Assessment of genetic markers for coronary thrombosis: promise and precaution

被引：33

作者：

Ridker, PM ^{[1
]}

Stampfer, MJ

机构：

[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med, Boston, MA 02115 USA

[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA

[3] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA

来源：

LANCET | 1999年 / 353卷 / 9154期

关键词：

D O I：

10.1016/S0140-6736(99)00067-7

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：687 / 688

页数：2

共 17 条

[1] DELETION POLYMORPHISM IN THE GENE FOR ANGIOTENSIN-CONVERTING ENZYME IS A POTENT RISK FACTOR FOR MYOCARDIAL-INFARCTION [J].

CAMBIEN, F ;

POIRIER, O ;

LECERF, L ;

EVANS, A ;

CAMBOU, JP ;

ARVEILER, D ;

LUC, G ;

BARD, JM ;

BARA, L ;

RICARD, S ;

TIRET, L ;

AMOUYEL, P ;

ALHENCGELAS, F ;

SOUBRIER, F .

NATURE, 1992, 359 (6396) :641-644

[2] Platelet glycoprotein IIIa PIA polymorphism in young men with myocardial infarction [J].

Carter, AM ;

OsseiGerning, N ;

Grant, PJ .

LANCET, 1996, 348 (9025) :485-486

[3] Association of the platelet PIA polymorphism of glycoprotein IIb/IIIa and the fibrinogen B beta 448 polymorphism with myocardial infarction and extent of coronary artery disease [J].

Carter, AM ;

OsseiGerning, N ;

Wilson, IJ ;

Grant, PJ .

CIRCULATION, 1997, 96 (05) :1424-1431

[4] A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].

FROSST, P ;

BLOM, HJ ;

MILOS, R ;

GOYETTE, P ;

SHEPPARD, CA ;

MATTHEWS, RG ;

BOERS, GJH ;

DENHEIJER, M ;

KLUIJTMANS, LAJ ;

VANDENHEUVEL, LP ;

ROZEN, R .

NATURE GENETICS, 1995, 10 (01) :111-113

[5]

HERRMANN SM, 1997, THROMB HAEMOSTASIS, V77, P1170

[6] MYOCARDIAL-INFARCTION ASSOCIATED WITH HOMOZYGOUS RESISTANCE TO ACTIVATED PROTEIN-C [J].

HOLM, J ;

ZOLLER, B ;

SVENSSON, PJ ;

BERNTORP, E ;

ERHARDT, L ;

DAHLBACK, B .

LANCET, 1994, 344 (8927) :952-953

[7] The role of a common variant of the cholesterol ester transfer protein gene in the progression of coronary atherosclerosis [J].

Kuivenhoven, JA ;

Jukema, JW ;

Zwinderman, AH ;

de Knijff, P ;

McPherson, R ;

Bruschke, VG ;

Lie, KI ;

Kastelein, JJP .

NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (02) :86-93

[8] Hereditary variation in platelet integrin alpha(2)beta(1) density is associated with two silent polymorphisms in the alpha(2) gene coding sequence [J].

Kunicki, TJ ;

Kritzik, M ;

Annis, DS ;

Nugent, DJ .

BLOOD, 1997, 89 (06) :1939-1943

[9] A PROSPECTIVE EVALUATION OF AN ANGIOTENSIN-CONVERTING-ENZYME GENE POLYMORPHISM AND THE RISK OF ISCHEMIC-HEART-DISEASE [J].

LINDPAINTNER, K ;

PFEFFER, MA ;

KREUTZ, R ;

STAMPFER, MJ ;

GRODSTEIN, F ;

LAMOTTE, F ;

BURING, J ;

HENNEKENS, CH .

NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (11) :706-711

[10] Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction:: a case-control study [J].

Moshfegh, K ;

Wuillemin, WA ;

Redondo, M ;

Lämmle, B ;

Beer, JH ;

Liechti-Gallati, S ;

Meyer, BJ .

LANCET, 1999, 353 (9150) :351-354

← 1 2 →