Mariem Ben Saïd

652 citations

26 papers · 369 indexed · h-index 11

Co-authors: Saber Masmoudi Abdelmonem Ghorbel Hammadi Ayadi Mounira Hmani‐Aifa Nabil Driss Abdelaziz Tlili Imen Chakchouk Z. Benzina
Topics: Hearing, Cochlea, Tinnitus, Genetics (14 papers)Genetics and Neurodevelopmental Disorders (6 papers)Ear Surgery and Otitis Media (5 papers)
Cited by: Sensory Systems Neurology Otorhinolaryngology
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Scientific Reports
Partner nations: Tunisia United States United Arab Emirates

In The Last Decade

Mariem Ben Saïd

24 papers receiving 363 citations

Peers

Countries citing papers authored by Mariem Ben Saïd

Since Specialization

Citations

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

Fields of papers citing papers by Mariem Ben Saïd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mariem Ben Saïd. 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 Mariem Ben Saïd. The network helps show where Mariem Ben Saïd may publish in the future.

Co-authorship network of co-authors of Mariem Ben Saïd

This figure shows the co-authorship network connecting the top 25 collaborators of Mariem Ben Saïd. A scholar is included among the top collaborators of Mariem Ben Saïd 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 Mariem Ben Saïd. Mariem Ben Saïd 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	Whole exome sequencing identifies ABHD14A and MRNIP as novel candidate genes for developmental language disorder 2025 ·Scientific Reports ·Amal Bouzid,(unknown),Amal Souissi,(unknown),Fakher Frikha,(unknown),Crystel Bonnet,(unknown),(unknown),Christine Petit,Saber Masmoudi,Rifat Hamoudi,Mariem Ben Saïd	0
2	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
3	Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy 2023 ·Epilepsia Open ·Mariem Ben Saïd,(unknown),(unknown),Amal Souissi,(unknown),Faiza Fakhfakh,Saber Masmoudi,Ikhlas Ben Ayed,Chahnez Triki	3
4	First report of Tunisian patients with CDKL5‐related encephalopathy 2023 ·Epilepsia Open ·Chahnez Triki,(unknown),(unknown),Mariem Ben Saïd,(unknown),Sarah Weckhuysen,(unknown),Faiza Fakhfakh	1
5	A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature 2023 ·International Journal of Developmental Neuroscience ·(unknown),Ikhlas Ben Ayed,(unknown),Amal Souissi,(unknown),Mariem Ben Saïd,(unknown),Saber Masmoudi,Chahnez Triki,Hassen Hadj Kacem,(unknown)	3
6	A Tunisian patient with CLCN2 ‐related leukoencephalopathy 2022 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),Samia Ben Sassi,Mariem Ben Saïd,Fatma Nabli,(unknown),(unknown),Saber Masmoudi,Rim Amouri	1
7	Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer 2022 ·PLoS ONE ·(unknown),Slim Ben Ahmed,(unknown),(unknown),(unknown),(unknown),Mariem Ben Saïd,Saber Masmoudi,(unknown),Angela Brieger,Stefan Zeuzem,Saad Hasan Mohammed Ali,Moez Gribaa,Guido Plotz	4
8	Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population 2021 ·Journal of Advanced Research ·Amal Souissi,Mariem Ben Saïd,Ikhlas Ben Ayed,(unknown),Amal Bouzid,Mohamed Ali Mosrati,(unknown),(unknown),(unknown),Hassen Kamoun,(unknown),Abdullah Ahmed Gibriel,Abdelaziz Tlili,Saber Masmoudi	18
9	Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene 2021 ·Genetic Testing and Molecular Biomarkers ·Amal Souissi,Mariem Ben Saïd,Fakher Frikha,(unknown),Saber Masmoudi,André Mégarbané	3
10	Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly 2021 ·European Journal of Medical Genetics ·Ikhlas Ben Ayed,(unknown),Amal Bouzid,(unknown),Amal Souissi,(unknown),Mariem Ben Saïd,(unknown),(unknown),(unknown),(unknown),(unknown),Hassen Kamoun,Abdelaziz Tlili,Saber Masmoudi,Chahnez Triki	4
