Author

Mark J. Daly

Primary ORCID profile (0000-0002-0949-8752 · 178 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Mark J. DalyiD178 papers · Broad Institute

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 3 Approach:statistical model· 3 Organism:human· 2 Research Focus:variant calling· 2 Research Focus:variant effect prediction· 2 Assay:whole-exome sequencing· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1

Frequent Co-Authors

Benjamin M. Neale· 2 shared Hailiang Huang· 2 shared Aarno Palotie· 1 shared Adam P. Levine· 1 shared Andre Franke· 1 shared Andrea Ganna· 1 shared Ann Pulver· 1 shared Anthony W. Segal· 1 shared

Activity by Year

2016-2016 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetics

Benjamin M. Neale

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3 papers

Recent·Most cited

Insights into the genetic epidemiology of Crohn’s and rare diseases in the Ashkenazi Jewish population

Manuel A. Rivas, Jukka Koskela, Hailiang Huang, Christine Stevens, Brandon E. Avila, Talin Haritunians, Benjamin M. Neale, Mitja Kurki, Andrea Ganna, Daniel Graham, Benjamin Glaser, Inga Peter, Gil Atzmon, Nir Barzilai, Adam P. Levine, , Mark J. Daly

The paper analyzes exome sequencing data from Ashkenazi Jews to identify enriched alleles and their association with genetic risk for Crohn’s disease and rare diseases.

bioRxiv · Sep 25, 2016 · PreprintGenetics

Bootstrat: Population Informed Bootstrapping for Rare Variant Tests

Hailiang Huang, Gina M. Peloso, Daniel Howrigan, Barbara Rakitsch, Carl Johann Simon-Gabriel, Jacqueline I. Goldstein, Mark J. Daly, Karsten Borgwardt, Benjamin M. Neale

Bootstrat corrects population stratification in rare variant tests by using genetic distance to create phenotype probabilities, maintaining statistical power while controlling type I error.

bioRxiv · Aug 11, 2016 · PreprintGenomics

Novel protective associations with age-related macular degeneration: A common variant near CTRB1 and a rare variant in PELI3

Erin K. Wagner, Yi Yu, Eric H. Souied, Sanna Seitsonen, Ilkka J. Immonen, Paavo Häppölä, Soumya Raychaudhuri, Mark J. Daly, Johanna M. Seddon

This study identifies new protective variants for age-related macular degeneration, including a common variant near CTRB1 and rare variants in PELI3 and CFH.

bioRxiv · Apr 9, 2016 · PreprintGenetics