Sarar Mohamed

811 total citations
27 papers, 184 citations indexed

About

Sarar Mohamed is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Sarar Mohamed has authored 27 papers receiving a total of 184 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Sarar Mohamed's work include Metabolism and Genetic Disorders (5 papers), Genomics and Rare Diseases (3 papers) and Neonatal Health and Biochemistry (3 papers). Sarar Mohamed is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Genomics and Rare Diseases (3 papers) and Neonatal Health and Biochemistry (3 papers). Sarar Mohamed collaborates with scholars based in Saudi Arabia, Egypt and Lebanon. Sarar Mohamed's co-authors include Rana Hasanato, Amir Babiker, Abdulrahman Alnemri, Tarek Kashour, Imran Ali Khan, Khalid Khalaf Alharbi, Waleed Tamimi, Amal Alhashem, Yasser Sami Amer and Aida I. Al‐Aqeel and has published in prestigious journals such as Lipids in Health and Disease, Journal of Evaluation in Clinical Practice and American Journal of Medical Genetics Part A.

In The Last Decade

Sarar Mohamed

25 papers receiving 181 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 8 49 42 29 27 25 27 184
Mitch Goldman United States 6 64 1.3× 5 0.1× 39 1.3× 11 0.4× 27 1.1× 8 423
Janine Bullard United States 7 65 1.3× 20 0.5× 202 7.0× 11 0.4× 47 1.9× 9 446
Evelina Maines Italy 10 67 1.4× 64 1.5× 42 1.4× 69 2.6× 43 1.7× 53 325
Deirdre E. Donnelly United Kingdom 7 51 1.0× 21 0.5× 23 0.8× 11 0.4× 2 0.1× 17 252
Jennie Harré Hindmarsh New Zealand 10 73 1.5× 7 0.2× 44 1.5× 14 0.5× 8 0.3× 17 282
Jolanta Sawicka-Powierza Poland 9 60 1.2× 30 0.7× 10 0.3× 10 0.4× 18 0.7× 35 243
N. Ben Achour Tunisia 10 31 0.6× 6 0.1× 28 1.0× 34 1.3× 16 0.6× 45 269
Maria Koutsaki Greece 9 153 3.1× 5 0.1× 32 1.1× 7 0.3× 79 3.2× 19 334
Ariunaa Togtokh Mongolia 7 57 1.2× 3 0.1× 20 0.7× 69 2.6× 11 0.4× 7 251
Jing Cheng China 11 63 1.3× 26 0.6× 58 2.0× 60 2.2× 41 1.6× 25 316

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
1.
Alhashem, Amal, et al.. (2022). A Biallelic Variant in FRA10AC1 Is Associated With Neurodevelopmental Disorder and Growth Retardation. Neurology Genetics. 8(4). e200010–e200010. 3 indexed citations
2.
Marais, Anett, Aida M. Bertoli‐Avella, Christian Beetz, et al.. (2022). Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European Journal of Medical Genetics. 65(8). 104537–104537. 4 indexed citations
3.
Mohamed, Sarar, et al.. (2022). A novel variant of RBCK1 gene causes mild polyglucosan myopathy. Neurosciences. 27(1). 45–49. 4 indexed citations
4.
Mohamed, Sarar, W Elsheikh, Aida I. Al‐Aqeel, et al.. (2020). Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. Saudi Medical Journal. 41(7). 703–708. 17 indexed citations
5.
Alhashem, Amal, et al.. (2020). Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis. Saudi Medical Journal. 41(2). 199–202. 4 indexed citations
6.
Mohamed, Sarar, et al.. (2019). Methionyl-tRNA synthetase novel mutation causes pulmonary alveolar proteinosis. Saudi Medical Journal. 40(2). 195–198. 7 indexed citations
7.
Abbas, Mohammed, et al.. (2019). Assessment of professionalism among medical students at a regional university in Saudi Arabia. PubMed. 19(2). 140–144. 2 indexed citations
8.
Hundallah, Khalid, et al.. (2018). A novel variant in ATM gene causes ataxia telangiectasia revealed by whole-exome sequencing. Neurosciences. 23(2). 162–164. 4 indexed citations
9.
Mohamed, Sarar, et al.. (2018). Prevalence of obesity, overweight, underweight, and stunting among school children in Argo city, Northern Sudan. PubMed. 18(2). 15–19. 5 indexed citations
10.
Amer, Yasser Sami, et al.. (2018). Perception, attitude, and satisfaction of paediatric physicians and nurses towards clinical practice guidelines at a university teaching hospital. Journal of Evaluation in Clinical Practice. 25(4). 543–549. 10 indexed citations
11.
Al-Jurayyan, Nasir A.M., et al.. (2017). Precocious puberty: An experience from a major teaching hospital in Central Saudi Arabia.. Europe PMC (PubMed Central). 17(1). 19–24. 6 indexed citations
12.
Mohamed, Sarar, et al.. (2016). The perception of safety culture among nurses in a tertiary hospital in Central Saudi Arabia.. PubMed. 16(2). 51–58. 20 indexed citations
13.
Kozak, Igor, Darren T. Oystreck, Khaled K. Abu‐Amero, et al.. (2016). NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS–SAYRE SYNDROME. Retinal Cases & Brief Reports. 12(4). 349–358. 7 indexed citations
14.
Mohamed, Sarar, et al.. (2015). Prevalence of Thinness, Stunting and Anemia Among Rural School-aged Sudanese Children: A Cross-sectional Study. Journal of Tropical Pediatrics. 61(4). 260–265. 11 indexed citations
15.
Mohamed, Sarar. (2014). From Concept to Bedside: What Pediatricians Should Know about Synthesis of Clinical Practice Guidelines?. PubMed. 24(5). 557–64. 2 indexed citations
16.
Mohamed, Sarar. (2013). Sanfilippo syndrome, glucose‐6‐phosphate dehydrogenase deficiency and sickle cell/β+ thalassemia in a child: The burden of consanguinity. American Journal of Medical Genetics Part A. 164(1). 267–269. 4 indexed citations
17.
Mohamed, Sarar, et al.. (2013). Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy. BMC Research Notes. 6(1). 362–362. 21 indexed citations
18.
Alharbi, Khalid Khalaf, Tarek Kashour, May Al-Nbaheen, et al.. (2013). Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population. Lipids in Health and Disease. 12(1). 177–177. 12 indexed citations
19.
Mohamed, Sarar. (2012). Cat eye syndrome: A mild phenotype with isolated growth hormone deficiency. Current Paediatrics. 16(1). 0. 1 indexed citations
20.
Mohamed, Sarar. (2012). A clinical and DNA study on patients with Neuronal ceroid lipofuscinosis in Eastern Province, Saudi Arabia.. Current Paediatrics. 16(1). 0.

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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