

Kennedy Family Professor of Pediatrics in Medicine, Columbia University
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SFARI Funded Publications
Recessive rare variants in deoxyhypusine synthase, an enzyme involved in the synthesis of hypusine, are associated with a neurodevelopmental disorder.
Ganapathi M., Padgett L.R., Yamada K., Devinsky O., Willaert R., Person R., Au P.B., Tagoe J., McDonald M., Karlowicz D., Wolf B., Lee J., Shen Y., Okur V., Deng L., LeDuc C.A., Wang J., Hanner A., Mirmira R.G., Park M.H., Mastracci T.L., Chung W.
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Niarchou M., Chawner S., Doherty J.L., Maillard A.M., Jacquemont S., Chung W., Green Snyder L., Bernier R., Goin-Kochel R., Hanson E., Linden D.E.J., Linden S.C., Raymond F.L., Skuse D., Hall J., Owen M.J., van den Bree M.B.M.
Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes.
Feliciano P., Zhou X., Astrovskaya I., Turner T., Wang T., Brueggeman L., Barnard R., Hsieh A., Green Snyder L., Muzny D., Sabo A., SPARK Consortium, Gibbs R., Eichler E., O'Roak B., Michaelson J., Volfovsky N., Shen Y., Chung W.