tamar
Publicado 2022

Ancestry-specific recent effective population size in the Americas

por Browning, Sharon R., Browning, Brian L., Daviglus, Martha L., Durazo-Arvizu, Ramon A., Schneiderman, Neil, Kaplan, Robert C., Laurie, Cathy C.
Publicado 2018

Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

por Nelson, Sarah C., Doheny, Kimberly F., Pugh, Elizabeth W., Romm, Jane M., Ling, Hua, Laurie, Cecelia A., Browning, Sharon R., Weir, Bruce S., Laurie, Cathy C.
Publicado 2013

Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

por Browning, Sharon R., Grinde, Kelsey, Plantinga, Anna, Gogarten, Stephanie M., Stilp, Adrienne M., Kaplan, Robert C., Avilés-Santa, M. Larissa, Browning, Brian L., Laurie, Cathy C.
Publicado 2016

Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes

por Li, Li, Li, Yun, Browning, Sharon R., Browning, Brian L., Slater, Andrew J., Kong, Xiangyang, Aponte, Jennifer L., Mooser, Vincent E., Chissoe, Stephanie L., Whittaker, John C., Nelson, Matthew R., Ehm, Margaret Gelder
Publicado 2011

Admixture mapping in the Hispanic Community Health Study/Study of Latinos reveals regions of genetic associations with blood pressure traits

por Sofer, Tamar, Baier, Leslie J., Browning, Sharon R., Thornton, Timothy A., Talavera, Gregory A., Wassertheil-Smoller, Sylvia, Daviglus, Martha L., Hanson, Robert, Kobes, Sayuko, Cooper, Richard S., Cai, Jianwen, Levy, Daniel, Reiner, Alex P., Franceschini, Nora
Publicado 2017

Ancestry-driven metabolite variation provides insights into disease states in admixed populations

por Reynolds, Kaylia M., Horimoto, Andrea R. V. R., Lin, Bridget M., Zhang, Ying, Kurniansyah, Nuzulul, Yu, Bing, Boerwinkle, Eric, Qi, Qibin, Kaplan, Robert, Daviglus, Martha, Hou, Lifang, Zhou, Laura Y., Cai, Jianwen, Shaikh, Saame Raza, Sofer, Tamar, Browning, Sharon R., Franceschini, Nora
Publicado 2023

Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations

por Horimoto, Andrea R.V.R., Boyken, Lisa A., Blue, Elizabeth E., Grinde, Kelsey E., Nafikov, Rafael A., Sohi, Harkirat K., Nato, Alejandro Q., Bis, Joshua C., Brusco, Luis I., Morelli, Laura, Ramirez, Alfredo, Dalmasso, Maria Carolina, Temple, Seth, Satizabal, Claudia, Browning, Sharon R., Seshadri, Sudha, Wijsman, Ellen M., Thornton, Timothy A.
Publicado 2023

A Polymorphism in the HLA-DPB1 Gene Is Associated with Susceptibility to Multiple Sclerosis

por Field, Judith, Browning, Sharon R., Johnson, Laura J., Danoy, Patrick, Varney, Michael D., Tait, Brian D., Gandhi, Kaushal S., Charlesworth, Jac C., Heard, Robert N., Stewart, Graeme J., Kilpatrick, Trevor J., Foote, Simon J., Bahlo, Melanie, Butzkueven, Helmut, Wiley, James, Booth, David R., Taylor, Bruce V., Brown, Matthew A., Rubio, Justin P., Stankovich, Jim
Publicado 2010

Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fat

por Lehnert, Klaus, Ward, Hamish, Berry, Sarah D., Ankersmit-Udy, Alex, Burrett, Alayna, Beattie, Elizabeth M., Thomas, Natalie L., Harris, Bevin, Ford, Christine A., Browning, Sharon R., Rawson, Pisana, Verkerk, Gwyneth A., van der Does, Yvonne, Adams, Linda F., Davis, Stephen R., Jordan, T. William, MacGibbon, Alastair K. H., Spelman, Richard J., Snell, Russell G.
Publicado 2015