

Funded Projects
SFARI Funded Publications
Phenotypic and ancestry-related assortative mating in autism.
Zhang J., Weissenkampen J.D., Kember R.L., iPSYCH Consortium, Grove J., Børglum A.D., Robinson E., Brodkin E.S., Almasy L., Bucan M., Sebro R.
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.