Home › Researcher directory › Rym Meddeb

Rym Meddeb

Affiliation : Hôpital Charles-Nicolle · Faculté de médecine de Tunis

• 11Publications (affiliation in Tunisia)
• 13Total publications
• 66Citations
• 4h-index

OpenAlex

Research profile

Rym Meddeb has 11 indexed publications (2014–2023). Their work appears mainly in “Indian Journal of Nephrology”, “Frontiers in Oncology” and “BMC Medical Genomics”. Their most cited article, “Exome sequencing and case–control analyses identify RCC1 as a candidate breast cancer susceptibility gene” (2018), has been cited 25 times. 5 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in Germany, Netherlands.

Is this you? Get your research seen

Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.

Create my free profile Add my publications

Research areas

• BRCA gene mutations in cancer
• Breast Lesions and Carcinomas
• Genomics and Rare Diseases
• Genetic factors in colorectal cancer
• Genomic variations and chromosomal abnormalities

Publications (11)

• Phenotype Spectrum in Tunisian Population with NPHP1 Deletion
  2023 · Indian Journal of Nephrology · cited 3 times
• Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report
  2023 · Frontiers in Oncology · cited 2 times
• Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation
  2022 · BMC Medical Genomics · cited 6 times
• Identification of Novel BRCA1 Germline Deleterious Variant Among a Tunisian Family
  2021 · Clinical Oncology and Research · cited 1 times
• Le syndrome Wolf–Hirschhorn : à propos de 9 cas
  2021 · Morphologie
• Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
  2020
• Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
  2020
• Exome sequencing and case–control analyses identify RCC1 as a candidate breast cancer susceptibility gene
  2018 · International Journal of Cancer · cited 25 times
• WDR73-related galloway mowat syndrome with collapsing glomerulopathy
  2018 · European Journal of Medical Genetics · cited 13 times
• Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene
  2018 · Geburtshilfe und Frauenheilkunde · cited 1 times
• Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients
  2014 · Open Journal of Genetics · cited 2 times

Publication venues

• Indian Journal of Nephrology × 1
• Frontiers in Oncology × 1
• BMC Medical Genomics × 1
• Clinical Oncology and Research × 1
• Morphologie × 1
• International Journal of Cancer × 1

Publications per year

• 20232
• 20221
• 20212
• 20202
• 20183
• 20141

Collaborations

Partner institutions : Tunis El Manar University · Tunis University · Institut Pasteur de Tunis · Institut Salah-Azaïz · Military Hospital of Tunis

Co-authors’ countries : Germany · Netherlands

Co-authors

• Ridha Mrad
• Neïla Belguith
• Médiha Trabelsi
• Inès Ouertani
• Faouzi Mâazoul
• Mariem Ben Rekaya
• Aouatef Riahi
• Lilia Kraoua
• Maryem Ferjani
• Abderazek Haddaoui
• Tahar Gargah
• Soumaya Labidi

Bibliographic data from OpenAlex (open database).