Moez Gribaa

1.8k total citations
51 papers, 679 citations indexed

About

Moez Gribaa is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Moez Gribaa has authored 51 papers receiving a total of 679 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Moez Gribaa's work include Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Moez Gribaa is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Moez Gribaa collaborates with scholars based in Tunisia, France and Germany. Moez Gribaa's co-authors include M. Kœnig, Saad Hasan Mohammed Ali, Mustafa A. Salih, Marie Fernet, Janet Hall, Ilhem Ben Charfeddine, Hatem Elghezal, Hanène Landolsi, Christine Bétard and Clotilde Lagier‐Tourenne and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Moez Gribaa

50 papers receiving 659 citations

Peers

Countries citing papers authored by Moez Gribaa

Since Specialization

Citations

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

Fields of papers citing papers by Moez Gribaa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moez Gribaa

This figure shows the co-authorship network connecting the top 25 collaborators of Moez Gribaa. A scholar is included among the top collaborators of Moez Gribaa 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 Moez Gribaa. Moez Gribaa 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	Functional analysis of MMR gene VUS from potential Lynch syndrome patients 2024 ·PLoS ONE ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mariem Ben Saïd, Saber Masmoudi, (unknown), (unknown), (unknown), Angela Brieger, Stefan Zeuzem, Saad Hasan Mohammed Ali, Hakan Gürkan, (unknown), Moez Gribaa, Guido Plotz	1
2	Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency in a Tunisian family 2020 ·Pan African Medical Journal ·(unknown), (unknown), (unknown), (unknown), Moez Gribaa, (unknown), (unknown)	6
3	Targeted next generation sequencing screening of Lynch syndrome in Tunisian population 2019 ·Familial Cancer ·(unknown), (unknown), (unknown), Tom van Wezel, (unknown), (unknown), (unknown), Slim Ben Ahmed, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Saad Hasan Mohammed Ali, (unknown), Moez Gribaa, Hans Morreau	8
4	c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis 2019 ·Cancer Genetics ·(unknown), Klaus Brusgaard, (unknown), (unknown), (unknown), Lilian Bomme Ousager, (unknown), (unknown), (unknown), (unknown), Saad Hasan Mohammed Ali, (unknown), Moez Gribaa	3
5	Genetic Analysis of Mu and Kappa Opioid Receptor and COMT Enzyme in Cancer Pain Tunisian Patients Under Opioid Treatment 2017 ·SHILAP Revista de lepidopterología ·(unknown), Jean‐Baptiste Woillard, A. Mili, Isabelle Creveaux, Ilhem Ben Charfeddine, (unknown), (unknown), (unknown), (unknown), Moez Gribaa, (unknown)	7
6	Sanjad-Sakati syndrome in a Tunisian child 2015 ·Archives de Pédiatrie ·Emna Kerkeni, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Moez Gribaa, Kamel Monastiri	9
7	Molecular characterization of piebaldism in a Tunisian family 2015 ·Pathologie Biologie ·Emna Kerkeni, S Boubaker, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Moez Gribaa, Kamel Monastiri	2
8	Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population 2015 ·Journal of Assisted Reproduction and Genetics ·(unknown), Moez Gribaa, Ons Mamaï, Ilhem Ben Charfeddine, (unknown), (unknown), Meriem Mehdi, Saad Hasan Mohammed Ali, Samira Ibala‐Romdhane	17
9	Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes 2014 ·PubMed ·Dorra H’mida-Ben Brahim, (unknown), (unknown), Imed Harrabi, Saoussen Trabelsi, (unknown), Moez Gribaa, (unknown), (unknown), (unknown), (unknown), (unknown), Saad Hasan Mohammed Ali	5
10	Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia 2012 ·European Journal of Medical Genetics ·(unknown), (unknown), Audrey Labalme, (unknown), Soumaya Mougou, (unknown), Moez Gribaa, Damien Sanlaville, Hatem Elghezal, Saad Hasan Mohammed Ali	21
11	Screening for NLRP7 Mutations in Familial and Sporadic Recurrent Hydatidiform Moles 2011 ·International Journal of Gynecological Pathology ·Hanène Landolsi, Cécile Rittore, Laurent Philibert, Nabiha Missaoui, Sihem Hmissa, Isabelle Touitou, Moez Gribaa, Mohamed Tahar Yacoubi	15
12	Cytogenetic and Molecular Aspects of Absolute Teratozoospermia: Comparison Between Polymorphic and Monomorphic Forms 2011 ·Urology ·Sonia Brahem, Hatem Elghezal, (unknown), Hanène Landolsi, (unknown), (unknown), Moez Gribaa, Saad Hasan Mohammed Ali, Meriem Mehdi	24
13	Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family 2011 ·General and Comparative Endocrinology ·Ilhem Ben Charfeddine, Felix G. Riepe, (unknown), Alexandra Kulle, (unknown), Ons Mamaï, (unknown), A. Mili, (unknown), Saad Hasan Mohammed Ali, Paul‐Martin Holterhus, Moez Gribaa	15
14	Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III 2011 ·Journal of Human Genetics ·A. Mili, Ilhem Ben Charfeddine, Ons Mamaï, (unknown), (unknown), (unknown), Serena Pagliarani, Sabrina Lucchiari, (unknown), Néji Tebib, (unknown), Jihène Bouguila, (unknown), Saad Hasan Mohammed Ali, Khalifa Limem, Giacomo P. Comi, Moez Gribaa	20
15	The usefulness of p57KIP2 immunohistochemical staining and genotyping test in the diagnosis of the hydatidiform mole 2011 ·Pathology - Research and Practice ·Hanène Landolsi, Nabiha Missaoui, Sonia Brahem, Sihem Hmissa, Moez Gribaa, Mohamed Tahar Yacoubi	22
16	Le syndrome de Li Fraumeni: à propos d'un cas familial avec cancers multiples et présentant une mutation germinale du gène p53 2010 ·Annales de biologie clinique ·(unknown), Olfa Gharbi, (unknown), Moez Gribaa, (unknown), Abdelfattah Zakhama, (unknown), Thierry Frébourg, Slim Ben Ahmed	3
17	An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation 2009 ·Journal of Bone and Mineral Metabolism ·Moez Gribaa, M. Younès, Yosra Bouyacoub, (unknown), Ilhem Ben Charfeddine, M. Touzi, (unknown), (unknown), N. Bergaoui, Saad Hasan Mohammed Ali	40
18	Placental Mesenchymal Dysplasia with Beckwith–Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines 2008 ·Placenta ·(unknown), Moez Gribaa, (unknown), A. Chaïeb, (unknown), Hatem Elghezal, A. Saad	33
19	Identification and functional consequences of a novel MRE11 mutation affecting 10 Saudi Arabian patients with the ataxia telangiectasia-like disorder 2004 ·Human Molecular Genetics ·Marie Fernet, Moez Gribaa, Mustafa A. Salih, (unknown), Janet Hall, M. Kœnig	96
20	Cytogenetic analysis in 139 Tunisian patients with de novo acute myeloid leukemia 2002 ·Annales de Génétique ·(unknown), Hatem Elghezal, (unknown), (unknown), Moez Gribaa, (unknown), (unknown), (unknown), Moez Elloumi, Saad Ali	11

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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