Author

Ricky Lali

Population Health Research InstituteORCID 0000-0002-9689-9414Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:polygenic risk· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Guillaume ParéiD· 3 shared Ann Le· 2 shared Michael ChongiD· 2 shared Pedrum Mohammadi‐ShemiraniiD· 2 shared Alice ManiD· 1 shared Arghavan Omidi· 1 shared Conor S. JudgeiD· 1 shared Edward Cui· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Guillaume ParéORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 20, 2026

Biobank-scale survey of gene-diet interactions informs precision nutrition polygenic scores

Matteo Di Scipio, Alice Man, Ricky Lali…·G P Pare

The paper assesses gene-diet interactions in UK Biobank data to derive polygenic scores that associate with cardiometabolic outcomes and clinical conditions like gout.

DOI 10.64898/2026.04.13.26350340

humanGWAS summary statistics

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Genetic & Genomic MedicineeLifePeer-reviewedJan 12, 2022

GWAS and ExWAS of blood Mitochondrial DNA copy number identifies 73 loci and highlights a potential causal role in dementia

Michael Chong, Pedrum Mohammadi‐Shemirani, Nicolas Perrot…·Guillaume Paré

This study identifies 73 genetic loci associated with blood mitochondrial DNA copy number and suggests a causal link between low mtDNA-CN and dementia risk.

128 citationstop 1%

humanwhole-genome sequencing

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GeneticsNature CommunicationsPeer-reviewedOct 6, 2021

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

Ricky Lali, Michael Chong, Arghavan Omidi…·Guillaume Paré

The paper develops a method to create calibrated rare variant genetic risk scores using exome data, showing strong association with coronary artery disease risk.

36 citations

humanwhole-exome sequencing

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