345 related articles for article (PubMed ID: 29505555)
1. Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES).
Liu Y; Cao Y; Li Y; Lei D; Li L; Hou ZL; Han S; Meng M; Shi J; Zhang Y; Wang Y; Niu Z; Xie Y; Xiao B; Wang Y; Li X; Yang L; Wang W; Jiang L
Med Sci Monit; 2018 Mar; 24():1340-1358. PubMed ID: 29505555
[TBL] [Abstract][Full Text] [Related]
2. Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease.
Razmara E; Garshasbi M
BMC Cardiovasc Disord; 2018 Jul; 18(1):137. PubMed ID: 29969989
[TBL] [Abstract][Full Text] [Related]
3. Novel insertion mutation (Arg1822_Glu1823dup) in MYH6 coiled-coil domain causing familial atrial septal defect.
Huang S; Wu Y; Chen S; Yang Y; Wang Y; Wang H; Li P; Zhuang J; Xia Y
Eur J Med Genet; 2021 Nov; 64(11):104314. PubMed ID: 34481090
[TBL] [Abstract][Full Text] [Related]
4. The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect.
Bu H; Sun G; Zhu Y; Yang Y; Tan Z; Zhao T; Hu S
BMC Cardiovasc Disord; 2021 Jan; 21(1):12. PubMed ID: 33413087
[TBL] [Abstract][Full Text] [Related]
5. Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
Granados-Riveron JT; Ghosh TK; Pope M; Bu'Lock F; Thornborough C; Eason J; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Armour JA; David Brook J
Hum Mol Genet; 2010 Oct; 19(20):4007-16. PubMed ID: 20656787
[TBL] [Abstract][Full Text] [Related]
6. Novel Mutation in MYH6 in 2 Unrelated Chinese Han Families With Familial Atrial Septal Defect.
Xia Y; Chen S; Yang Y; Wu Y; Huang S; Wang Y; Ding H; He W; Li P; Zhuang J
Circ Genom Precis Med; 2019 Nov; 12(11):e002732. PubMed ID: 31638415
[No 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. Identification and functional analysis of variants of MYH6 gene promoter in isolated ventricular septal defects.
Zuo JY; Chen HX; Liu ZG; Yang Q; He GW
BMC Med Genomics; 2022 Oct; 15(1):213. PubMed ID: 36209093
[TBL] [Abstract][Full Text] [Related]
9. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
[TBL] [Abstract][Full Text] [Related]
10. Identification of LBX2 as a novel causal gene of atrial septal defect.
Wang J; Luo J; Chen Q; Wang X; He J; Zhang W; Yin Z; Zheng F; Pan H; Li T; Lou Q; Wang B
Int J Cardiol; 2018 Aug; 265():188-194. PubMed ID: 29669692
[TBL] [Abstract][Full Text] [Related]
11. Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients.
Fichna JP; Macias A; Piechota M; Korostyński M; Potulska-Chromik A; Redowicz MJ; Zekanowski C
Hum Genomics; 2018 Jul; 12(1):34. PubMed ID: 29970176
[TBL] [Abstract][Full Text] [Related]
12. A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect.
Chen Y; Han ZQ; Yan WD; Tang CZ; Xie JY; Chen H; Hu DY
J Thorac Cardiovasc Surg; 2010 Sep; 140(3):684-7. PubMed ID: 20347099
[TBL] [Abstract][Full Text] [Related]
13. Identification of Two Mutations in PCDHGA4 and SLFN14 Genes in an Atrial Septal Defect Family.
Su W; Wang RC; Lohano MK; Wang L; Zhu P; Luo Y; Guo LJ; Lv Q; Jiang H; Wang JH; Mei L; Weng J; Su L; Dong NG
Curr Med Sci; 2018 Dec; 38(6):989-996. PubMed ID: 30536060
[TBL] [Abstract][Full Text] [Related]
14. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
[TBL] [Abstract][Full Text] [Related]
15. Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.
Greenway SC; McLeod R; Hume S; Roslin NM; Alvarez N; Giuffre M; Zhan SH; Shen Y; Preuss C; Andelfinger G; ; Jones SJ; Gerull B
Can J Cardiol; 2014 Feb; 30(2):181-7. PubMed ID: 24461919
[TBL] [Abstract][Full Text] [Related]
16. Whole-exome sequencing identify a new mutation of MYH7 in a Chinese family with left ventricular noncompaction.
Yang J; Zhu M; Wang Y; Hou X; Wu H; Wang D; Shen H; Hu Z; Zou J
Gene; 2015 Mar; 558(1):138-42. PubMed ID: 25550050
[TBL] [Abstract][Full Text] [Related]
17. Identification of a novel MYO6 mutation associated with autosomal dominant non-syndromic hearing loss in a Chinese family by whole-exome sequencing.
Tian T; Lu Y; Yao J; Cao X; Wei Q; Li Q
Genes Genet Syst; 2018 Dec; 93(5):171-179. PubMed ID: 30175721
[TBL] [Abstract][Full Text] [Related]
18. Whole exome sequencing reveals novel
Xiao X; Cao Y; Chen S; Chen M; Mai X; Zheng Y; Zhuang X; Ng TK; Chen H
Mol Vis; 2019; 25():35-46. PubMed ID: 30804660
[TBL] [Abstract][Full Text] [Related]
19. Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.
Cao Y; Wang J; Wei C; Hou Z; Li Y; Zou H; Meng M; Wang W; Jiang L
Gene; 2016 Jan; 575(1):29-33. PubMed ID: 26297999
[TBL] [Abstract][Full Text] [Related]
20. Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.
Posch MG; Waldmuller S; Müller M; Scheffold T; Fournier D; Andrade-Navarro MA; De Geeter B; Guillaumont S; Dauphin C; Yousseff D; Schmitt KR; Perrot A; Berger F; Hetzer R; Bouvagnet P; Özcelik C
PLoS One; 2011; 6(12):e28872. PubMed ID: 22194935
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
