BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 33240314)

  • 1. Identification of Novel
    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
    Front Genet; 2020; 11():552971. PubMed ID: 33240314
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa.
    ElBiad O; Laraqui A; El Boukhrissi F; Mounjid C; Lamsisi M; Bajjou T; Elannaz H; Lahlou AI; Kouach J; Benchekroune K; Oukabli M; Chahdi H; Ennaji MM; Tanz R; Sbitti Y; Ichou M; Ennibi K; Badaoui B; Sekhsokh Y
    BMC Cancer; 2022 Feb; 22(1):208. PubMed ID: 35216584
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals.
    Kuusisto KM; Bebel A; Vihinen M; Schleutker J; Sallinen SL
    Breast Cancer Res; 2011 Feb; 13(1):R20. PubMed ID: 21356067
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Globally Rare
    Oosthuizen J; Kotze MJ; Van Der Merwe N; Myburgh EJ; Bester P; van der Merwe NC
    Front Oncol; 2020; 10():619469. PubMed ID: 33643918
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary breast cancer in Middle Eastern and North African (MENA) populations: identification of novel, recurrent and founder BRCA1 mutations in the Tunisian population.
    Mahfoudh W; Bouaouina N; Ahmed SB; Gabbouj S; Shan J; Mathew R; Uhrhammer N; Bignon YJ; Troudi W; Elgaaied AB; Hassen E; Chouchane L
    Mol Biol Rep; 2012 Feb; 39(2):1037-46. PubMed ID: 21603858
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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;
    J Transl Med; 2018 Jun; 16(1):158. PubMed ID: 29879995
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Screening for common mutations in BRCA1 and BRCA2 genes: interest in genetic testing of Tunisian families with breast and/or ovarian cancer.
    Fourati A; Louchez MM; Fournier J; Gamoudi A; Rahal K; El May MV; El May A; Revillion F; Peyrat JP
    Bull Cancer; 2014 Nov; 101(11):E36-40. PubMed ID: 25418591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of
    Hamdi Y; Boujemaa M; Mighri N; Mejri N; Jaidane O; Ben Nasr S; Bouaziz H; Hassouna JB; Zribi A; Berrazaga Y; Rachdi H; Daoud N; El Benna H; Labidi S; Haddaoui A; Rahal K; Benna F; Boussen H; Abdelhak S; Boubaker S
    Front Genet; 2021; 12():674990. PubMed ID: 34456966
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutation spectrum and prevalence of BRCA1 and BRCA2 genes in patients with familial and early-onset breast/ovarian cancer from Tunisia.
    Riahi A; Kharrat M; Ghourabi ME; Khomsi F; Gamoudi A; Lariani I; May AE; Rahal K; Chaabouni-Bouhamed H
    Clin Genet; 2015 Feb; 87(2):155-60. PubMed ID: 24372583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of Eleven Novel
    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
    Front Oncol; 2021; 11():674965. PubMed ID: 34490083
    [TBL] [Abstract][Full Text] [Related]  

  • 11. First application of next-generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the
    Jouali F; Laarabi FZ; Marchoudi N; Ratbi I; Elalaoui SC; Rhaissi H; Fekkak J; Sefiani A
    Oncol Lett; 2016 Aug; 12(2):1192-1196. PubMed ID: 27446417
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer families.
    Riahi A; Ghourabi ME; Fourati A; Chaabouni-Bouhamed H
    Breast Cancer; 2017 Mar; 24(2):238-244. PubMed ID: 27025497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complete mutation screening and haplotype characterization of BRCA1 gene in Tunisian patients with familial breast cancer.
    Troudi W; Uhrhammer N; Romdhane KB; Sibille C; Amor MB; Khodjet El Khil H; Jalabert T; Mahfoudh W; Chouchane L; Ayed FB; Bignon YJ; Elgaaied AB
    Cancer Biomark; 2008; 4(1):11-8. PubMed ID: 18334730
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of novel BRCA founder mutations in Middle Eastern breast cancer patients using capture and Sanger sequencing analysis.
    Bu R; Siraj AK; Al-Obaisi KA; Beg S; Al Hazmi M; Ajarim D; Tulbah A; Al-Dayel F; Al-Kuraya KS
    Int J Cancer; 2016 Sep; 139(5):1091-7. PubMed ID: 27082205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Contribution of the BRCA1 and BRCA2 mutations to breast cancer in Tunisia.
    Troudi W; Uhrhammer N; Sibille C; Dahan C; Mahfoudh W; Bouchlaka Souissi C; Jalabert T; Chouchane L; Bignon YJ; Ben Ayed F; Ben Ammar Elgaaied A
    J Hum Genet; 2007; 52(11):915-920. PubMed ID: 17922257
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.
    Pinto P; Paulo P; Santos C; Rocha P; Pinto C; Veiga I; Pinheiro M; Peixoto A; Teixeira MR
    Breast Cancer Res Treat; 2016 Sep; 159(2):245-56. PubMed ID: 27553368
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy.
    Cini G; Mezzavilla M; Della Puppa L; Cupelli E; Fornasin A; D'Elia AV; Dolcetti R; Damante G; Bertok S; Miolo G; Maestro R; de Paoli P; Amoroso A; Viel A
    BMC Med Genet; 2016 Feb; 17():11. PubMed ID: 26852130
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2 deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age.
    Turkovic L; Gurrin LC; Bahlo M; Dite GS; Southey MC; Hopper JL
    BMC Cancer; 2010 Sep; 10():466. PubMed ID: 20807450
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of mutations in BRCA genes and other candidate genes in high-risk probands or probands with breast or ovarian cancer in the Czech Republic.
    Riedlova P; Janoutova J; Hermanova B
    Mol Biol Rep; 2020 Apr; 47(4):2763-2769. PubMed ID: 32180084
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.