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ERIC BOERWINKLE to Multifactorial Inheritance

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This is a "connection" page, showing publications ERIC BOERWINKLE has written about Multifactorial Inheritance.
ERIC BOERWINKLE
Connection Strength
2.331
Multifactorial Inheritance
  1. Admixture-informed polygenic risk reporting using the ePRS framework. Nat Commun. 2026 Apr 30; 17(1).
    View in: PubMed
    Score: 0.216
  2. Polygenic prediction of body mass index and obesity through the life course and across ancestries. Nat Med. 2025 Sep; 31(9):3151-3168.
    View in: PubMed
    Score: 0.205
  3. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. Nat Genet. 2024 May; 56(5):778-791.
    View in: PubMed
    Score: 0.188
  4. Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature. 2022 12; 612(7941):720-724.
    View in: PubMed
    Score: 0.171
  5. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data. Nat Genet. 2022 Mar; 54(3):263-273.
    View in: PubMed
    Score: 0.162
  6. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. Genome Biol. 2021 06 29; 22(1):194.
    View in: PubMed
    Score: 0.155
  7. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nat Commun. 2021 06 07; 12(1):3417.
    View in: PubMed
    Score: 0.154
  8. The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance. Am J Hum Genet. 2019 07 03; 105(1):132-150.
    View in: PubMed
    Score: 0.134
  9. Genetic analyses of diverse populations improves discovery for complex traits. Nature. 2019 06; 570(7762):514-518.
    View in: PubMed
    Score: 0.134
  10. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nat Commun. 2018 05 29; 9(1):2098.
    View in: PubMed
    Score: 0.125
  11. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genet. 2017 May; 13(5):e1006728.
    View in: PubMed
    Score: 0.116
  12. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat Genet. 2024 Jul; 56(7):1397-1411.
    View in: PubMed
    Score: 0.048
  13. Power of a simplified multivariate test for genetic linkage. Ann Hum Genet. 2002 Nov; 66(Pt 5-6):407-17.
    View in: PubMed
    Score: 0.042
  14. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Mol Psychiatry. 2022 Nov; 27(11):4419-4431.
    View in: PubMed
    Score: 0.042
  15. Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation. 2022 05 17; 145(20):1524-1533.
    View in: PubMed
    Score: 0.041
  16. 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: 0.040
  17. Genetic susceptibility, obesity and lifetime risk of type 2 diabetes: The ARIC study and Rotterdam Study. Diabet Med. 2021 10; 38(10):e14639.
    View in: PubMed
    Score: 0.039
  18. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. Nat Commun. 2021 06 09; 12(1):3505.
    View in: PubMed
    Score: 0.039
  19. The trans-ancestral genomic architecture of glycemic traits. Nat Genet. 2021 06; 53(6):840-860.
    View in: PubMed
    Score: 0.038
  20. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nat Commun. 2020 05 21; 11(1):2542.
    View in: PubMed
    Score: 0.036
  21. Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample. Hum Mol Genet. 2019 04 01; 28(7):1212-1224.
    View in: PubMed
    Score: 0.033
  22. Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence. JAMA Psychiatry. 2017 11 01; 74(11):1153-1160.
    View in: PubMed
    Score: 0.030
  23. Rare and low-frequency coding variants alter human adult height. Nature. 2017 02 09; 542(7640):186-190.
    View in: PubMed
    Score: 0.029
  24. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. N Engl J Med. 2016 12 15; 375(24):2349-2358.
    View in: PubMed
    Score: 0.028
  25. Integrating GWASs and human protein interaction networks identifies a gene subnetwork underlying alcohol dependence. Am J Hum Genet. 2013 Dec 05; 93(6):1027-34.
    View in: PubMed
    Score: 0.023
  26. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 2012 Apr 04; 485(7397):242-5.
    View in: PubMed
    Score: 0.020
  27. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 2010 Oct 14; 467(7317):832-8.
    View in: PubMed
    Score: 0.018
  28. Genetics of ultrasonographic carotid atherosclerosis. Arterioscler Thromb Vasc Biol. 2004 Sep; 24(9):1567-77.
    View in: PubMed
    Score: 0.012
  29. Diagnostic tools in linkage analysis for quantitative traits. Genet Epidemiol. 2003 May; 24(4):302-8.
    View in: PubMed
    Score: 0.011
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.