Alexandre Reymond, Ph.D.

Professor, University of Lausanne

SFARI Investigator Website

Funded Projects

SFARI Funded Publications

Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus. Männik K., Arbogast T., Lepamets M., Lepik K., Pellaz A., Ademi H., Kupchinsky Z.A., Ellegood J., Attanasio C., Messina A., Rotman S., Martin-Brevet S., Dubruc E., Chrast J., Lerch J., Qiu L.R., Laisk T., The 16p11.2 European Consortium, The Simons VIP Consortium, The eQTLGen Consortium, Henkelman R.M., Jacquemon S., Herault Y., Lindgren C.M., Peterson H., Stehle J.C., Katsanis N., Kutalik Z., Nef S., Draganski B., Davis E.E., Mägi R., Reymond A.
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.
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