Kathryn Roeder, Ph.D.

Professor of Statistics and Computational Biology, Carnegie Mellon University

SFARI Investigator Website

Funded Projects

SFARI Funded Publications

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Werling D.M., Brand H., An J.Y., Stone M.R., Zhu L., Glessner J.T., Collins R.L., Dong S., Layer R.M., Markenscoff-Papadimitriou E., Farrell A., Schwartz G.B., Wang H.Z., Currall B.B., Zhao X., Dea J., Duhn C., Erdman C.A., Gilson M.C., Yadav R., Handsaker R.E., Kashin S., Klei L., Mandell J.D., Nowakowski T., Liu Y., Pochareddy S., Smith L., Walker M.F., Waterman M.J., He X., Kriegstein A., Rubenstein J., Sestan N., McCarroll S., Neale B.M., Coon H., Willsey J., Buxbaum J., Daly M., State M., Quinlan A., Marth G., Roeder K., Devlin B., Talkowski M., Sanders S.
Common risk variants identified in autism spectrum disorder. Grove J., Ripke S., Als T.D., Mattheisen M., Walters R., Won H., Pallesen J., Agerbo E., Andreassen O.A., Anney R., Belliveau R., Bettella F., Buxbaum J., Grauholm B.J., Bækved-Hansen M., Cerrato F., Chambert K., Christensen J.H., Churchhouse C., Dellenvall K., Demontis D., De Rubeis S., Devlin B., Djurovic S., Dumont A., Goldstein J., Hansen C.S., Hauberg M.E., Hollegaard M.V., Hope S., Howrigan D.P., Huang H., Hultman C., Klei L., Maller J., Martin J., Martin A.R., Moran J., Nyegaard M., Nærland T., Palmer D.S., Palotie A., Pedersen C.B., Pedersen M.G., Poterba T., Poulsen J.B., Saint Pourcain B., Qvist P., Rehnström K., Reichenberg A., Reichert J., Robinson E., Roeder K., Roussos P., Saemundsen E., Sandin S., Satterstrom F.K., Smith G.D., Stefansson H., Stefansson K., Steinberg S., Stevens C., Sullivan P.F., Turley P., Walters B.G., Xu X., ASD Working Group of the PGC, BUPGEN, Major Depressive Disorder Working Group of the PGC, 23andMe Research Team, Geschwind D., Nordentoft M., Hougaard D.M., Werge T., Mors O., Mortensen P.B., Neale B.M., Daly M., Børglum A.D.
Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families. Werling D.M., Brand H., An J., Stone M.R., Glessner J.T., Zhu L., Collins R.L., Dong S., Layer R.M., Markenscoff-Papadimitriou E., Farrell A., Schwartz G.B., Currall B.B., Dea J., Duhn C., Erdman C., Gilson M., Handsaker R.E., Kashin S., Klei L., Mandell J.D., Nowakowski T., Liu Y., Pochareddy S., Smith L., Walker M.F., Wang H.Z., Waterman M.J., He X., Kriegstein A., Rubenstein J., Sestan N., McCarroll S., Neale B.M., Coon H., Willsey J., Buxbaum J., Daly M., State M., Quinlan A., Marth G., Roeder K., Devlin B., Talkowski M., Sanders S.
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