Wafaa Eyaid

5.5k total citations
55 papers, 2.4k citations indexed

About

Wafaa Eyaid is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Wafaa Eyaid has authored 55 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 14 papers in Genetics. Recurrent topics in Wafaa Eyaid's work include Metabolism and Genetic Disorders (16 papers), Mitochondrial Function and Pathology (9 papers) and Neonatal Health and Biochemistry (7 papers). Wafaa Eyaid is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Mitochondrial Function and Pathology (9 papers) and Neonatal Health and Biochemistry (7 papers). Wafaa Eyaid collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Wafaa Eyaid's co-authors include Majid Alfadhel, Mohammed Al Balwi, Simeon A. Boyadjiev, Christopher A. Walsh, Mariella Ravazzola, J. Christopher Fromme, Adria Bodell, Susan Hamamoto, Lelio Orci and Randy Schekman and has published in prestigious journals such as Nature Genetics, Developmental Cell and The American Journal of Human Genetics.

In The Last Decade

Wafaa Eyaid

54 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wafaa Eyaid Saudi Arabia 25 1.5k 889 459 288 255 55 2.4k
Stavit A. Shalev Israel 29 1.8k 1.2× 709 0.8× 378 0.8× 287 1.0× 126 0.5× 88 2.6k
Yoshinori Tsurusaki Japan 37 2.6k 1.7× 1.6k 1.8× 392 0.9× 181 0.6× 197 0.8× 146 3.9k
Eissa Faqeih Saudi Arabia 28 1.5k 1.0× 920 1.0× 238 0.5× 222 0.8× 136 0.5× 80 2.2k
Roberta Biancheri Italy 31 1.3k 0.8× 377 0.4× 339 0.7× 264 0.9× 308 1.2× 100 2.5k
Katrin Õunap Estonia 25 1.0k 0.7× 857 1.0× 126 0.3× 249 0.9× 264 1.0× 106 1.8k
Takeshi Mizuguchi Japan 28 1.6k 1.1× 1.2k 1.3× 266 0.6× 111 0.4× 198 0.8× 126 2.7k
Adeline Vanderver United States 33 2.6k 1.7× 373 0.4× 320 0.7× 227 0.8× 134 0.5× 149 3.5k
Mordechai Shohat Israel 26 1.7k 1.1× 540 0.6× 154 0.3× 331 1.1× 432 1.7× 83 2.9k
Maha S. Zaki Egypt 27 1.2k 0.8× 679 0.8× 326 0.7× 81 0.3× 388 1.5× 147 2.4k
Andreas Tzschach Germany 30 2.1k 1.4× 1.8k 2.0× 266 0.6× 80 0.3× 255 1.0× 104 3.3k

Countries citing papers authored by Wafaa Eyaid

Since Specialization
Citations

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

Fields of papers citing papers by Wafaa Eyaid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wafaa Eyaid

