285 related articles for article (PubMed ID: 22010865)
1. Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.
Goldmuntz E; Paluru P; Glessner J; Hakonarson H; Biegel JA; White PS; Gai X; Shaikh TH
Congenit Heart Dis; 2011; 6(6):592-602. PubMed ID: 22010865
[TBL] [Abstract][Full Text] [Related]
2. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
Wayhelova M; Smetana J; Vallova V; Hladilkova E; Filkova H; Hanakova M; Vilemova M; Nikolova P; Gromesova B; Gaillyova R; Kuglik P
BMC Med Genomics; 2019 Jul; 12(1):111. PubMed ID: 31337399
[TBL] [Abstract][Full Text] [Related]
3. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
[TBL] [Abstract][Full Text] [Related]
4. [Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease].
Mei M; Yang L; Zhan G; Wang H; Ma D; Zhou W; Huang G
Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):460-3. PubMed ID: 25190168
[TBL] [Abstract][Full Text] [Related]
5. Rare copy number variants in patients with congenital conotruncal heart defects.
Xie HM; Werner P; Stambolian D; Bailey-Wilson JE; Hakonarson H; White PS; Taylor DM; Goldmuntz E
Birth Defects Res; 2017 Mar; 109(4):271-295. PubMed ID: 28398664
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease.
Warburton D; Ronemus M; Kline J; Jobanputra V; Williams I; Anyane-Yeboa K; Chung W; Yu L; Wong N; Awad D; Yu CY; Leotta A; Kendall J; Yamrom B; Lee YH; Wigler M; Levy D
Hum Genet; 2014 Jan; 133(1):11-27. PubMed ID: 23979609
[TBL] [Abstract][Full Text] [Related]
8. Rare copy number variants in a population-based investigation of hypoplastic right heart syndrome.
Dimopoulos A; Sicko RJ; Kay DM; Rigler SL; Druschel CM; Caggana M; Browne ML; Fan R; Romitti PA; Brody LC; Mills JL
Birth Defects Res; 2017 Jan; 109(1):8-15. PubMed ID: 28009100
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Genome-wide copy number scan in Chinese patients with premature ovarian failure].
Zhen XM; Sun YM; Qiao J; Li R; Wang LN; Liu P
Beijing Da Xue Xue Bao Yi Xue Ban; 2013 Dec; 45(6):841-7. PubMed ID: 24343059
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience.
Liang B; Yu D; Zhao W; Wang Y; Wu X; Chen L; Lin N; Huang H; Xu L
BMC Med Genomics; 2022 Dec; 15(1):268. PubMed ID: 36544138
[TBL] [Abstract][Full Text] [Related]
14. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.
An Y; Duan W; Huang G; Chen X; Li L; Nie C; Hou J; Gui Y; Wu Y; Zhang F; Shen Y; Wu B; Wang H
BMC Med Genomics; 2016 Jan; 9():2. PubMed ID: 26742958
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
[TBL] [Abstract][Full Text] [Related]
19. Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
Derwińska K; Bartnik M; Wiśniowiecka-Kowalnik B; Jagła M; Rudziński A; Pietrzyk JJ; Kawalec W; Ziółkowska L; Kutkowska-Kaźmierczak A; Gambin T; Sykulski M; Shaw CA; Gambin A; Mazurczak T; Obersztyn E; Bocian E; Stankiewicz P
Med Wieku Rozwoj; 2012; 16(3):175-82. PubMed ID: 23378395
[TBL] [Abstract][Full Text] [Related]
20. Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.
Maini I; Ivanovski I; Djuric O; Caraffi SG; Errichiello E; Marinelli M; Franchi F; Bizzarri V; Rosato S; Pollazzon M; Gelmini C; Malacarne M; Fusco C; Gargano G; Bernasconi S; Zuffardi O; Garavelli L
Ital J Pediatr; 2018 Mar; 44(1):34. PubMed ID: 29523172
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
