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Amal Abu-Rayyan

Bethlehem University

15

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727

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Genomic analysis of inherited hearing loss in the Palestinian population.

2020 Proceedings of the National Academy of Sciences of the United States of America
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Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities.

2020
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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

2020 Clinical Genetics
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Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

2017 International Journal of Cancer
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The GPSM2/LGN GoLoco motifs are essential for hearing

2016 Mammalian Genome
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Mutation of KREMEN1 , a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

2016 European Journal of Human Genetics
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Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure

2015 Journal of Medical Genetics
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A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis

2015 Journal of Clinical Investigation
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Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing

2014 European Journal of Human Genetics
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Serotype distribution and drug resistance in Streptococcus pneumoniae, Palestinian Territories.

2011 Emerging Infectious Diseases
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Citations (8)