157 related articles for article (PubMed ID: 35451555)
1. A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
Rashkin SR; Cleves M; Shaw GM; Nembhard WN; Nestoridi E; Jenkins MM; Romitti PA; Lou XY; Browne ML; Mitchell LE; Olshan AF; Lomangino K; Bhattacharyya S; Witte JS; Hobbs CA;
Am J Med Genet A; 2022 Aug; 188(8):2303-2314. PubMed ID: 35451555
[TBL] [Abstract][Full Text] [Related]
2. Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.
Patel J; Bircan E; Tang X; Orloff M; Hobbs CA; Browne ML; Botto LD; Finnell RH; Jenkins MM; Olshan A; Romitti PA; Shaw GM; Werler MM; Li J; Nembhard WN;
PLoS Genet; 2021 Mar; 17(3):e1009413. PubMed ID: 33684136
[TBL] [Abstract][Full Text] [Related]
3. Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation.
Tang X; Cleves MA; Nick TG; Li M; MacLeod SL; Erickson SW; Li J; Shaw GM; Mosley BS; Hobbs CA;
Am J Med Genet A; 2015 Jun; 167(6):1231-42. PubMed ID: 25846410
[TBL] [Abstract][Full Text] [Related]
4. Assessing the Associations of Blood Metabolites With Osteoporosis: A Mendelian Randomization Study.
Liu L; Wen Y; Zhang L; Xu P; Liang X; Du Y; Li P; He A; Fan Q; Hao J; Wang W; Guo X; Shen H; Tian Q; Zhang F; Deng HW
J Clin Endocrinol Metab; 2018 May; 103(5):1850-1855. PubMed ID: 29506141
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A genetic association study detects haplotypes associated with obstructive heart defects.
Li M; Cleves MA; Mallick H; Erickson SW; Tang X; Nick TG; Macleod SL; Hobbs CA;
Hum Genet; 2014 Sep; 133(9):1127-38. PubMed ID: 24894164
[TBL] [Abstract][Full Text] [Related]
7. PDGFRA gene, maternal binge drinking and obstructive heart defects.
Tang X; Eberhart JK; Cleves MA; Li J; Li M; MacLeod S; Nembhard WN; Hobbs CA
Sci Rep; 2018 Jul; 8(1):11083. PubMed ID: 30038270
[TBL] [Abstract][Full Text] [Related]
8. Maternal and infant genetic variants, maternal periconceptional use of selective serotonin reuptake inhibitors, and risk of congenital heart defects in offspring: population based study.
Nembhard WN; Tang X; Hu Z; MacLeod S; Stowe Z; Webber D;
BMJ; 2017 Mar; 356():j832. PubMed ID: 28264803
[No Abstract] [Full Text] [Related]
9. Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.
Agopian AJ; Goldmuntz E; Hakonarson H; Sewda A; Taylor D; Mitchell LE;
Circ Cardiovasc Genet; 2017 Jun; 10(3):e001449. PubMed ID: 28468790
[TBL] [Abstract][Full Text] [Related]
10. Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways.
Hobbs CA; Cleves MA; Macleod SL; Erickson SW; Tang X; Li J; Li M; Nick T; Malik S;
Birth Defects Res A Clin Mol Teratol; 2014 Feb; 100(2):116-26. PubMed ID: 24535845
[TBL] [Abstract][Full Text] [Related]
11. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.
Noth I; Zhang Y; Ma SF; Flores C; Barber M; Huang Y; Broderick SM; Wade MS; Hysi P; Scuirba J; Richards TJ; Juan-Guardela BM; Vij R; Han MK; Martinez FJ; Kossen K; Seiwert SD; Christie JD; Nicolae D; Kaminski N; Garcia JGN
Lancet Respir Med; 2013 Jun; 1(4):309-317. PubMed ID: 24429156
[TBL] [Abstract][Full Text] [Related]
12. Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects.
van Beynum IM; Mooij C; Kapusta L; Heil S; den Heijer M; Blom HJ
Clin Chem Lab Med; 2008; 46(10):1369-75. PubMed ID: 18844489
[TBL] [Abstract][Full Text] [Related]
13. A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects.
Nembhard WN; Tang X; Li J; MacLeod SL; Levy J; Schaefer GB; Hobbs CA;
Am J Med Genet A; 2018 Mar; 176(3):609-617. PubMed ID: 29399948
[TBL] [Abstract][Full Text] [Related]
14. Four pleiotropic loci associated with fat mass and lean mass.
Liu Y; Ran S; Lin Y; Zhang YX; Yang XL; Wei XT; Jiang ZX; He X; Zhang H; Feng GJ; Shen H; Tian Q; Deng HW; Zhang L; Pei YF
Int J Obes (Lond); 2020 Oct; 44(10):2113-2123. PubMed ID: 32719433
[TBL] [Abstract][Full Text] [Related]
15. A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
Wang H; St Julien KR; Stevenson DK; Hoffmann TJ; Witte JS; Lazzeroni LC; Krasnow MA; Quaintance CC; Oehlert JW; Jelliffe-Pawlowski LL; Gould JB; Shaw GM; O'Brodovich HM
Pediatrics; 2013 Aug; 132(2):290-7. PubMed ID: 23897914
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.
Mitchell LE; Agopian AJ; Bhalla A; Glessner JT; Kim CE; Swartz MD; Hakonarson H; Goldmuntz E
Hum Mol Genet; 2015 Jan; 24(1):265-73. PubMed ID: 25138779
[TBL] [Abstract][Full Text] [Related]
17. Maternal smoking and congenital heart defects.
Malik S; Cleves MA; Honein MA; Romitti PA; Botto LD; Yang S; Hobbs CA;
Pediatrics; 2008 Apr; 121(4):e810-6. PubMed ID: 18381510
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Integrating genome-wide association study with regulatory SNP annotations identified novel candidate genes for osteoporosis.
Jia Y; Qi X; Ma M; Cheng S; Cheng B; Liang C; Guo X; Zhang F
Bone Joint Res; 2023 Feb; 12(2):147-154. PubMed ID: 37051837
[TBL] [Abstract][Full Text] [Related]
20. Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.
Li M; Erickson SW; Hobbs CA; Li J; Tang X; Nick TG; Macleod SL; Cleves MA;
Genet Epidemiol; 2014 Apr; 38(3):198-208. PubMed ID: 24585533
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]