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Page 1
Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report.
Akrout F, Achour A, Tops CMJ, Gallon R, Meddeb R, Achoura S, Ben Rekaya M, Hamdeni E, Rammeh S, Chkili R, Mansouri N, Belguith N, Mrad R. Akrout F, et al. Among authors: ben rekaya m. Front Oncol. 2023 Aug 17;13:1195814. doi: 10.3389/fonc.2023.1195814. eCollection 2023. Front Oncol. 2023. PMID: 37664053 Free PMC article.
Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers.
Hamdi Y, Mighri N, Boujemaa M, Mejri N, Ben Nasr S, Ben Rekaya M, Messaoud O, Bouaziz H, Berrazega Y, Rachdi H, Jaidane O, Daoud N, Zribi A, Ayari J, El Benna H, Labidi S, Ben Hassouna J, Haddaoui A, Rahal K, Benna F, Mrad R, Ben Ahmed S, Boussen H, Boubaker S, Abdelhak S. Hamdi Y, et al. Among authors: ben rekaya m. Front Oncol. 2021 Aug 20;11:674965. doi: 10.3389/fonc.2021.674965. eCollection 2021. Front Oncol. 2021. PMID: 34490083 Free PMC article.
PIK3CA mutations in breast cancer: A Tunisian series.
Ben Rekaya M, Sassi F, Saied E, Bel Haj Kacem L, Mansouri N, Zarrouk S, Azouz S, Rammeh S. Ben Rekaya M, et al. PLoS One. 2023 May 17;18(5):e0285413. doi: 10.1371/journal.pone.0285413. eCollection 2023. PLoS One. 2023. PMID: 37195967 Free PMC article.
Identification of Novel BRCA1 and RAD50 Mutations Associated With Breast Cancer Predisposition in Tunisian Patients.
Mighri N, Hamdi Y, Boujemaa M, Othman H, Ben Nasr S, El Benna H, Mejri N, Labidi S, Ayari J, Jaidene O, Bouaziz H, Ben Rekaya M, M'rad R, Haddaoui A, Rahal K, Boussen H, Boubaker S, Abdelhak S. Mighri N, et al. Among authors: ben rekaya m. Front Genet. 2020 Nov 6;11:552971. doi: 10.3389/fgene.2020.552971. eCollection 2020. Front Genet. 2020. PMID: 33240314 Free PMC article.
Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases.
Hamdi Y, Boujemaa M, Ben Rekaya M, Ben Hamda C, Mighri N, El Benna H, Mejri N, Labidi S, Daoud N, Naouali C, Messaoud O, Chargui M, Ghedira K, Boubaker MS, Mrad R, Boussen H, Abdelhak S; PEC Consortium. Hamdi Y, et al. Among authors: ben rekaya m. J Transl Med. 2018 Jun 7;16(1):158. doi: 10.1186/s12967-018-1504-9. J Transl Med. 2018. PMID: 29879995 Free PMC article.
Specific aspects of consanguinity: some examples from the Tunisian population.
Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, Abdelhak S. Romdhane L, et al. Among authors: ben halim n, ben rekaya m, ben rhouma f. Hum Hered. 2014;77(1-4):167-74. doi: 10.1159/000362167. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060280 Review.
Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis.
Ben Rekaya M, Naouali C, Messaoud O, Jones M, Bouyacoub Y, Nagara M, Pippucci T, Jmel H, Chargui M, Jerbi M, Alibi M, Dallali H, Bashamboo A, McElreavey K, Romeo G, Barakat A, Zghal M, Yacoub-Youssef H, Abdelhak S. Ben Rekaya M, et al. J Dermatol Sci. 2018 Feb;89(2):172-180. doi: 10.1016/j.jdermsci.2017.10.015. Epub 2017 Nov 2. J Dermatol Sci. 2018. PMID: 29169765
24 results