Rosan Kenana

Statistics

Publications

Citations

268

H-Index

Active since

2013

Affiliations

King Faisal Specialist Hospital & Research Centre(Current)

Alfaisal University

King Fahd Medical City

Rosan Kenana is an author at King Faisal Specialist Hospital & Research Centre specializing in genetic syndromes, life sciences, and molecular genetics.

Publications per year

2013–2016

Publications

Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay

Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet et al. · The American Journal of Human Genetics · 2013 · 120 citations

Life Sciences, Genetics, Molecular Genetics +14

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder

Zuhair N. Al‐Hassnan, Mazhor Aldosary, Majid Alfadhel et al. · Journal of Medical Genetics · 2014 · 99 citations

Life Sciences, Genetics, Molecular Genetics +17

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

Namik Kaya, Maysoon Alsagob, Maria Cristina D’Adamo et al. · Journal of Medical Genetics · 2016 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly

Eissa Faqeih, Mohammed Al‐Owain, Dilek Çolak et al. · American Journal of Medical Genetics Part A · 2014 · 23 citations

Life Sciences, Genetics, Molecular Genetics +17

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