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Ernst C., Nagy C., Kim S., Yang J.P., Deng X., Hellstrom I.C., Choi K.H., Gershenfeld H., Meaney M., Turecki G. (2011). Dysfunction of astrocyte connexins 30 and 43 in dorsal lateral prefrontal cortex of suicide completers, Biol Psychiatry, 70(4), 312-319. En savoir plus.

Ernst C., Wanner B., Brezo J., Vitaro F., Tremblay R., Turecki G. (2011). A deletion in tropomyosin-related kinase B and the development of human anxiety, Biol Psychiatry, 69(6), 604-607. En savoir plus.

Talkowski M.E., Ernst C., Heilbut A., Chiang C., Hanscom C., Lindgren A., Kirby A., Liu S., Muddukrishna B., Ohsumi T.K., Shen Y., Borowsky M., Daly M.J., Morton C.C., Gusella J.F. (2011). Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research, Am J Hum Genet, 88(4), 469-481. En savoir plus.

Talkowski M.E., Mullegama S.V., Rosenfeld J.A., van Bon B.W., Shen Y., Repnikova E.A., Gastier-Foster J., Thrush D.L., Kathiresan S., Ruderfer D.M., Chiang C., Hanscom C., Ernst C., Lindgren A.M., Morton C.C., An Y., Astbury C., Brueton L.A., Lichtenbelt K.D., Ades L.C., Fichera M., Romano C., Innis J.W., Williams C.A., Bartholomew D., Van Allen M.I., Parikh A., Zhang L., Wu L., Pyatt R.E., Schwartz S., Shaffer L.G., de Vries B.B., Gusella J.F., Elsea S.H. (2011). Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder, Am J Hum Genet, 89(4), 551-563. En savoir plus.