188 related articles for article (PubMed ID: 38313678)
1. Uncovering the clinical relevance of unclassified variants in DNA repair genes: a focus on
Boujemaa M; Nouira F; Jandoubi N; Mejri N; Bouaziz H; Charfeddine C; Ben Nasr S; Labidi S; El Benna H; Berrazega Y; Rachdi H; Daoud N; Benna F; Haddaoui A; Abdelhak S; Samir Boubaker M; Boussen H; Hamdi Y
Front Genet; 2024; 15():1327894. PubMed ID: 38313678
[No Abstract] [Full Text] [Related]
2. Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
Zuntini R; Ferrari S; Bonora E; Buscherini F; Bertonazzi B; Grippa M; Godino L; Miccoli S; Turchetti D
Front Genet; 2018; 9():378. PubMed ID: 30254663
[No Abstract] [Full Text] [Related]
3. Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population.
da Costa E Silva Carvalho S; Cury NM; Brotto DB; de Araujo LF; Rosa RCA; Texeira LA; Plaça JR; Marques AA; Peronni KC; Ruy PC; Molfetta GA; Moriguti JC; Carraro DM; Palmero EI; Ashton-Prolla P; de Faria Ferraz VE; Silva WA
BMC Med Genomics; 2020 Feb; 13(1):21. PubMed ID: 32039725
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction.
Caleca L; Catucci I; Figlioli G; De Cecco L; Pesaran T; Ward M; Volorio S; Falanga A; Marchetti M; Iascone M; Tondini C; Zambelli A; Azzollini J; Manoukian S; Radice P; Peterlongo P
Front Oncol; 2018; 8():480. PubMed ID: 30410870
[TBL] [Abstract][Full Text] [Related]
6. The Identification by Exome Sequencing of Candidate Genes in
BenAyed-Guerfali D; Kifagi C; BenKridis-Rejeb W; Ammous-Boukhris N; Ayedi W; Khanfir A; Daoud J; Mokdad-Gargouri R
Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 35893033
[TBL] [Abstract][Full Text] [Related]
7. Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics.
Ernst C; Hahnen E; Engel C; Nothnagel M; Weber J; Schmutzler RK; Hauke J
BMC Med Genomics; 2018 Mar; 11(1):35. PubMed ID: 29580235
[TBL] [Abstract][Full Text] [Related]
8. Characteristics of Germline Non-BRCA Mutation Status of High-Risk Breast Cancer Patients in China and Correlation with High-Risk Factors and Multigene Testing Suggestions.
Su Y; Yao Q; Xu Y; Yu C; Zhang J; Wang Q; Li J; Shi D; Yu B; Zeng Y; Zhu X; Bai Q; Zhou X
Front Genet; 2021; 12():674094. PubMed ID: 34917121
[No Abstract] [Full Text] [Related]
9. The Clinical Significance of Unknown Sequence Variants in BRCA Genes.
Calò V; Bruno L; La Paglia L; Perez M; Margarese N; Di Gaudio F; Russo A
Cancers (Basel); 2010 Sep; 2(3):1644-60. PubMed ID: 24281179
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins.
Jaballah-Gabteni A; Tounsi H; Kabbage M; Hamdi Y; Elouej S; Ben Ayed I; Medhioub M; Mahmoudi M; Dallali H; Yaiche H; Ben Jemii N; Maaloul A; Mezghani N; Abdelhak S; Hamzaoui L; Azzouz M; Boubaker S
J Transl Med; 2019 Jun; 17(1):212. PubMed ID: 31248416
[TBL] [Abstract][Full Text] [Related]
11. Germline mismatch repair gene variants analyzed by universal sequencing in Japanese cancer patients.
Kiyozumi Y; Matsubayashi H; Horiuchi Y; Higashigawa S; Oishi T; Abe M; Ohnami S; Urakami K; Nagashima T; Kusuhara M; Miyake H; Yamaguchi K
Cancer Med; 2019 Sep; 8(12):5534-5543. PubMed ID: 31386297
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients.
Grasel RS; Felicio PS; de Paula AE; Campacci N; Garcia FAO; de Andrade ES; Evangelista AF; Fernandes GC; Sabato CDS; De Marchi P; Souza CP; de Paula CAA; Torrezan GT; Galvão HCR; Carraro DM; Palmero EI
Front Oncol; 2020; 10():571330. PubMed ID: 33134171
[TBL] [Abstract][Full Text] [Related]
