146 related articles for article (PubMed ID: 22923420)
1. Pooled DNA resequencing of 68 myocardial infarction candidate genes in French canadians.
Beaudoin M; Lo KS; N'Diaye A; Rivas MA; Dubé MP; Laplante N; Phillips MS; Rioux JD; Tardif JC; Lettre G
Circ Cardiovasc Genet; 2012 Oct; 5(5):547-54. PubMed ID: 22923420
[TBL] [Abstract][Full Text] [Related]
2. Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits.
Golbus JR; Stitziel NO; Zhao W; Xue C; Farrall M; McPherson R; Erdmann J; Deloukas P; Watkins H; Schunkert H; Samani NJ; Saleheen D; Kathiresan S; Reilly MP;
Circ Cardiovasc Genet; 2016 Jun; 9(3):250-8. PubMed ID: 27013693
[TBL] [Abstract][Full Text] [Related]
3. Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).
Ferguson JF; Matthews GJ; Townsend RR; Raj DS; Kanetsky PA; Budoff M; Fischer MJ; Rosas SE; Kanthety R; Rahman M; Master SR; Qasim A; Li M; Mehta NN; Shen H; Mitchell BD; O'Connell JR; Shuldiner AR; Ho WK; Young R; Rasheed A; Danesh J; He J; Kusek JW; Ojo AO; Flack J; Go AS; Gadegbeku CA; Wright JT; Saleheen D; Feldman HI; Rader DJ; Foulkes AS; Reilly MP;
J Am Coll Cardiol; 2013 Aug; 62(9):789-98. PubMed ID: 23727086
[TBL] [Abstract][Full Text] [Related]
4. Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.
Ichihara S; Yamamoto K; Asano H; Nakatochi M; Sukegawa M; Ichihara G; Izawa H; Hirashiki A; Takatsu F; Umeda H; Iwase M; Inagaki H; Hirayama H; Sone T; Nishigaki K; Minatoguchi S; Cho MC; Jang Y; Kim HS; Park JE; Tada-Oikawa S; Kitajima H; Matsubara T; Sunagawa K; Shimokawa H; Kimura A; Lee JY; Murohara T; Inoue I; Yokota M
Circ Cardiovasc Genet; 2013 Dec; 6(6):569-78. PubMed ID: 24122612
[TBL] [Abstract][Full Text] [Related]
5. A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.
Shen GQ; Girelli D; Li L; Rao S; Archacki S; Olivieri O; Martinelli N; Park JE; Chen Q; Topol EJ; Wang QK
Circ Cardiovasc Genet; 2014 Aug; 7(4):514-20. PubMed ID: 24867879
[TBL] [Abstract][Full Text] [Related]
6. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.
Hahn J; Fu YP; Brown MR; Bis JC; de Vries PS; Feitosa MF; Yanek LR; Weiss S; Giulianini F; Smith AV; Guo X; Bartz TM; Becker DM; Becker LC; Boerwinkle E; Brody JA; Chen YI; Franco OH; Grove M; Harris TB; Hofman A; Hwang SJ; Kral BG; Launer LJ; Markus MRP; Rice KM; Rich SS; Ridker PM; Rivadeneira F; Rotter JI; Sotoodehnia N; Taylor KD; Uitterlinden AG; Völker U; Völzke H; Yao J; Chasman DI; Dörr M; Gudnason V; Mathias RA; Post W; Psaty BM; Dehghan A; O'Donnell CJ; Morrison AC
PLoS One; 2020; 15(11):e0230035. PubMed ID: 33186364
[TBL] [Abstract][Full Text] [Related]
7. Genetic and Functional Sequence Variants of the SIRT3 Gene Promoter in Myocardial Infarction.
Yin X; Pang S; Huang J; Cui Y; Yan B
PLoS One; 2016; 11(4):e0153815. PubMed ID: 27078640
[TBL] [Abstract][Full Text] [Related]
8. Association of the genetic variants of endothelial nitric oxide synthase gene with angiographically defined coronary artery disease and myocardial infarction in South Indian patients with type 2 diabetes mellitus.
Narne P; Ponnaluri KC; Singh S; Siraj M; Ishaq M
J Diabetes Complications; 2013; 27(3):255-61. PubMed ID: 23182401
[TBL] [Abstract][Full Text] [Related]
9. Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.
Preuss M; König IR; Thompson JR; Erdmann J; Absher D; Assimes TL; Blankenberg S; Boerwinkle E; Chen L; Cupples LA; Hall AS; Halperin E; Hengstenberg C; Holm H; Laaksonen R; Li M; März W; McPherson R; Musunuru K; Nelson CP; Burnett MS; Epstein SE; O'Donnell CJ; Quertermous T; Rader DJ; Roberts R; Schillert A; Stefansson K; Stewart AF; Thorleifsson G; Voight BF; Wells GA; Ziegler A; Kathiresan S; Reilly MP; Samani NJ; Schunkert H;
Circ Cardiovasc Genet; 2010 Oct; 3(5):475-83. PubMed ID: 20923989
[TBL] [Abstract][Full Text] [Related]
10. Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population.
