Sarar Mohamed

417 total citations
37 papers, 289 citations indexed

About

Sarar Mohamed is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Sarar Mohamed has authored 37 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 12 papers in Clinical Biochemistry. Recurrent topics in Sarar Mohamed's work include Metabolism and Genetic Disorders (12 papers), Neonatal Health and Biochemistry (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Sarar Mohamed is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Neonatal Health and Biochemistry (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Sarar Mohamed collaborates with scholars based in Saudi Arabia, Sudan and United Kingdom. Sarar Mohamed's co-authors include Mohamed Khaldi, Khaled K. Abu‐Amero, Mohammed Al‐Owain, Jaak Jaeken, Gert Matthijs, Namik Kaya, M. A. Al Karawi, Mustafa A. Salih, Muddathir H. Hamad and Abdulrahman Alnemri and has published in prestigious journals such as Diabetes, Cochrane Database of Systematic Reviews and Endoscopy.

In The Last Decade

Sarar Mohamed

35 papers receiving 280 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarar Mohamed Saudi Arabia 11 105 79 74 62 49 37 289
Luísa Barros Portugal 11 69 0.7× 85 1.1× 73 1.0× 217 3.5× 20 0.4× 30 442
Nobuaki Takeda Japan 9 95 0.9× 52 0.7× 60 0.8× 110 1.8× 14 0.3× 21 542
P Bouchard France 15 75 0.7× 130 1.6× 26 0.4× 109 1.8× 14 0.3× 28 794
Fu S China 8 56 0.5× 33 0.4× 15 0.2× 8 0.1× 4 0.1× 19 411
S. Degl’Innocenti Italy 12 139 1.3× 50 0.6× 55 0.7× 74 1.2× 26 0.5× 22 405
Inés Camacho Spain 8 34 0.3× 127 1.6× 5 0.1× 12 0.2× 19 0.4× 8 336
Clelia Cipolla Italy 11 90 0.9× 62 0.8× 20 0.3× 58 0.9× 6 0.1× 46 422
Xiaoni Meng China 12 114 1.1× 26 0.3× 68 0.9× 70 1.1× 2 0.0× 33 369
Lars Hynsjö Sweden 9 66 0.6× 46 0.6× 12 0.2× 69 1.1× 11 0.2× 12 344
Fatma Dursun Türkiye 9 63 0.6× 25 0.3× 37 0.5× 60 1.0× 9 0.2× 37 218

Countries citing papers authored by Sarar Mohamed

Since Specialization
Citations

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

Fields of papers citing papers by Sarar Mohamed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarar Mohamed

This figure shows the co-authorship network connecting the top 25 collaborators of Sarar Mohamed. A scholar is included among the top collaborators of Sarar Mohamed 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 Sarar Mohamed. Sarar Mohamed 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
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Abbas, Mohamed, et al.. (2022). The Pattern of Management of Nocturnal Enuresis in a Tertiary Hospital in Sudan. 16(1). 394–396. 2 indexed citations
4.
Alhashem, Amal, et al.. (2020). Molecular and clinical characteristics of very long-chain acyl-CoA dehydrogenase deficiency. Saudi Medical Journal. 41(6). 590–596. 2 indexed citations
5.
Elawad, Mamoun, et al.. (2020). Screening for Fabry disease among 619 hemodialysis patients in Saudi Arabia. Saudi Medical Journal. 41(8). 813–818. 6 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.
Alnemri, Abdulrahman, et al.. (2018). Perinatal and neonatal morbidity among infants of diabetic mothers at a university hospital in Central Saudi Arabia. Saudi Medical Journal. 39(6). 592–597. 11 indexed citations
8.
Mohamed, Sarar, et al.. (2016). Autoimmune thyroiditis associated with Sanjad-Sakati syndrome: A call for regular thyroid screening.. Europe PMC (PubMed Central). 16(2). 41–44. 4 indexed citations
9.
Mohamed, Sarar, et al.. (2015). A CYP21A2 Gene Mutation in Patients with Congenital Adrenal Hyperplasia: Molecular Genetics Report from Saudi Arabia. 84. 1 indexed citations
10.
Mohamed, Sarar, Muddathir H. Hamad, & Khaled K. Abu‐Amero. (2015). Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients. Saudi Medical Journal. 36(9). 1110–1114. 4 indexed citations
11.
Mohamed, Sarar, et al.. (2015). Neurometabolic Disorders-Related Early Childhood Epilepsy: A Single-Center Experience in Saudi Arabia. Pediatrics & Neonatology. 56(6). 393–401. 15 indexed citations
12.
Mohamed, Sarar, et al.. (2015). A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia. Saudi Medical Journal. 36(1). 113–116. 10 indexed citations
13.
Mohamed, Sarar, Muddathir H. Hamad, Altaf A. Kondkar, & Khaled K. Abu‐Amero. (2015). A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia. Saudi Medical Journal. 36(10). 1229–1232. 3 indexed citations
14.
Mohamed, Sarar, et al.. (2014). Congenital toxoplasmosis presenting as central diabetes insipidus in an infant: a case report. BMC Research Notes. 7(1). 184–184. 13 indexed citations
15.
Mohamed, Sarar. (2012). Newborn screening for Glucose-6-Phosphate Dehydrogenase Deficiencyin Eastern Province, Saudi Arabia.. Current Pediatric Research. 16(2). 0. 2 indexed citations
16.
Al-Jurayyan, Nasir A.M., et al.. (2012). Osteomalacia in adolescents presenting as proximal myopathy. Current Paediatrics. 16(1). 0. 2 indexed citations
17.
Mohamed, Sarar, et al.. (2012). Neonatal hyperbilirubinemia and elevated liver enzymes associated withthyroid hormone deficiency in neonates.. Current Pediatric Research. 16(2). 0.
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Al‐Owain, Mohammed, et al.. (2010). A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report. Orphanet Journal of Rare Diseases. 5(1). 7–7. 28 indexed citations
20.
Mohamed, Sarar, et al.. (1997). Therapeutic Endoscopic Retrograde Cholangiopancreatography with Ultra-Short Fluoroscopy: Report of Two Cases. Endoscopy. 29(5). S 31–S 31. 5 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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