BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

551 related articles for article (PubMed ID: 27558279)

  • 1. Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.
    Cohen PA; Flowers N; Tong S; Hannan N; Pertile MD; Hui L
    BMC Med; 2016 Aug; 14(1):126. PubMed ID: 27558279
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
    Bianchi DW; Chudova D; Sehnert AJ; Bhatt S; Murray K; Prosen TL; Garber JE; Wilkins-Haug L; Vora NL; Warsof S; Goldberg J; Ziainia T; Halks-Miller M
    JAMA; 2015 Jul; 314(2):162-9. PubMed ID: 26168314
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.
    Yin AH; Peng CF; Zhao X; Caughey BA; Yang JX; Liu J; Huang WW; Liu C; Luo DH; Liu HL; Chen YY; Wu J; Hou R; Zhang M; Ai M; Zheng L; Xue RQ; Mai MQ; Guo FF; Qi YM; Wang DM; Krawczyk M; Zhang D; Wang YN; Huang QF; Karin M; Zhang K
    Proc Natl Acad Sci U S A; 2015 Nov; 112(47):14670-5. PubMed ID: 26554006
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
    Lefkowitz RB; Tynan JA; Liu T; Wu Y; Mazloom AR; Almasri E; Hogg G; Angkachatchai V; Zhao C; Grosu DS; McLennan G; Ehrich M
    Am J Obstet Gynecol; 2016 Aug; 215(2):227.e1-227.e16. PubMed ID: 26899906
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.
    Liu H; Gao Y; Hu Z; Lin L; Yin X; Wang J; Chen D; Chen F; Jiang H; Ren J; Wang W
    PLoS One; 2016; 11(7):e0159233. PubMed ID: 27415003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
    Li R; Wan J; Zhang Y; Fu F; Ou Y; Jing X; Li J; Li D; Liao C
    Ultrasound Obstet Gynecol; 2016 Jan; 47(1):53-7. PubMed ID: 26033469
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Massively parallel sequencing of cell-free DNA in plasma for detecting gynaecological tumour-associated copy number alteration.
    Nakabayashi M; Kawashima A; Yasuhara R; Hayakawa Y; Miyamoto S; Iizuka C; Sekizawa A
    Sci Rep; 2018 Jul; 8(1):11205. PubMed ID: 30046040
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Non invasive prenatal test (NIPT) in maternal blood by parallel massive sequencing. Initial experience in Mexican women and literature review].
    Hernández-Gómez M; Ramirez-Arroyo E; Meléndez-Hernández R; Garduño-Zaraza LM; Mayén-Molina DG
    Ginecol Obstet Mex; 2015 May; 83(5):277-88. PubMed ID: 26233973
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women.
    Kølvraa S; Singh R; Normand EA; Qdaisat S; van den Veyver IB; Jackson L; Hatt L; Schelde P; Uldbjerg N; Vestergaard EM; Zhao L; Chen R; Shaw CA; Breman AM; Beaudet AL
    Prenat Diagn; 2016 Dec; 36(12):1127-1134. PubMed ID: 27761919
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low-pass whole-genome sequencing.
    Yu D; Zhang K; Han M; Pan W; Chen Y; Wang Y; Jiao H; Duan L; Zhu Q; Song X; Hong Y; Chen C; Wang J; Hui F; Huang L; Chen C; Du Y
    Mol Genet Genomic Med; 2019 Jun; 7(6):e674. PubMed ID: 31004415
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Combining Effects of Cell-Free Circulating Tumor DNA of Breast Tumor to the Noninvasive Prenatal Testing Results: A Simulating Investigation.
    Cai YH; Yao GY; Chen LJ; Gan HY; Ye CS; Yang XX
    DNA Cell Biol; 2018 Jul; 37(7):626-633. PubMed ID: 29957029
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.
    Amant F; Verheecke M; Wlodarska I; Dehaspe L; Brady P; Brison N; Van Den Bogaert K; Dierickx D; Vandecaveye V; Tousseyn T; Moerman P; Vanderstichele A; Vergote I; Neven P; Berteloot P; Putseys K; Danneels L; Vandenberghe P; Legius E; Vermeesch JR
    JAMA Oncol; 2015 Sep; 1(6):814-9. PubMed ID: 26355862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Non-Invasive Prenatal Testing (NIPT) in pregnancies with trisomy 21, 18 and 13 performed in a public setting - factors of importance for correct interpretation of results.
    Hartwig TS; Ambye L; Werge L; Weiergang MK; Nørgaard P; Sørensen S; Jørgensen FS
    Eur J Obstet Gynecol Reprod Biol; 2018 Jul; 226():35-39. PubMed ID: 29804026
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations.
    Neveling K; Tjwan Thung D; Beulen L; van Rens-Buijsman W; Gomes I; van den Heuvel S; Mieloo H; Derks-Prinsen I; Kater-Baats E; Faas BH
    Prenat Diagn; 2016 Mar; 36(3):216-23. PubMed ID: 26774010
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Breast Cancer Detection and Treatment Monitoring Using a Noninvasive Prenatal Testing Platform: Utility in Pregnant and Nonpregnant Populations.
    Lenaerts L; Che H; Brison N; Neofytou M; Jatsenko T; Lefrère H; Maggen C; Villela D; Verheecke M; Dehaspe L; Croitor A; Hatse S; Wildiers H; Neven P; Vandecaveye V; Floris G; Vermeesch JR; Amant F
    Clin Chem; 2020 Nov; 66(11):1414-1423. PubMed ID: 33141904
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.
    Zhang J; Tang X; Hu J; He G; Wang J; Zhu Y; Zhu B
    BMC Pregnancy Childbirth; 2021 Jul; 21(1):496. PubMed ID: 34238233
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variation profile in noninvasive prenatal testing (NIPT) can identify co-existing maternal malignancies: Case reports and a literature review.
    Ji X; Chen F; Zhou Y; Li J; Yuan Y; Mo Y; Liu Q; Tseng JY; Shih-Chieh Lin D; Shen SH; Liu Y; Ye W; Cheung YN; Yuen KY; Lin S; Fu M; Zhang H; Liu N; Wang J; Yang H; Wang Y; Li S; Fan S; Jin X; Mao M; Sung PL
    Taiwan J Obstet Gynecol; 2018 Dec; 57(6):871-877. PubMed ID: 30545544
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.
    Wang S; Huang S; Ma L; Liang L; Zhang J; Zhang J; Cram DS
    Clin Chim Acta; 2015 Apr; 444():113-6. PubMed ID: 25689220
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.
    Tamminga S; van Maarle M; Henneman L; Oudejans CB; Cornel MC; Sistermans EA
    Adv Clin Chem; 2016; 74():63-102. PubMed ID: 27117661
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
    Beulen L; Faas BHW; Feenstra I; van Vugt JMG; Bekker MN
    Ultrasound Obstet Gynecol; 2017 Jun; 49(6):721-728. PubMed ID: 27515011
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.