S. Browning

发表

A fast, powerful method for detecting identity by descent.

B. Browning, S. Browning, 2011, American journal of human genetics.

On reducing the statespace of hidden Markov models for the identity by descent process.

B. Browning, S. Browning, 2002, Theoretical population biology.

Haplotype phasing: existing methods and new developments

B. Browning, S. Browning, 2011, Nature Reviews Genetics.

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.

Kathleen F. Kerr, Stephanie A. Bien, Sarah C. Nelson, 2016, American journal of human genetics.

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

R. Kaplan, A. Stilp, C. Laurie, 2016, G3: Genes, Genomes, Genetics.

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering.

B. Browning, S. Browning, 2007, American journal of human genetics.

Efficient multilocus association testing for whole genome association studies using localized haplotype clustering

B. Browning, S. Browning, 2007, Genetic epidemiology.

Robust Inference of Identity by Descent from Exome-Sequencing Data.

Wenqing Fu, Brian L Browning, Sharon R Browning, 2016, American journal of human genetics.

Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent.

Brian L Browning, Sharon R Browning, B. Browning, 2015, American journal of human genetics.

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

B. Browning, S. Browning, 2013, Genetics.

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

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

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals.

B. Browning, S. Browning, 2009, American journal of human genetics.

Population Structure With Localized Haplotype Clusters

B. Weir, S. Browning, 2010, Genetics.

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

S. Browning, B. Madsen, B. E. Madsen, 2009, PLoS genetics.

Admixture Mapping Identifies an Amerindian Ancestry Locus Associated with Albuminuria in Hispanics in the United States.

D. Levy, S. Redline, T. Thornton, 2017, Journal of the American Society of Nephrology : JASN.

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.

Kathleen F. Kerr, Sarah C. Nelson, Caitlin P. McHugh, 2016, American journal of human genetics.

Ancestry-specific recent effective population size in the Americas

N. Schneiderman, C. Laurie, R. Kaplan, 2018, PLoS genetics.

De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population

Andrew D. Johnson, Ryan D. Hernandez, S. Redline, 2019, bioRxiv.

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

Andrew D. Johnson, Ryan D. Hernandez, S. Redline, 2020, Proceedings of the National Academy of Sciences.

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

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

A one penny imputed genome from next generation reference panels

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

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

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

Haplotypic analysis of Wellcome Trust Case Control Consortium data

B. Browning, S. Browning, 2008, Human Genetics.

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

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

Estimation of Pairwise Identity by Descent From Dense Genetic Marker Data in a Population Sample of Haplotypes

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

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

A. Reiner, D. Levy, R. Cooper, 2017, PloS one.

Population-Specific Recombination Maps from Segments of Identity by Descent.

B. Browning, S. Browning, Yingxiao Zhou, 2020, American journal of human genetics.

Population-specific recombination maps from segments of identity by descent

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

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.

Population structure can inflate SNP-based heritability estimates.

Brian L Browning, Sharon R Browning, B. Browning, 2011, American journal of human genetics.

Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture

J. Akey, B. Browning, S. Browning, 2018, Cell.

Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.

Qian S. Zhang, Kathleen F. Kerr, Henry J. Lin, 2017, Heart rhythm.

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

B. Browning, S. Browning, 2013, Human Genetics.

Admixture mapping screening of CKD traits and risk factors in U.S. Hispanic/Latino individuals from Central America country-of-origin

T. Thornton, S. Cole, N. Franceschini, 2022, medRxiv.

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

B. Browning, S. Browning, 2020, The American Journal of Human Genetics.

IBD-based estimation of X chromosome effective population size with application to sex-specific demographic history

B. Browning, S. Browning, Ruoyi Cai, 2022, bioRxiv.

Fast, accurate local ancestry inference with FLARE

B. Browning, S. Browning, R. Waples, 2022, bioRxiv.

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

R. Snell, S. Davis, S. Browning, 2015, Scientific Reports.

A canine model of inherited myopia: familial aggregation of refractive error in labrador retrievers.

S. Browning, J. Black, J. Phillips, 2008, Investigative ophthalmology & visual science.

Estimating the genome-wide mutation rate from thousands of unrelated individuals

S. Browning, Xiaowen Tian, Ruoyi Cai, 2022, bioRxiv.

Statistical phasing of 150,119 sequenced genomes in the UK Biobank

B. Browning, S. Browning, 2022, bioRxiv.

Pedigree data analysis with crossover interference.