14. BRCA1 and BRCA2 unclassified variants and missense polymorphisms in Algerian breast/ovarian cancer families.
Cherbal F; Salhi N; Bakour R; Adane S; Boualga K; Maillet P
Dis Markers; 2012; 32(6):343-53. PubMed ID: 22684231
[TBL] [Abstract][Full Text] [Related]
15. Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
Caputo SM; Golmard L; Léone M; Damiola F; Guillaud-Bataille M; Revillion F; Rouleau E; Derive N; Buisson A; Basset N; Schwartz M; Vilquin P; Garrec C; Privat M; Gay-Bellile M; Abadie C; Abidallah K; Airaud F; Allary AS; Barouk-Simonet E; Belotti M; Benigni C; Benusiglio PR; Berthemin C; Berthet P; Bertrand O; Bézieau S; Bidart M; Bignon YJ; Birot AM; Blanluet M; Bloucard A; Bombled J; Bonadona V; Bonnet F; Bonnet-Dupeyron MN; Boulaire M; Boulouard F; Bouras A; Bourdon V; Brahimi A; Brayotel F; Bressac de Paillerets B; Bronnec N; Bubien V; Buecher B; Cabaret O; Carriere J; Chiesa J; Chieze-Valéro S; Cohen C; Cohen-Haguenauer O; Colas C; Collonge-Rame MA; Conoy AL; Coulet F; Coupier I; Crivelli L; Cusin V; De Pauw A; Dehainault C; Delhomelle H; Delnatte C; Demontety S; Denizeau P; Devulder P; Dreyfus H; d'Enghein CD; Dupré A; Durlach A; Dussart S; Fajac A; Fekairi S; Fert-Ferrer S; Fiévet A; Fouillet R; Mouret-Fourme E; Gauthier-Villars M; Gesta P; Giraud S; Gladieff L; Goldbarg V; Goussot V; Guibert V; Guillerm E; Guy C; Hardouin A; Heude C; Houdayer C; Ingster O; Jacquot-Sawka C; Jones N; Krieger S; Lacoste S; Lallaoui H; Larbre H; Laugé A; Le Guyadec G; Le Mentec M; Lecerf C; Le Gall J; Legendre B; Legrand C; Legros A; Lejeune S; Lidereau R; Lignon N; Limacher JM; Doriane Livon ; Lizard S; Longy M; Lortholary A; Macquere P; Mailliez A; Malsa S; Margot H; Mari V; Maugard C; Meira C; Menjard J; Molière D; Moncoutier V; Moretta-Serra J; Muller E; Nevière Z; Nguyen Minh Tuan TV; Noguchi T; Noguès C; Oca F; Popovici C; Prieur F; Raad S; Rey JM; Ricou A; Salle L; Saule C; Sevenet N; Simaga F; Sobol H; Suybeng V; Tennevet I; Tenreiro H; Tinat J; Toulas C; Turbiez I; Uhrhammer N; Vande Perre P; Vaur D; Venat L; Viellard N; Villy MC; Warcoin M; Yvard A; Zattara H; Caron O; Lasset C; Remenieras A; Boutry-Kryza N; Castéra L; Stoppa-Lyonnet D
Am J Hum Genet; 2021 Oct; 108(10):1907-1923. PubMed ID: 34597585
[TBL] [Abstract][Full Text] [Related]
16. In silico analysis for determining the deleterious nonsynonymous single nucleotide polymorphisms of
Yadegari F; Majidzadeh K
Mol Biol Res Commun; 2019 Dec; 8(4):141-150. PubMed ID: 32042831
[TBL] [Abstract][Full Text] [Related]
17. Structural Biology Helps Interpret Variants of Uncertain Significance in Genes Causing Endocrine and Metabolic Disorders.
Ittisoponpisan S; David A
J Endocr Soc; 2018 Aug; 2(8):842-854. PubMed ID: 30019023
[TBL] [Abstract][Full Text] [Related]
18. A Rare
Kabbage M; Ben Aissa-Haj J; Othman H; Jaballah-Gabteni A; Laarayedh S; Elouej S; Medhioub M; Kettiti HT; Khsiba A; Mahmoudi M; BelFekih H; Maaloul A; Touinsi H; Hamzaoui L; Chelbi E; Abdelhak S; Boubaker MS; Azzouz MM
Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 36011265
[TBL] [Abstract][Full Text] [Related]
19. Classification of genetic variants in genes associated with Lynch syndrome using a clinical history weighting algorithm.
Morris B; Hughes E; Rosenthal E; Gutin A; Bowles KR
BMC Genet; 2016 Jul; 17(1):99. PubMed ID: 27363726
[TBL] [Abstract][Full Text] [Related]
20. Estimating risks for variants of unknown significance according to their predicted pathogenicity classes with application to BRCA1.
Dowty JG; Lee E; McKean-Cowdin R; Henderson BE; Bernstein L; Ursin G; Hopper JL
Breast Cancer Res Treat; 2014 Feb; 144(1):171-7. PubMed ID: 24481681
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
