Banan Al‐Younes

1.7k citations

18 papers · 387 indexed · h-index 12

Clinical Biochemistry
- Metabolism and Genetic Disorders 2
Hematology
Genetics
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 2
Molecular Biology
Ophthalmology top 10%
- Retinal Diseases and Treatments 2
Infectious Diseases
- COVID-19 Clinical Research Studies 2
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 2
Plant Science
- Chromosomal and Genetic Variations 2

Co-authors: Brian F. Meyer Dorota Monies Dilek Çolak Mohamed Abouelhoda Namik Kaya Albandary AlBakheet Salma M. Wakil Nada Al Tassan
Cited by: Clinical Biochemistry Hematology Genetics
Journals: Gene (1 paper)Investigative Ophthalmology & Visual Science (1 paper)Genomics (1 paper)
Partner nations: Saudi Arabia Türkiye United Kingdom

In The Last Decade

Banan Al‐Younes

18 papers receiving 379 citations

Peers

Countries citing papers authored by Banan Al‐Younes

Since Specialization

Citations

This map shows the geographic impact of Banan Al‐Younes's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Banan Al‐Younes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Banan Al‐Younes more than expected).

Fields of papers citing papers by Banan Al‐Younes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Banan Al‐Younes. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Banan Al‐Younes. The network helps show where Banan Al‐Younes may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Banan Al‐Younes, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Banan Al‐Younes Line = papers co-authored together Banan Al‐Younes links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Clinical characteristics, risk factors, and rate of severity of a nationwide COVID-19 Saudi cohort Saudi Journal of Biological Sciences ·Nouf S. Al‐Numair,Banan Al‐Younes,Haya Al‐Saud,Rabih Halwani,Saleh Al‐Muhsen	2022	5
2	Favipiravir Effectiveness and Safety in Hospitalized Moderate-Severe COVID-19 Patients: Observational Prospective Multicenter Investigation in Saudi Arabia Frontiers in Medicine ·Saleh Al‐Muhsen,Nouf S. Al‐Numair,Narjes Saheb Sharif‐Askari,Roaa Basamh,Banan Al‐Younes,Amjad Jabaan,Fatemeh Saheb Sharif‐Askari,Mohammed F. Alosaimi,Fahad Alsohime,Rabih Halwani,Haya Al‐Saud	2022	8
3	Identification of a novel genetic locus underlying tremor and dystonia Human Genomics ·Dorota Monies,Hussam Abou‐Al‐Shaar,Ewa Goljan,Banan Al‐Younes,Muna Albreacan,Maher Al‐Saif,Salma M. Wakil,Brian F. Meyer,Khalid S.A. Khabar,Saeed Bohlega	2017	5
4	Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism Human Genomics ·Abdulaziz Alsemari,Banan Al‐Younes,Ewa Goljan,Dyala Jaroudi,Faisal S. BinHumaid,Brian F. Meyer,Stefan T. Arold,Dorota Monies	2017	13
5	A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies Human Genomics ·Dorota Monies,Hindi Al‐Hindi,Mohamed Almuhaizea,Mohamed Abouelhoda,Anas M. Alazami,Ewa Goljan,Banan Al‐Younes,Dyala Jaroudi,Abdulelah AlIssa,Khalid Alabdulrahman,Shazia Subhani,Mohamed El-Kalioby,Tariq Faquih,Salma M. Wakil,Nada Al Tassan,Brian F. Meyer,Saeed Bohlega	2016	29
6	Exome-based case–control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy Human Genetics ·Corina Shtir,Mohammed A. Aldahmesh,Saad Al-Dahmash,Emad B. Abboud,Hisham Alkuraya,Marwan A. Abouammoh,Sawsan R. Nowailaty,Ghazai Al-Thubaiti,Ewa A. Naim,Banan Al‐Younes,Faisal S. BinHumaid,Alanoud Alotaibi,Anfal Altamimi,F. H. Alamer,Mais Hashem,Mohamed Abouelhoda,Dorota Monies,Fowzan S. Alkuraya	2015	35
7	Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome Neuromuscular Disorders ·Dorota Monies,Hindi Al‐Hindi,Mohamed Almuhaizea,Dyala Jaroudi,Banan Al‐Younes,Ewa A. Naim,Salma M. Wakil,Brian F. Meyer,Saeed Bohlega	2014	20
8	Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis Arthritis & Rheumatology ·Salma M. Wakil,Dorota Monies,Mohamed Abouelhoda,Nada Al Tassan,Haya Al‐Dusery,Ewa A. Naim,Banan Al‐Younes,Jameela Shinwari,Futwan A. Al‐Mohanna,Brian F. Meyer,Sulaiman M. Al‐Mayouf	2014	88
