Ellen Grant, M.D.

Director, Fetal-Neonatal Neuroimaging and Developmental Science Center, Boston Children’s Hospital
Associate Professor, Harvard Medical School

SFARI Investigator, SFARI Scientific Review Board Website

Funded Projects

SFARI Funded Publications

Defining the effect of the 16p11.2 duplication on cognition, behavior, and medical comorbidities. D'Angelo D., Lebon S., Chen Q., Martin-Brevet S., Snyder L.G., Hippolyte L., Hanson E., Maillard A.M., Faucett W.A., Macé A., Pain A., Bernier R., Chawner S.J., David A., Andrieux J., Aylward E., Baujat G., Caldeira I., Conus P., Ferrari C., Forzano F., Gérard M., Goin-Kochel R., Grant E., Hunter J., Isidor B., Jacquette A., Jonch A.E., Keren B., Lacombe D., Le Caignec C., Martin C.L., Männik K., Metspalu A., Mignot C., Mukherjee P., Owen M.J., Passeggeri M., Rooryck-Thambo C., Rosenfeld J.A., Spence S., Steinman K.J., Tjernagel J., Van Haelst M., Shen Y., Draganski B., Sherr E., Ledbetter D., van den Bree M.B., Beckmann J.S., Spiro J., Reymond A., Jacquemont S., Chung W., Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, the 16p11, 2 European Consortium, and the Simons Variation in Individuals Project (VIP) Consortium.
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. Zufferey F., Sherr E., Beckmann N.D., Hanson E., Maillard A.M., Hippolyte L., Macé A., Ferrari C., Kutalik Z., Andrieux J., Aylward E., Barker M., Bernier R., Bouquillon S., Conus P., Delobel B., Faucett A., Goin-Kochel R., Grant E., Harewood L., Hunter J., Lebon S., Ledbetter D., Martin C. L., Mannik K., Martinet D., Mukherjee P., Ramocki M.B., Spence S., Steinman K., Tjernagel J., Spiro J., Reymond A., Beckmann J.S., Chung W., Jacquemont S., Simons VIP Consortium, 16p11.2 European Consortium.
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