BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 36037157)

  • 21. Italian Precision Medicine in Pediatric Oncology: Moving beyond Actionable Alterations.
    Pastorino F; Capasso M; Brignole C; Giglio S; Bensa V; Cantalupo S; Lasorsa VA; Tondo A; Mura R; Sementa AR; Garaventa A; Ponzoni M; Amoroso L
    Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232538
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole-exome sequencing identified mutational profiles of high-grade colon adenomas.
    Lee SH; Jung SH; Kim TM; Rhee JK; Park HC; Kim MS; Kim SS; An CH; Lee SH; Chung YJ
    Oncotarget; 2017 Jan; 8(4):6579-6588. PubMed ID: 28179590
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Whole exome sequencing reveals intertumor heterogeneity and distinct genetic origins of sporadic synchronous colorectal cancer.
    Di J; Yang H; Jiang B; Wang Z; Ji J; Su X
    Int J Cancer; 2018 Mar; 142(5):927-939. PubMed ID: 29105743
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Unbiased Detection of Driver Mutations in Extramammary Paget Disease.
    Ishida Y; Kakiuchi N; Yoshida K; Inoue Y; Irie H; Kataoka TR; Hirata M; Funakoshi T; Matsushita S; Hata H; Uchi H; Yamamoto Y; Fujisawa Y; Fujimura T; Saiki R; Takeuchi K; Shiraishi Y; Chiba K; Tanaka H; Otsuka A; Miyano S; Kabashima K; Ogawa S
    Clin Cancer Res; 2021 Mar; 27(6):1756-1765. PubMed ID: 33323405
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Whole-exome sequencing of rectal cancer identifies locally recurrent mutations in the Wnt pathway.
    Yang Y; Gu X; Li Z; Zheng C; Wang Z; Zhou M; Chen Z; Li M; Li D; Xiang J
    Aging (Albany NY); 2021 Oct; 13(19):23262-23283. PubMed ID: 34642262
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Comparison study of whole exome sequencing and targeted panel sequencing in molecular diagnosis of inherited retinal dystrophies].
    Liu XZ; Li YY; Yang LP
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):836-844. PubMed ID: 33047716
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genomic characterization of Chinese ovarian clear cell carcinoma identifies driver genes by whole exome sequencing.
    Yang Q; Zhang C; Ren Y; Yi H; Luo T; Xing F; Bai X; Cui L; Zhu L; Ouyang J; Jiang P; Fan W; Qiu J; Wang F; Xing X; Zhang Z; Zhang X; Zhang R
    Neoplasia; 2020 Sep; 22(9):399-430. PubMed ID: 32650224
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy.
    Zammataro L; Lopez S; Bellone S; Pettinella F; Bonazzoli E; Perrone E; Zhao S; Menderes G; Altwerger G; Han C; Zeybek B; Bianchi A; Manzano A; Manara P; Cocco E; Buza N; Hui P; Wong S; Ravaggi A; Bignotti E; Romani C; Todeschini P; Zanotti L; Odicino F; Pecorelli S; Donzelli C; Ardighieri L; Angioli R; Raspagliesi F; Scambia G; Choi J; Dong W; Bilguvar K; Alexandrov LB; Silasi DA; Huang GS; Ratner E; Azodi M; Schwartz PE; Pirazzoli V; Stiegler AL; Boggon TJ; Lifton RP; Schlessinger J; Santin AD
    Proc Natl Acad Sci U S A; 2019 Nov; 116(45):22730-22736. PubMed ID: 31624127
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Whole-exome sequencing identifies unique mutations and copy number losses in calcifying fibrous tumor of the pleura: report of 3 cases and review of the literature.
    Mehrad M; LaFramboise WA; Lyons MA; Trejo Bittar HE; Yousem SA
    Hum Pathol; 2018 Aug; 78():36-43. PubMed ID: 29689243
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients.
    Fichna JP; Macias A; Piechota M; Korostyński M; Potulska-Chromik A; Redowicz MJ; Zekanowski C
    Hum Genomics; 2018 Jul; 12(1):34. PubMed ID: 29970176
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole-exome sequencing identified mutational profiles of squamous cell carcinomas of anus.
    Shin S; Park HC; Kim MS; Han MR; Lee SH; Jung SH; Lee SH; Chung YJ
    Hum Pathol; 2018 Oct; 80():1-10. PubMed ID: 29555573
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.
    Chang YS; Lin CY; Huang HY; Chang JG; Kuo HT
    Mol Genet Genomic Med; 2019 Dec; 7(12):e996. PubMed ID: 31595719
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Exploration of the molecular characteristics of the tumor-immune interaction and the development of an individualized immune prognostic signature for neuroblastoma.
    Jin W; Zhang Y; Liu Z; Che Z; Gao M; Peng H
    J Cell Physiol; 2021 Jan; 236(1):294-308. PubMed ID: 32510620
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma.
    Seo SH; Kim JH; Kim MJ; Cho SI; Kim SJ; Kang H; Shin CS; Park SS; Lee KE; Seong MW
    Endocrinol Metab (Seoul); 2020 Dec; 35(4):909-917. PubMed ID: 33397043
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The landscape of genetic aberrations in myxofibrosarcoma.
    Takeuchi Y; Yoshida K; Halik A; Kunitz A; Suzuki H; Kakiuchi N; Shiozawa Y; Yokoyama A; Inoue Y; Hirano T; Yoshizato T; Aoki K; Fujii Y; Nannya Y; Makishima H; Pfitzner BM; Bullinger L; Hirata M; Jinnouchi K; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Okamoto T; Haga H; Ogawa S; Damm F
    Int J Cancer; 2022 Aug; 151(4):565-577. PubMed ID: 35484982
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Reliable Analysis of Clinical Tumor-Only Whole-Exome Sequencing Data.
    Oh S; Geistlinger L; Ramos M; Morgan M; Waldron L; Riester M
    JCO Clin Cancer Inform; 2020 Apr; 4():321-335. PubMed ID: 32282230
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma.
    Ülgen E; Can Ö; Bilguvar K; Akyerli Boylu C; Kılıçturgay Yüksel Ş; Erşen Danyeli A; Sezerman OU; Yakıcıer MC; Pamir MN; Özduman K
    BMC Med Genomics; 2021 Feb; 14(1):54. PubMed ID: 33622343
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The identification of novel gene mutations for degenerative lumbar spinal stenosis using whole-exome sequencing in a Chinese cohort.
    Jiang X; Chen D
    BMC Med Genomics; 2021 May; 14(1):134. PubMed ID: 34020649
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Copy Number Changes Identified Using Whole Exome Sequencing in Nonsyndromic Cleft Lip and Palate in a Honduran Population.
    Cai Y; Patterson KE; Reinier F; Keesecker SE; Blue E; Bamshad M; Haddad J
    Birth Defects Res; 2017 Oct; 109(16):1257-1267. PubMed ID: 28748635
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in
    Robyns T; Willems R; Van Cleemput J; Jhangiani S; Muzny D; Gibbs R; Lupski JR; Breckpot J; Devriendt K; Corveleyn A
    Acta Cardiol; 2020 Dec; 75(8):748-753. PubMed ID: 31583969
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.