Taghreed Shuaib

621 total citations
13 papers, 243 citations indexed

About

Taghreed Shuaib is a scholar working on Genetics, Rheumatology and Molecular Biology. According to data from OpenAlex, Taghreed Shuaib has authored 13 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Rheumatology and 3 papers in Molecular Biology. Recurrent topics in Taghreed Shuaib's work include Connective tissue disorders research (3 papers), Genomics and Rare Diseases (2 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Taghreed Shuaib is often cited by papers focused on Connective tissue disorders research (3 papers), Genomics and Rare Diseases (2 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Taghreed Shuaib collaborates with scholars based in Saudi Arabia, Egypt and United Kingdom. Taghreed Shuaib's co-authors include Dilek Çolak, Fowzan S. Alkuraya, Mohammed Al‐Owain, Mohammad Al-Owain, Hesham Aldhalaan, Saleh M. Al‐Qahtani, Namik Kaya, Anas M. Alazami, Fatema Alzahrani and Tarfa Al‐Sheddi and has published in prestigious journals such as Gene, Journal of the Neurological Sciences and Human Mutation.

In The Last Decade

Taghreed Shuaib

13 papers receiving 238 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Taghreed Shuaib Saudi Arabia 9 133 74 45 27 25 13 243
Mohammad Al-Owain Saudi Arabia 10 170 1.3× 65 0.9× 19 0.4× 34 1.3× 41 1.6× 15 264
Saeed Al-Turki Saudi Arabia 4 114 0.9× 102 1.4× 41 0.9× 36 1.3× 17 0.7× 7 250
Elisa Rahikkala Finland 9 163 1.2× 81 1.1× 37 0.8× 13 0.5× 61 2.4× 38 269
Ohad Wormser Israel 11 173 1.3× 65 0.9× 20 0.4× 46 1.7× 31 1.2× 28 275
Heiko Brennenstuhl Germany 11 180 1.4× 74 1.0× 47 1.0× 19 0.7× 99 4.0× 25 315
Shinobu Fukumura Japan 11 149 1.1× 55 0.7× 44 1.0× 43 1.6× 9 0.4× 29 272
Malavika Hebbar India 9 207 1.6× 70 0.9× 28 0.6× 22 0.8× 39 1.6× 19 290
Michael Yourshaw United States 9 166 1.2× 86 1.2× 24 0.5× 34 1.3× 32 1.3× 10 347
Riitta Sallinen Finland 9 97 0.7× 35 0.5× 59 1.3× 10 0.4× 10 0.4× 12 212
A. Al‐Memar United Kingdom 9 138 1.0× 24 0.3× 125 2.8× 31 1.1× 29 1.2× 13 336

Countries citing papers authored by Taghreed Shuaib

Since Specialization
Citations

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

Fields of papers citing papers by Taghreed Shuaib

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taghreed Shuaib

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

All Works

13 of 13 papers shown
1.
2.
Parveen, Asia, et al.. (2020). A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients. Frontiers in Pediatrics. 8. 383–383. 9 indexed citations
3.
Al‐Mayouf, Sulaiman M., et al.. (2020). Management of Mucopolysaccharidosis Type I in Saudi Arabia: Insights from Saudi Arabia. Open Access Macedonian Journal of Medical Sciences. 8(F). 304–309. 1 indexed citations
4.
5.
Ahmed, Saleem, Mona Mohammad Almramhi, Taghreed Shuaib, et al.. (2016). The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family. Journal of the Neurological Sciences. 363. 240–244. 18 indexed citations
6.
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
7.
Al‐Owain, Mohammed, et al.. (2012). Identification of a novel ZNF469 mutation in a large family with Ehlers–Danlos phenotype. Gene. 511(2). 447–450. 22 indexed citations
8.
Alhashmi, Nadia, Faiqa Imtiaz, Khushnooda Ramzan, et al.. (2012). Novel splice (IVS18+1G>C) mutation in COL2A1 causing Kniest dysplasia. Clinical Dysmorphology. 22(1). 39–41. 7 indexed citations
9.
Kaya, Namik, Hesham Aldhalaan, Banan Al‐Younes, et al.. (2011). Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(7). 826–834. 53 indexed citations
10.
Al-Owain, Mohammad, Dilek Çolak, Taghreed Shuaib, et al.. (2011). Novel mutation in GLRB in a large family with hereditary hyperekplexia. Clinical Genetics. 81(5). 479–484. 26 indexed citations
11.
Al-Owain, Mohammad, Faiqa Imtiaz, Taghreed Shuaib, et al.. (2011). Smith–Lemli–Opitz syndrome among Arabs. Clinical Genetics. 82(2). 165–172. 8 indexed citations
12.
Faiyaz‐Ul‐Haque, Muhammad, et al.. (2011). Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria. Clinical Genetics. 81(6). 563–570. 12 indexed citations
13.
Shuaib, Taghreed, Nadia Alhashmi, Mohammad Ghaziuddin, et al.. (2011). Propionic Acidemia Associated With Visual Hallucinations. Journal of Child Neurology. 27(6). 799–803. 20 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 Mohammad Al-Owain Breakdown of academic impact, for papers by Saeed Al-Turki Breakdown of academic impact, for papers by Elisa Rahikkala Breakdown of academic impact, for papers by Ohad Wormser Breakdown of academic impact, for papers by Heiko Brennenstuhl Breakdown of academic impact, for papers by Shinobu Fukumura Breakdown of academic impact, for papers by Malavika Hebbar Breakdown of academic impact, for papers by Michael Yourshaw Breakdown of academic impact, for papers by Riitta Sallinen Breakdown of academic impact, for papers by A. Al‐Memar
Rankless by CCL
2026