Amal Abu Rayyan

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

T. Walsh, M. King, N. Shomron, 2011, Genome Biology.

Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

T. Walsh, M. King, Ming K. Lee, 2016, European Journal of Human Genetics.

Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

M. King, S. Pierce, B. Norquist, 2020, Cold Spring Harbor molecular case studies.

Serotype Distribution and Drug Resistance in Streptococcus pneumoniae

Palestinian Territories, M. Hindiyeh, Amal Abu Rayyan, 2011 .

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

C. Baker, T. Walsh, M. King, 2010, European Journal of Human Genetics.