Genetics of cardiovascular diseases - From single mutations to the whole genome

被引：79

作者：

Cambien, Francois

Tiret, Laurence

机构：

[1] INSERM, U525, Fac Med Pitie Salpetriere, F-75634 Paris, France

[2] Univ Paris 06, Paris, France

来源：

CIRCULATION | 2007年 / 116卷 / 15期

关键词：

D O I：

10.1161/CIRCULATIONAHA.106.661751

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1714 / 1724

页数：11

共 80 条

[1] Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam study [J].

Aarnoudse, Albert-Jan L. H. J. ;

Newton-Cheh, Christopher ;

de Bakker, Paul I. W. ;

Straus, Sabine M. J. M. ;

Kors, Jan A. ;

Hofman, Albert ;

Uitterlinden, Andre G. ;

Witteman, Jacqueline C. M. ;

Stricker, Bruno H. C. .

CIRCULATION, 2007, 116 (01) :10-16

[2] Mutations in PCSK9 cause autosomal dominant hypercholesterolemia [J].

Abifadel, M ;

Varret, M ;

Rabès, JP ;

Allard, D ;

Ouguerram, K ;

Devillers, M ;

Cruaud, C ;

Benjannet, S ;

Wickham, L ;

Erlich, D ;

Derré, A ;

Villéger, L ;

Farnier, M ;

Beucler, I ;

Bruckert, E ;

Chambaz, J ;

Chanu, B ;

Lecerf, JM ;

Luc, G ;

Moulin, P ;

Weissenbach, J ;

Prat, A ;

Krempf, M ;

Junien, C ;

Seidah, NG ;

Boileau, C .

NATURE GENETICS, 2003, 34 (02) :154-156

[3] A haplotype map of the human genome [J].

Altshuler, D ;

Brooks, LD ;

Chakravarti, A ;

Collins, FS ;

Daly, MJ ;

Donnelly, P ;

Gibbs, RA ;

Belmont, JW ;

Boudreau, A ;

Leal, SM ;

Hardenbol, P ;

Pasternak, S ;

Wheeler, DA ;

Willis, TD ;

Yu, FL ;

Yang, HM ;

Zeng, CQ ;

Gao, Y ;

Hu, HR ;

Hu, WT ;

Li, CH ;

Lin, W ;

Liu, SQ ;

Pan, H ;

Tang, XL ;

Wang, J ;

Wang, W ;

Yu, J ;

Zhang, B ;

Zhang, QR ;

Zhao, HB ;

Zhao, H ;

Zhou, J ;

Gabriel, SB ;

Barry, R ;

Blumenstiel, B ;

Camargo, A ;

Defelice, M ;

Faggart, M ;

Goyette, M ;

Gupta, S ;

Moore, J ;

Nguyen, H ;

Onofrio, RC ;

Parkin, M ;

Roy, J ;

Stahl, E ;

Winchester, E ;

Ziaugra, L ;

Shen, Y .

NATURE, 2005, 437 (7063) :1299-1320

[4]

AMETT DK, 2007, CIRCULATION, V115, P2878

[5] Drug-metabolizing enzymes: Evidence for clinical utility of pharmacogenomic tests [J].

Andersson, T ;

Flockhart, DA ;

Goldstein, DB ;

Huang, SM ;

Kroetz, DL ;

Milos, PM ;

Ratain, MJ ;

Thummel, K .

CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 78 (06) :559-581

[6] A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization [J].

Arking, Dan E. ;

Pfeufer, Arne ;

Post, Wendy ;

Kao, W. H. Linda ;

Newton-Cheh, Christopher ;

Ikeda, Morna ;

West, Kristen ;

Kashuk, Carl ;

Akyol, Mahmut ;

Perz, Siegfried ;

Jalilzadeh, Shapour ;

Illig, Thomas ;

Gieger, Christian ;

Guo, Chao-Yu ;

Larson, Martin G. ;

Wichmann, H. Erich ;

Marban, Eduardo ;

O'Donnell, Christopher J. ;

Hirschhorn, Joel N. ;

Kaeaeb, Stefan ;

Spooner, Peter M. ;

Meitinger, Thomas ;

Chakravarti, Aravinda .

NATURE GENETICS, 2006, 38 (06) :644-651

[7] Genetic causes of monogenic heterozygous familial hypercholesterolemia: A HuGE prevalence review [J].

Austin, MA ;

Hutter, CM ;

Zimmern, RL ;

Humphries, SE .

AMERICAN JOURNAL OF EPIDEMIOLOGY, 2004, 160 (05) :407-420

[8]

BARBAUX S, IN PRESS J MOL MED

[9] The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease [J].

Bodzioch, M ;

Orsó, E ;

Klucken, T ;

Langmann, T ;

Böttcher, L ;

Diederich, W ;

Drobnik, W ;

Barlage, S ;

Büchler, C ;

Porsch-Özcürümez, M ;

Kaminski, WE ;

Hahmann, HW ;

Oette, K ;

Rothe, G ;

Aslanidis, C ;

Lackner, KJ ;

Schmitz, G .

NATURE GENETICS, 1999, 22 (04) :347-351

[10] Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease [J].

Botstein, D ;

Risch, N .

NATURE GENETICS, 2003, 33 (Suppl 3) :228-237

← 1 2 3 4 5 6 7 8 →