Guella I; Asselta R; Ardissino D; Merlini PA; Peyvandi F; Kathiresan S; Mannucci PM; Tubaro M; Duga S
J Lipid Res; 2010 Nov; 51(11):3342-9. PubMed ID: 20699424
[TBL] [Abstract][Full Text] [Related]
11. Differential effects of PCSK9 loss of function variants on serum lipid and PCSK9 levels in Caucasian and African Canadian populations.
Mayne J; Ooi TC; Raymond A; Cousins M; Bernier L; Dewpura T; Sirois F; Mbikay M; Davignon J; Chrétien M
Lipids Health Dis; 2013 May; 12():70. PubMed ID: 23663650
[TBL] [Abstract][Full Text] [Related]
12. An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.
Shen GQ; Li L; Girelli D; Seidelmann SB; Rao S; Fan C; Park JE; Xi Q; Li J; Hu Y; Olivieri O; Marchant K; Barnard J; Corrocher R; Elston R; Cassano J; Henderson S; Hazen SL; Plow EF; Topol EJ; Wang QK
Am J Hum Genet; 2007 Oct; 81(4):780-91. PubMed ID: 17847002
[TBL] [Abstract][Full Text] [Related]
13. Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans.
Saleheen D; Alexander M; Rasheed A; Wormser D; Soranzo N; Hammond N; Butterworth A; Zaidi M; Haycock P; Bumpstead S; Potter S; Blackburn H; Gray E; Di Angelantonio E; Kaptoge S; Shah N; Samuel M; Janjua A; Sheikh N; Haider SR; Murtaza M; Ahmad U; Hakeem A; Memon MA; Mallick NH; Azhar M; Samad A; Rasheed SZ; Gardezi AR; Memon NA; Ghaffar A; Memon FU; Zaman KS; Kundi A; Yaqoob Z; Cheema LA; Qamar N; Faruqui A; Jooma R; Niazi JH; Hussain M; Kumar K; Saleem A; Kumar K; Daood MS; Memon F; Gul AA; Abbas S; Zafar J; Shahid F; Memon Z; Bhatti SM; Kayani W; Ali SS; Fahim M; Ishaq M; Frossard P; Deloukas P; Danesh J
Arterioscler Thromb Vasc Biol; 2010 Jul; 30(7):1467-73. PubMed ID: 20395598
[TBL] [Abstract][Full Text] [Related]
14. Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
Lieb W; Zeller T; Mangino M; Götz A; Braund P; Wenzel JJ; Horn C; Proust C; Linsel-Nitschke P; Amouyel P; Bruse P; Arveiler D; König IR; Ferrières J; Ziegler A; Balmforth AJ; Evans A; Ducimetière P; Cambien F; Hengstenberg C; Stark K; Hall AS; Schunkert H; Blankenberg S; Samani NJ; Erdmann J; Tiret L
J Mol Med (Berl); 2008 Oct; 86(10):1163-70. PubMed ID: 18592168
[TBL] [Abstract][Full Text] [Related]
15. The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population.
Kashyap S; Kumar S; Agarwal V; Misra DP; Rai MK; Kapoor A
Gene; 2018 Mar; 648():89-96. PubMed ID: 29309886
[TBL] [Abstract][Full Text] [Related]
16. Strong association of the APOA5-1131T>C gene variant and early-onset acute myocardial infarction.
De Caterina R; Talmud PJ; Merlini PA; Foco L; Pastorino R; Altshuler D; Mauri F; Peyvandi F; Lina D; Kathiresan S; Bernardinelli L; Ardissino D;
Atherosclerosis; 2011 Feb; 214(2):397-403. PubMed ID: 21130994
[TBL] [Abstract][Full Text] [Related]
17. [Genetic factors in myocardial infarction--Results from a candidate gene and a genome-wide approach between beta blockers].
Hengstenberg C; Bröckel U; Holmer S; Mayer B; Fischer M; Baessler A; Erdmann J; Lieb W; Löwel H; Riegger G; Schunkert H
Herz; 2002 Nov; 27(7):649-61. PubMed ID: 12439636
[TBL] [Abstract][Full Text] [Related]
18. Association of six genetic variants with myocardial infarction.
Matsuoka R; Abe S; Tokoro F; Arai M; Noda T; Watanabe S; Horibe H; Fujimaki T; Oguri M; Kato K; Minatoguchi S; Yamada Y
Int J Mol Med; 2015 May; 35(5):1451-9. PubMed ID: 25738804
[TBL] [Abstract][Full Text] [Related]
19. Large-scale gene-centric analysis identifies novel variants for coronary artery disease.
IBC 50K CAD Consortium
PLoS Genet; 2011 Sep; 7(9):e1002260. PubMed ID: 21966275
[TBL] [Abstract][Full Text] [Related]
20. Performance of genotype imputation for rare variants identified in exons and flanking regions of genes.
Li L; Li Y; Browning SR; Browning BL; Slater AJ; Kong X; Aponte JL; Mooser VE; Chissoe SL; Whittaker JC; Nelson MR; Ehm MG
PLoS One; 2011; 6(9):e24945. PubMed ID: 21949800
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
