Louis Kunkel, Ph.D.

Director, Genomics Program, Boston Children’s Hospital
Professor of Genetics and Pediatrics, Harvard Medical School

SFARI Investigator, SFARI Scientific Review Board Website

Divergent dysregulation of gene expression in murine models of fragile x syndrome and tuberous sclerosis. Kong S.W., Sahin M., Collins C.D., Wertz M.H., Campbell M.G., Leech J.D., Krueger D., Bear M., Kunkel L., Kohane I.S.

Peripheral blood gene expression signature differentiates children with autism from unaffected siblings. Kong S.W., Shimizu-Motohashi Y., Campbell M.G., Lee I.H., Collins C.D., Brewster S.J., Holm I.A., Rappaport L., Kohane I.S., Kunkel L.

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders. Kong S.W., Collins C.D., Shimizu-Motohashi Y., Holm I.A., Campbell M.G., Lee I.H., Brewster S.J., Hanson E., Harris H.K., Lowe K.R., Saada A., Mora A., Madison K., Hundley R., Egan J., McCarthy J., Eran A., Galdzicki M., Rappaport L., Kunkel L., Kohane I.S.