Solving genetic heterogeneity in extended families by identifying sub-types of complex diseases. - Arafat Tayeb; Aurélie Labbe; Alexandre Bureau; Chantal Mérette (Comput. Stat., 2011)

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. - Alexandre Bureau; Samuel G. Younkin; Margaret M. Parker; Joan E. Bailey-Wilson; Mary L. Marazita; Jeffrey C. Murray; Elisabeth Mangold; Hasan Albacha-Hejazi; Terri H. Beaty; Ingo Ruczinski (Bioinform., 2014)

Detection of rare disease variants in extended pedigrees using RVS. - Thomas Sherman; Jack M. Fu; Robert B. Scharpf; Alexandre Bureau; Ingo Ruczinski (Bioinform., 2019)

Exploring polypharmacy with artificial intelligence: data analysis protocol. - Caroline Sirois; Richard Khoury; Audrey Durand; Pierre-Luc Déziel; Olga Bukhtiyarova; Yohann Chiu; Denis Talbot; Alexandre Bureau; Philippe Després; Christian Gagné 001; François Laviolette; Anne-Marie Savard; et al. (BMC Medical Informatics Decis. Mak., 2021)