Sharon R. Browning

发表

ASAFE: ancestry-specific allele frequency estimation

Qian S. Zhang, Brian L. Browning, Sharon R. Browning, 2016, Bioinform..

Faculty Opinions recommendation of High-throughput inference of pairwise coalescence times identifies signals of selection and enriched disease heritability.

Sharon R. Browning, 2020 .

A fast and simple method for detecting identity by descent segments in large-scale data

Ying Zhou, Brian L. Browning, Sharon R. Browning, 2019, bioRxiv.

IBDkin: fast estimation of kinship coefficients from identity by descent segments

Russell Schwartz, Ying Zhou, Brian L. Browning, 2020, Bioinform..

Efficient clustering of identity-by-descent between multiple individuals

Yu Qian, Brian L. Browning, Sharon R. Browning, 2014, Bioinform..

POPdemog: visualizing population demographic history from simulation scripts

Ying Zhou, Brian L. Browning, Sharon R. Browning, 2018, Bioinform..

A Multi-feature Reproducibility Assessment of Mass Spectral Data in Clinical Proteomic Studies

Sharon R. Browning, Martin Middleditch, Irene S. L. Zeng, 2009, Clinical Proteomics.

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

Brian L. Browning, Sharon R. Browning, B. Browning, 2020, bioRxiv.

Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

Bruce S. Weir, Sharon R. Browning, Cathy C. Laurie, 2013, G3: Genes, Genomes, Genetics.

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

Yun Li, Brian L. Browning, Sharon R. Browning, 2011, PloS one.

High-resolution detection of identity by descent in unrelated individuals.

Brian L. Browning, Sharon R. Browning, B. Browning, 2010, American journal of human genetics.

Missing data imputation and haplotype phase inference for genome-wide association studies

Sharon R. Browning, S. Browning, 2008, Human Genetics.

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

Sharon R. Browning, Patrick Danoy, Melanie Bahlo, 2010, PloS one.

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

Brian L. Browning, Sharon R. Browning, B. Browning, 2013, Human Genetics.

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Deborah L. Levy, Gregory M. Cooper, Brian L. Browning, 2010, Nature Genetics.

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

Sharon R. Browning, Elizabeth A. Thompson, E. Thompson, 2012, Genetics.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Brian E. Cade, Zachary A. Szpiech, Shannon Kelly, 2019, Nature.

Case‐control single‐marker and haplotypic association analysis of pedigree data

Sharon R. Browning, Gyan Chandra, Andrew J. Karter, 2005, Genetic epidemiology.

A one penny imputed genome from next generation reference panels

Brian L. Browning, Sharon R. Browning, B. Browning, 2018, bioRxiv.

Population-specific recombination maps from segments of identity by descent

Brian L. Browning, Sharon R. Browning, B. Browning, 2019, bioRxiv.

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

Pablo Moscato, Rodney J. Scott, Brian L. Browning, 2009, Nature Genetics.