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2018

A. Bureau, Begum, F., Taub, M. A., Hetmanski, J. B., Parker, M. M., Albacha-Hejazi, H., Scott, A. F., Murray, J. C., Marazita, M. L., Bailey-Wilson, J. E., Beaty, T. H., and Ruczinski, I., “Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.”, Genet Epidemiol, 2018.

2014

A. Bureau, Younkin, S. G., Parker, M. M., Bailey-Wilson, J. E., Marazita, M. L., Murray, J. C., Mangold, E., Albacha-Hejazi, H., Beaty, T. H., and Ruczinski, I., “Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.”, Bioinformatics, vol. 30, no. 15, pp. 2189-96, 2014.

A. Bureau, Parker, M. M., Ruczinski, I., Taub, M. A., Marazita, M. L., Murray, J. C., Mangold, E., Noethen, M. M., Ludwig, K. U., Hetmanski, J. B., Bailey-Wilson, J. E., Cropp, C. D., Li, Q., Szymczak, S., Albacha-Hejazi, H., Alqosayer, K., L Field, L., Wu-Chou, Y. - H., Doheny, K. F., Ling, H., Scott, A. F., and Beaty, T. H., “Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.”, Genetics, vol. 197, no. 3, pp. 1039-44, 2014.

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