S. Browning, 2003, Genetics.

A Monte Carlo approach to calculating probabilities for continuous identity by descent data

S. Browning, 2000, Journal of Applied Probability.

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

M. Brown, M. Bahlo, S. Browning, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos

Caitlin P. McHugh, A. Reiner, Yun Li, 2017, PLoS genetics.

Genotype Imputation with Millions of Reference Samples.

Brian L Browning, Sharon R Browning, B. Browning, 2016, American journal of human genetics.

Fast two-stage phasing of large-scale sequence data.

B. Browning, S. Browning, Xiaowen Tian, 2021, American journal of human genetics.

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.

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

B. Browning, S. Browning, 2012, 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.

Estimating the Genome-wide Mutation Rate with Three-Way Identity by Descent.

Brian L Browning, Sharon R Browning, B. Browning, 2019, American journal of human genetics.

Evolutionary history of modern Samoans

D. Weeks, T. O’Connor, S. Browning, 2020, Proceedings of the National Academy of Sciences.

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

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

Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos

Tamar Sofer, Brian L Browning, Sharon R Browning, 2017, Human molecular genetics.

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

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

A One-Penny Imputed Genome from Next-Generation Reference Panels.

Brian L Browning, Sharon R Browning, B. Browning, 2018, American journal of human genetics.

Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

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

Multilocus association mapping using variable-length Markov chains.

Sharon R Browning, S. Browning, 2006, American journal of human genetics.

Detecting identity by descent and estimating genotype error rates in sequence data.

Brian L Browning, Sharon R Browning, B. Browning, 2013, American journal of human genetics.

A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects

E. Reiman, S. Browning, R. Sánchez-Valle, 2022, Genome medicine.

Deletion at the SLC1A1 glutamate transporter gene co‐segregates with schizophrenia and bipolar schizoaffective disorder in a 5‐generation family

F. Middleton, S. Faraone, S. Browning, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

Xihong Lin, T. Sofer, S. Browning, 2022, HGG advances.

Genotype error biases trio-based estimates of haplotype phase accuracy

B. Browning, S. Browning, 2022, bioRxiv.

Genome-wide Significance Thresholds for Admixture Mapping Studies.

Kelsey E. Grinde, A. Reiner, T. Thornton, 2019, American journal of human genetics.

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.

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.

Identity by descent between distant relatives: detection and applications.

Brian L Browning, Sharon R Browning, B. Browning, 2012, Annual review of genetics.

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

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

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.

Benjamin D. Heavner, Kelsey E. Grinde, A. Reiner, 2021, EBioMedicine.

Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans

Xihong Lin, S. Purcell, S. Sunyaev, 2018, Human molecular genetics.

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.

Monte Carlo likelihood calculation for identity by descent data

Sharon Browning, S. Browning, 1999 .

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

E. Wijsman, T. Thornton, L. Brusco, 2023, HGG advances.

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

E. Boerwinkle, T. Sofer, N. Franceschini, 2023, Genome Medicine.

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

B. Browning, S. Browning, 2013, Human Genetics.

AFA: Computationally efficient Ancestral Frequency estimation in Admixed populations: the Hispanic Community Health Study/Study of Latinos

Xihong Lin, T. Sofer, S. Browning, 2021 .

IBD-based estimation of X chromosome effective population size with application to sex-specific demographic history

B. Browning, S. Browning, Ruoyi Cai, 2023, bioRxiv.

Genome-wide haplotypic testing in a Finnish cohort identifies a novel association with low-density lipoprotein cholesterol

Qian S. Zhang, Brian L Browning, Sharon R Browning, 2014, European Journal of Human Genetics.

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

M. Brown, M. Bahlo, S. Browning, 2010, Cancer Epidemiology, Biomarkers & Prevention.

A one penny imputed genome from next generation reference panels

B. Browning, S. Browning, Yingxiao Zhou, 2018, bioRxiv.

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

B. Browning, S. Browning, 2013, Genetics.

Efficient clustering of identity-by-descent between multiple individuals

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

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

B. Browning, S. Browning, 2020, The American Journal of Human Genetics.

Population structure can inflate SNP-based heritability estimates.

B. Browning, S. Browning, 2011, American journal of human genetics.

Adjusting for principal components can induce spurious associations in genome-wide association studies in admixed populations

Kelsey E. Grinde, B. Browning, S. Browning, 2024, bioRxiv.