Publications | Centre de recherche CERVO

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Filtres: Author is Parker, Margaret M [Enlever les filtres]

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., et Ruczinski, I., « Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. », Genet Epidemiol, 2018.

2017

J. Fu, Beaty, T. H., Scott, A. F., Hetmanski, J., Parker, M. M., Wilson, J. E. Bailey, Marazita, M. L., Mangold, E., Albacha-Hejazi, H., Murray, J. C., Bureau, A., Carey, J., Cristiano, S., Ruczinski, I., et Scharpf, R. B., « Whole exome association of rare deletions in multiplex oral cleft families. », Genet Epidemiol, vol. 41, nᵒ 1, p. 61-69, 2017.

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., et Ruczinski, I., « Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. », Bioinformatics, vol. 30, nᵒ 15, p. 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., et 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, p. 1039-44, 2014.

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