Nour Ewida

1.9k total citations
9 papers, 328 citations indexed

About

Nour Ewida is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nour Ewida has authored 9 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nour Ewida's work include Genetic and Kidney Cyst Diseases (3 papers), RNA modifications and cancer (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). Nour Ewida is often cited by papers focused on Genetic and Kidney Cyst Diseases (3 papers), RNA modifications and cancer (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). Nour Ewida collaborates with scholars based in Saudi Arabia, United States and Egypt. Nour Ewida's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Eman Alobeid, Eissa Faqeih, Eric M. Phizicky, Lu Han, Ghada M. H. Abdel‐Salam, Sateesh Maddirevula, Firdous Abdulwahab and Niema Ibrahim and has published in prestigious journals such as Hepatology, The American Journal of Human Genetics and Human Genetics.

In The Last Decade

Nour Ewida

9 papers receiving 328 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nour Ewida Saudi Arabia	9	255	138	37	33	28	9	328
Mariko Yamane Japan	10	308 1.2×	86 0.6×	27 0.7×	21 0.6×	20 0.7×	17	388
Jennifer McDaid United Kingdom	8	271 1.1×	99 0.7×	17 0.5×	29 0.9×	21 0.8×	8	325
Resie van Spaendonk Netherlands	3	197 0.8×	181 1.3×	24 0.6×	53 1.6×	21 0.8×	3	321
Alexandre Z. Daly United States	6	157 0.6×	86 0.6×	11 0.3×	31 0.9×	10 0.4×	9	282
Jane M. vanWert United States	11	370 1.5×	158 1.1×	13 0.4×	40 1.2×	26 0.9×	12	446
Silvia Moleri Italy	8	180 0.7×	41 0.3×	70 1.9×	34 1.0×	57 2.0×	9	308
Shingo Usuki Japan	9	277 1.1×	63 0.5×	31 0.8×	21 0.6×	17 0.6×	22	362
Anna Hammarsjö Sweden	9	164 0.6×	115 0.8×	8 0.2×	59 1.8×	16 0.6×	21	264
M. Lutz Germany	10	475 1.9×	185 1.3×	38 1.0×	26 0.8×	22 0.8×	10	542
Jennifer L. Smedberg United States	10	366 1.4×	35 0.3×	79 2.1×	25 0.8×	36 1.3×	14	422

Countries citing papers authored by Nour Ewida

Since Specialization

Citations

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

Fields of papers citing papers by Nour Ewida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nour Ewida

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

All Works

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9 of 9 papers shown

Shamseldin, Hanan E., Turki H. Albatti, Mais Hashem, et al.. (2021). PLXNA2 as a candidate gene in patients with intellectual disability. American Journal of Medical Genetics Part A. 185(12). 3859–3865. 9 indexed citations

Maddirevula, Sateesh, Seham Alameer, Nour Ewida, et al.. (2021). Insight into ALKBH8-related intellectual developmental disability based on the first pathogenic missense variant. Human Genetics. 141(2). 209–215. 13 indexed citations

Alhathal, Naif, Sateesh Maddirevula, Serdar Coşkun, et al.. (2020). A genomics approach to male infertility. Genetics in Medicine. 22(12). 1967–1975. 51 indexed citations

Abdel‐Salam, Ghada M. H., Inas Mazen, Maha M. Eid, et al.. (2019). Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia. American Journal of Medical Genetics Part A. 179(6). 1053–1057. 14 indexed citations

Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations

Shaheen, Ranad, Saud Alsahli, Nour Ewida, et al.. (2019). Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in Humans. Hepatology. 71(6). 2067–2079. 23 indexed citations

Alkanderi, Sumaya, Elisa Molinari, Ranad Shaheen, et al.. (2018). ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition. The American Journal of Human Genetics. 103(4). 612–620. 59 indexed citations

Shaheen, Ranad, et al.. (2016). Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans. Human Genetics. 135(10). 1191–1197. 25 indexed citations

Shaheen, Ranad, Lu Han, Eissa Faqeih, et al.. (2016). A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognition. Human Genetics. 135(7). 707–713. 113 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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