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Rym Meddeb

Observed names: Meddeb, Rym, R Meddeb
OpenAlex ID: A5084357207
Exome sequencing and case–control analyses identify RCC1 as a candidate breast cancer susceptibility gene
2018 · Aouatef Riahi, Hoda Radmanesh, et al. · International Journal of Cancer · 25
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WDR73-related galloway mowat syndrome with collapsing glomerulopathy
2018 · Mariem El Younsi, Lilia Kraoua, et al. · European Journal of Medical Genetics · 13
Genome Tunisia Project: paving the way for precision medicine in North Africa
2024 · Yosr Hamdi, Mediha Trabelsi, et al. · Genome Medicine · 12
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Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation
2022 · Hela Sassi, Rym Meddeb, et al. · BMC Medical Genomics · 6
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Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report
2023 · Firas Akrout, Ahlem Achour, et al. · Frontiers in Oncology · 2
Phenotype Spectrum in Tunisian Population with NPHP1 Deletion
2023 · Yousra Hammi, Maryem Ferjani, et al. · Indian Journal of Nephrology · 2
Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients
2014 · Ines Ouertani, Myriam Chaabouni, et al. · Open Journal of Genetics · 2
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Identification of Novel BRCA1 Germline Deleterious Variant Among a Tunisian Family
2021 · Hela Sassi, Hela Sassi, et al. · Clinical Oncology and Research · 1
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Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene
2018 · A Riahi, H Radmanesh, et al. · Geburtshilfe und Frauenheilkunde · 1
Rare 9q21.33q22.33 deletion due to an unbalanced transmission of a maternal chromosomal insertion
2025 · Bellil, Hela, Ben Yahia, Salwa, et al. · HAL (Le Centre pour la Communication Scientifique Directe)
Le syndrome Wolf–Hirschhorn : à propos de 9 cas
2021 · Hana Fredj, Lilia Kraoua, et al. · Morphologie
Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
2020 · Mariem Ben rekaya, Yosr Hamdi, et al.
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Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
2020 · Mariem Ben rekaya, Yosr Hamdi, et al.
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Works count: 13
Citation count: 64
H-index: 4
I10-index: 3
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