Khader Badarneh

Carrier frequency of autosomal‐recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?

F. Fares, R. Diukman, Khader Badarneh, 2008, Prenatal diagnosis.

Whole-Exome Sequencing Identifies a Novel Homozygous Frameshift Mutation in the MTMR2 Gene as a Causative Mutation in a Patient with Charcot-Marie-Tooth Disease Type 4B1

F. Fares, A. Peleg, O. Sadeh, 2018, Molecular Neurobiology.

Comparative screening of FMF mutations in various communities of the Israeli society.

A. Azem, M. Mahajnah, R. Sharkia, 2013, European journal of medical genetics.