182 related articles for article (PubMed ID: 36205932)
1. 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]
2. Copy number variant analysis for syndromic congenital heart disease in the Chinese population.
Li P; Chen W; Li M; Zhao Z; Feng Z; Gao H; Suo M; Xu Z; Tian G; Wu F; Wei S; Huang G
Hum Genomics; 2022 Oct; 16(1):51. PubMed ID: 36316717
[TBL] [Abstract][Full Text] [Related]
3. Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Glessner JT; Bick AG; Ito K; Homsy J; Rodriguez-Murillo L; Fromer M; Mazaika E; Vardarajan B; Italia M; Leipzig J; DePalma SR; Golhar R; Sanders SJ; Yamrom B; Ronemus M; Iossifov I; Willsey AJ; State MW; Kaltman JR; White PS; Shen Y; Warburton D; Brueckner M; Seidman C; Goldmuntz E; Gelb BD; Lifton R; Seidman J; Hakonarson H; Chung WK
Circ Res; 2014 Oct; 115(10):884-896. PubMed ID: 25205790
[TBL] [Abstract][Full Text] [Related]
4. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
Geng J; Picker J; Zheng Z; Zhang X; Wang J; Hisama F; Brown DW; Mullen MP; Harris D; Stoler J; Seman A; Miller DT; Fu Q; Roberts AE; Shen Y
BMC Genomics; 2014 Dec; 15(1):1127. PubMed ID: 25516202
[TBL] [Abstract][Full Text] [Related]
5. Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
Cai M; Huang H; Su L; Lin N; Wu X; Xie X; An G; Li Y; Lin Y; Xu L
Medicine (Baltimore); 2018 Dec; 97(50):e13617. PubMed ID: 30558042
[TBL] [Abstract][Full Text] [Related]
6. Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.
Xia Y; Yang Y; Huang S; Wu Y; Li P; Zhuang J
Prenat Diagn; 2018 May; 38(6):406-413. PubMed ID: 29573438
[TBL] [Abstract][Full Text] [Related]
7. Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
Kim DS; Kim JH; Burt AA; Crosslin DR; Burnham N; Kim CE; McDonald-McGinn DM; Zackai EH; Nicolson SC; Spray TL; Stanaway IB; Nickerson DA; Heagerty PJ; Hakonarson H; Gaynor JW; Jarvik GP
J Thorac Cardiovasc Surg; 2016 Apr; 151(4):1147-51.e4. PubMed ID: 26704054
[TBL] [Abstract][Full Text] [Related]
8. Systemic Screening for 22q11.2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare Pathogenic Patterns in the Region.
Zodanu GKE; Oszlánczi M; Havasi K; Kalapos A; Rácz G; Katona M; Ujfalusi A; Nagy O; Széll M; Nagy D
Front Genet; 2021; 12():635480. PubMed ID: 33995479
[TBL] [Abstract][Full Text] [Related]
9. Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification.
Mutlu ET; Aykan HH; Karagöz T
Anatol J Cardiol; 2018 Jul; 20(1):9-15. PubMed ID: 29952356
[TBL] [Abstract][Full Text] [Related]
10. Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects.
Liu C; Cao R; Xu Y; Li T; Li F; Chen S; Xu R; Sun K
Genome Med; 2018 May; 10(1):40. PubMed ID: 29843777
[TBL] [Abstract][Full Text] [Related]
11. Identification of Novel Congenital Heart Disease Candidate Genes Using Chromosome Microarray.
Shanshen E; Rosenberg J; Van Bergen AH
Pediatr Cardiol; 2018 Jan; 39(1):148-159. PubMed ID: 28993849
[TBL] [Abstract][Full Text] [Related]
12. Effect of copy number variants on outcomes for infants with single ventricle heart defects.
Carey AS; Liang L; Edwards J; Brandt T; Mei H; Sharp AJ; Hsu DT; Newburger JW; Ohye RG; Chung WK; Russell MW; Rosenfeld JA; Shaffer LG; Parides MK; Edelmann L; Gelb BD
Circ Cardiovasc Genet; 2013 Oct; 6(5):444-51. PubMed ID: 24021551
[TBL] [Abstract][Full Text] [Related]
13. Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect.
Zhu C; Yang Y; Pan B; Wei H; Ju J; Si N; Xu Q
Genes (Basel); 2023 Apr; 14(4):. PubMed ID: 37107637
[TBL] [Abstract][Full Text] [Related]
14. Rare de novo copy number variants in patients with congenital pulmonary atresia.
Xie L; Chen JL; Zhang WZ; Wang SZ; Zhao TL; Huang C; Wang J; Yang JF; Yang YF; Tan ZP
PLoS One; 2014; 9(5):e96471. PubMed ID: 24826987
[TBL] [Abstract][Full Text] [Related]
15. A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.
Landis BJ; Helvaty LR; Geddes GC; Lin JI; Yatsenko SA; Lo CW; Border WL; Wechsler SB; Murali CN; Azamian MS; Lalani SR; Hinton RB; Garg V; McBride KL; Hodge JC; Ware SM
J Am Heart Assoc; 2023 Sep; 12(18):e029340. PubMed ID: 37681527
[TBL] [Abstract][Full Text] [Related]
16. Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.
Hanchard NA; Umana LA; D'Alessandro L; Azamian M; Poopola M; Morris SA; Fernbach S; Lalani SR; Towbin JA; Zender GA; Fitzgerald-Butt S; Garg V; Bowman J; Zapata G; Hernandez P; Arrington CB; Furthner D; Prakash SK; Bowles NE; McBride KL; Belmont JW
Am J Med Genet A; 2017 Aug; 173(8):2176-2188. PubMed ID: 28653806
[TBL] [Abstract][Full Text] [Related]
17. Human gene copy number spectra analysis in congenital heart malformations.
Tomita-Mitchell A; Mahnke DK; Struble CA; Tuffnell ME; Stamm KD; Hidestrand M; Harris SE; Goetsch MA; Simpson PM; Bick DP; Broeckel U; Pelech AN; Tweddell JS; Mitchell ME
Physiol Genomics; 2012 May; 44(9):518-41. PubMed ID: 22318994
[TBL] [Abstract][Full Text] [Related]
18. A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome.
Meerschaut I; Vergult S; Dheedene A; Menten B; De Groote K; De Wilde H; Muiño Mosquera L; Panzer J; Vandekerckhove K; Coucke PJ; De Wolf D; Callewaert B
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356064
[TBL] [Abstract][Full Text] [Related]
19. Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.
Zhang X; Wang B; You G; Xiang Y; Fu Q; Yu Y; Zhang X
BMC Med Genomics; 2021 Oct; 14(1):243. PubMed ID: 34627233
[TBL] [Abstract][Full Text] [Related]
20. New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.
Dasouki MJ; Wakil SM; Al-Harazi O; Alkorashy M; Muiya NP; Andres E; Hagos S; Aldusery H; Dzimiri N; Colak D
OMICS; 2020 Jan; 24(1):16-28. PubMed ID: 31855513
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]