Hateley, Shannon

Carrier testing for severe childhood recessive diseases by next-generation sequencing

Bell, C. J., Dinwiddie, D. L., Miller, N. A., Hateley, S. L., Ganusova, E. E., Mudge, J., Langley, R. J., Zhang, L., Lee, C. C., Schilkey, F. D., et al. (2011) · Science Translational Medicine

Genomics and Rare DiseasesPrenatal Screening and Diagnostics

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Genetic diversity loss in the Anthropocene

Exposito-Alonso, M., Booker, T. R., Czech, L., Gillespie, L., Hateley, S., Kyriazis, C. C., Lang, P. L. M., Leventhal, L., Nogues-Bravo, D., Pagowski, V., et al. (2022) · Science

Genetic diversity and population structureEcology and Vegetation Dynamics Studies

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The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele

Hateley, S., Lopez-Izquierdo, A., Jou, C. J., Cho, S., Schraiber, J. G., Song, S., Maguire, C. T., Torres, N., Riedel, M., Bowles, N. E., et al. (2021) · Nature Communications

Cardiac electrophysiology and arrhythmiasGenetic Associations and Epidemiology

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