Andrew Faucett, M.S.

Genetic Counselor & Director of Policy and Education, Autism & Developmental Medicine Institute, Geisinger Health System

SFARI Investigator Website

Funded Projects

Simons Variation in Individuals Project (Simons VIP)

Awarded: 2011
Award Type: Simons Searchlight

SFARI Funded Publications

Incorporating social media into your support tool box: Points to consider from genetics-based communities. Rocha H.M., Savatt J.M., Riggs E.R., Wagner J.K., Faucett A., Martin C. L., Valdivia Espino J.

The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. Moreno-De-Luca A., Evans D.W., Boomer K.B., Hanson E., Bernier R., Goin-Kochel R., Myers S.M., Challman T.D., Moreno-De-Luca D., Slane M.M., Hare A.E., Chung W., Spiro J., Faucett A., Martin C. L., Ledbetter D.

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.