Soumaya Mougou-Zerelli

1.2k total citations
23 papers, 337 citations indexed

About

Soumaya Mougou-Zerelli is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Soumaya Mougou-Zerelli has authored 23 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Soumaya Mougou-Zerelli's work include Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (6 papers). Soumaya Mougou-Zerelli is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (6 papers). Soumaya Mougou-Zerelli collaborates with scholars based in Tunisia, France and Netherlands. Soumaya Mougou-Zerelli's co-authors include Saad Hasan Mohammed Ali, Molka Kammoun, Amira Sallem, Sonia Brahem, Samira Ibala‐Romdhane, M. Fékih, Damien Sanlaville, Hatem Elghezal, A. Saad and Nadia Boutry‐Kryza and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Fertility and Sterility.

In The Last Decade

Soumaya Mougou-Zerelli

23 papers receiving 331 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Soumaya Mougou-Zerelli Tunisia 8 164 115 108 108 78 23 337
Marina Cunha-Silva Brazil 7 207 1.3× 48 0.4× 209 1.9× 232 2.1× 52 0.7× 7 393
Shangang Li China 11 80 0.5× 80 0.7× 252 2.3× 36 0.3× 52 0.7× 32 396
Mingru Yin China 14 55 0.3× 254 2.2× 186 1.7× 217 2.0× 128 1.6× 35 563
Ann M. Ratchford United States 5 39 0.2× 187 1.6× 137 1.3× 81 0.8× 111 1.4× 6 356
Harsh Sheth India 9 93 0.6× 43 0.4× 97 0.9× 31 0.3× 56 0.7× 34 277
Danielle S. Bessa Brazil 8 208 1.3× 52 0.5× 214 2.0× 252 2.3× 53 0.7× 9 411
Colleen Buggs United States 7 175 1.1× 91 0.8× 221 2.0× 173 1.6× 12 0.2× 8 431
Maria Rosa Maduro United States 7 257 1.6× 163 1.4× 286 2.6× 276 2.6× 62 0.8× 24 488
A. Saad Tunisia 9 130 0.8× 71 0.6× 97 0.9× 58 0.5× 42 0.5× 24 255
Weili Wang China 12 199 1.2× 183 1.6× 171 1.6× 234 2.2× 44 0.6× 23 453

Countries citing papers authored by Soumaya Mougou-Zerelli

Since Specialization
Citations

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

Fields of papers citing papers by Soumaya Mougou-Zerelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Soumaya Mougou-Zerelli. 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 Soumaya Mougou-Zerelli. The network helps show where Soumaya Mougou-Zerelli may publish in the future.

Co-authorship network of co-authors of Soumaya Mougou-Zerelli

This figure shows the co-authorship network connecting the top 25 collaborators of Soumaya Mougou-Zerelli. A scholar is included among the top collaborators of Soumaya Mougou-Zerelli 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 Soumaya Mougou-Zerelli. Soumaya Mougou-Zerelli 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.
Turki, Ilhem, Saad Hasan Mohammed Ali, Christian G. Bouwkamp, et al.. (2024). Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome. World Journal of Clinical Cases. 12(3). 503–516. 1 indexed citations
2.
3.
Dimassi, Sarra, et al.. (2022). Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review. Molecular Cytogenetics. 15(1). 42–42. 5 indexed citations
4.
Hassine, Ikbel Hadj, et al.. (2022). Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis. Journal of Clinical Research in Pediatric Endocrinology. 15(1). 25–34. 3 indexed citations
5.
Kammoun, Molka, et al.. (2021). Further report of MEDS syndrome: Clinical and molecular delineation of a new Tunisian case. European Journal of Medical Genetics. 64(9). 104285–104285. 5 indexed citations
6.
Ali, Saad Hasan Mohammed, et al.. (2021). Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene. Molecular Cytogenetics. 14(1). 12–12. 4 indexed citations
7.
Dimassi, Sarra, et al.. (2020). Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype. BMC Medical Genetics. 21(1). 26–26. 2 indexed citations
8.
Al‐Rikabi, Ahmed, et al.. (2020). Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives. Journal of Assisted Reproduction and Genetics. 37(7). 1729–1736. 6 indexed citations
9.
Dimassi, Sarra, et al.. (2019). Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization. Molecular Cytogenetics. 12(1). 5–5. 6 indexed citations
10.
Kammoun, Molka, et al.. (2018). Subtelomeric Rearrangements in Patients with Recurrent Miscarriage.. SHILAP Revista de lepidopterología. 12(3). 218–222. 2 indexed citations
11.
12.
Mougou-Zerelli, Soumaya, Sarra Dimassi, Molka Kammoun, et al.. (2016). Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrhea. Fertility and Sterility. 106(1). 225–229.e11. 11 indexed citations
13.
Mougou-Zerelli, Soumaya, Molka Kammoun, Amira Sallem, et al.. (2015). Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy loss. Fertility and Sterility. 105(1). 58–64. 125 indexed citations
14.
Kammoun, Molka, et al.. (2015). Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits. Journal of Pediatric Genetics. 4(4). 187–193. 3 indexed citations
15.
Dimassi, Sarra, Thomas Simonet, Audrey Jalabert, et al.. (2015). Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA. PubMed. 7. 19–25. 19 indexed citations
16.
Mougou-Zerelli, Soumaya, et al.. (2013). Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients.. PubMed. 2(3). 147–55. 7 indexed citations
17.
18.
Mougou-Zerelli, Soumaya, et al.. (2011). Clinical and Molecular Characterization of a Combined 17p13.3 Microdeletion with Partial Monosomy 21q21.3 in a 26-Year-Old Man. Cytogenetic and Genome Research. 135(2). 102–110. 6 indexed citations
19.
Mougou-Zerelli, Soumaya, Sonia Brahem, Molka Kammoun, et al.. (2011). Detection of aneuploidy rate for chromosomes X, Y and 8 by fluorescence in-situ hybridization in spermatozoa from patients with severe non-obstructive oligozoospermia. Journal of Assisted Reproduction and Genetics. 28(10). 971–977. 12 indexed citations
20.
Putoux, Audrey, Soumaya Mougou-Zerelli, Sophie Thomas, et al.. (2010). BBS10 mutations are common in ‘Meckel’-type cystic kidneys. Journal of Medical Genetics. 47(12). 848–852. 20 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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