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Bhérer, Claude; Eveleigh, Robert; Trajanoska, Katerina; St-Cyr, Janick; Paccard, Antoine; Nadukkalam Ravindran, Praveen; Caron, Elizabeth; Bader Asbah, Nimara; McClelland, Peyton; Wei, Clare; Baumgartner, Iris; Schindewolf, Marc; Döring, Yvonne; Perley, Danielle; Lefebvre, François; Lepage, Pierre; Bourgey, Mathieu; Bourque, Guillaume; Ragoussis, Jiannis; Mooser, Vincent; ... (2024). A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome. NPJ genomic medicine, 9(8) Springer Nature 10.1038/s41525-024-00390-3
Parolin Schnekenberg, Ricardo; Perkins, Emma M.; Miller, Jack W.; Davies, Wayne I. L.; D’Adamo, Maria Cristina; Pessia, Mauro; Fawcett, Katherine A.; Sims, David; Gillard, Elodie; Hudspith, Karl; Skehel, Paul; Williams, Jonathan; O’Regan, Mary; Jayawant, Sandeep; Jefferson, Rosalind; Hughes, Sarah; Lustenberger, Andrea; Ragoussis, Jiannis; Jackson, Mandy; Tucker, Stephen J.; ... (2015). De novo point mutations in patients diagnosed with ataxic cerebral palsy. Brain, 138(7), pp. 1817-1832. Oxford University Press 10.1093/brain/awv117
Bhérer, Claude; Eveleigh, Robert; Trajanoska, Katerina; St-Cry, Janick; Paccard, Antoine; Ravindran, Praveen Nadukkalam; Caron, Elizabeth; Asbah, Nimara Bader; Wei, Claire; Baumgartner, Iris; Schindewolf, Marc; Döring, Yvonne; Perley, Danielle; Lefebvre, François; Lepage, Pierre; Bourgey, Mathieu; Bourque, Guillaume; Ragoussis, Jiannis; Mooser, Vincent and Taliun, Daniel (2023). WEGS: a cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome (In Press) (bioRxiv). Cold Spring Harbor Laboratory 10.1101/2023.04.27.538531
