Sharon R. Browning
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Statistical geneticist
Sharon R. Browning's AcademicInfluence.com Rankings
Sharon R. Browningmathematics Degrees
Mathematics
#7829
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#10633
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Statistics
#999
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#1096
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Sharon R. Browningbiology Degrees
Biology
#14335
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#18058
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Genetics
#1646
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#1754
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Mathematics Biology
Sharon R. Browning's Degrees
- PhD Biostatistics University of Washington
- Masters Biostatistics University of Washington
- Bachelors Mathematics University of California, Berkeley
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Why Is Sharon R. Browning Influential?
(Suggest an Edit or Addition)According to Wikipedia, Sharon Ruth Browning is a statistical geneticist at the University of Washington, and a research professor with its Department of Biostatistics. Her research has various implications for the field of biogenetics.
Sharon R. Browning's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. (2007) (2648)
- A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (2009) (1550)
- A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic (2009) (1052)
- Genotype Imputation with Millions of Reference Samples. (2016) (803)
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) (785)
- A One-Penny Imputed Genome from Next-Generation Reference Panels. (2018) (601)
- A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay (2010) (561)
- Haplotype phasing: existing methods and new developments (2011) (549)
- Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 (2009) (540)
- Improving the Accuracy and Efficiency of Identity-by-Descent Detection in Population Data (2013) (466)
- A fast, powerful method for detecting identity by descent. (2011) (343)
- A one penny imputed genome from next generation reference panels (2018) (327)
- Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos. (2016) (231)
- Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture (2018) (218)
- High-resolution detection of identity by descent in unrelated individuals. (2010) (211)
- Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent. (2015) (193)
- Multilocus association mapping using variable-length Markov chains. (2006) (161)
- Efficient multilocus association testing for whole genome association studies using localized haplotype clustering (2007) (160)
- Missing data imputation and haplotype phase inference for genome-wide association studies (2008) (160)
- Identity by descent between distant relatives: detection and applications. (2012) (135)
- Detecting identity by descent and estimating genotype error rates in sequence data. (2013) (124)
- Detecting Rare Variant Associations by Identity-by-Descent Mapping in Case-Control Studies (2012) (104)
- Population structure can inflate SNP-based heritability estimates. (2011) (93)
- Fast two-stage phasing of large-scale sequence data. (2021) (92)
- Ancestry-specific recent effective population size in the Americas (2018) (88)
- A Polymorphism in the HLA-DPB1 Gene Is Associated with Susceptibility to Multiple Sclerosis (2010) (86)
- Haplotypic analysis of Wellcome Trust Case Control Consortium data (2008) (83)
- Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans. (2016) (68)
- Estimation of Pairwise Identity by Descent From Dense Genetic Marker Data in a Population Sample of Haplotypes (2008) (61)
- Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies (2010) (60)
- Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes (2011) (58)
- Case‐control single‐marker and haplotypic association analysis of pedigree data (2005) (53)
- A fast and simple method for detecting identity by descent segments in large-scale data (2019) (52)
- De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population (2020) (51)
- Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays (2013) (44)
- Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL) (2016) (44)
- Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos (2017) (43)
- Deletion at the SLC1A1 glutamate transporter gene co‐segregates with schizophrenia and bipolar schizoaffective disorder in a 5‐generation family (2013) (38)
- Population Structure With Localized Haplotype Clusters (2010) (33)
- Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort (2012) (28)
- Admixture Mapping Identifies an Amerindian Ancestry Locus Associated with Albuminuria in Hispanics in the United States. (2017) (27)
- Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans (2018) (27)
- Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos (2017) (26)
- A canine model of inherited myopia: familial aggregation of refractive error in labrador retrievers. (2008) (25)
- Estimating the Genome-wide Mutation Rate with Three-Way Identity by Descent. (2019) (23)
- Admixture mapping in the Hispanic Community Health Study/Study of Latinos reveals regions of genetic associations with blood pressure traits (2017) (23)
- Genome-wide Significance Thresholds for Admixture Mapping Studies. (2019) (18)
- Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. (2021) (18)
- Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts. (2017) (18)
- Erratum to: Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort (2013) (17)
- Population-specific recombination maps from segments of identity by descent (2019) (17)
- On reducing the statespace of hidden Markov models for the identity by descent process. (2002) (16)
- Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fat (2015) (15)
- Relationship Information Contained in Gamete Identiti by Descent Data (1998) (14)
- Evolutionary history of modern Samoans (2020) (13)
- Genome-wide haplotypic testing in a Finnish cohort identifies a novel association with low-density lipoprotein cholesterol (2014) (10)
- IBDkin: fast estimation of kinship coefficients from identity by descent segments (2020) (9)
- Efficient clustering of identity-by-descent between multiple individuals (2014) (9)
- Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection (2020) (8)
- ASAFE: ancestry-specific allele frequency estimation (2016) (7)
- A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects (2022) (6)
- A Monte Carlo approach to calculating probabilities for continuous identity by descent data (2000) (6)
- Robust Inference of Identity by Descent from Exome-Sequencing Data. (2016) (5)
- POPdemog: visualizing population demographic history from simulation scripts (2018) (5)
- Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort (2012) (3)
- Protocol for detecting introgressed archaic variants with SPrime (2021) (3)
- Sprime results for 1000 Genomes non-African populations and SGDP Papuans (2018) (3)
- Documentation for BEAGLE 2.1 (2007) (2)
- Genotype error biases trio-based estimates of haplotype phase accuracy (2022) (2)
- Monte Carlo likelihood calculation for identity by descent data (1999) (2)
- A Multi-feature Reproducibility Assessment of Mass Spectral Data in Clinical Proteomic Studies (2009) (2)
- Fast, accurate local ancestry inference with FLARE (2022) (2)
- AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos (2022) (2)
- Multilocus analysis of GAW15 NARAC chromosome 18 case-control data (2007) (2)
- De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population (2019) (1)
- Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection (2020) (1)
- A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects (2022) (1)
- Estimating the genome-wide mutation rate from thousands of unrelated individuals (2022) (1)
- Pedigree data analysis with crossover interference. (2003) (1)
- 100 years of quantitative genetics theory and its applications: celebrating the centenary of Fisher 1918 (2018) (0)
- Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci | NOVA. The University of Newcastle's Digital Repository (2011) (0)
- Statistical phasing of 150,119 sequenced genomes in the UK Biobank (2022) (0)
- AFA: Computationally efficient Ancestral Frequency estimation in Admixed populations: the Hispanic Community Health Study/Study of Latinos (2021) (0)
- IBD-based estimation of X chromosome effective population size with application to sex-specific demographic history (2022) (0)
- Faculty Opinions recommendation of Non-crossover gene conversions show strong GC bias and unexpected clustering in humans. (2022) (0)
- Erratum to: Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort (2013) (0)
- Searching for rare variants conferring susceptibility to multiple sclerosis (2012) (0)
- Evolutionary Genomics of Samoans (2019) (0)
- Faculty Opinions recommendation of Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups. (2020) (0)
- Effect of litter size and birth weight on naturally occurring myopia in the Labrador retriever (2008) (0)
- Admixture mapping screening of CKD traits and risk factors in U.S. Hispanic/Latino individuals from Central America country-of-origin (2022) (0)
- Faculty Opinions recommendation of High-throughput inference of pairwise coalescence times identifies signals of selection and enriched disease heritability. (2020) (0)
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