660 related articles for article (PubMed ID: 27476653)
1. Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
Adam R; Spier I; Zhao B; Kloth M; Marquez J; Hinrichsen I; Kirfel J; Tafazzoli A; Horpaopan S; Uhlhaas S; Stienen D; Friedrichs N; Altmüller J; Laner A; Holzapfel S; Peters S; Kayser K; Thiele H; Holinski-Feder E; Marra G; Kristiansen G; Nöthen MM; Büttner R; Möslein G; Betz RC; Brieger A; Lifton RP; Aretz S
Am J Hum Genet; 2016 Aug; 99(2):337-51. PubMed ID: 27476653
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
Spier I; Kerick M; Drichel D; Horpaopan S; Altmüller J; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Holinski-Feder E; Perner S; Thiele H; Nöthen MM; Hoffmann P; Timmermann B; Schweiger MR; Aretz S
Fam Cancer; 2016 Apr; 15(2):281-8. PubMed ID: 26780541
[TBL] [Abstract][Full Text] [Related]
3. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
[TBL] [Abstract][Full Text] [Related]
4. Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.
Tanskanen T; Gylfe AE; Katainen R; Taipale M; Renkonen-Sinisalo L; Mecklin JP; Järvinen H; Tuupanen S; Kilpivaara O; Vahteristo P; Aaltonen LA
Scand J Gastroenterol; 2013 Jun; 48(6):672-8. PubMed ID: 23544471
[TBL] [Abstract][Full Text] [Related]
5.
Villy MC; Masliah-Planchon J; Schnitzler A; Delhomelle H; Buecher B; Filser M; Merchadou K; Golmard L; Melaabi S; Vacher S; Blanluet M; Suybeng V; Corsini C; Dhooge M; Hamzaoui N; Farelly S; Ait Omar A; Benamouzig R; Caumette V; Bahuau M; Cucherousset J; Allory Y; Stoppa-Lyonnet D; Bieche I; Colas C
J Med Genet; 2023 Nov; 60(12):1198-1205. PubMed ID: 37402566
[TBL] [Abstract][Full Text] [Related]
6. Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Spier I; Holzapfel S; Altmüller J; Zhao B; Horpaopan S; Vogt S; Chen S; Morak M; Raeder S; Kayser K; Stienen D; Adam R; Nürnberg P; Plotz G; Holinski-Feder E; Lifton RP; Thiele H; Hoffmann P; Steinke V; Aretz S
Int J Cancer; 2015 Jul; 137(2):320-31. PubMed ID: 25529843
[TBL] [Abstract][Full Text] [Related]
7. Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis.
Perne C; Peters S; Cartolano M; Horpaopan S; Grimm C; Altmüller J; Sommer AK; Hillmer AM; Thiele H; Odenthal M; Möslein G; Adam R; Sivalingam S; Kirfel J; Schweiger MR; Peifer M; Spier I; Aretz S
PLoS One; 2021; 16(11):e0259185. PubMed ID: 34843512
[TBL] [Abstract][Full Text] [Related]
8. Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.
Morak M; Käsbauer S; Kerscher M; Laner A; Nissen AM; Benet-Pagès A; Schackert HK; Keller G; Massdorf T; Holinski-Feder E
Fam Cancer; 2017 Oct; 16(4):491-500. PubMed ID: 28528517
[TBL] [Abstract][Full Text] [Related]
9. Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Yurgelun MB; Kulke MH; Fuchs CS; Allen BA; Uno H; Hornick JL; Ukaegbu CI; Brais LK; McNamara PG; Mayer RJ; Schrag D; Meyerhardt JA; Ng K; Kidd J; Singh N; Hartman AR; Wenstrup RJ; Syngal S
J Clin Oncol; 2017 Apr; 35(10):1086-1095. PubMed ID: 28135145
[TBL] [Abstract][Full Text] [Related]
10. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
Rohlin A; Rambech E; Kvist A; Törngren T; Eiengård F; Lundstam U; Zagoras T; Gebre-Medhin S; Borg Å; Björk J; Nilbert M; Nordling M
Fam Cancer; 2017 Apr; 16(2):195-203. PubMed ID: 27696107
[TBL] [Abstract][Full Text] [Related]
11. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.
