Jordan DM - Search Results

1

Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human disease.

Petrazzini BO, Balick DJ, Forrest IS, Cho J, Rocheleau G, Jordan DM, Do R. Petrazzini BO, et al. Among authors: jordan dm. Cell Rep Methods. 2024 Dec 16;4(12):100914. doi: 10.1016/j.crmeth.2024.100914. Epub 2024 Dec 9. Cell Rep Methods. 2024. PMID: 39657681 Free article.

2

Overcoming constraints on the detection of recessive selection in human genes from population frequency data.

Balick DJ, Jordan DM, Sunyaev S, Do R. Balick DJ, et al. Among authors: jordan dm. Am J Hum Genet. 2022 Jan 6;109(1):33-49. doi: 10.1016/j.ajhg.2021.12.001. Epub 2021 Dec 23. Am J Hum Genet. 2022. PMID: 34951958 Free PMC article.

3

Population-Based Penetrance of Deleterious Clinical Variants.

Forrest IS, Chaudhary K, Vy HMT, Petrazzini BO, Bafna S, Jordan DM, Rocheleau G, Loos RJF, Nadkarni GN, Cho JH, Do R. Forrest IS, et al. Among authors: jordan dm. JAMA. 2022 Jan 25;327(4):350-359. doi: 10.1001/jama.2021.23686. JAMA. 2022. PMID: 35076666 Free PMC article.

4

Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts.

Forrest IS, Petrazzini BO, Duffy Á, Park JK, Marquez-Luna C, Jordan DM, Rocheleau G, Cho JH, Rosenson RS, Narula J, Nadkarni GN, Do R. Forrest IS, et al. Among authors: jordan dm. Lancet. 2023 Jan 21;401(10372):215-225. doi: 10.1016/S0140-6736(22)02079-7. Epub 2022 Dec 20. Lancet. 2023. PMID: 36563696 Free PMC article.

5

A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.

Forrest IS, Petrazzini BO, Duffy Á, Park JK, O'Neal AJ, Jordan DM, Rocheleau G, Nadkarni GN, Cho JH, Blazer AD, Do R. Forrest IS, et al. Among authors: jordan dm. Nat Commun. 2023 Apr 25;14(1):2385. doi: 10.1038/s41467-023-37996-7. Nat Commun. 2023. PMID: 37169741 Free PMC article.

6

A deep learning transformer model predicts high rates of undiagnosed rare disease in large electronic health systems.

Jordan DM, Vy HMT, Do R. Jordan DM, et al. medRxiv [Preprint]. 2023 Dec 24:2023.12.21.23300393. doi: 10.1101/2023.12.21.23300393. medRxiv. 2023. PMID: 38196638 Free PMC article. Preprint.

7

Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease.

Petrazzini BO, Forrest IS, Rocheleau G, Vy HMT, Márquez-Luna C, Duffy Á, Chen R, Park JK, Gibson K, Goonewardena SN, Malick WA, Rosenson RS, Jordan DM, Do R. Petrazzini BO, et al. Among authors: jordan dm. Nat Genet. 2024 Jul;56(7):1412-1419. doi: 10.1038/s41588-024-01791-x. Epub 2024 Jun 11. Nat Genet. 2024. PMID: 38862854

8

Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases.

Jordan DM, Do R. Jordan DM, et al. Annu Rev Genomics Hum Genet. 2018 Aug 31;19:289-301. doi: 10.1146/annurev-genom-083117-021136. Epub 2018 Apr 11. Annu Rev Genomics Hum Genet. 2018. PMID: 29641912 Review.

9

HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases.

Jordan DM, Verbanck M, Do R. Jordan DM, et al. Genome Biol. 2019 Oct 25;20(1):222. doi: 10.1186/s13059-019-1844-7. Genome Biol. 2019. PMID: 31653226 Free PMC article.

10

Probing the aggregated effects of purifying selection per individual on 1,380 medical phenotypes in the UK Biobank.

Vy HMT, Jordan DM, Balick DJ, Do R. Vy HMT, et al. Among authors: jordan dm. PLoS Genet. 2021 Jan 25;17(1):e1009337. doi: 10.1371/journal.pgen.1009337. eCollection 2021 Jan. PLoS Genet. 2021. PMID: 33493176 Free PMC article.

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