This figure shows the co-authorship network connecting the top 25 collaborators of Wafaa Eyaid. A scholar is included among the top collaborators of Wafaa Eyaid 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 Wafaa Eyaid. Wafaa Eyaid 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.
Khan, Amjad, et al.. (2024). Further delineation of Wiedemann‐Rautenstrauch syndrome linked with POLR3A. Molecular Genetics & Genomic Medicine. 12(3). e2274–e2274. 1 indexed citations
2.
Almannai, Mohammed, Abdulrahman Alswaid, Wafaa Eyaid, et al.. (2024). Consanguinity and Occurrence of Monogenic Diseases in a Single Tertiary Centre in Riyadh, Saudi Arabia: A 2 Years Cross-Sectional Study. The Application of Clinical Genetics. Volume 17. 151–158.
3.
Alfadhel, Majid, Marwan Nashabat, Ahmed Alfares, et al.. (2021). Long-term effectiveness of carglumic acid in patients with propionic acidemia (PA) and methylmalonic acidemia (MMA): a randomized clinical trial. Orphanet Journal of Rare Diseases. 16(1). 422–422. 18 indexed citations
4.
Khan, Amjad, et al.. (2020). PDCD6IP , encoding a regulator of the ESCRT complex, is mutated in microcephaly. Clinical Genetics. 98(1). 80–85. 9 indexed citations
5.
Alkuraya, Hisham, Nisha Patel, Niema Ibrahim, et al.. (2019). Phenotypic delineation of the retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome. Clinical Genetics. 97(3). 447–456. 5 indexed citations
6.
7.
Williams, Monique, Vassili Valayannopoulos, Ruqaiah Altassan, et al.. (2018). Clinical, biochemical, and molecular overview of transaldolase deficiency and evaluation of the endocrine function: update of 34 patients. Journal of Inherited Metabolic Disease. 2 indexed citations
8.
Almannai, Mohammed, Ali Alasmari, Eissa Faqeih, et al.. (2018). Expanding the phenotype of SLC25A42‐associated mitochondrial encephalomyopathy. Clinical Genetics. 93(5). 1097–1102. 24 indexed citations
9.
Eyaid, Wafaa, Kimberli J. Kamer, Rehab Ali, et al.. (2018). A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. JIMD Reports. 43. 79–83. 43 indexed citations
10.
Hossain, Mohammad Arif, et al.. (2017). Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula. Human Genome Variation. 4(1). 17018–17018. 7 indexed citations
11.
Nashabat, Marwan, Majid Alfadhel, Ali Alasmari, et al.. (2017). Clinical, Biochemical, and Molecular Features in 37 Saudi Patients with Very Long Chain Acyl CoA Dehydrogenase Deficiency. JIMD Reports. 40. 47–53. 16 indexed citations
12.
Imtiaz, Faiqa, Mohamed H. Al‐Hamed, Zuhair N. Al‐Hassnan, et al.. (2014). Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia. JIMD Reports. 29. 39–46. 5 indexed citations
13.
Al‐Hussaini, Abdulrahman, Eissa Faqeih, Ayman W. El‐Hattab, et al.. (2013). Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure. The Journal of Pediatrics. 164(3). 553–559.e2. 36 indexed citations
14.
Alfadhel, Majid, Fahad A. Bashiri, Mahmoud Al Rifai, et al.. (2013). Biotin-responsive basal ganglia disease should be renamed biotin-thiamine-responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of 18 new cases. Orphanet Journal of Rare Diseases. 8(1). 83–83. 101 indexed citations
15.
AL-QATTAN, M. M., Wafaa Eyaid, & Mohammed Al Balwi. (2007). Congenital Duplication of the Palm Syndrome. Annals of Plastic Surgery. 59(3). 341–343. 10 indexed citations
16.
Frank, Christian, Wafaa Eyaid, Eric G. Berger, et al.. (2004). Identification and Functional Analysis of a Defect in the Human ALG9 Gene: Definition of Congenital Disorder of Glycosylation Type IL. The American Journal of Human Genetics. 75(1). 146–150. 70 indexed citations
17.
Rashed, Mohamed S., Amal Saadallah, Zuhair Rahbeeni, et al.. (2004). Determination of urinary S‐sulphocysteine, xanthine and hypoxanthine by liquid chromatography–electrospray tandem mass spectrometry. Biomedical Chromatography. 19(3). 223–230. 34 indexed citations
18.
Ferland, Russell J., Wafaa Eyaid, Randall V. Collura, et al.. (2004). Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. Nature Genetics. 36(9). 1008–1013. 286 indexed citations
19.
Eyaid, Wafaa, et al.. (2004). An inborn error of metabolism presenting as hypoxic-ischemic insult. Pediatric Neurology. 32(2). 134–136. 10 indexed citations
20.
Eyaid, Wafaa, Mark V. Clough, Kathleen M. Scott, et al.. (1998). Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs. Human Genetics. 103(4). 525–526. 4 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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