Deciphering the fine-structure of tribal admixture in the Bedouin population using genomic data

Keywords

Pedigree chart, Biology, Population, Genetics, Evolutionary biology

References

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Cited by

• Kuwaiti population subgroup of nomadic Bedouin ancestry—Whole genome sequence and analysisSumi Elsa John, Gaurav Thareja, Prashantha Hebbar — 2014
• A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4ADina Fine, Hagit Flusser, Barak Markus — 2014
• Prevalence of Keratoconus among Young Arab students in IsraelRamez Barbara, Ariela Gordon‐Shaag, Michel Millodot — 2014
• UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCNYonatan Perez, Rotem Kadir, Michael Volodarsky — 2015
• CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay.Michael Volodarsky, Hava Lichtig, Tom Leibson — 2015
• Indigenous Arabs are descendants of the earliest split from ancient Eurasian populationsJuan L. Rodríguez-Flores, Khalid A. Fakhro, Francisco Agosto-Perez — 2016
• SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndromeYonatan Perez, Zamir Shorer, Keren Liani-Leibson — 2017
• Testing support for the northern and southern dispersal routes out of Africa: an analysis of Levantine and southern Arabian populations.Deven N. Vyas, Ali Al‐Meeri, Connie J. Mulligan — 2017
• Fast and Accurate Genomic Analyses using Genome GraphsGoran Rakočević, Vladimir Semenyuk, James Spencer — 2017
• A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous CarriersYonatan Perez, Ohad Wormser, Yair Sadaka — 2017
• Genetic history of Latin America : fine-scale population structure, sub-continental ancestry and phenotypic diversityChacon Duque, Juan Camilo — 2018
• Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindredMax Drabkin, Ohad S. Birk, Ruth Birk — 2018
• Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribeOhad Wormser, Libe Gradstein, Einat Kadar — 2018
• SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndromeOhad Wormser, Libe Gradstein, Yuval Yogev — 2019
• Novel MTMR2 mutation causing severe Charcot-Marie-Tooth type 4B1 disease: a case reportDaniel Halpérin, Aviad Sapir, Ohad Wormser — 2020
• Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathyOdeya David, Marina Eskin‐Schwartz, Galina Ling — 2020
• Bioarchaeological analysis of one of the earliest Islamic burials in the LevantMegha Srigyan, Héctor Bolívar, Irène Ureña — 2020
• Forty‐seven pathogenic variants causing autosomal recessive disorders are shared by Israeli and Saudi Arabian ArabsJoël Zlotogora — 2021
• Population structure and inherited genetic disorders in the Bedouin of the NegevA.H. Bittles — 2019
• A syndrome of severe intellectual disability, hypotonia, failure to thrive, dysmorphism, and thinning of corpus callosum maps to chromosome 7q21.13‐q21.3Daniel Halpérin, Nadav Agam, Maher Hallak — 2022

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