Maha M. Eid

566 total citations
52 papers, 318 citations indexed

About

Maha M. Eid is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maha M. Eid has authored 52 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 26 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maha M. Eid's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Hedgehog Signaling Pathway Studies (5 papers). Maha M. Eid is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Hedgehog Signaling Pathway Studies (5 papers). Maha M. Eid collaborates with scholars based in Egypt, United States and France. Maha M. Eid's co-authors include Ghada M. H. Abdel‐Salam, Hanan H. Afifi, Ioannis Livieratos, Daniela Tsikou, Mohamed S. Abdel‐Hamid, Ibrahim A. Abdel‐Hamid, Mohamed Sobh, Samia A. Temtamy, Hala T. El‐Bassyouni and Laila K. Effat and has published in prestigious journals such as SHILAP Revista de lepidopterología, Reproductive BioMedicine Online and Cytogenetic and Genome Research.

In The Last Decade

Maha M. Eid

45 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maha M. Eid Egypt 10 154 92 55 35 34 52 318
Eran Cohen‐Barak Israel 13 133 0.9× 99 1.1× 43 0.8× 22 0.6× 46 1.4× 41 414
Luise Landreh Sweden 8 163 1.1× 94 1.0× 12 0.2× 13 0.4× 93 2.7× 9 401
Ayumi Uematsu Japan 10 171 1.1× 143 1.6× 26 0.5× 10 0.3× 10 0.3× 18 391
Christos Shammas Cyprus 14 281 1.8× 140 1.5× 7 0.1× 15 0.4× 11 0.3× 38 408
Ana Lı́a Errecalde Argentina 10 78 0.5× 21 0.2× 20 0.4× 9 0.3× 134 3.9× 24 354
DD Farhud Iran 12 156 1.0× 192 2.1× 46 0.8× 3 0.1× 12 0.4× 48 498
Lihui Wu China 10 207 1.3× 24 0.3× 39 0.7× 36 1.0× 15 0.4× 17 415
Małgorzata Szczepańska Poland 14 185 1.2× 207 2.3× 16 0.3× 3 0.1× 137 4.0× 31 787
Laura McMahon United States 13 345 2.2× 31 0.3× 23 0.4× 6 0.2× 27 0.8× 17 609
Sónia Costa Brazil 15 137 0.9× 116 1.3× 45 0.8× 4 0.1× 463 13.6× 30 672

Countries citing papers authored by Maha M. Eid

Since Specialization
Citations

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

Fields of papers citing papers by Maha M. Eid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maha M. Eid. 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 Maha M. Eid. The network helps show where Maha M. Eid may publish in the future.

Co-authorship network of co-authors of Maha M. Eid

This figure shows the co-authorship network connecting the top 25 collaborators of Maha M. Eid. A scholar is included among the top collaborators of Maha M. Eid 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 Maha M. Eid. Maha M. Eid 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.
Aboulghar, Mona M., Mona L. Essawi, Engy A. Ashaat, et al.. (2025). Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing. Clinical Genetics. 108(4). 433–449.
2.
Vallée, Alexandre, et al.. (2025). Maternal vaping and pregnancy adverse outcomes: A systematic review and meta-analysis. Women and Birth. 38(5). 101951–101951. 1 indexed citations
3.
Eid, Maha M., et al.. (2024). Generation of Dual-Color FISH probes targeting 9p21, Xp21, and 17p13.1 loci as diagnostic markers for some genetic disorders and cancer in Egypt. Journal of Genetic Engineering and Biotechnology. 23(1). 100449–100449.
4.
Eid, Maha M., Adrien Lemoine, Lise Selleret, et al.. (2024). Pain after oocyte retrieval in women with endometriosis undergoing fertility preservation or IVF. Reproductive BioMedicine Online. 49(3). 104100–104100. 1 indexed citations
5.
Hamdy, Mona, et al.. (2023). Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients. Journal of Genetic Engineering and Biotechnology. 21(1). 149–149. 1 indexed citations
6.
Eid, Maha M., et al.. (2023). Detection of AZFc gene deletion in a cohort of Egyptian patients with idiopathic male infertility. Journal of Genetic Engineering and Biotechnology. 21(1). 111–111.
7.
8.
Eid, Maha M., et al.. (2022). MLPA as a genetic assay for the prenatal diagnosis of common aneuploidy: the first Egyptian experience. Journal of Genetic Engineering and Biotechnology. 20(1). 112–112. 2 indexed citations
9.
Abdel‐Salam, Ghada M. H., et al.. (2022). A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasia. Journal of Human Genetics. 67(11). 669–673.
10.
Eid, Maha M., et al.. (2021). Evaluation of MLPA as a comprehensive molecular cytogenetic tool to detect cytogenetic markers of chronic lymphocytic leukemia in Egyptian patients. Journal of Genetic Engineering and Biotechnology. 19(1). 98–98. 5 indexed citations
11.
Eid, Maha M., et al.. (2020). Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic Aberrations. Current Pharmaceutical Biotechnology. 21(13). 1394–1401. 3 indexed citations
12.
Eid, Maha M., et al.. (2020). Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation. Cytogenetic and Genome Research. 160(3). 124–133. 1 indexed citations
13.
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
14.
Zaki, Maha S., et al.. (2019). Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features. Cytogenetic and Genome Research. 159(3). 130–136. 3 indexed citations
15.
Mazen, Inas, et al.. (2018). A Homozygous Missense Mutation in <b><i>FANCA</i></b> Gene in a 46,XY Female with Gonadal Dysgenesis. Sexual Development. 12(5). 239–243. 2 indexed citations
16.
Eid, Maha M., et al.. (2013). Ring chromosome 15: expanding the phenotype.. PubMed. 24(4). 417–25. 5 indexed citations
17.
18.
Abdel‐Salam, Ghada M. H., et al.. (2011). Ectodermal Abnormalities in Patients with Kabuki Syndrome. Pediatric Dermatology. 28(5). 507–511. 7 indexed citations
19.
Abdel‐Salam, Ghada M. H., Noriko Miyake, Maha M. Eid, et al.. (2011). A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder. American Journal of Medical Genetics Part A. 155(11). 2885–2896. 21 indexed citations
20.
Abdel‐Salam, Ghada M. H., Laura Flores‐Sarnat, Jillian S. Parboosingh, et al.. (2010). Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype. American Journal of Medical Genetics Part A. 155(1). 207–214. 15 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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