Harvard Catalyst Profiles

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

Peter Kraft, Ph.D.

Co-Author

This page shows the publications co-authored by Peter Kraft and Alkes Price.
Connection Strength

1.971
  1. Deep targeted sequencing of 12 breast cancer susceptibility regions in 4611 women across four different ethnicities. Breast Cancer Res. 2016 11 05; 18(1):109.
    View in: PubMed
    Score: 0.179
  2. Response to Day et al. Am J Hum Genet. 2016 Feb 04; 98(2):394-5.
    View in: PubMed
    Score: 0.169
  3. Meta-Analysis of Rare Variant Association Tests in Multiethnic Populations. Genet Epidemiol. 2016 Jan; 40(1):57-65.
    View in: PubMed
    Score: 0.168
  4. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. Am J Hum Genet. 2015 Oct 01; 97(4):576-92.
    View in: PubMed
    Score: 0.165
  5. Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction. Genet Epidemiol. 2015 Sep; 39(6):427-38.
    View in: PubMed
    Score: 0.161
  6. Adjusting for heritable covariates can bias effect estimates in genome-wide association studies. Am J Hum Genet. 2015 Feb 05; 96(2):329-39.
    View in: PubMed
    Score: 0.158
  7. Genetic and environmental components of family history in type 2 diabetes. Hum Genet. 2015 Feb; 134(2):259-67.
    View in: PubMed
    Score: 0.157
  8. Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits. PLoS Genet. 2013 May; 9(5):e1003520.
    View in: PubMed
    Score: 0.141
  9. Improved ancestry inference using weights from external reference panels. Bioinformatics. 2013 Jun 01; 29(11):1399-406.
    View in: PubMed
    Score: 0.139
  10. Informed conditioning on clinical covariates increases power in case-control association studies. PLoS Genet. 2012; 8(11):e1003032.
    View in: PubMed
    Score: 0.135
  11. Analysis of case-control association studies with known risk variants. Bioinformatics. 2012 Jul 01; 28(13):1729-37.
    View in: PubMed
    Score: 0.131
  12. Shared heritability and functional enrichment across six solid cancers. Nat Commun. 2019 01 25; 10(1):431.
    View in: PubMed
    Score: 0.052
  13. Quantifying the Genetic Correlation between Multiple Cancer Types. Cancer Epidemiol Biomarkers Prev. 2017 09; 26(9):1427-1435.
    View in: PubMed
    Score: 0.047
  14. 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: 0.046
  15. Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation. Nat Commun. 2016 Apr 07; 7:10979.
    View in: PubMed
    Score: 0.043
  16. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat Genet. 2015 Nov; 47(11):1294-1303.
    View in: PubMed
    Score: 0.041
  17. Integrating functional data to prioritize causal variants in statistical fine-mapping studies. PLoS Genet. 2014 Oct; 10(10):e1004722.
    View in: PubMed
    Score: 0.039
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.