Abdulrahman Swaid

479 total citations
6 papers, 112 citations indexed

About

Abdulrahman Swaid is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Abdulrahman Swaid has authored 6 papers receiving a total of 112 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Abdulrahman Swaid's work include Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Syndromes and Imprinting (1 paper). Abdulrahman Swaid is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Syndromes and Imprinting (1 paper). Abdulrahman Swaid collaborates with scholars based in Saudi Arabia, United Arab Emirates and Lebanon. Abdulrahman Swaid's co-authors include Fowzan S. Alkuraya, Hanan E. Shamseldin, Mohammed Zain Seidahmed, Chantal Farra, Wesam Kurdi, Sameera Sogaty, Muneera Alshammari, Ahmed Alfares, Shinu Ansari and Eissa Faqeih and has published in prestigious journals such as Genetics in Medicine, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Abdulrahman Swaid

6 papers receiving 111 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Abdulrahman Swaid Saudi Arabia	5	66	59	33	10	9	6	112
Michelle Steinraths Canada	8	104 1.6×	60 1.0×	60 1.8×	6 0.6×	6 0.7×	12	168
Ali Alothaim Saudi Arabia	6	81 1.2×	48 0.8×	16 0.5×	6 0.6×	7 0.8×	9	139
Houda Karmous‐Benailly France	6	96 1.5×	61 1.0×	33 1.0×	7 0.7×	10 1.1×	11	157
Christel Thauvin-Robinet France	6	69 1.0×	65 1.1×	26 0.8×	17 1.7×	32 3.6×	7	124
Lara Al-Olabi United Kingdom	4	28 0.4×	34 0.6×	32 1.0×	9 0.9×	4 0.4×	4	87
Katharina Löhner Netherlands	4	87 1.3×	59 1.0×	28 0.8×	5 0.5×	2 0.2×	5	137
Mar Borregán Spain	5	92 1.4×	76 1.3×	11 0.3×	4 0.4×	3 0.3×	11	160
Mohandas Nair India	6	51 0.8×	70 1.2×	21 0.6×	17 1.7×	4 0.4×	12	127
Flávia Piazzon Brazil	6	56 0.8×	74 1.3×	26 0.8×	7 0.7×	4 0.4×	21	135
Arne Jahn Germany	7	40 0.6×	69 1.2×	11 0.3×	5 0.5×	3 0.3×	19	148

Countries citing papers authored by Abdulrahman Swaid

Since Specialization

Citations

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

Fields of papers citing papers by Abdulrahman Swaid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdulrahman Swaid

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

All Works

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6 of 6 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.

Babiker, Amir, Abdulrahman Swaid, Majid Alfadhel, et al.. (2021). Short stature with low insulin‐like growth factor 1 availability due to pregnancy‐associated plasma protein A2 deficiency in a Saudi family. Clinical Genetics. 100(5). 601–606. 11 indexed citations

3.

Alsubaie, Lamia, Abdulrahman Swaid, Fuad Al Mutairi, et al.. (2020). Genomic testing and counseling: The contribution of next‐generation sequencing to epilepsy genetics. Annals of Human Genetics. 84(6). 431–436. 7 indexed citations

4.

Alsubaie, Lamia, Abdulrahman Swaid, Fuad Al Mutairi, et al.. (2020). MEFV c.2230G>T p.(Ala744Ser) rs61732874 previously misclassified as pathogenic variant due to lack of a population specific database. Annals of Human Genetics. 84(5). 370–379. 1 indexed citations

5.

Shaheen, Ranad, Eissa Faqeih, Muneera Alshammari, et al.. (2012). Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes. European Journal of Human Genetics. 21(7). 762–768. 42 indexed citations

6.

Shamseldin, Hanan E., Abdulrahman Swaid, & Fowzan S. Alkuraya. (2012). Lifting the lid on unborn lethal Mendelian phenotypes through exome sequencing. Genetics in Medicine. 15(4). 307–309. 35 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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