Funded Projects
SFARI Funded Publications
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Pizzo L., Jensen M., Polyak A., Rosenfeld J.A., Mannik K., Krishnan A., McCready E., Pichon O., Le Caignec C., Van Dijck A., Pope K., Voorhoeve E., Yoon J., Stankiewicz P., Wai Cheung S., Pazuchanics D., Huber E., Kumar V., Kember R., Mari F., Curró A., Castiglia L., Galesi O., Avola E., Mattina T., Fichera M., Mandarà L., Vincent M., Nizon M., Mercier S., Bénéteau C., Blesson S., Martin-Coignard D., Mosca-Boidron A-L., Caberg J.H., Bucan M., Zeesman S., Nowaczyk M.J.M., Lefebvre M., Faivre L., Callier P., Skinner C., Keren B., Perrine C., Prontera P., Marle N., Renieri A., Reymond A., Kooy F.R., Isidor B., Schwartz B., Romano C., Sistermans E., Amor D.J., Andrieux J., Girirajan S.
Functional significance of rare neuroligin 1 variants found in autism.
Nakanishi M., Nomura J., Ji X., Tamada K., Arai T., Takahashi E., Bucan M., Takumi T.
Increased burden of deleterious variants in essential genes in autism spectrum disorder.
Ji X., Kember R.L., Brown C.D., Bucan M.