Forrest IS - 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: forrest is. 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

Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system.

Forrest IS, Duffy Á, Park JK, Vy HMT, Pasquale LR, Nadkarni GN, Cho JH, Do R. Forrest IS, et al. Cell Rep Med. 2024 May 21;5(5):101518. doi: 10.1016/j.xcrm.2024.101518. Epub 2024 Apr 19. Cell Rep Med. 2024. PMID: 38642551 Free PMC article.

3

Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries.

Forrest IS, Chaudhary K, Vy HMT, Bafna S, Kim S, Won HH, Loos RJF, Cho J, Pasquale LR, Nadkarni GN, Rocheleau G, Do R. Forrest IS, et al. Hum Mutat. 2021 Aug;42(8):969-977. doi: 10.1002/humu.24220. Epub 2021 May 31. Hum Mutat. 2021. PMID: 34005834 Free PMC article.

4

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. JAMA. 2022 Jan 25;327(4):350-359. doi: 10.1001/jama.2021.23686. JAMA. 2022. PMID: 35076666 Free PMC article.

5

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records.

Petrazzini BO, Chaudhary K, Márquez-Luna C, Forrest IS, Rocheleau G, Cho J, Narula J, Nadkarni G, Do R. Petrazzini BO, et al. Among authors: forrest is. J Am Coll Cardiol. 2022 Mar 29;79(12):1155-1166. doi: 10.1016/j.jacc.2022.01.021. J Am Coll Cardiol. 2022. PMID: 35331410 Free PMC article.

6

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. 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.

7

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. Nat Commun. 2023 Apr 25;14(1):2385. doi: 10.1038/s41467-023-37996-7. Nat Commun. 2023. PMID: 37169741 Free PMC article.

8

Machine learning-based markers for CAD - Authors' reply.

Forrest IS, Petrazzini BO, Do R. Forrest IS, et al. Lancet. 2023 Jul 15;402(10397):184. doi: 10.1016/S0140-6736(23)01059-0. Lancet. 2023. PMID: 37453750 No abstract available.

9

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: forrest is. Nat Genet. 2024 Jul;56(7):1412-1419. doi: 10.1038/s41588-024-01791-x. Epub 2024 Jun 11. Nat Genet. 2024. PMID: 38862854

10

Tissue-specific genetic features inform prediction of drug side effects in clinical trials.

Duffy Á, Verbanck M, Dobbyn A, Won HH, Rein JL, Forrest IS, Nadkarni G, Rocheleau G, Do R. Duffy Á, et al. Among authors: forrest is. Sci Adv. 2020 Sep 10;6(37):eabb6242. doi: 10.1126/sciadv.abb6242. Print 2020 Sep. Sci Adv. 2020. PMID: 32917698 Free PMC article.

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