BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 29536580)

  • 1. Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
    Hu P; Qiao F; Wang Y; Meng L; Ji X; Luo C; Xu T; Zhou R; Zhang J; Yu B; Wang L; Wang T; Pan Q; Ma D; Liang D; Xu Z
    Ultrasound Obstet Gynecol; 2018 Aug; 52(2):205-211. PubMed ID: 29536580
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The uncertainty of copy number variants: pregnancy decisions and clinical follow-up.
    Shi P; Liang H; Hou Y; Chen D; Ren H; Wang C; Xia Y; Zhang D; Leigh D; Cram DS; Kong X
    Am J Obstet Gynecol; 2023 Aug; 229(2):170.e1-170.e8. PubMed ID: 36716986
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosomal microarray analysis in the investigation of prenatally diagnosed congenital heart disease.
    Mustafa HJ; Jacobs KM; Tessier KM; Narasimhan SL; Tofte AN; McCarter AR; Cross SN
    Am J Obstet Gynecol MFM; 2020 Feb; 2(1):100078. PubMed ID: 33345990
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The yield of SNP microarray analysis for fetal ultrasound cardiac abnormalities.
    Ye F; Xu X; Wang Y; Chen L; Shan Q; Wang Q; Jin F
    BMC Pregnancy Childbirth; 2024 Apr; 24(1):244. PubMed ID: 38580914
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting.
    Westenius E; Conner P; Pettersson M; Sahlin E; Papadogiannakis N; Lindstrand A; Iwarsson E
    Ultrasound Obstet Gynecol; 2024 May; 63(5):658-663. PubMed ID: 38268232
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exploring the clinical utility of exome sequencing/Mono, Duo, Trio in prenatal testing: a retrospective study in a tertiary care centre in South India.
    Ilangovan H; Elangovan J; Danda S; Beck MM; Navaneethan P; Athiyarath R
    J Perinat Med; 2024 Jun; 52(5):520-529. PubMed ID: 38709224
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome microarray analysis in the investigation of children with congenital heart disease.
    Wu XL; Li R; Fu F; Pan M; Han J; Yang X; Zhang YL; Li FT; Liao C
    BMC Pediatr; 2017 May; 17(1):117. PubMed ID: 28472932
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing.
    Wang Y; Li R; Fu F; Huang R; Li D; Liao C
    Front Genet; 2023; 14():1260995. PubMed ID: 38075692
    [No Abstract]   [Full Text] [Related]  

  • 9. Contribution of genetic variants to congenital heart defects in both singleton and twin fetuses: a Chinese cohort study.
    Lin S; Shi S; Lu J; He Z; Li D; Huang L; Huang X; Zhou Y; Luo Y
    Mol Cytogenet; 2024 Jan; 17(1):2. PubMed ID: 38178226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease.
    Tambi R; Zehra B; Nandkishore S; Sharafat S; Kader F; Nassir N; Mohamed N; Ahmed A; Abdel Hameid R; Alasrawi S; Brueckner M; Kuebler WM; Chung WK; Alsheikh-Ali A; Di Donato RM; Uddin M; Berdiev BK
    Physiol Genomics; 2023 Dec; 55(12):634-646. PubMed ID: 37811720
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficiency of copy number variation sequencing combined with karyotyping in fetuses with congenital heart disease and the following outcomes.
    Wang X; Sha J; Han Y; Pang M; Liu M; Liu M; Zhang B; Zhai J
    Mol Cytogenet; 2024 May; 17(1):12. PubMed ID: 38741090
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.
    Griffin EL; Nees SN; Morton SU; Wynn J; Patel N; Jobanputra V; Robinson S; Kochav SM; Tao A; Andrews C; Cross N; Geva J; Lanzilotta K; Ritter A; Taillie E; Thompson A; Meyer C; Akers R; King EC; Cnota JF; Kim RW; Porter GA; Brueckner M; Seidman CE; Shen Y; Gelb BD; Goldmuntz E; Newburger JW; Roberts AE; Chung WK
    Circ Genom Precis Med; 2023 Apr; 16(2):e003791. PubMed ID: 36803080
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex genetics and the etiology of human congenital heart disease.
    Gelb BD; Chung WK
    Cold Spring Harb Perspect Med; 2014 Jul; 4(7):a013953. PubMed ID: 24985128
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Genetics and Complex Inheritance of Congenital Heart Disease.
    Diab NS; Barish S; Dong W; Zhao S; Allington G; Yu X; Kahle KT; Brueckner M; Jin SC
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34209044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Specification for genetic diagnosis of congenital heart disease].
    Cardiovascular Medicine Professional Committee Of The Chinese Medical Education Association ; Medical Genetics Branch Of Chinese Medical Association ; Cardiology Group Of Pediatric Surgery Branch Of Chinese Medical Association ; He G; Qi M; Yang D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jun; 41(6):641-650. PubMed ID: 38818547
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects.
    Saacks NA; Eales J; Spracklen TF; Aldersley T; Human P; Verryn M; Lawrenson J; Cupido B; Comitis G; De Decker R; Fourie B; Swanson L; Joachim A; Brooks A; Ramesar R; Shaboodien G; Keavney BD; Zühlke LJ
    Circ Genom Precis Med; 2022 Dec; 15(6):e003510. PubMed ID: 36205932
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
    Jin SC; Homsy J; Zaidi S; Lu Q; Morton S; DePalma SR; Zeng X; Qi H; Chang W; Sierant MC; Hung WC; Haider S; Zhang J; Knight J; Bjornson RD; Castaldi C; Tikhonoa IR; Bilguvar K; Mane SM; Sanders SJ; Mital S; Russell MW; Gaynor JW; Deanfield J; Giardini A; Porter GA; Srivastava D; Lo CW; Shen Y; Watkins WS; Yandell M; Yost HJ; Tristani-Firouzi M; Newburger JW; Roberts AE; Kim R; Zhao H; Kaltman JR; Goldmuntz E; Chung WK; Seidman JG; Gelb BD; Seidman CE; Lifton RP; Brueckner M
    Nat Genet; 2017 Nov; 49(11):1593-1601. PubMed ID: 28991257
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Risk factor analysis for adverse prognosis of the fetal ventricular septal defect (VSD).
    Shan W; Yuanqing X; Jing Z; Xi W; Huifeng G; Yi W
    BMC Pregnancy Childbirth; 2023 Sep; 23(1):683. PubMed ID: 37735364
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Experience with genomic sequencing in pediatric patients with congenital cardiac defects in a large community hospital.
    Hauser NS; Solomon BD; Vilboux T; Khromykh A; Baveja R; Bodian DL
    Mol Genet Genomic Med; 2018 Mar; 6(2):200-212. PubMed ID: 29368431
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic testing and diagnostic strategies of fetal skeletal dysplasia: a preliminary study in Wuhan, China.
    Liu W; Cao J; Shi X; Li Y; Qiao F; Wu Y
    Orphanet J Rare Dis; 2023 Oct; 18(1):336. PubMed ID: 37875969
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.