257 related articles for article (PubMed ID: 23708191)
1. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Cordell HJ; Bentham J; Topf A; Zelenika D; Heath S; Mamasoula C; Cosgrove C; Blue G; Granados-Riveron J; Setchfield K; Thornborough C; Breckpot J; Soemedi R; Martin R; Rahman TJ; Hall D; van Engelen K; Moorman AF; Zwinderman AH; Barnett P; Koopmann TT; Adriaens ME; Varro A; George AL; dos Remedios C; Bishopric NH; Bezzina CR; O'Sullivan J; Gewillig M; Bu'Lock FA; Winlaw D; Bhattacharya S; Devriendt K; Brook JD; Mulder BJ; Mital S; Postma AV; Lathrop GM; Farrall M; Goodship JA; Keavney BD
Nat Genet; 2013 Jul; 45(7):822-4. PubMed ID: 23708191
[TBL] [Abstract][Full Text] [Related]
2. Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations.
Zhao B; Lin Y; Xu J; Ni B; Da M; Ding C; Hu Y; Zhang K; Yang S; Wang X; Yu S; Chen Y; Mo X; Liu J; Shen H; Sha J; Ma H
PLoS One; 2014; 9(9):e107411. PubMed ID: 25215500
[TBL] [Abstract][Full Text] [Related]
3. Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis.
Zhao L; Li B; Dian K; Ying B; Lu X; Hu X; An Q; Chen C; Huang C; Tan B; Qin L
PLoS One; 2015; 10(4):e0123959. PubMed ID: 25875170
[TBL] [Abstract][Full Text] [Related]
4. Association Between the 4p16 Susceptibility Locus and the Risk of Atrial Septal Defect in Population from Southeast China.
Pei K; Huang Q; Zhang G; Lu C; Yu B; Yang L
Pediatr Cardiol; 2016 Jan; 37(1):120-4. PubMed ID: 26283177
[TBL] [Abstract][Full Text] [Related]
5. Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank.
Córdova-Palomera A; Priest JR
Sci Rep; 2019 Nov; 9(1):16515. PubMed ID: 31712678
[TBL] [Abstract][Full Text] [Related]
6. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
[TBL] [Abstract][Full Text] [Related]
7. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
[TBL] [Abstract][Full Text] [Related]
8. Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population.
Muroke V; Jalanko M; Ruotsalainen S; Perola M; Helle E; Sinisalo J
Circ Genom Precis Med; 2023 Oct; 16(5):486-489. PubMed ID: 37577800
[No Abstract] [Full Text] [Related]
9. 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]
10. Genome-wide compound heterozygosity analysis highlighted 4 novel susceptibility loci for congenital heart disease in Chinese population.
Jiang T; Huang M; Jiang T; Gu Y; Wang Y; Wu Y; Ma H; Jin G; Dai J; Hu Z
Clin Genet; 2018 Oct; 94(3-4):296-302. PubMed ID: 29774522
[TBL] [Abstract][Full Text] [Related]
11. A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Hanchard NA; Swaminathan S; Bucasas K; Furthner D; Fernbach S; Azamian MS; Wang X; Lewin M; Towbin JA; D'Alessandro LC; Morris SA; Dreyer W; Denfield S; Ayres NA; Franklin WJ; Justino H; Lantin-Hermoso MR; Ocampo EC; Santos AB; Parekh D; Moodie D; Jeewa A; Lawrence E; Allen HD; Penny DJ; Fraser CD; Lupski JR; Popoola M; Wadhwa L; Brook JD; Bu'Lock FA; Bhattacharya S; Lalani SR; Zender GA; Fitzgerald-Butt SM; Bowman J; Corsmeier D; White P; Lecerf K; Zapata G; Hernandez P; Goodship JA; Garg V; Keavney BD; Leal SM; Cordell HJ; Belmont JW; McBride KL
Hum Mol Genet; 2016 Jun; 25(11):2331-2341. PubMed ID: 26965164
[TBL] [Abstract][Full Text] [Related]
