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Export 3 results:
Filters: Author is Scott, Alan F  [Clear All Filters]
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.
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., and Scharpf, R. B., “Whole exome association of rare deletions in multiplex oral cleft families.”, Genet Epidemiol, vol. 41, no. 1, pp. 61-69, 2017.
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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