9	Expanding Phenotypic and Allelic Heterogeneity of Tricho‐Hepato‐Enteric Syndrome Journal of Pediatric Gastroenterology and Nutrition ·Dorota Monies,Zuhair Rahbeeni,Mohamed Abouelhoda,Ewa A. Naim,Banan Al‐Younes,Brian F. Meyer,Ali Al‐Mehaidib	2014	17
10	Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia Gene ·Namik Kaya,Dilek Çolak,Albandary AlBakheet,Banan Al‐Younes,Sahar Tulbah,Maha H. Daghestani,Fuad Al-Mutairi,Mohammed Uthman A. Alamoudi,Ali Al‐Odaib,Aida I. Al‐Aqeel	2012	3
11	A novel syndrome of abnormal striatum and congenital cataract: evidence for linkage to chromosomes 11 Clinical Genetics ·Mohammad Al-Owain,Jawaher Al‐Zahrani,A Al‐Bakheet,Nada AbuDheim,Banan Al‐Younes,Hesham Aldhalaan,Hamad Alzaidan,Dilek Çolak,Fahad Al‐Mohaileb,Mohei Abouzied,Fatima Alfadhli,Brian F. Meyer,Namik Kaya	2012	5
12	Genome-Wide Expression Profiling of Patients with Primary Open Angle Glaucoma Investigative Ophthalmology & Visual Science ·Dilek Çolak,J.M. Morales,Thomas M. Bosley,Albandary AlBakheet,Banan Al‐Younes,Namik Kaya,Khaled K. Abu‐Amero	2012	13
13	Clinical and biochemical features associated with BCS1L mutation Journal of Inherited Metabolic Disease ·Mohammed Al‐Owain,Dilek Çolak,Albandary AlBakheet,Banan Al‐Younes,Zainab Alhumaidi,Moeen Al‐Sayed,Hindi Al‐Hindi,Abdulaziz Al‐Sugair,Ahmed Almuhaideb,Zuhair Rahbeeni,Abdullah Al‐Sehli,Fatima Alfadhli,Pinar T. Ozand,Robert W. Taylor,Namik Kaya	2012	28
14	Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Namik Kaya,Hesham Aldhalaan,Banan Al‐Younes,Dilek Çolak,Taghreed Shuaib,Fahad Al‐Mohaileb,Abdulaziz Al‐Sugair,Michael Nester,Suad Alyamani,Albandary AlBakheet,Nadia Alhashmi,Moeen Al‐Sayed,Brian F. Meyer,Heinz Jungbluth,Mohammed Al‐Owain	2011	53
15	Novel mutation in GLRB in a large family with hereditary hyperekplexia Clinical Genetics ·Mohammad Al-Owain,Dilek Çolak,A Al‐Bakheet,N Al‐Hashmi,Taghreed Shuaib,Amal Al‐Hemidan,Hesham Aldhalaan,Zuhair Rahbeeni,Moeen Al‐Sayed,Banan Al‐Younes,PT Ozand,Namik Kaya	2011	26
16	A novel interstitial microdeletion of 7q22.1‐7q22.3 detected by array comparative genomic hybridization American Journal of Medical Genetics Part A ·Zuhair N. Al‐Hassnan,Albandary AlBakheet,Nada AbuDheim,Banan Al‐Younes,Dilek Çolak,Namik Kaya	2011	7
17	Novel V97G ASAH1 mutation found in Farber disease patients: Unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral nervous system Brain and Development ·Aziza Chedrawi,Zuhair N. Al‐Hassnan,Muhammad Al-Muhaizea,Dilek Çolak,Banan Al‐Younes,Albandary AlBakheet,Sahar Tulba,Namik Kaya	2011	14
18	Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways Genomics ·Dilek Çolak,Hesham Aldhalaan,Michael Nester,Albandary AlBakheet,Banan Al‐Younes,Zohair Al-Hassnan,Mohammad Aldosari,Aziza Chedrawi,Muhammad Al-Owain,Nada AbuDheim,Laila Al‐Alwan,Ali Al‐Odaib,Pinar T. Ozand,Mehmet Sait Inan,Namik Kaya	2010	18

About Banan Al‐Younes

Banan Al‐Younes is a scholar working on Clinical Biochemistry, Genetics and Ophthalmology, having authored 18 papers that have together received 387 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Metabolism and Genetic Disorders (2 papers), Retinal Diseases and Treatments (2 papers), COVID-19 Clinical Research Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Clinical Biochemistry (35 citations), Hematology (49 citations) and Genetics (92 citations). Banan Al‐Younes has collaborated with scholars based in Saudi Arabia, Türkiye and United Kingdom. Frequent co-authors include Brian F. Meyer, Dorota Monies, Dilek Çolak, Mohamed Abouelhoda, Namik Kaya, Albandary AlBakheet, Salma M. Wakil, Nada Al Tassan, Sulaiman M. Al‐Mayouf and Jameela Shinwari. Their work appears in journals such as Gene, Investigative Ophthalmology & Visual Science and Genomics.

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