

Funded Projects
SFARI Funded Publications
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Einson J., Glinos D., Boerwinkle E., Castaldi P., Darbar D., de Andrade M., Ellinor P., Fornage M., Gabriel S., Germer S., Gibbs R., Hersh C.P., Johnsen J., Pstay B., Vasan R.S., Rich S.S., Rienstra M., Rotter J.I., Saferali A., Shoemaker M.B., Silverman E., Smith A.V., NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Mohammadi P., Castel S.E., Iossifov I., Lappalainen T.
Sharing parental genomes by siblings concordant or discordant for autism.
Wroten M., Yoon S., Andrews P., Yamrom B., Ronemus A., Buja A., Krieger A., Levy D., Ye K., Wigler M., Iossifov I.
Rates of contributory de novo mutation in high and low-risk autism families.
Yoon S., Munoz A., Yamrom B., Lee Y.-h., Andrews P., Marks S., Wang Z., Reeves C., Winterkorn L., Krieger A., Buja A., Pradhan K., Ronemus M., Baldwin K.K., Levy D., Wigler M., Iossifov I.
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