Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Irmarie Chazaro"'
Autor:
Anita L. DeStefano, Jing Cui, Lindsay A. Farrer, Irmarie Chazaro, Athanasios J. Manolis, Xiaofeng C. Zhou, Haralambos Gavras, Clinton T. Baldwin
Publikováno v:
Disease Markers
Disease Markers, Vol 21, Iss 1, Pp 3-7 (2005)
Disease Markers, Vol 21, Iss 1, Pp 3-7 (2005)
Genetic variations that predispose individuals to complex disorders, such as essential hypertension, may be found in gene coding regions, intronic regions or in gene promoter regions. Most studies have focused on gene variations that result in amino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da8b2d2eabd6684a1c7cef53a8bf8b61
https://doi.org/10.1155/2005/487014
https://doi.org/10.1155/2005/487014
Autor:
Philip A. Wolf, Joseph F. Polak, Ralph B. D'Agostino, Irmarie Chazaro, Christopher J. O'Donnell, L. Adrienne Cupples, Caroline S. Fox, Jose M. Ordovas
Publikováno v:
The American Journal of Human Genetics. 74:253-261
Carotid intimal medial thickness (IMT) is a heritable quantitative measure of atherosclerosis. A genomewide linkage analysis was conducted to localize a quantitative-trait locus (QTL) influencing carotid IMT. Carotid IMT was measured in 596 men and 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d4c71e6bb108b140a4ef843c61d5ff
https://doi.org/10.1086/381559
https://doi.org/10.1086/381559
Autor:
Irmarie Chazaro, Anita L. DeStefano, Jing Cui, Clinton T. Baldwin, Athanasios J. Manolis, Xiaofeng C. Zhou, Haralambos Gavras
Publikováno v:
American Journal of Hypertension. 16:859-863
Background Several studies have indicated that a region on human chromosome 17 may influence blood pressure. Our group reported positive linkage for hypertension to the region on human chromosome 17, between D17S1814 and D17S800 in white sibling pair
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80ede5b32a0e2c937bbff9f04c96e855
https://doi.org/10.1016/s0895-7061(03)01026-4
https://doi.org/10.1016/s0895-7061(03)01026-4
Autor:
Jing Cui, Anita L. DeStefano, Irmarie Chazaro, Haralambos Gavras, Lindsay A. Farrer, Porat M. Erlich, Clinton T. Baldwin
Publikováno v:
Hypertension. 41:1191-1195
Human chromosome 17q has been implicated to contain a gene that influences hypertension susceptibility. This region contains the WNK4 gene that causes the mendelian disorder pseudohypoaldosteronism type II, characterized by high potassium levels and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b076e0ed76319bba4b07d076d0ed1b3
https://doi.org/10.1161/01.hyp.0000070025.30572.91
https://doi.org/10.1161/01.hyp.0000070025.30572.91
Autor:
Adrienne Cupples, Joseph F. Polak, Christopher J. O'Donnell, R. D'Agostino, Philip A. Wolf, Irmarie Chazaro, Caroline S. Fox
Publikováno v:
Stroke. 34:397-401
Background and Purpose— Carotid intima-media thickness (IMT) is a quantitative measure of subclinical atherosclerosis that is predictive of subsequent myocardial infarction and stroke. There is controversy regarding the proportion of variability in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f11a33c5d9c5cd78aaccab183c00d70
https://doi.org/10.1161/01.str.0000048214.56981.6f
https://doi.org/10.1161/01.str.0000048214.56981.6f
Autor:
Christopher J. O'Donnell, Peter W. F. Wilson, L. Adrienne Cupples, Marian T. Hannan, Irmarie Chazaro, Caroline S. Fox, Douglas P. Kiel
Publikováno v:
Circulation. 106:337-341
Background — Atherosclerosis is a systemic disease that underlies clinical cardiovascular disease. The radiographic finding of abdominal aortic calcific deposits is an indicator of the presence of aortic atherosclerosis and an independent predictor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4e4345eec12c5939e02ef56a41b684
https://doi.org/10.1161/01.cir.0000022663.26468.5b
https://doi.org/10.1161/01.cir.0000022663.26468.5b
Publikováno v:
BMC Genetics, Vol 6, Iss Suppl 1, p S134 (2005)
BMC Genetics
BMC Genetics
In genome-wide genetic studies with a large number of markers, balancing the type I error rate and power is a challenging issue. Recently proposed false discovery rate (FDR) approaches are promising solutions to this problem. Using the 100 simulated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b325dee1b23d3860d0695bb0a41a2e89
http://www.gaworkshop.org/
http://www.gaworkshop.org/
Autor:
Athanasios J. Manolis, Efthymia Melista, Yuejian Zhang, Irmarie Chazaro, Haralambos Gavras, Clinton T. Baldwin, Jing Cui, Xiaofeng C. Zhou, Anita L. DeStefano
Publikováno v:
Journal of hypertension. 23(1)
OBJECTIVE To identify variants in the complete genomic sequence of the two subtypes of bradykinin receptors: B1 (BDKRB1) and B2 (BDKRB2) and to examine the association of these variants with essential hypertension. DESIGN A case-control design compar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0da3ac2cc30c909808b3b277c609d87
https://pubmed.ncbi.nlm.nih.gov/15643125
https://pubmed.ncbi.nlm.nih.gov/15643125
Autor:
Irmarie Chazaro, A DeSefano, Haralambos Gavras, Clinton T. Baldwin, Jing Cui, Xiaofeng C. Zhou, A.J. Manolis
Publikováno v:
Journal of Hypertension. 22:S179
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0e9234b09c883e6650c37aa9a0df506
https://doi.org/10.1097/00004872-200402001-00761
https://doi.org/10.1097/00004872-200402001-00761
Autor:
Jing Cui, Chao-Yu Guo, Serkalem Demissie, Martin G. Larson, Qiong Yang, Larry D. Atwood, Irmarie Chazaro, L. Adrienne Cupples, Anita L. DeStefano
Publikováno v:
BMC Genetics, Vol 4, Iss Suppl 1, p S29 (2003)
BMC Genetics
BMC Genetics
Background We explored three approaches to heritability and linkage analyses of longitudinal total cholesterol levels (CHOL) in the Genetic Analysis Workshop 13 simulated data without knowing the answers. The first two were univariate approaches and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82a8b31c0627d84f011267ed8612ec33
https://doi.org/10.1186/1471-2156-4-s1-s29
https://doi.org/10.1186/1471-2156-4-s1-s29