Wafa Eyaid

488 total citations
5 papers, 42 citations indexed

About

Wafa Eyaid is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wafa Eyaid has authored 5 papers receiving a total of 42 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Wafa Eyaid's work include Amino Acid Enzymes and Metabolism (1 paper), Genetic Syndromes and Imprinting (1 paper) and Porphyrin Metabolism and Disorders (1 paper). Wafa Eyaid is often cited by papers focused on Amino Acid Enzymes and Metabolism (1 paper), Genetic Syndromes and Imprinting (1 paper) and Porphyrin Metabolism and Disorders (1 paper). Wafa Eyaid collaborates with scholars based in Saudi Arabia and Qatar. Wafa Eyaid's co-authors include Majid Alfadhel, Marwan Nashabat, Ali Alothaim, Fuad Al Mutairi, Abdulrahman Swaid, Ahmed Alfares, Lamia Alsubaie, Fowzan S. Alkuraya, Mariam Al‐Mureikhi and Hessa S. Alsaif and has published in prestigious journals such as American Journal of Medical Genetics Part A, Annals of Saudi Medicine and Molecular Genetics and Metabolism Reports.

In The Last Decade

Wafa Eyaid

5 papers receiving 41 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wafa Eyaid Saudi Arabia	5	14	12	9	9	8	5	42
Kathleen Wallace United States	4	50 3.6×	17 1.4×	16 1.8×	4 0.4×	17 2.1×	7	75
Theresia Herget Germany	4	22 1.6×	29 2.4×	7 0.8×	4 0.4×	6 0.8×	6	54
Peter Durda United States	4	9 0.6×	20 1.7×	4 0.4×	4 0.4×	1 0.1×	7	44
Oana Moldovan Portugal	4	20 1.4×	12 1.0×	2 0.2×	3 0.3×	3 0.4×	18	46
Fanchao Wei China	4	7 0.5×	15 1.3×	4 0.4×	7 0.8×	1 0.1×	5	38
Wai Ming Lai China	4	3 0.2×	21 1.8×	5 0.6×	3 0.3×	13 1.6×	5	45
Christopher M. Richmond Australia	4	14 1.0×	28 2.3×	6 0.7×	4 0.4×	9 1.1×	9	49
Thomas Battram United Kingdom	3	19 1.4×	25 2.1×	5 0.6×	8 0.9×		3	55
Colleen Morse Kripke United States	3	22 1.6×	12 1.0×	4 0.4×	3 0.3×	1 0.1×	7	53
Lindsay Guare United States	3	18 1.3×	18 1.5×	3 0.3×	3 0.3×	1 0.1×	6	56

Countries citing papers authored by Wafa Eyaid

Since Specialization

Citations

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

Fields of papers citing papers by Wafa Eyaid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wafa Eyaid

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

All Works

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5 of 5 papers shown

1.

Alsubaie, Lamia, Abdulrahman Swaid, Wafa Eyaid, et al.. (2022). Common disease-associated gene variants in a Saudi Arabian population. Annals of Saudi Medicine. 42(1). 29–35. 16 indexed citations

2.

Maddirevula, Sateesh, Tawfeg Ben‐Omran, Mariam Al‐Mureikhi, et al.. (2020). Further delineation of HIDEA syndrome. American Journal of Medical Genetics Part A. 182(12). 2999–3006. 5 indexed citations

3.

Alfadhel, Majid, et al.. (2020). Clinical presentation of seven patients with Methylenetetrahydrofolate reductase deficiency. Molecular Genetics and Metabolism Reports. 25. 100644–100644. 6 indexed citations

4.

Alothaim, Ali, et al.. (2019). Cord blood versus heel-stick sampling for measuring thyroid stimulating hormone for newborn screening of congenital hypothyroidism. Annals of Saudi Medicine. 39(5). 291–294. 9 indexed citations

5.

Eyaid, Wafa, et al.. (2005). Hypoparathyroidism–retardation–dysmorphism (HRD) syndrome in triplets. American Journal of Medical Genetics Part A. 135A(2). 200–201. 6 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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