Publications | Page 5 | Cervo Brain Research Centre

Export 5 results:

Filters: Author is Ruczinski, Ingo [Clear All Filters]

2018

Sherman T, Fu J, Scharpf RB, Bureau A, Ruczinski I. Detection of rare disease variants in extended pedigrees using RVS. Bioinformatics. 2018.

Bureau A, Begum F, Taub MA, Hetmanski JB, Parker MM, Albacha-Hejazi H, Scott AF, Murray JC, Marazita ML, Bailey-Wilson JE, Beaty TH, Ruczinski I. Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genet Epidemiol. 2018.

2017

Fu J, Beaty TH, Scott AF, Hetmanski J, Parker MM, Wilson JEB, Marazita ML, Mangold E, Albacha-Hejazi H, Murray JC, Bureau A, Carey J, Cristiano S, Ruczinski I, Scharpf RB. Whole exome association of rare deletions in multiplex oral cleft families. Genet Epidemiol. 2017;41(1):61-69.

2014

Bureau A, Younkin SG, Parker MM, Bailey-Wilson JE, Marazita ML, Murray JC, Mangold E, Albacha-Hejazi H, Beaty TH, Ruczinski I. Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics. 2014;30(15):2189-96.

Bureau A, Parker MM, Ruczinski I, Taub MA, Marazita ML, Murray JC, Mangold E, Noethen MM, Ludwig KU, Hetmanski JB, Bailey-Wilson JE, Cropp CD, Li Q, Szymczak S, Albacha-Hejazi H, Alqosayer K, L Field L, Wu-Chou Y-H, Doheny KF, Ling H, Scott AF, Beaty TH. Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. Genetics. 2014;197(3):1039-44.

Participate in
clinical studies

Funding / Support / Partners

© Gouvernement du Québec, 2018