BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

423 related articles for article (PubMed ID: 28152582)

  • 1. Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.
    Zhou X; Sui L; Xu Y; Song Y; Qi Q; Zhang J; Zhu H; Sun H; Tian F; Xu M; Cram DS; Liu J
    Prenat Diagn; 2017 Apr; 37(4):318-322. PubMed ID: 28152582
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
    Lau TK; Cheung SW; Lo PS; Pursley AN; Chan MK; Jiang F; Zhang H; Wang W; Jong LF; Yuen OK; Chan HY; Chan WS; Choy KW
    Ultrasound Obstet Gynecol; 2014 Mar; 43(3):254-64. PubMed ID: 24339153
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.
    Lau TK; Chen F; Pan X; Pooh RK; Jiang F; Li Y; Jiang H; Li X; Chen S; Zhang X
    J Matern Fetal Neonatal Med; 2012 Aug; 25(8):1370-4. PubMed ID: 22070770
    [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. Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
    Zhang H; Gao Y; Jiang F; Fu M; Yuan Y; Guo Y; Zhu Z; Lin M; Liu Q; Tian Z; Zhang H; Chen F; Lau TK; Zhao L; Yi X; Yin Y; Wang W
    Ultrasound Obstet Gynecol; 2015 May; 45(5):530-8. PubMed ID: 25598039
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnancies.
    Chen Y; Lu L; Zhang Y; Wang F; Ni Y; Wang Q; Ying C
    Am J Med Genet A; 2022 May; 188(5):1426-1434. PubMed ID: 35107205
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation.
    Zhang H; Zhao YY; Song J; Zhu QY; Yang H; Zheng ML; Xuan ZL; Wei Y; Chen Y; Yuan PB; Yu Y; Li DW; Liang JB; Fan L; Chen CJ; Qiao J
    Sci Rep; 2015 Nov; 5():16106. PubMed ID: 26534864
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.
    Mao J; Wang T; Wang BJ; Liu YH; Li H; Zhang J; Cram D; Chen Y
    Clin Chim Acta; 2014 Jun; 433():190-3. PubMed ID: 24667696
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.
    Dheedene A; Sante T; De Smet M; Vanbellinghen JF; Grisart B; Vergult S; Janssens S; Menten B
    Prenat Diagn; 2016 Aug; 36(8):699-707. PubMed ID: 27176606
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
    Liu S; Song L; Cram DS; Xiong L; Wang K; Wu R; Liu J; Deng K; Jia B; Zhong M; Yang F
    Ultrasound Obstet Gynecol; 2015 Oct; 46(4):472-7. PubMed ID: 25767059
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population.
    Song Y; Liu C; Qi H; Zhang Y; Bian X; Liu J
    Prenat Diagn; 2013 Jul; 33(7):700-6. PubMed ID: 23703459
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?
    Cong X; Zhang T; Li Z; Luo X; Hu L; Liu W
    BMC Pregnancy Childbirth; 2024 May; 24(1):338. PubMed ID: 38702634
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Performance of prenatal screening by non-invasive cell-free fetal DNA testing for women with various indications].
    Zhang B; Pan L; Wang H; Liu J; Lu B; Chen Y; Long W; Yu B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):51-55. PubMed ID: 29419860
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.