Tarfa Alshidi

756 total citations
10 papers, 305 citations indexed

About

Tarfa Alshidi is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Tarfa Alshidi has authored 10 papers receiving a total of 305 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Clinical Biochemistry. Recurrent topics in Tarfa Alshidi's work include Mitochondrial Function and Pathology (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Metabolism and Genetic Disorders (2 papers). Tarfa Alshidi is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Metabolism and Genetic Disorders (2 papers). Tarfa Alshidi collaborates with scholars based in Saudi Arabia, Oman and Kuwait. Tarfa Alshidi's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Eissa Faqeih, Rana Alomar, Ghada M. H. Abdel‐Salam, Zuhair N. Al‐Hassnan, Shinu Ansari, Sameera Sogaty, Hanan E. Shamseldin and Mais Hashem and has published in prestigious journals such as Brain, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Tarfa Alshidi

10 papers receiving 303 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 Alshidi Saudi Arabia 8 253 98 35 29 22 10 305
Ok‐Hwa Kim South Korea 10 194 0.8× 124 1.3× 33 0.9× 17 0.6× 17 0.8× 12 318
Pablo Villavicencio‐Lorini Germany 11 282 1.1× 109 1.1× 23 0.7× 36 1.2× 13 0.6× 17 384
Björn Fischer‐Zirnsak Germany 13 316 1.2× 158 1.6× 68 1.9× 38 1.3× 40 1.8× 26 426
Yu Ding China 12 219 0.9× 170 1.7× 22 0.6× 35 1.2× 38 1.7× 38 359
Majdi Nagara Tunisia 10 161 0.6× 140 1.4× 37 1.1× 26 0.9× 11 0.5× 25 343
Ian Berry United Kingdom 11 226 0.9× 192 2.0× 20 0.6× 53 1.8× 8 0.4× 24 370
Adam C. Gunning United Kingdom 7 179 0.7× 151 1.5× 16 0.5× 36 1.2× 11 0.5× 12 291
Nagarajan Paramasivam Germany 13 239 0.9× 165 1.7× 27 0.8× 43 1.5× 18 0.8× 41 408
Ewelina Bukowska‐Olech Poland 11 157 0.6× 147 1.5× 20 0.6× 25 0.9× 6 0.3× 41 273
Shinu Ansari Saudi Arabia 8 304 1.2× 232 2.4× 86 2.5× 34 1.2× 9 0.4× 8 447

Countries citing papers authored by Tarfa Alshidi

Since Specialization
Citations

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

Fields of papers citing papers by Tarfa Alshidi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tarfa Alshidi

This figure shows the co-authorship network connecting the top 25 collaborators of Tarfa Alshidi. A scholar is included among the top collaborators of Tarfa Alshidi 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 Alshidi. Tarfa Alshidi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Marafi, Dana, Mais Hashem, Firdous Abdulwahab, et al.. (2023). Human ‘knockouts’ of CSF3 display severe congenital neutropenia. British Journal of Haematology. 203(3). 477–480. 3 indexed citations
2.
Aldosary, Mazhor, Rawan Almass, Maysoon Alsagob, et al.. (2021). SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion. JIMD Reports. 60(1). 75–87. 12 indexed citations
3.
Patel, Nisha, Eman Alobeid, Tarfa Alshidi, et al.. (2020). Confirming the recessive inheritance of PERP‐related erythrokeratoderma. Clinical Genetics. 97(4). 661–665. 4 indexed citations
4.
Shamseldin, Hanan E., Ali Alasmari, Mohammed A. Salih, et al.. (2017). A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder. Brain. 140(11). 2806–2813. 40 indexed citations
5.
Patel, Nisha, Hanan E. Shamseldin, Nadia Sakati, et al.. (2017). GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome. The American Journal of Human Genetics. 100(5). 831–836. 13 indexed citations
6.
Patel, Nisha, Arif O. Khan, Maher Al‐Saif, et al.. (2017). A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation. Genome biology. 18(1). 144–144. 17 indexed citations
7.
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
8.
Shaheen, Ranad, Eissa Faqeih, Shinu Ansari, et al.. (2014). Genomic analysis of primordial dwarfism reveals novel disease genes. Genome Research. 24(2). 291–299. 122 indexed citations
9.
Shamseldin, Hanan E., Anna Rajab, Amal Alhashem, et al.. (2013). Mutations in DDX59 Implicate RNA Helicase in the Pathogenesis of Orofaciodigital Syndrome. The American Journal of Human Genetics. 93(3). 555–560. 39 indexed citations
10.
Aldosari, Naji, Tarfa Alshidi, Dilek Çolak, et al.. (2011). Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects. Molecular Cytogenetics. 4(1). 9–9. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ok‐Hwa Kim Breakdown of academic impact, for papers by Pablo Villavicencio‐Lorini Breakdown of academic impact, for papers by Björn Fischer‐Zirnsak Breakdown of academic impact, for papers by Yu Ding Breakdown of academic impact, for papers by Majdi Nagara Breakdown of academic impact, for papers by Ian Berry Breakdown of academic impact, for papers by Adam C. Gunning Breakdown of academic impact, for papers by Nagarajan Paramasivam Breakdown of academic impact, for papers by Ewelina Bukowska‐Olech Breakdown of academic impact, for papers by Shinu Ansari
Rankless by CCL
2026