Banan Al‐Younes - Concepedia

Author

Banan Al‐Younes

King Faisal Specialist Hospital & Research Centre

Also Known As

B Al‐Younes, B. ALYounes, Banan Al-Younes, Banan AlYounes, Banan Alyounes, Banan Al‐Younes

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre King Abdulaziz City for Science and Technology Alfaisal University King Saud University Riyadh Armed Forces Hospital

About

Banan Al‐Younes is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, genetics, and systems biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	300
2	Natural Sciences	1	1	50
3	Diabetes	1	1	53
4	Molecular Biology	1	1	50
5	Molecular Genetics	1	1	11

Banan Al‐Younes

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin, Cell Reports	2014	465
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Human Genetics	2017	296
Association of a Mutation in <i>LACC1</i> With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis Salma M. Wakil, Dorota Monies, Mohamed Abouelhoda, Arthritis & Rheumatology	2014	136
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Genetics in Medicine Ocular DiseaseRetinaOphthalmologyGeneticsLocus Heterogeneity	2015	109
A novel X‐linked disorder with developmental delay and autistic features Namik Kaya, Dilek Çolak, Albandary AlBakheet, Annals of Neurology	2011	72
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the <i>CA8</i> gene, encoding carbonic anhydrase (CA) VIII Namik Kaya, Hesham Aldhalaan, Banan Al‐Younes, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2011	62
Exome-based case–control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy Corina Shtir, Mohammed A. Aldahmesh, Saad Al-Dahmash, Human Genetics Genome-wide Association StudyDiabetic RetinopathyOcular DiseaseOphthalmologyDiabetes	2015	53
METTL23, a transcriptional partner of GABPA, is essential for human cognition Rachel E. Reiff, Bassam R. Ali, Byron Baron, Human Molecular Genetics Transcriptional RegulationSystems BiologyGenetic DisorderArab OriginGenetics	2014	50
Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking Leslie E. Sanderson, Kristina Lanko, Maysoon Alsagob, Brain	2021	50
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies Dorota Monies, Hindi Al‐Hindi, Mohamed Almuhaizea, Human Genomics	2016	38

Page 1