Research Topics
| E A StreetenSummaryAffiliation: University of Maryland Country: USA Publications
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Detail Information
Publications
Reduced parathyroid hormone-stimulated 1,25-dihydroxyvitamin d production in vitamin d sufficient postmenoposual women with low bone mass and idiopathic secondary hyperparathyroidismElizabeth A Streeten
University of Maryland School of Medicine, Baltimore, MD 21201, USA
Endocr Pract 19:91-9. 2013....
Osteoporosis-pseudoglioma syndrome: description of 9 new cases and beneficial response to bisphosphonatesElizabeth A Streeten
Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, USA
Bone 43:584-90. 2008....
Autosome-wide linkage analysis of hip structural phenotypes in the Old Order AmishE A Streeten
University of Maryland School of Medicine, Department of Medicine, Division of Endocrinology, Diabetes and Nutrition, Baltimore, MD, USA
Bone 43:607-12. 2008..We derived hip structural phenotypes using the Hip Structural Analysis program (HSA) and performed autosome-wide linkage analysis of hip geometric structural phenotypes...
Reduced incidence of hip fracture in the Old Order AmishElizabeth A Streeten
Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA
J Bone Miner Res 19:308-13. 2004..The incidence of hip fracture was estimated in a community of Old Order Amish and compared with available data from non-Amish whites. Hip fracture rates were 40% lower in the Amish, and the Amish also experienced higher BMD...
The inpatient consultation approach to osteoporosis treatment in patients with a fracture. Is automatic consultation needed?Elizabeth A Streeten
Department of Medicine, Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Room N3W130, 22 South Greene Street, Baltimore, MD 21201, USA
J Bone Joint Surg Am 88:1968-74. 2006..Osteoporosis has been described as a "silent epidemic." We describe an osteoporosis consultation program to facilitate the evaluation and treatment of inpatients with fragility fractures...
Quantitative trait loci for BMD identified by autosome-wide linkage scan to chromosomes 7q and 21q in men from the Amish Family Osteoporosis StudyElizabeth A Streeten
Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA
J Bone Miner Res 21:1433-42. 2006..Using autosome-wide linkage analysis in 964 Amish, strong evidence was found for the presence of genes affecting hip and spine BMD in men on chromosomes 7q31 and 21q22 (LOD = 4.15 and 3.36, respectively)...
The relationship between parity and bone mineral density in women characterized by a homogeneous lifestyle and high parityElizabeth A Streeten
Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Room N3W130, 22 South Greene Street, Baltimore, Maryland 21201, USA
J Clin Endocrinol Metab 90:4536-41. 2005..We reported previously that Old Order Amish (OOA) women have fewer hip fractures and higher bone mineral density (BMD) than non-Amish Caucasian women...
Relationship between vascular calcification and bone mineral density in the Old-order AmishH Shen
Division of Endocrinology, Diabetes, and Nutrition, Department of Medicine, University of Maryland, 660 W Redwood Street, Room 492, Baltimore, MD 21201, USA
Calcif Tissue Int 80:244-50. 2007..003). We detected no evidence for shared genes affecting the joint distribution of bone and vascular calcification. However, our results do reveal a lower BMD in subjects with a prior history of CVD in the Old-Order Amish...
Does having children extend life span? A genealogical study of parity and longevity in the AmishPatrick F McArdle
Department of Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA
J Gerontol A Biol Sci Med Sci 61:190-5. 2006..We evaluated this issue by using genealogical data from an Old Order Amish community in Lancaster, Pennsylvania, a population characterized by large nuclear families, homogeneous lifestyle, and extensive genealogical records...
Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amishErin D Michos
Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA
Calcif Tissue Int 84:195-202. 2009..Either there is no causal relationship between 25(OH)D and CVD risk, or if there is, it may be mediated through mechanisms other than subclinical vascular disease severity...
A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitroNicole Hoppman
Division of Endocrinology, Diabetes and Nutrition, University of Maryland School of Medicine, Baltimore, MD 21201, USA
Bone 47:272-80. 2010..Collectively, these findings suggest that sequence variation in FGFBP1 may contribute to variation in BMD, possibly influencing osteoporosis risk...
Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcificationHaiqing Shen
Division of Endocrinology, University of Maryland School of Medicine, Baltimore, MD 21201, USA
Arterioscler Thromb Vasc Biol 30:2648-54. 2010..We hypothesized that DNA sequence variation in genes regulating vitamin D metabolism and signaling pathways might influence variation in coronary artery calcification (CAC)...
Genetic and environmental influences on bone mineral density in pre- and post-menopausal womenLillian B Brown
Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA
Osteoporos Int 16:1849-56. 2005..Overall, these analyses suggest that many, but not all, of the genetic factors influencing variation in BMD are common to both pre- and post-menopausal women...
Assessment of sex-specific genetic and environmental effects on bone mineral densityLillian B Brown
Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan 21201, USA
Genet Epidemiol 27:153-61. 2004..Overall, these analyses do not provide evidence for sex-specific genetic effects, suggesting that many of the genes influencing variation in BMD should be detectable in both men and women...
