Shinya Yamamoto, D.V.M., Ph.D.

Assistant Professor, Baylor College of Medicine

SFARI Investigator Website

Funded Projects

SFARI Funded Publications

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases. Marcogliese P.C., Deal S.L., Andrews J., Harnish J.M., Bhavana V.H., Graves H.K., Jangam S., Luo X., Liu N., Bei D., Chao Y.-H., Hull B., Lee P.-T., Pan H., Longley C.M., Chao H.-T., Chung H., Haelterman N.A., Kanca O., Manivannan S.N., Rossetti L.Z., Gerard A., Schwaibold E.M.C., Guerrini R., Vetro A., England E., Murali C.N., Barakat T.S., van Dooren M.F., Wilke M., van Slegtenhorst M., Lesca G., Sabatier I., Chatron N., Brownstein C.A., Madden J.A., Agrawal P.B., Pavinato L., Brusco A., Rosenfeld J.A., Marom R., Wangler M., Yamamoto S.
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders Guo H., Bettella E., Marcogliese P.C., Zhao R., Andrews J.C., Nowakowski T., Gillentine M.A., Hoekzema K., Wang T., Wu H., Jangam S., Liu C., Ni H., Willemsen M.H., van Bon B.W., Rinne T., Stevens S.J.C., Kleefstra T., Brunner H.G., Yntema H.G., Long M., Zhao W., Hu Z., Colson C., Richard N., Schwartz C.E., Romano C., Castiglia L., Bottitta M., Dhar S.U., Erwin D.J., Emrick L., Keren B., Afenjar A., Zhu B., Bai B., Stankiewicz P., Herman K., University of Washington Center for Mendelian Genomics, Mercimek-Andrews S., Juusola J., Wilfert A.B., Abou Jamra R., Büttner B., Mefford H., Muir A.M., Scheffer I.E., Regan B.M., Malone S., Gecz J., Cobben J., Weiss M.M., Waisfisz Q., Bijlsma E.K., Hoffer M.J.V., Ruivenkamp C.A.L., Sartori S., Xia F., Rosenfeld J.A., Bernier R., Wangler M., Yamamoto S., Xia K., Stegmann A.P.A., Bellen H.J., Murgia A., Eichler E.
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