SFARI Funded Publications
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou X., Feliciano P., Shu C., Wang T., Astrovskaya I., Hall J., Obiajulu J.U., Wright J., Murali S., Xuming Xu S., Brueggeman L., Thomas T.R., Marchenko O., Fleisch C., Barns S.D., Green Snyder L., Han B., Chang T.S., Turner T., Harvey W.T., Nishida A., O'Roak B., Geschwind D., SPARK Consortium, Michaelson J., Volfovsky N., Eichler E., Shen Y., Chung W.
De novo variant calling identifies cancer mutation profiles in the 1000 Genomes Project.
Ng J., Vats P., Fritz-Waters E., Sarkar S., Sams E.I., Padhi E.M., Payne Z.L., Leonard S., West M., Prince C., Trani L., Jansen M., Vacek G., Samadi M., Harkins T.T., Pohl C., Turner T.