Trial of carnitine therapy in TMLHE deficiency and non-dysmorphic autism

Awarded: 2012
Award Type: Research

Simons Variation in Individuals Project (Simons VIP)

Awarded: 2011
Award Type: Simons Searchlight

A genome-wide search for autism genes in the Simons Simplex Collection

Awarded: 2008
Award Type: Research

Brain carnitine deficiency causes nonsyndromic autism with an extreme male bias: A hypothesis. Beaudet A.

Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci. Sanders S., He X., Willsey A. J., Ercan-Sencicek A.G., Samocha K.E., Çiçek A. E., Murtha M.T., Bal V.H., Bishop S., Dong S., Goldberg A.P., Jinlu C., Keaney J.F. 3rd, Klei L., Mandell J.D., Moreno-De-Luca D., Poultney C.S., Robinson E., Smith L., Solli-Nowlan T., Su M.Y., Teran N.A., Walker M.F., Werling D., Beaudet A., Cantor R.M., Fombonne E., Geschwind D., Grice D.E., Lord C., Lowe J.K., Mane S.M., Martin D.M., Morrow E., Talkowski M., Sutcliffe J., Walsh C., Yu T., Autism Sequencing Consortium, Ledbetter D., Martin C. L., Cook E. H., Buxbaum J., Daly M., Devlin B., Roeder K., State M.

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Chaste P., Klei L., Sanders S., Hus V., Murtha M.T., Lowe J.K., Willsey A. J., Moreno-De-Luca D., Yu T., Fombonne E., Geschwind D., Grice D.E., Ledbetter D., Mane S.M., Martin D.M., Morrow E., Walsh C., Sutcliffe J., Martin C. L., Beaudet A., Lord C., State M., Cook E. H., Devlin B.