Agaadir Almoisheer

Statistics

Publications

Citations

449

H-Index

Active since

2014

Affiliations

King Faisal Specialist Hospital & Research Centre(Current)

Alfaisal University

Riyadh Armed Forces Hospital

Security Forces Hospital

King Fahd Medical City

Agaadir Almoisheer is an author at King Faisal Specialist Hospital & Research Centre specializing in genetics, molecular genetics, and genetic disorders.

Publications per year

2014–2017

Publications

Neu-Laxova Syndrome, an Inborn Error of Serine Metabolism, Is Caused by Mutations in PHGDH

Ranad Shaheen, Zuhair Rahbeeni, Amal Alhashem et al. · The American Journal of Human Genetics · 2014 · 122 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism

John J. Reynolds, Louise S. Bicknell, Paula Carroll et al. · Nature Genetics · 2017 · 113 citations · Full text

Life Sciences, Genetics, Molecular Biology +13

A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies

Ranad Shaheen, Miriam Schmidts, Eissa Faqeih et al. · Human Molecular Genetics · 2014 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Identification of a novel MKS locus defined by<i>TMEM107</i>mutation

Ranad Shaheen, Agaadir Almoisheer, Eissa Faqeih et al. · Human Molecular Genetics · 2015 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutation in <i>PLK4</i>, encoding a master regulator of centriole formation, defines a novel locus for primordial dwarfism

Ranad Shaheen, Saeed Al Tala, Agaadir Almoisheer et al. · Journal of Medical Genetics · 2014 · 38 citations

Life Sciences, Genetics, Molecular Genetics +17

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