Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Alkes Price, Ph.D.

Co-Author

This page shows the publications co-authored by Alkes Price and Po-Ru Loh.
Connection Strength

7.906
  1. Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations. Nature. 2018 07; 559(7714):350-355.
    View in: PubMed
    Score: 0.769
  2. Mixed-model association for biobank-scale datasets. Nat Genet. 2018 07; 50(7):906-908.
    View in: PubMed
    Score: 0.768
  3. Fast and accurate long-range phasing in a UK Biobank cohort. Nat Genet. 2016 07; 48(7):811-6.
    View in: PubMed
    Score: 0.665
  4. Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis. Nat Genet. 2015 Dec; 47(12):1385-92.
    View in: PubMed
    Score: 0.638
  5. Efficient Bayesian mixed-model analysis increases association power in large cohorts. Nat Genet. 2015 Mar; 47(3):284-90.
    View in: PubMed
    Score: 0.606
  6. Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets. Nat Commun. 2021 10 18; 12(1):6052.
    View in: PubMed
    Score: 0.241
  7. Annotations capturing cell type-specific TF binding explain a large fraction of disease heritability. Hum Mol Genet. 2020 05 08; 29(7):1057-1067.
    View in: PubMed
    Score: 0.218
  8. Liability threshold modeling of case-control status and family history of disease increases association power. Nat Genet. 2020 05; 52(5):541-547.
    View in: PubMed
    Score: 0.217
  9. Genes with High Network Connectivity Are Enriched for Disease Heritability. Am J Hum Genet. 2019 Dec 05; 105(6):1302.
    View in: PubMed
    Score: 0.212
  10. Author Correction: Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection. Nat Genet. 2019 Aug; 51(8):1295.
    View in: PubMed
    Score: 0.207
  11. Genes with High Network Connectivity Are Enriched for Disease Heritability. Am J Hum Genet. 2019 05 02; 104(5):896-913.
    View in: PubMed
    Score: 0.203
  12. Quantification of frequency-dependent genetic architectures in 25 UK Biobank traits reveals action of negative selection. Nat Commun. 2019 02 15; 10(1):790.
    View in: PubMed
    Score: 0.200
  13. Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Am J Hum Genet. 2019 01 03; 104(1):65-75.
    View in: PubMed
    Score: 0.199
  14. Estimating cross-population genetic correlations of causal effect sizes. Genet Epidemiol. 2019 03; 43(2):180-188.
    View in: PubMed
    Score: 0.197
  15. Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations. Nat Genet. 2018 11; 50(11):1600-1607.
    View in: PubMed
    Score: 0.196
  16. Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk. Nat Genet. 2018 10; 50(10):1483-1493.
    View in: PubMed
    Score: 0.194
  17. Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits. Nat Genet. 2018 07; 50(7):1041-1047.
    View in: PubMed
    Score: 0.192
  18. Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. Nat Genet. 2018 04; 50(4):621-629.
    View in: PubMed
    Score: 0.189
  19. Multiethnic polygenic risk scores improve risk prediction in diverse populations. Genet Epidemiol. 2017 12; 41(8):811-823.
    View in: PubMed
    Score: 0.183
  20. Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection. Nat Genet. 2017 Oct; 49(10):1421-1427.
    View in: PubMed
    Score: 0.182
  21. Mixed Model Association with Family-Biased Case-Control Ascertainment. Am J Hum Genet. 2017 Jan 05; 100(1):31-39.
    View in: PubMed
    Score: 0.173
  22. Response to Shen et al. Am J Hum Genet. 2016 11 03; 99(5):1220-1221.
    View in: PubMed
    Score: 0.171
  23. Population Structure of UK Biobank and Ancient Eurasians Reveals Adaptation at Genes Influencing Blood Pressure. Am J Hum Genet. 2016 Nov 03; 99(5):1130-1139.
    View in: PubMed
    Score: 0.171
  24. Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia. Am J Hum Genet. 2016 Mar 03; 98(3):456-472.
    View in: PubMed
    Score: 0.163
  25. Two-Variance-Component Model Improves Genetic Prediction in Family Datasets. Am J Hum Genet. 2015 Nov 05; 97(5):677-90.
    View in: PubMed
    Score: 0.160
  26. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. Am J Hum Genet. 2015 Oct 01; 97(4):576-92.
    View in: PubMed
    Score: 0.159
  27. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat Genet. 2015 Nov; 47(11):1228-35.
    View in: PubMed
    Score: 0.159
  28. Mixed model with correction for case-control ascertainment increases association power. Am J Hum Genet. 2015 May 07; 96(5):720-30.
    View in: PubMed
    Score: 0.154
  29. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat Genet. 2017 Jun; 49(6):834-841.
    View in: PubMed
    Score: 0.044
  30. An atlas of genetic correlations across human diseases and traits. Nat Genet. 2015 Nov; 47(11):1236-41.
    View in: PubMed
    Score: 0.040
  31. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat Genet. 2015 Mar; 47(3):291-5.
    View in: PubMed
    Score: 0.038
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.