Sieber OM; Lipton L; Crabtree M; Heinimann K; Fidalgo P; Phillips RK; Bisgaard ML; Orntoft TF; Aaltonen LA; Hodgson SV; Thomas HJ; Tomlinson IP
N Engl J Med; 2003 Feb; 348(9):791-9. PubMed ID: 12606733
[TBL] [Abstract][Full Text] [Related]
12. A large family with MSH3-related polyposis.
Aelvoet AS; Hoekman DR; Redeker BJW; Weegenaar J; Dekker E; van Noesel CJM; Duijkers FAM
Fam Cancer; 2023 Jan; 22(1):49-54. PubMed ID: 35675019
[TBL] [Abstract][Full Text] [Related]
13. Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients.
Russell AM; Zhang J; Luz J; Hutter P; Chappuis PO; Berthod CR; Maillet P; Mueller H; Heinimann K
Int J Cancer; 2006 Apr; 118(8):1937-40. PubMed ID: 16287072
[TBL] [Abstract][Full Text] [Related]
14. Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients.
Ciavarella M; Miccoli S; Prossomariti A; Pippucci T; Bonora E; Buscherini F; Palombo F; Zuntini R; Balbi T; Ceccarelli C; Bazzoli F; Ricciardiello L; Turchetti D; Piazzi G
Eur J Hum Genet; 2018 Mar; 26(3):387-395. PubMed ID: 29367705
[TBL] [Abstract][Full Text] [Related]
15. New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis.
Valle L; Hernández-Illán E; Bellido F; Aiza G; Castillejo A; Castillejo MI; Navarro M; Seguí N; Vargas G; Guarinos C; Juarez M; Sanjuán X; Iglesias S; Alenda C; Egoavil C; Segura Á; Juan MJ; Rodriguez-Soler M; Brunet J; González S; Jover R; Lázaro C; Capellá G; Pineda M; Soto JL; Blanco I
Hum Mol Genet; 2014 Jul; 23(13):3506-12. PubMed ID: 24501277
[TBL] [Abstract][Full Text] [Related]
16. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
Spier I; Drichel D; Kerick M; Kirfel J; Horpaopan S; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Perner S; Hoffmann P; Kristiansen G; Timmermann B; Nöthen MM; Holinski-Feder E; Schweiger MR; Aretz S
J Med Genet; 2016 Mar; 53(3):172-9. PubMed ID: 26613750
[TBL] [Abstract][Full Text] [Related]
17. Update on genetic predisposition to colorectal cancer and polyposis.
Valle L; de Voer RM; Goldberg Y; Sjursen W; Försti A; Ruiz-Ponte C; Caldés T; Garré P; Olsen MF; Nordling M; Castellvi-Bel S; Hemminki K
Mol Aspects Med; 2019 Oct; 69():10-26. PubMed ID: 30862463
[TBL] [Abstract][Full Text] [Related]
18. Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.
Lorca V; Rueda D; Martín-Morales L; Fernández-Aceñero MJ; Grolleman J; Poves C; Llovet P; Tapial S; García-Barberán V; Sanz J; Pérez-Segura P; de Voer RM; Díaz-Rubio E; de la Hoya M; Caldés T; Garre P
Sci Rep; 2019 Jul; 9(1):9814. PubMed ID: 31285513
[TBL] [Abstract][Full Text] [Related]
19. NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Belhadj S; Quintana I; Mur P; Munoz-Torres PM; Alonso MH; Navarro M; Terradas M; Piñol V; Brunet J; Moreno V; Lázaro C; Capellá G; Valle L
Sci Rep; 2019 Jun; 9(1):9020. PubMed ID: 31227763
[TBL] [Abstract][Full Text] [Related]
20. Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.
Chubb D; Broderick P; Frampton M; Kinnersley B; Sherborne A; Penegar S; Lloyd A; Ma YP; Dobbins SE; Houlston RS
J Clin Oncol; 2015 Feb; 33(5):426-32. PubMed ID: 25559809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