12. Congenital heart defects in molecularly proven Kabuki syndrome patients.
Digilio MC; Gnazzo M; Lepri F; Dentici ML; Pisaneschi E; Baban A; Passarelli C; Capolino R; Angioni A; Novelli A; Marino B; Dallapiccola B
Am J Med Genet A; 2017 Nov; 173(11):2912-2922. PubMed ID: 28884922
[TBL] [Abstract][Full Text] [Related]
13. A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Hu Z; Shi Y; Mo X; Xu J; Zhao B; Lin Y; Yang S; Xu Z; Dai J; Pan S; Da M; Wang X; Qian B; Wen Y; Wen J; Xing J; Guo X; Xia Y; Ma H; Jin G; Yu S; Liu J; Zhou Z; Wang X; Chen Y; Sha J; Shen H
Nat Genet; 2013 Jul; 45(7):818-21. PubMed ID: 23708190
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci.
Flaquer A; Baumbach C; Piñero E; García Algas F; de la Fuente Sanchez MA; Rosell J; Toquero J; Alonso-Pulpon L; Garcia-Pavia P; Strauch K; Heine-Suñer D
BMC Genet; 2013 May; 14():44. PubMed ID: 23705960
[TBL] [Abstract][Full Text] [Related]
15. Molecular genetics of congenital atrial septal defects.
Posch MG; Perrot A; Berger F; Ozcelik C
Clin Res Cardiol; 2010 Mar; 99(3):137-47. PubMed ID: 20012542
[TBL] [Abstract][Full Text] [Related]
16. Congenital heart disease risk loci identified by genome-wide association study in European patients.
Lahm H; Jia M; Dreßen M; Wirth F; Puluca N; Gilsbach R; Keavney BD; Cleuziou J; Beck N; Bondareva O; Dzilic E; Burri M; König KC; Ziegelmüller JA; Abou-Ajram C; Neb I; Zhang Z; Doppler SA; Mastantuono E; Lichtner P; Eckstein G; Hörer J; Ewert P; Priest JR; Hein L; Lange R; Meitinger T; Cordell HJ; Müller-Myhsok B; Krane M
J Clin Invest; 2021 Jan; 131(2):. PubMed ID: 33201861
[TBL] [Abstract][Full Text] [Related]
17. Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects.
Benson DW; Sharkey A; Fatkin D; Lang P; Basson CT; McDonough B; Strauss AW; Seidman JG; Seidman CE
Circulation; 1998 May; 97(20):2043-8. PubMed ID: 9610535
[TBL] [Abstract][Full Text] [Related]
18. Severity and recurrence risk of congenital heart defects exemplified by atrial septal defect secundum.
Gold RJ; Rose V; Yau Y
Clin Genet; 1987 Sep; 32(3):148-55. PubMed ID: 3621660
[TBL] [Abstract][Full Text] [Related]
19. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
Elliott DA; Kirk EP; Yeoh T; Chandar S; McKenzie F; Taylor P; Grossfeld P; Fatkin D; Jones O; Hayes P; Feneley M; Harvey RP
J Am Coll Cardiol; 2003 Jun; 41(11):2072-6. PubMed ID: 12798584
[TBL] [Abstract][Full Text] [Related]
20. Association analysis identifies new risk loci for congenital heart disease in Chinese populations.
Lin Y; Guo X; Zhao B; Liu J; Da M; Wen Y; Hu Y; Ni B; Zhang K; Yang S; Xu J; Dai J; Wang X; Xia Y; Ma H; Jin G; Yu S; Liu J; Keavney BD; Goodship JA; Cordell HJ; Wang X; Shen H; Sha J; Zhou Z; Chen Y; Mo X; Luo L; Hu Z
Nat Commun; 2015 Aug; 6():8082. PubMed ID: 26283027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]