Hassan Rouba

2.3k total citations
83 papers, 1.4k citations indexed

About

Hassan Rouba is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Hassan Rouba has authored 83 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 31 papers in Genetics and 15 papers in Sensory Systems. Recurrent topics in Hassan Rouba's work include Hearing, Cochlea, Tinnitus, Genetics (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers) and Sexual Differentiation and Disorders (11 papers). Hassan Rouba is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers) and Sexual Differentiation and Disorders (11 papers). Hassan Rouba collaborates with scholars based in Morocco, France and Tunisia. Hassan Rouba's co-authors include Abdelhamid Barakat, Ken McElreavey, Hicham Charoute, Omar Abidi, Anu Bashamboo, Brahim El Houate, Abdelaziz Chafik, Redouane Boulouiz, Houda Benrahma and Lluís Quintana‐Murci and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Hassan Rouba

79 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hassan Rouba Morocco 22 762 739 419 176 170 83 1.4k
Andréa Trevas Maciel‐Guerra Brazil 20 1.2k 1.6× 1.1k 1.5× 379 0.9× 64 0.4× 220 1.3× 146 1.7k
B.J. Otten Netherlands 26 987 1.3× 594 0.8× 244 0.6× 141 0.8× 102 0.6× 55 1.7k
Beverly J. White United States 26 660 0.9× 935 1.3× 412 1.0× 22 0.1× 324 1.9× 61 1.9k
Lawrence C. Layman United States 26 762 1.0× 778 1.1× 1.2k 2.9× 30 0.2× 466 2.7× 76 2.0k
Louise Tee United Kingdom 18 801 1.1× 781 1.1× 87 0.2× 13 0.1× 153 0.9× 31 1.5k
Lawrence C. Layman United States 23 825 1.1× 841 1.1× 664 1.6× 19 0.1× 362 2.1× 54 1.8k
Boleslaw Goldman Israel 22 746 1.0× 575 0.8× 125 0.3× 8 0.0× 94 0.6× 74 1.7k
Jean Amos United States 11 565 0.7× 418 0.6× 66 0.2× 53 0.3× 38 0.2× 24 1.3k
Antonia Paula Marques‐de‐Faria Brazil 15 383 0.5× 391 0.5× 81 0.2× 20 0.1× 34 0.2× 51 617
Rima Slim Canada 27 1.3k 1.7× 838 1.1× 71 0.2× 285 1.6× 1.2k 7.1× 75 2.7k

Countries citing papers authored by Hassan Rouba

Since Specialization
Citations

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

Fields of papers citing papers by Hassan Rouba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hassan Rouba

This figure shows the co-authorship network connecting the top 25 collaborators of Hassan Rouba. A scholar is included among the top collaborators of Hassan Rouba 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 Hassan Rouba. Hassan Rouba 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.
Charoute, Hicham, et al.. (2023). Exploring the impact of CYP11A1’s missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study. Computational Biology and Chemistry. 106. 107937–107937. 2 indexed citations
2.
Charif, Majida, Hicham Charoute, Hassan Rouba, et al.. (2022). A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability. European Journal of Medical Genetics. 65(6). 104515–104515. 2 indexed citations
3.
4.
5.
Charoute, Hicham, et al.. (2019). Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience. American Journal of Medical Genetics Part A. 179(8). 1516–1524. 2 indexed citations
6.
Charoute, Hicham, Hassan Rouba, Mostafa Kabine, et al.. (2018). A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family. Gene. 659. 89–92. 3 indexed citations
7.
Nasser, Boubker, et al.. (2018). Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review. Journal of Assisted Reproduction and Genetics. 36(3). 499–507. 28 indexed citations
8.
Charoute, Hicham, et al.. (2017). Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family. Molecular Biology Reports. 44(5). 429–434. 10 indexed citations
9.
Charif, Majida, Omar Abidi, Redouane Boulouiz, et al.. (2013). Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss. Gene. 523(1). 103–105. 8 indexed citations
10.
Abidi, Omar, Majida Charif, Brahim El Houate, et al.. (2012). Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility. PLoS ONE. 7(3). e34111–e34111. 39 indexed citations
11.
Houate, Brahim El, Omar Abidi, Majida Charif, et al.. (2012). Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion. PLoS ONE. 7(4). e34902–e34902. 35 indexed citations
12.
Benrahma, Houda, Omar Abidi, Hassan Rouba, et al.. (2011). Association of the C677T Polymorphism in the Human Methylenetetrahydrofolate Reductase ( MTHFR ) Gene with the Genetic Predisposition for Type 2 Diabetes Mellitus in a Moroccan Population. Genetic Testing and Molecular Biomarkers. 16(5). 383–387. 29 indexed citations
13.
Bashamboo, Anu, Bruno Ferraz‐de‐Souza, Diana Lourenço, et al.. (2010). Human Male Infertility Associated with Mutations in NR5A1Encoding Steroidogenic Factor 1. The American Journal of Human Genetics. 87(5). 736–736. 3 indexed citations
14.
Vinci, G, Raja Brauner, Attila Tar, et al.. (2009). Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility. Fertility and Sterility. 92(4). 1347–1350. 17 indexed citations
15.
Abidi, Omar, Redouane Boulouiz, Lahcen Wakrim, et al.. (2008). Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene ( GJB2 ) in the Moroccan Population. Genetic Testing. 12(4). 569–574. 13 indexed citations
16.
Houate, Brahim El, Hassan Rouba, Abdelaziz Chafik, et al.. (2008). No Association between T222P/LGR8 Mutation and Cryptorchidism in the Moroccan Population. Hormone Research in Paediatrics. 70(4). 236–239. 23 indexed citations
17.
Abidi, Omar, Redouane Boulouiz, Abdelaziz Tlili, et al.. (2007). GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation. International Journal of Pediatric Otorhinolaryngology. 71(8). 1239–1245. 35 indexed citations
18.
Orvig, Anne Salazar, et al.. (2005). Une étude sur les premières expressions référentielles. Le cas des pronoms. 41(41). 15–31. 2 indexed citations
19.
Manni, Franz, Étienne Patin, Houssein Khodjet‐El‐Khil, et al.. (2005). A Y-chromosome portrait of the population of Jerba (Tunisia) to elucidate its complex demographic history. Bulletins et Mémoires de la Société d anthropologie de Paris. 17(1-2). 103–114. 4 indexed citations
20.
Krausz, Csilla, Lluís Quintana‐Murci, Sandrine Barbaux, et al.. (1999). A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility1. The Journal of Clinical Endocrinology & Metabolism. 84(10). 3606–3612. 73 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Andréa Trevas Maciel‐Guerra Breakdown of academic impact, for papers by B.J. Otten Breakdown of academic impact, for papers by Beverly J. White Breakdown of academic impact, for papers by Lawrence C. Layman Breakdown of academic impact, for papers by Louise Tee Breakdown of academic impact, for papers by Lawrence C. Layman Breakdown of academic impact, for papers by Boleslaw Goldman Breakdown of academic impact, for papers by Jean Amos Breakdown of academic impact, for papers by Antonia Paula Marques‐de‐Faria Breakdown of academic impact, for papers by Rima Slim
Rankless by CCL
2026