Tarfa Al‐Sheddi

1.5k total citations
21 papers, 664 citations indexed

About

Tarfa Al‐Sheddi is a scholar working on Molecular Biology, Genetics and Mechanical Engineering. According to data from OpenAlex, Tarfa Al‐Sheddi has authored 21 papers receiving a total of 664 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Mechanical Engineering. Recurrent topics in Tarfa Al‐Sheddi's work include RNA regulation and disease (3 papers), RNA modifications and cancer (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). Tarfa Al‐Sheddi is often cited by papers focused on RNA regulation and disease (3 papers), RNA modifications and cancer (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). Tarfa Al‐Sheddi collaborates with scholars based in Saudi Arabia, Egypt and Tunisia. Tarfa Al‐Sheddi's co-authors include Fowzan S. Alkuraya, Hanan E. Shamseldin, Mais Hashem, Ranad Shaheen, Muneera Alshammari, Mustafa A. Salih, Eissa Faqeih, Hisham Alkhalidi, Amal Y. Kentab and Gabriela M. Repetto and has published in prestigious journals such as Hepatology, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Tarfa Al‐Sheddi

19 papers receiving 660 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tarfa Al‐Sheddi Saudi Arabia 13 456 166 87 80 51 21 664
Yoshihiro Ujihara Japan 11 264 0.6× 31 0.2× 101 1.2× 13 0.2× 20 0.4× 48 510
Ming-min Gu China 9 181 0.4× 75 0.5× 21 0.2× 50 0.6× 16 0.3× 19 355
John Wiseman Sweden 15 588 1.3× 130 0.8× 57 0.7× 16 0.2× 76 1.5× 28 787
Matthew R. Paul United States 12 267 0.6× 27 0.2× 90 1.0× 7 0.1× 66 1.3× 17 570
Abdelaziz Tlili United Arab Emirates 17 496 1.1× 72 0.4× 19 0.2× 46 0.6× 101 2.0× 61 801
Theresa C. Swayne United States 16 883 1.9× 26 0.2× 201 2.3× 69 0.9× 33 0.6× 31 1.1k
Ghazanfar Ali Pakistan 18 739 1.6× 257 1.5× 289 3.3× 5 0.1× 99 1.9× 74 1.2k
Yantao Wei China 18 262 0.6× 51 0.3× 76 0.9× 10 0.1× 36 0.7× 75 1.3k
Monika Valtink Germany 20 413 0.9× 46 0.3× 75 0.9× 23 0.3× 16 0.3× 50 1.0k
Daisuke Yamashita Japan 13 484 1.1× 85 0.5× 83 1.0× 4 0.1× 62 1.2× 20 627

Countries citing papers authored by Tarfa Al‐Sheddi

Since Specialization
Citations

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

Fields of papers citing papers by Tarfa Al‐Sheddi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tarfa Al‐Sheddi. 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 Tarfa Al‐Sheddi. The network helps show where Tarfa Al‐Sheddi may publish in the future.

