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Connection

Co-Authors

This is a "connection" page, showing publications co-authored by Peter Carbonetto and Matthew Stephens.
Connection Strength

5.803
  1. Non-negative matrix factorization algorithms generally improve topic model fits. Stat Comput. 2026; 36(3):131.
    View in: PubMed
    Score: 0.970
  2. GoM DE: interpreting structure in sequence count data with differential expression analysis allowing for grades of membership. Genome Biol. 2023 10 19; 24(1):236.
    View in: PubMed
    Score: 0.813
  3. Integrated enrichment analysis of variants and pathways in genome-wide association studies indicates central role for IL-2 signaling genes in type 1 diabetes, and cytokine signaling genes in Crohn's disease. PLoS Genet. 2013; 9(10):e1003770.
    View in: PubMed
    Score: 0.405
  4. Fast and flexible joint fine-mapping of multiple traits via the Sum of Single Effects model. Nat Genet. 2026 Feb; 58(2):454-462.
    View in: PubMed
    Score: 0.238
  5. ebnm: An R Package for Solving the Empirical Bayes Normal Means Problem Using a Variety of Prior Families. J Stat Softw. 2025; 114.
    View in: PubMed
    Score: 0.232
  6. fSuSiE enables fine-mapping of QTLs from genome-scale molecular profiles. bioRxiv. 2025 Aug 17.
    View in: PubMed
    Score: 0.231
  7. BAYESIAN VARIABLE SELECTION IN A COX PROPORTIONAL HAZARDS MODEL WITH THE "SUM OF SINGLE EFFECTS" PRIOR. ArXiv. 2025 Jun 06.
    View in: PubMed
    Score: 0.228
  8. Dissecting tumor transcriptional heterogeneity from single-cell RNA-seq data by generalized binary covariance decomposition. Nat Genet. 2025 01; 57(1):263-273.
    View in: PubMed
    Score: 0.221
  9. Accelerated dimensionality reduction of single-cell RNA sequencing data with fastglmpca. Bioinformatics. 2024 08 02; 40(8).
    View in: PubMed
    Score: 0.215
  10. Accelerated dimensionality reduction of single-cell RNA sequencing data with fastglmpca. bioRxiv. 2024 Jul 04.
    View in: PubMed
    Score: 0.213
  11. Fast and flexible joint fine-mapping of multiple traits via the Sum of Single Effects model. bioRxiv. 2024 Jun 18.
    View in: PubMed
    Score: 0.213
  12. Dissecting tumor transcriptional heterogeneity from single-cell RNA-seq data by generalized binary covariance decomposition. bioRxiv. 2024 May 26.
    View in: PubMed
    Score: 0.212
  13. A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes. PLoS Genet. 2023 07; 19(7):e1010539.
    View in: PubMed
    Score: 0.199
  14. Fine-mapping from summary data with the "Sum of Single Effects" model. PLoS Genet. 2022 07; 18(7):e1010299.
    View in: PubMed
    Score: 0.186
  15. Flexible Signal Denoising via Flexible Empirical Bayes Shrinkage. J Mach Learn Res. 2021 Jan-Dec; 22.
    View in: PubMed
    Score: 0.167
  16. A simple new approach to variable selection in regression, with application to genetic fine mapping. J R Stat Soc Series B Stat Methodol. 2020 Dec; 82(5):1273-1300.
    View in: PubMed
    Score: 0.162
  17. Creating and sharing reproducible research code the workflowr way. F1000Res. 2019; 8:1749.
    View in: PubMed
    Score: 0.154
  18. Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions. Nat Genet. 2019 01; 51(1):187-195.
    View in: PubMed
    Score: 0.145
  19. Accurate genomic prediction of Coffea canephora in multiple environments using whole-genome statistical models. Heredity (Edinb). 2019 03; 122(3):261-275.
    View in: PubMed
    Score: 0.141
  20. Polygenic modeling with bayesian sparse linear mixed models. PLoS Genet. 2013; 9(2):e1003264.
    View in: PubMed
    Score: 0.097
  21. SuSiE 2.0: improved methods and implementations for genetic fine-mapping and phenotype prediction. bioRxiv. 2025 Dec 25.
    View in: PubMed
    Score: 0.059
  22. Genetic contributions to epigenetic-defined endotypes of allergic phenotypes in children. Am J Hum Genet. 2025 07 03; 112(7):1610-1624.
    View in: PubMed
    Score: 0.057
  23. Covariate-moderated Empirical Bayes Matrix Factorization. Adv Neural Inf Process Syst. 2025; 38:47219-47250.
    View in: PubMed
    Score: 0.055
  24. Genetic contributions to epigenetic-defined endotypes of allergic phenotypes in children. medRxiv. 2024 Oct 04.
    View in: PubMed
    Score: 0.054
  25. A pairwise cytokine code explains the organism-wide response to sepsis. Nat Immunol. 2024 Feb; 25(2):226-239.
    View in: PubMed
    Score: 0.052
  26. Fine-mapping studies distinguish genetic risks for childhood- and adult-onset asthma in the HLA region. Genome Med. 2022 05 24; 14(1):55.
    View in: PubMed
    Score: 0.046
  27. A Fast Algorithm for Maximum Likelihood Estimation of Mixture Proportions Using Sequential Quadratic Programming. J Comput Graph Stat. 2020; 29(2):261-273.
    View in: PubMed
    Score: 0.039
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.