11	NADf Chip, a Two-Color Microarray for Simultaneous Screening of Multigene Mutations Associated with Hearing Impairment in North African Mediterranean Countries 2015 ·Journal of Molecular Diagnostics ·Imen Chakchouk,Mariem Ben Saïd,(unknown),(unknown),(unknown),Ibtihel Smeti,(unknown),Abdullah Ahmed Gibriel,Abdelmonem Ghorbel,(unknown),Saber Masmoudi	18
12	A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation 2015 ·Human Molecular Genetics ·M’hamed Grati,Imen Chakchouk,Qi Ma,Mariem Ben Saïd,Alexandra A. DeSmidt,(unknown),Denise Yan,(unknown),Rahul Mittal,Nabil Driss,Susan H. Blanton,Amjad Farooq,Zhongmin Lu,Xue Zhong Liu,Saber Masmoudi	75
13	Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene 2013 ·Gene ·Mariem Ben Saïd,(unknown),Salma Ben‐Salem,(unknown),(unknown),W. Bouassida,Z. Benzina,Hammadi Ayadi,Peter Söderkvist,L. El Matri,Mounira Hmani‐Aifa	17
14	Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21 2012 ·Journal of Human Genetics ·Mohamed Ali Mosrati,Isabelle Schrauwen,Mariem Ben Saïd,Mounira Hmani‐Aifa,Erik Fransén,(unknown),Abdelmonem Ghorbel,Guy Van Camp,Saber Masmoudi	3
15	Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome 2012 ·International Journal of Pediatric Otorhinolaryngology ·Mariem Ben Saïd,(unknown),Z. Benzina,(unknown),Felipe Moreno,Saber Masmoudi,Hammadi Ayadi,Mounira Hmani‐Aifa	13
16	DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss 2011 ·European Journal of Medical Genetics ·Mariem Ben Saïd,Mounira Hmani‐Aifa,B. Hammami,Abdelaziz Tlili,(unknown),Ilhem Charfeddine,Hammadi Ayadi,Abdelmonem Ghorbel,Ignacio del Castillo,Saber Masmoudi	8
17	A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family 2011 ·European Journal of Medical Genetics ·Mariem Ben Saïd,(unknown),Malek Mnejja,(unknown),(unknown),Ilhem Charfeddine,(unknown),(unknown),Hammadi Ayadi,Z. Benzina,Abdelmonem Ghorbel,Ignacio del Castillo,Saber Masmoudi,(unknown)	19
18	High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects 2010 ·Genetic Testing and Molecular Biomarkers ·Mariem Ben Saïd,Mounira Hmani‐Aifa,(unknown),Shahid Mahmood Baig,Mirna Mustapha,Sedigheh Delmaghani,Abdelaziz Tlili,Abdelmonem Ghorbel,Hammadi Ayadi,Guy Van Camp,Richard J. Smith,Mustafa Tekin,Saber Masmoudi	37
19	Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus 2009 ·Genetic Testing and Molecular Biomarkers ·(unknown),Mounira Hmani‐Aifa,(unknown),Mariem Ben Saïd,Mohamed Ali Mosrati,(unknown),(unknown),Ilhem Charfeddine,Nabil Driss,Saïda Ben Arab,Abdelmonem Ghorbel,Hammadi Ayadi,Saber Masmoudi	36
20	<i>TMC1</i> but Not <i>TMC2</i> Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families 2008 ·Audiology and Neurotology ·Abdelaziz Tlili,(unknown),Mounira Hmani‐Aifa,(unknown),(unknown),(unknown),Mariem Ben Saïd,(unknown),Z. Benzina,(unknown),Nabil Driss,Abdelmonem Ghorbel,Hammadi Ayadi,Saber Masmoudi	52

About Mariem Ben Saïd

Mariem Ben Saïd is a scholar working on Sensory Systems, Otorhinolaryngology and Neurology, having authored 26 papers that have together received 369 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Ear Surgery and Otitis Media (5 papers). The work is most often cited by research in Sensory Systems (214 citations), Neurology (101 citations) and Otorhinolaryngology (46 citations). Mariem Ben Saïd has collaborated with scholars based in Tunisia, United States and United Arab Emirates. Frequent co-authors include Saber Masmoudi, Abdelmonem Ghorbel, Hammadi Ayadi, Mounira Hmani‐Aifa, Nabil Driss, Abdelaziz Tlili, Imen Chakchouk, Z. Benzina, Qi Ma and M’hamed Grati. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

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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