Author

Laurence Baret

McGill University Health Centre

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1

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Organism:human· 1 Research Focus:imputation· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam J. ShapiroiD· 1 shared Alejandro Mejía‐GarcíaiD· 1 shared Alex Diaz-PapkovichiD· 1 shared Anne‐Laure ChongiD· 1 shared Daniel TaliuniD· 1 shared Daniela D’AgostinoiD· 1 shared George Chong· 1 shared Guillaume LettreiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Adam J. ShapiroORCID

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1 paper

Recent·Most cited

Using the ancestral recombination graph to study the history of rare variants in founder populations

Alejandro Mejía‐García, Alex Diaz-Papkovich, Guillaume Sillon, Daniela D’Agostino, Anne‐Laure Chong, George Chong, Ken Sin Lo, Laurence Baret, Nancy Hamel, Vincent Chapdelaine, William David Foulkes, Daniel Taliun, Adam J. Shapiro, Guillaume Lettre, Simon Gravel

This paper uses ancestral recombination graphs to impute and trace rare variants in founder populations, showing high accuracy in mutation age and regional frequency estimation.

bioRxiv · Mar 13, 2025 · PreprintGenetics