Connection

ERIC BOERWINKLE to Genetics, Population

This is a "connection" page, showing publications ERIC BOERWINKLE has written about Genetics, Population.
Connection Strength

1.612
  1. Estimating population genetic parameters and comparing model goodness-of-fit using DNA sequences with error. Genome Res. 2010 Jan; 20(1):101-9.
    View in: PubMed
    Score: 0.285
  2. Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. Genetics. 2021 05 17; 218(1).
    View in: PubMed
    Score: 0.157
  3. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. Am J Hum Genet. 2014 Mar 06; 94(3):349-60.
    View in: PubMed
    Score: 0.095
  4. Clan genomics and the complex architecture of human disease. Cell. 2011 Sep 30; 147(1):32-43.
    View in: PubMed
    Score: 0.081
  5. Association studies for next-generation sequencing. Genome Res. 2011 Jul; 21(7):1099-108.
    View in: PubMed
    Score: 0.078
  6. Population genetics of hypervariable loci: analysis of PCR based VNTR polymorphism within a population. EXS. 1991; 58:127-43.
    View in: PubMed
    Score: 0.077
  7. Genome-wide distribution of ancestry in Mexican Americans. Hum Genet. 2008 Oct; 124(3):207-14.
    View in: PubMed
    Score: 0.065
  8. Explaining the unexplained admixture mapping signals via rare variants: the HCHS/SOL. Hum Mol Genet. 2026 Sep 25; 35(20).
    View in: PubMed
    Score: 0.057
  9. Mining genetic epidemiology data with Bayesian networks application to APOE gene variation and plasma lipid levels. J Comput Biol. 2005; 12(1):1-11.
    View in: PubMed
    Score: 0.051
  10. Ethnicity and human genetic linkage maps. Am J Hum Genet. 2005 Feb; 76(2):276-90.
    View in: PubMed
    Score: 0.051
  11. Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. Am J Hum Genet. 2005 Feb; 76(2):268-75.
    View in: PubMed
    Score: 0.051
  12. Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies. Am J Hum Genet. 2024 10 03; 111(10):2129-2138.
    View in: PubMed
    Score: 0.050
  13. Haplotype block linkage disequilibrium mapping. Front Biosci. 2003 May 01; 8:a85-93.
    View in: PubMed
    Score: 0.045
  14. Power of a simplified multivariate test for genetic linkage. Ann Hum Genet. 2002 Nov; 66(Pt 5-6):407-17.
    View in: PubMed
    Score: 0.044
  15. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. Am J Hum Genet. 2022 01 06; 109(1):81-96.
    View in: PubMed
    Score: 0.041
  16. Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. Am J Hum Genet. 2001 Jan; 68(1):198-207.
    View in: PubMed
    Score: 0.038
  17. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. PLoS Genet. 2019 12; 15(12):e1008500.
    View in: PubMed
    Score: 0.036
  18. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. Am J Hum Genet. 2019 02 07; 104(2):260-274.
    View in: PubMed
    Score: 0.033
  19. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet. 2018 10; 50(10):1412-1425.
    View in: PubMed
    Score: 0.033
  20. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. Am J Hum Genet. 1998 Aug; 63(2):595-612.
    View in: PubMed
    Score: 0.032
  21. Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology. Nat Genet. 2017 10 27; 49(11):1560-1563.
    View in: PubMed
    Score: 0.031
  22. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 2015 Feb 05; 518(7537):102-6.
    View in: PubMed
    Score: 0.025
  23. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet. 2014 Nov; 46(11):1173-86.
    View in: PubMed
    Score: 0.025
  24. Neutral genomic regions refine models of recent rapid human population growth. Proc Natl Acad Sci U S A. 2014 Jan 14; 111(2):757-62.
    View in: PubMed
    Score: 0.024
  25. Comprehensive evaluation of imputation performance in African Americans. J Hum Genet. 2012 Jul; 57(7):411-21.
    View in: PubMed
    Score: 0.021
  26. The landscape of recombination in African Americans. Nature. 2011 Jul 20; 476(7359):170-5.
    View in: PubMed
    Score: 0.020
  27. Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet. 2011 Jun; 43(6):519-25.
    View in: PubMed
    Score: 0.020
  28. Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. Lancet. 2008 Dec 06; 372(9654):1953-61.
    View in: PubMed
    Score: 0.016
  29. The role of the genetics of sodium lithium countertransport in the determination of blood pressure variability in the population at large. Prog Clin Biol Res. 1984; 165:479-507.
    View in: PubMed
    Score: 0.012
  30. Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sample. Hum Genet. 2002 Jul; 111(1):75-87.
    View in: PubMed
    Score: 0.011
  31. Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene. Genome Res. 2000 Oct; 10(10):1532-45.
    View in: PubMed
    Score: 0.009
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.