MMP-2 and TIMP-2 gene polymorphisms and susceptibility to atrial fibrillation in Chinese Han patients with hypertensive heart disease

References

Page 1

	Year	Citations
The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure<SUBTITLE>The JNC 7 Report</SUBTITLE> Aram V. Chobanian JAMA HypertensionCardiovascular PharmacologyPharmacotherapyBlood PressureHypertension Prevention	2003	25.4K
Echocardiographic assessment of left ventricular hypertrophy: Comparison to necropsy findings Richard B. Devereux, Daniel R. Alonso, Elizabeth M. Lutas, The American Journal of Cardiology CardiomyopathyHeart FailureStructural Heart DiseaseCardiovascular DiseaseCardiac Pathology	1986	6.2K
Relation of Left Ventricular Mass and Geometry to Morbidity and Mortality in Uncomplicated Essential Hypertension Michael J. Koren, Richard B. Devereux, Paul N. Casale, Annals of Internal Medicine	1991	2.4K
KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation Yi-Han Chen, Shi-Jie Xu, Saı̈d Bendahhou, Science	2003	990
Variants conferring risk of atrial fibrillation on chromosome 4q25 Daníel F. Guðbjartsson, Davíð O. Arnar, Anna Helgadóttir, Nature Genetic DisorderGeneticsGenetic EpidemiologyAtrial FibrillationPublic Health	2007	943
Sample Size Requirements for Association Studies of Gene-Gene Interaction W. James Gauderman American Journal of Epidemiology	2002	625
Parental Atrial Fibrillation as a Risk Factor for Atrial Fibrillation in Offspring Caroline S. Fox JAMA	2004	594
Identification of Novel, Functional Genetic Variants in the Human Matrix Metalloproteinase-2 Gene Simon Price, David R. Greaves, Hugh Watkins Journal of Biological Chemistry EngineeringGeneticsHuman PolymorphismPathologyMatrix Metalloproteinase-2	2001	399
Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation Yiqing Yang, Min Xia, Qingfeng Jin, The American Journal of Human Genetics GeneticsPhysiologyFamilial Atrial FibrillationKcne2 Gain-of-function MutationCongenital Heart Anomaly	2004	389
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Emelia J. Benjamin, Kenneth Rice, Dan E. Arking, Nature Genetics Cardiovascular DiseaseGenetic EpidemiologyMedical GeneticsEuropean AncestryAtrial Fibrillation	2009	385

Page 1