Under the mentorship of Prof. Yair Anikster and Prof. Annick Raas-Rothschild, his research over the past decade has focused on the molecular basis of inborn errors of metabolism and other rare genetic disorders affecting infants and children. He took part in the discovery of several new genes and previously unrecognized genetic disorders, including DNAJC12-associated movement disorder with hyperphenylalaninemia, PPCS-related autosomal recessive dilated cardiomyopathy, as well as RALGAPA1, TBCD, DNAJC30, TRAK1, COQ5 and SCUBE3 related phenotypes, among others.