Rehab Ali

1.3k total citations
21 papers, 554 citations indexed

About

Rehab Ali is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Rehab Ali has authored 21 papers receiving a total of 554 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Genetics. Recurrent topics in Rehab Ali's work include Genomics and Rare Diseases (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Metabolism and Genetic Disorders (3 papers). Rehab Ali is often cited by papers focused on Genomics and Rare Diseases (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Metabolism and Genetic Disorders (3 papers). Rehab Ali collaborates with scholars based in Qatar, United States and Saudi Arabia. Rehab Ali's co-authors include Mariam Al‐Mureikhi, Noora Shahbeck, Tawfeg Ben‐Omran, Tawfeg Ben‐Omran, Fowzan S. Alkuraya, Mariam AlMulla, Laila Mahmoud, Nader Al‐Dewik, Shenela Lakhani and Zafar Nawaz and has published in prestigious journals such as Journal of the American College of Cardiology, The American Journal of Human Genetics and Gene Therapy.

In The Last Decade

Rehab Ali

19 papers receiving 548 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rehab Ali Qatar 14 286 212 62 54 51 21 554
Tawfeg Ben‐Omran Qatar 11 353 1.2× 225 1.1× 61 1.0× 36 0.7× 43 0.8× 24 584
Gözde Yeşil Türkiye 15 290 1.0× 205 1.0× 30 0.5× 67 1.2× 30 0.6× 78 679
Noora Shahbeck Qatar 11 193 0.7× 143 0.7× 104 1.7× 38 0.7× 62 1.2× 14 426
Adam Mp 6 180 0.6× 113 0.5× 56 0.9× 30 0.6× 37 0.7× 286 388
Bean Ljh 6 180 0.6× 113 0.5× 56 0.9× 30 0.6× 37 0.7× 285 386
Almundher Al‐Maawali Oman 14 312 1.1× 142 0.7× 57 0.9× 18 0.3× 62 1.2× 55 605
Geetha Anand United Kingdom 13 303 1.1× 105 0.5× 77 1.2× 60 1.1× 58 1.1× 34 565
A Amemiya Japan 6 173 0.6× 104 0.5× 53 0.9× 30 0.6× 37 0.7× 269 377
Bird Td United States 6 162 0.6× 90 0.4× 51 0.8× 28 0.5× 35 0.7× 244 342
Mefford Hc 6 163 0.6× 90 0.4× 51 0.8× 27 0.5× 35 0.7× 239 337

Countries citing papers authored by Rehab Ali

Since Specialization
Citations

This map shows the geographic impact of Rehab Ali'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 Rehab Ali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rehab Ali more than expected).

Fields of papers citing papers by Rehab Ali

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rehab Ali. 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 Rehab Ali. The network helps show where Rehab Ali may publish in the future.

Co-authorship network of co-authors of Rehab Ali

This figure shows the co-authorship network connecting the top 25 collaborators of Rehab Ali. A scholar is included among the top collaborators of Rehab Ali based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rehab Ali. Rehab Ali is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ali, Rehab, et al.. (2023). Mucopolysaccharidosis Type VI with Recurrent Chest Infection. Cureus. 15(2). e35229–e35229.
2.
Ali, Rehab, et al.. (2022). Comparison of the Antiseptic Effects of Betadine and Sterillium on Microbial Load of Surgical Hands. Mansoura Nursing Journal. 9(2). 213–222.
3.
4.
Ibrahim, Khalid, Mahmoud F. Elsaid, Mariam AlMulla, et al.. (2021). Gene therapy for spinal muscular atrophy: the Qatari experience. Gene Therapy. 28(10-11). 676–680. 32 indexed citations
5.
Al‐Mureikhi, Mariam, Noora Shahbeck, Rehab Ali, et al.. (2020). A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families. American Journal of Medical Genetics Part A. 182(11). 2570–2580. 8 indexed citations
6.
Almannai, Mohammed, Mohammed A. Saleh, Eissa Faqeih, et al.. (2019). 6-Pyruvoyltetrahydropterin Synthase Deficiency: Review and Report of 28 Arab Subjects. Pediatric Neurology. 96. 40–47. 13 indexed citations
7.
Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2019). Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. American Journal of Medical Genetics Part A. 179(6). 927–935. 32 indexed citations
8.
Eyaid, Wafaa, Kimberli J. Kamer, Rehab Ali, et al.. (2018). A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. JIMD Reports. 43. 79–83. 43 indexed citations
9.
Salem, Hosni, et al.. (2018). WORLDWIDE PREVALENCE OF HYPERTENSION: A POOLED META-ANALYSIS OF 1670 STUDIES IN 71 COUNTRIES WITH 29.5 MILLION PARTICIPANTS. Journal of the American College of Cardiology. 71(11). A1819–A1819. 42 indexed citations
10.
Al‐Dewik, Nader, Mariam Al‐Mureikhi, Noora Shahbeck, et al.. (2018). Clinical genetics and genomic medicine in Qatar. Molecular Genetics & Genomic Medicine. 6(5). 702–712. 20 indexed citations
11.
Gramer, Gwendolyn, Ghassan Abdoh, Tawfeg Ben‐Omran, et al.. (2017). Newborn screening for remethylation disorders and vitamin B12 deficiency-evaluation of new strategies in cohorts from Qatar and Germany. World Journal of Pediatrics. 13(2). 136–143. 18 indexed citations
12.
Mutairi, Fuad Al, Majid Alfadhel, Marwan Nashabat, et al.. (2017). Phenotypic and Molecular Spectrum of Aicardi-Goutières Syndrome: A Study of 24 Patients. Pediatric Neurology. 78. 35–40. 35 indexed citations
13.
Elsaid, Mahmoud F., et al.. (2016). W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report. BMC Medical Genetics. 17(1). 53–53. 21 indexed citations
14.
Shaheen, Ranad, Shams Anazi, Tawfeg Ben‐Omran, et al.. (2016). Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice. The American Journal of Human Genetics. 98(4). 643–652. 47 indexed citations
15.
Al‐Dewik, Nader, Mariam Al‐Mureikhi, Rehab Ali, et al.. (2015). High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders. Human Genetics. 134(9). 967–980. 140 indexed citations
16.
Ali, Rehab, et al.. (2015). Pierson syndrome: A case report with a neonatal cardiac association based on a novel mutation in the LAMB2 gene. Journal of Clinical Neonatology. 4(4). 281–281. 1 indexed citations
17.
Kambouris, Marios, Rachid C. Maroun, Tawfeg Ben‐Omran, et al.. (2014). Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome. Orphanet Journal of Rare Diseases. 9(1). 80–80. 16 indexed citations
18.
Ben‐Omran, Tawfeg, Rehab Ali, Mariam Al‐Mureikhi, et al.. (2011). Phenotypic heterogeneity in Woodhouse–Sakati syndrome: Two new families with a mutation in the C2orf37 gene. American Journal of Medical Genetics Part A. 155(11). 2647–2653. 24 indexed citations
19.
Anastasio, Natascia, Tawfeg Ben‐Omran, Ahmad S. Teebi, et al.. (2010). Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome. The American Journal of Human Genetics. 87(4). 553–559. 45 indexed citations
20.
Ali, Rehab, et al.. (2010). Further delineation of the Van den Ende–Gupta syndrome. American Journal of Medical Genetics Part A. 152A(12). 3095–3100. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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