Hassan Rouba

2.3k citations

83 papers · 1.4k indexed · h-index 22

Molecular Biology top 10%
Genetics top 2%
Reproductive Medicine top 2%
Sensory Systems top 2%
Public Health, Environmental and Occupational Health top 10%

Co-authors: Abdelhamid Barakat Ken McElreavey Hicham Charoute Omar Abidi Anu Bashamboo Brahim El Houate Abdelaziz Chafik Redouane Boulouiz
Topics: Hearing, Cochlea, Tinnitus, Genetics (15 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers)Sexual Differentiation and Disorders (11 papers)
Cited by: Reproductive Medicine Sensory Systems Genetics
Journals: SHILAP Revista de lepidopterologíaPLoS ONE The Journal of Clinical Endocrinology & Metabolism
Partner nations: Morocco France Tunisia

In The Last Decade

Hassan Rouba

79 papers receiving 1.4k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Exploring the impact of CYP11A1’s missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study 2023 ·Computational Biology and Chemistry ·(unknown),(unknown),(unknown),Hicham Charoute,Abderrahim Malki,Abdelhamid Barakat,Hassan Rouba	2
2	A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability 2022 ·European Journal of Medical Genetics ·(unknown),(unknown),Majida Charif,(unknown),Hicham Charoute,Hassan Rouba,Rachida Roky,Guy Lenaers,Abdelhamid Barakat,(unknown)	2
3	Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis 2020 ·Cardiology Research and Practice ·(unknown),Hicham Charoute,(unknown),(unknown),Houda Benrahma,Rachid Saı̈le,Hassan Rouba,Abdelhamid Barakat	6
4	Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity 2019 ·BioMed Research International ·(unknown),(unknown),(unknown),(unknown),Hicham Charoute,Hassan Rouba,Rachid Saı̈le,(unknown),Abdelhamid Barakat	11
5	Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21‐year single‐center experience 2019 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Hicham Charoute,(unknown),(unknown),(unknown),(unknown),(unknown),Boubker Nasser,Abdelhamid Barakat,Hassan Rouba	2
6	A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family 2018 ·Gene ·(unknown),(unknown),(unknown),(unknown),Hicham Charoute,(unknown),Hassan Rouba,Mostafa Kabine,Crystel Bonnet,Christine Petit,Abdelhamid Barakat	3
7	Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review 2018 ·Journal of Assisted Reproduction and Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Boubker Nasser,Abdelhamid Barakat,Hassan Rouba	28
8	Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family 2017 ·Molecular Biology Reports ·(unknown),(unknown),Hicham Charoute,(unknown),Hassan Rouba,Majida Charif,Guy Lenaers,Abdelhamid Barakat	10
9	Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss 2013 ·Gene ·Majida Charif,(unknown),Omar Abidi,Redouane Boulouiz,(unknown),Rachida Roky,Hassan Rouba,Mostafa Kandil,Guy Lenaers,Abdelhamid Barakat	8
10	Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility 2012 ·PLoS ONE ·(unknown),Omar Abidi,Majida Charif,Brahim El Houate,Houda Benrahma,Noureddine Louanjli,(unknown),(unknown),Abdelhamid Barakat,Anu Bashamboo,Ken McElreavey,(unknown),Hassan Rouba	39
11	Association of Spermatogenic Failure with the b2/b3 Partial AZFc Deletion 2012 ·PLoS ONE ·(unknown),(unknown),(unknown),(unknown),Brahim El Houate,Omar Abidi,Majida Charif,Noureddine Louanjli,(unknown),Abdelhamid Barakat,Anu Bashamboo,Ken McElreavey,Hassan Rouba	35
12	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 2011 ·Genetic Testing and Molecular Biomarkers ·Houda Benrahma,Omar Abidi,(unknown),(unknown),Hassan Rouba,Asma Chadli,Mounia Oudghiri,(unknown),Abdelhamid Barakat	29
13	Human Male Infertility Associated with Mutations in NR5A1Encoding Steroidogenic Factor 1 2010 ·The American Journal of Human Genetics ·Anu Bashamboo,Bruno Ferraz‐de‐Souza,Diana Lourenço,(unknown),Neil J. Sebire,Debbie Montjean,Joëlle Bignon‐Topalovic,Jacqueline Mandelbaum,Jean‐Pierre Siffroi,(unknown),Uppala Radhakrishna,Hassan Rouba,Célia Ravel,Jacob-S. Seeler,John C. Achermann,Ken McElreavey	3
14	Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility 2009 ·Fertility and Sterility ·G Vinci,Raja Brauner,Attila Tar,Hassan Rouba,Jayesh Sheth,Frenny Sheth,Célia Ravel,Ken McElreavey,Anu Bashamboo	17
15	Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene ( GJB2 ) in the Moroccan Population 2008 ·Genetic Testing ·Omar Abidi,Redouane Boulouiz,(unknown),(unknown),Lahcen Wakrim,Hassan Rouba,Abdelaziz Chafik,Mohammed Hassar,Abdelhamid Barakat	13
16	No Association between T222P/LGR8 Mutation and Cryptorchidism in the Moroccan Population 2008 ·Hormone Research in Paediatrics ·Brahim El Houate,Hassan Rouba,(unknown),(unknown),Abdelaziz Chafik,Redouane Boulouiz,(unknown),(unknown),Ken McElreavey,Abdelhamid Barakat	23
17	GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation 2007 ·International Journal of Pediatric Otorhinolaryngology ·Omar Abidi,Redouane Boulouiz,(unknown),(unknown),(unknown),Abdelaziz Tlili,Hassan Rouba,Saber Masmoudi,Abdelaziz Chafik,Mohammed Hassar,Abdelhamid Barakat	35
18	Une étude sur les premières expressions référentielles. Le cas des pronoms 2005 ·Anne Salazar Orvig,Hassan Rouba,(unknown),Haydée Marcos,Aliyah Morgenstern,(unknown)	2
19	A Y-chromosome portrait of the population of Jerba (Tunisia) to elucidate its complex demographic history 2005 ·Bulletins et Mémoires de la Société d anthropologie de Paris ·Franz Manni,(unknown),Étienne Patin,(unknown),Houssein Khodjet‐El‐Khil,Karl Skorecki,Dror Rosengarten,Hassan Rouba,Évelyne Heyer,(unknown)	4
20	A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility¹ 1999 ·The Journal of Clinical Endocrinology & Metabolism ·Csilla Krausz,Lluís Quintana‐Murci,Sandrine Barbaux,Jean‐Pierre Siffroi,Hassan Rouba,D Delafontaine,(unknown),(unknown),J.-M. Antoine,(unknown),(unknown),Attila Tar,Éric Jeandidier,Ghislaine Plessis,Thomas Bourgeron,J. P. Dadoune,Marc Fellous,Ken McElreavey	73

About Hassan Rouba

Hassan Rouba is a scholar working on Sensory Systems, Linguistics and Language and Genetics, having authored 83 papers that have together received 1.4k indexed citations. Recurring topics across this 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). The work is most often cited by research in Reproductive Medicine (419 citations), Sensory Systems (176 citations) and Genetics (739 citations). Hassan Rouba has collaborated with scholars based in Morocco, France and Tunisia. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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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