Lali R - Search Results

1

Frameshift mutation in the APOA5 gene causing hypertriglyceridemia in a Pakistani family: Management and considerations for cardiovascular risk.

Thériault S, Don-Wauchope A, Chong M, Lali R, Morrison KM, Paré G. Thériault S, et al. Among authors: lali r. J Clin Lipidol. 2016 Sep-Oct;10(5):1272-7. doi: 10.1016/j.jacl.2016.07.009. Epub 2016 Aug 9. J Clin Lipidol. 2016. PMID: 27678447

2

Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease.

Thériault S, Lali R, Chong M, Velianou JL, Natarajan MK, Paré G. Thériault S, et al. Among authors: lali r. Circ Genom Precis Med. 2018 Jan;11(1):e001849. doi: 10.1161/CIRCGEN.117.001849. Epub 2018 Jan 8. Circ Genom Precis Med. 2018. PMID: 29874178

3

Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome.

Chong M, Sjaarda J, Pigeyre M, Mohammadi-Shemirani P, Lali R, Shoamanesh A, Gerstein HC, Paré G. Chong M, et al. Among authors: lali r. Circulation. 2019 Sep 9;140(10):819-830. doi: 10.1161/CIRCULATIONAHA.119.040180. Epub 2019 Jun 18. Circulation. 2019. PMID: 31208196

4

Genetics of early-onset coronary artery disease: from discovery to clinical translation.

Lali R, Cui E, Ansarikaleibari A, Pigeyre M, Paré G. Lali R, et al. Curr Opin Cardiol. 2019 Nov;34(6):706-713. doi: 10.1097/HCO.0000000000000676. Curr Opin Cardiol. 2019. PMID: 31436558 Review.

5

Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups.

Grami N, Chong M, Lali R, Mohammadi-Shemirani P, Henshall DE, Rannikmäe K, Paré G. Grami N, et al. Among authors: lali r. Stroke. 2020 Apr;51(4):1290-1293. doi: 10.1161/STROKEAHA.119.028840. Epub 2020 Feb 28. Stroke. 2020. PMID: 32106772 Free article.

6

Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics.

Sariya S, Felsky D, Reyes-Dumeyer D, Lali R, Lantigua RA, Vardarajan B, Jiménez-Velázquez IZ, Haines JL, Shellenberg GD, Pericak-Vance MA, Paré G, Mayeux R, Tosto G. Sariya S, et al. Among authors: lali r. Ann Neurol. 2021 Sep;90(3):366-376. doi: 10.1002/ana.26131. Epub 2021 Jun 17. Ann Neurol. 2021. PMID: 34038570 Free PMC article.

7

Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories.

Lali R, Chong M, Omidi A, Mohammadi-Shemirani P, Le A, Cui E, Paré G. Lali R, et al. Nat Commun. 2021 Oct 6;12(1):5852. doi: 10.1038/s41467-021-26114-0. Nat Commun. 2021. PMID: 34615865 Free PMC article.

8

Mitochondrial DNA Copy Number as a Marker and Mediator of Stroke Prognosis: Observational and Mendelian Randomization Analyses.

Chong MR, Narula S, Morton R, Judge C, Akhabir L, Cawte N, Pathan N, Lali R, Mohammadi-Shemirani P, Shoamanesh A, O'Donnell M, Yusuf S, Langhorne P, Paré G. Chong MR, et al. Among authors: lali r. Neurology. 2022 Feb 1;98(5):e470-e482. doi: 10.1212/WNL.0000000000013165. Epub 2021 Dec 8. Neurology. 2022. PMID: 34880091 Free PMC article.

9

GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia.

Chong M, Mohammadi-Shemirani P, Perrot N, Nelson W, Morton R, Narula S, Lali R, Khan I, Khan M, Judge C, Machipisa T, Cawte N, O'Donnell M, Pigeyre M, Akhabir L, Paré G. Chong M, et al. Among authors: lali r. Elife. 2022 Jan 13;11:e70382. doi: 10.7554/eLife.70382. Elife. 2022. PMID: 35023831 Free PMC article.

10

Cost-Effectiveness of Polygenic Risk Scores to Guide Statin Therapy for Cardiovascular Disease Prevention.

Kiflen M, Le A, Mao S, Lali R, Narula S, Xie F, Paré G. Kiflen M, et al. Among authors: lali r. Circ Genom Precis Med. 2022 Oct;15(5):e003423. doi: 10.1161/CIRCGEN.121.003423. Epub 2022 Jul 29. Circ Genom Precis Med. 2022. PMID: 35904973

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