These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 37270869)

  • 1. Corrigendum to "Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center": [ESMO Open 7 (2022) 100607].
    Poliani L; Greco L; Barile M; Buono AD; Bianchi P; Basso G; Giatti V; Genuardi M; Malesci A; Laghi L;
    ESMO Open; 2023 Jun; 8(3):101581. PubMed ID: 37270869
    [No Abstract]   [Full Text] [Related]  

  • 2. Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center.
    Poliani L; Greco L; Barile M; Dal Buono A; Bianchi P; Basso G; Giatti V; Genuardi M; Malesci A; Laghi L;
    ESMO Open; 2022 Dec; 7(6):100607. PubMed ID: 36356413
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germline sequencing for presumed germline pathogenic variants via tumor-only comprehensive genomic profiling.
    Kondo T; Yamamoto Y; Fukuyama K; Kanai M; Yamada A; Matsubara J; Quy PN; Yoshioka M; Yamada T; Minamiguchi S; Matsumoto S; Kosugi S; Muto M
    Int J Clin Oncol; 2022 Aug; 27(8):1256-1263. PubMed ID: 35567649
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline variants screening of MLH1, MSH2, MSH6 and PMS2 genes in 64 Algerian Lynch syndrome families: The first nationwide study.
    Boumehdi AL; Cherbal F; Khider F; Oukkal M; Mahfouf H; Zebboudj F; Maaoui M
    Ann Hum Genet; 2022 Nov; 86(6):328-352. PubMed ID: 36073783
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Prevalence of Pathogenic or Likely Pathogenic Germline Variants in a Nationwide Cohort of Young Colorectal Cancer Patients Using a Panel of 18 Genes Associated with Colorectal Cancer.
    Frostberg E; Petersen AH; Bojesen A; Rahr HB; Lindebjerg J; Rønlund K
    Cancers (Basel); 2021 Oct; 13(20):. PubMed ID: 34680242
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Susceptibility study on the germline rare variants of bromodomain and extraterminal domain protein family-encoding genes and patients with cancer living in some regions of China].
    Huang Y; Li JH; Wang X; Zou Y; Huang WF; Liu C; Zhang H
    Zhonghua Yi Xue Za Zhi; 2022 Nov; 102(42):3374-3381. PubMed ID: 36372767
    [No Abstract]   [Full Text] [Related]  

  • 7. Investigation of clinically relevant germline variants detected by next-generation sequencing in patients with childhood cancer: a review of the literature.
    Sylvester DE; Chen Y; Jamieson RV; Dalla-Pozza L; Byrne JA
    J Med Genet; 2018 Dec; 55(12):785-793. PubMed ID: 30287599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline Genetic Features of Young Individuals With Colorectal Cancer.
    Stoffel EM; Koeppe E; Everett J; Ulintz P; Kiel M; Osborne J; Williams L; Hanson K; Gruber SB; Rozek LS
    Gastroenterology; 2018 Mar; 154(4):897-905.e1. PubMed ID: 29146522
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NRAS germline variant G138R and multiple rare somatic mutations on APC in colorectal cancer patients in Taiwan by next generation sequencing.
    Chang PY; Chen JS; Chang NC; Chang SC; Wang MC; Tsai SH; Wen YH; Tsai WS; Chan EC; Lu JJ
    Oncotarget; 2016 Jun; 7(25):37566-37580. PubMed ID: 27121310
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Germline-focussed analysis of tumour-only sequencing: recommendations from the ESMO Precision Medicine Working Group.
    Mandelker D; Donoghue M; Talukdar S; Bandlamudi C; Srinivasan P; Vivek M; Jezdic S; Hanson H; Snape K; Kulkarni A; Hawkes L; Douillard JY; Wallace SE; Rial-Sebbag E; Meric-Bersntam F; George A; Chubb D; Loveday C; Ladanyi M; Berger MF; Taylor BS; Turnbull C
    Ann Oncol; 2019 Aug; 30(8):1221-1231. PubMed ID: 31050713
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients.
    Elsayed FA; Tops CMJ; Nielsen M; Morreau H; Hes FJ; van Wezel T
    Fam Cancer; 2022 Jan; 21(1):79-83. PubMed ID: 33683519
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Incidental germline findings during molecular profiling of tumor tissues for precision oncology: molecular survey and methodological obstacles.
    Lebedeva A; Shaykhutdinova Y; Seriak D; Ignatova E; Rozhavskaya E; Vardhan D; Manicka S; Sharova M; Grigoreva T; Baranova A; Mileyko V; Ivanov M
    J Transl Med; 2022 Jan; 20(1):29. PubMed ID: 35033101
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma.
    Yalcintepe S; Gurkan H; Korkmaz FN; Demir S; Atli E; Eker D; Guler HS; Zhuri D; Atli EI; Salt SA; Sahin M; Guldiken S
    J Kidney Cancer VHL; 2021; 8(1):19-24. PubMed ID: 33777662
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Corrigendum to 'Single-nucleotide variants, tumour mutational burden and microsatellite instability in patients with metastatic colorectal cancer: Next-generation sequencing results of the FIRE-3 trial'. [European Journal of Cancer 137 (2020) 250-259].
    Stahler A; Stintzing S; von Einem JC; Westphalen Benedikt CB; Heinrich K; Krämer N; Michl M; Modest DP; Fischer von Weikersthal L; Decker T; Kiani A; Heintges T; Kahl C; Kullmann F; Scheithauer W; Moehler M; Kaiser F; Kirchner T; Jung A; Heinemann V
    Eur J Cancer; 2022 Jul; 169():223-225. PubMed ID: 35570084
    [No Abstract]   [Full Text] [Related]  

  • 16. The prevalence of germline pathogenic variants in Estonian colorectal cancer patients: results from routine clinical setting 2016-2021.
    Roht L; Tooming M; Rekker K; Roomere H; Toome K; Murumets Ü; Šamarina U; Õunap K; Kahre T
    Front Genet; 2022; 13():1020543. PubMed ID: 36425062
    [No Abstract]   [Full Text] [Related]  

  • 17. Impact of gene-specific germline pathogenic variants on presentation of endometrial cancer in Lynch syndrome.
    Bogani G; Ricci MT; Vitellaro M; Ditto A; Chiappa V; Raspagliesi F
    Int J Gynecol Cancer; 2019 May; 29(4):705-710. PubMed ID: 30772826
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Germline pathogenic variant spectrum in 25 cancer susceptibility genes in Turkish breast and colorectal cancer patients and elderly controls.
    Akcay IM; Celik E; Agaoglu NB; Alkurt G; Kizilboga Akgun T; Yildiz J; Enc F; Kir G; Canbek S; Kilic A; Zemheri E; Ezberci F; Ozcelik M; Dinler Doganay G; Doganay L
    Int J Cancer; 2021 Jan; 148(2):285-295. PubMed ID: 32658311
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Scoring Model and Protocol to Adapt Universal Screening for Lynch Syndrome to Identify Germline Pathogenic Variants by Next Generation Sequencing from Colorectal Cancer Patients and Cascade Screening.
    Chambuso R; Robertson B; Ramesar R
    Cancers (Basel); 2022 Jun; 14(12):. PubMed ID: 35740566
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome.
    Dos Santos W; de Andrade ES; Garcia FAO; Campacci N; Sábato CDS; Melendez ME; Reis RM; Galvão HCR; Palmero EI
    Cancers (Basel); 2022 Aug; 14(17):. PubMed ID: 36077770
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.