Co-authorship network of co-authors of Tarfa Al‐Sheddi

This figure shows the co-authorship network connecting the top 25 collaborators of Tarfa Al‐Sheddi. A scholar is included among the top collaborators of Tarfa Al‐Sheddi 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 Tarfa Al‐Sheddi. Tarfa Al‐Sheddi 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.
Al–Muhaizea, Mohammad A., Anoud Albader, Rawan Almass, et al.. (2025). Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness. Orphanet Journal of Rare Diseases. 20(1). 415–415.
2.
3.
Hendi, Awatif A., Meznah M. Alanazi, Manal A. Awad, et al.. (2023). Dye-sensitized solar cells constructed using titanium oxide nanoparticles and green dyes as photosensitizers. Journal of King Saud University - Science. 35(3). 102555–102555. 30 indexed citations
4.
Al‐Sheddi, Tarfa, et al.. (2022). NUTRITIONAL COMPOSITION OF THE EDIBLE WILD PLANT OPUNTIA LITTORALIS (ENGELM.) IN RELATION TO DIFFERENT SEASONS AND EDAPHIC FACTORS. Applied Ecology and Environmental Research. 20(4). 3655–3669. 4 indexed citations
5.
Souayeh, Basma, Zulqurnain Sabir, Najib Hdhiri, et al.. (2022). A Stochastic Bayesian Regularization Approach for the Fractional Food Chain Supply System with Allee Effects. Fractal and Fractional. 6(10). 553–553. 6 indexed citations
6.
Souayeh, Basma, Kashif Ali Abro, Najib Hdhiri, et al.. (2022). Role of copper and alumina for heat transfer in hybrid nanofluid by using Fourier sine transform. Scientific Reports. 12(1). 11307–11307. 25 indexed citations
7.
Gharbi, F., K. Benthami, Tarfa Al‐Sheddi, et al.. (2022). Structural, Thermal, and Optical Studies of Gamma Irradiated Polyvinyl Alcohol-, Lignosulfonate-, and Palladium Nanocomposite Film. Polymers. 14(13). 2613–2613. 5 indexed citations
8.
Al‐Sheddi, Tarfa, et al.. (2022). THE RADIOLOGICAL IMPACT OF THE USE OF PHOSPHATE FERTILIZERS IN GERMINATION AND GROWTH OF ERUCA SATIVA (ROCKET PLANT). Applied Ecology and Environmental Research. 20(6). 5059–5071. 1 indexed citations
9.
Al‐Sheddi, Tarfa, et al.. (2022). Test Model for Analysis of the Elastic and Inelastic Scattering of 11Li on Proton at 6 to 75 MeV/nucleon. Journal of the Physical Society of Japan. 91(12). 1 indexed citations
10.
Gharbi, F., et al.. (2020). Combination of 137Cs and 210Pb Radioactive Atmospheric Fallouts to Estimate Soil Erosion for the Same Time Scale. International Journal of Environmental Research and Public Health. 17(22). 8292–8292. 3 indexed citations
11.
Shaheen, Ranad, Sateesh Maddirevula, Ghada M. H. Abdel‐Salam, et al.. (2019). PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly. Human Genetics. 138(3). 231–239. 68 indexed citations
12.
Shamseldin, Hanan E., Nawal Makhseed, Niema Ibrahim, et al.. (2019). NUP214 deficiency causes severe encephalopathy and microcephaly in humans. Human Genetics. 138(3). 221–229. 14 indexed citations
13.
Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations
14.
Shaheen, Ranad, Saud Alsahli, Nour Ewida, et al.. (2019). Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans. Hepatology. 71(6). 2067–2079. 23 indexed citations
15.
AlSayed, Moeenaldeen, Hamad Alzaidan, Albandary AlBakheet, et al.. (2013). Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay. The American Journal of Human Genetics. 93(4). 721–726. 69 indexed citations
16.
Alazami, Anas M., Mohammad Al-Owain, Fatema Alzahrani, et al.. (2012). Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism. Human Mutation. 33(10). 1429–1434. 64 indexed citations
17.
Shamseldin, Hanan E., Muneera Alshammari, Tarfa Al‐Sheddi, et al.. (2012). Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes. Journal of Medical Genetics. 49(4). 234–241. 143 indexed citations
18.
Shaheen, Ranad, Eissa Faqeih, Hanan E. Shamseldin, et al.. (2012). POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism. The American Journal of Human Genetics. 91(2). 330–336. 63 indexed citations
19.
Shaheen, Ranad, Eissa Faqeih, Heba Morsy, et al.. (2011). Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome. The American Journal of Human Genetics. 89(2). 328–333. 95 indexed citations
20.
Shaheen, Ranad, Mohammed Al‐Owain, Mustafa A. Salih, et al.. (2010). Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs. Clinical Genetics. 79(1). 60–70. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Yoshihiro Ujihara Breakdown of academic impact, for papers by Ming-min Gu Breakdown of academic impact, for papers by John Wiseman Breakdown of academic impact, for papers by Matthew R. Paul Breakdown of academic impact, for papers by Abdelaziz Tlili Breakdown of academic impact, for papers by Theresa C. Swayne Breakdown of academic impact, for papers by Ghazanfar Ali Breakdown of academic impact, for papers by Yantao Wei Breakdown of academic impact, for papers by Monika Valtink Breakdown of academic impact, for papers by Daisuke Yamashita
Rankless by CCL
2026