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Mariem Ben Rekaya

Observed names: Ben Rekaya, Ben Rekaya Meriam, Ben Rekaya, Mariem, M Ben Rekaya, M. Ben Rekaya, M. Ben-Rekaya, M. BenRekaya, MARIEM BEN REKAYA, Mariem B. Rekaya, Mariem Ben rekaya, Mariem Ben Rekaya, Meriam Rekaya Ben, Meriem Ben Rekaya
Observed institutions: Tunis University, Hôpital Farhat Hached, Hôpital Charles-Nicolle, Institut Pasteur de Tunis, Faculté de médecine de Tunis, Tunis El Manar University
ORCID: 0000-0001-7176-5201
Observed ORCID: 0000-0001-7176-5201
OpenAlex ID: A5076125834
High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis
2009 · M Ben Rekaya, O Messaoud, et al. · Journal of Human Genetics · 55
Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases
2018 · Yosr Hamdi, Maroua Boujemaa, et al. · Journal of Translational Medicine · 48
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Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia
2015 · Nizar Ben Halim, Sana Hsouna, et al. · American Journal of Human Biology · 33
Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia
2015 · M. Jerbi, M. Ben Rekaya, et al. · British Journal of Dermatology · 28
Specific Aspects of Consanguinity: Some Examples from the Tunisian Population
2014 · Lilia Romdhane, Nizar Ben Halim, et al. · Human Heredity · 27
Genetic homogeneity of mutational spectrum of group‐A xeroderma pigmentosum in Tunisian patients
2010 · Olfa Messaoud, Mariem Ben Rekaya, et al. · International Journal of Dermatology · 26
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity
2011 · O. Messaoud, M. Ben Rekaya, et al. · Archives of Dermatological Research · 24
Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family
2010 · O. Messaoud, M. Ben Rekaya, et al. · British Journal of Dermatology · 21
Identification of Novel BRCA1 and RAD50 Mutations Associated With Breast Cancer Predisposition in Tunisian Patients
2020 · Najah Mighri, Yosr Hamdi, et al. · Frontiers in Genetics · 20
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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci
2018 · Yosr Hamdi, Mariem Ben Rekaya, et al. · BMC Cancer · 20
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Further Evidence of Mutational Heterogeneity of theXPCGene in Tunisian Families: A Spectrum of Private and Ethnic Specific Mutations
2013 · Mariem Ben Rekaya, Manel Jerbi, et al. · BioMed Research International · 19
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Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
2017 · Mariem Ben Rekaya, Chokri Naouali, et al. · Journal of Dermatological Science · 18
Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia
2007 · Elghezal Hatem, Ben Rekaya Meriam, et al. · Prenatal Diagnosis · 18
Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers
2021 · Yosr Hamdi, Najah Mighri, et al. · Frontiers in Oncology · 17
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Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome
2013 · Yosra Bouyacoub, Hela Zribi, et al. · Gene · 17
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum
2012 · Mohamed Amine Senhaji, Omar Abidi, et al. · Archives of Dermatological Research · 17
Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype
2019 · Asma Chikhaoui, Sahar Elouej, et al. · Frontiers in Genetics · 14
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A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype–genotype correlation
2011 · MARIEM BEN REKAYA, OLFA MESSAOUD, et al. · Journal of Genetics · 14
High frequency of exon 15 deletion in the FANCA gene in T unisian patients affected with F anconi anemia disease: implication for diagnosis
2014 · Ahlem Amouri, Faten Talmoudi, et al. · Molecular Genetics & Genomic Medicine · 13
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A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy
2014 · Mariem Ben Rekaya, Nadia Laroussi, et al. · BioMed Research International · 13
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Performances of single tube nested polymerase chain reaction and GeneXpert ultra on Formalin fixed paraffin embedded tissues in the diagnosis of tuberculous spondylodiscitis
2021 · Emna Romdhane, Soumaya Rammeh, et al. · Clinical Rheumatology · 11
Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients
2016 · Chokri Naouali, Meriem Jones, et al. · International Journal of Dermatology · 11
PIK3CA mutations in breast cancer: A Tunisian series
2023 · Mariem Ben Rekaya, Farah Sassi, et al. · PLoS ONE · 10
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The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of Xeroderma pigmentosum
2013 · O. Messaoud, M. Ben Rekaya, et al. · Public Health Genomics · 10
Pathologically confirmed women's breast cancer: A descriptive study of Tunisian and Algerian series
2023 · Farah Sassi, Meriem Ben Rekaya, et al. · Cancer Reports · 6
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Works count: 53
Citation count: 526
H-index: 16
I10-index: 24
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