| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1024227590 |
| P356 | DOI | 10.1186/1471-2350-8-S1-S14 |
| P3181 | OpenCitations bibliographic resource ID | 1694803 |
| P932 | PMC publication ID | 1995606 |
| P698 | PubMed publication ID | 17903296 |
| P50 | author | Douglas P. Kiel | Q46935730 |
| Joanne M Murabito | Q47502296 | ||
| David Karasik | Q47502312 | ||
| Josée Dupuis | Q29840575 | ||
| Serkalem Demissie | Q37389793 | ||
| Kathryn L. Lunetta | Q37630755 | ||
| P2860 | cites work | Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene | Q24311919 |
| Meta-analysis of COL1A1 Sp1 polymorphism in relation to bone mineral density and osteoporotic fracture | Q28179668 | ||
| Multipoint quantitative-trait linkage analysis in general pedigrees | Q29614967 | ||
| Estrogen receptor beta polymorphisms are associated with bone mass in women and men: the Framingham Study | Q47806301 | ||
| Genetic and environmental correlations of bone mineral density at different skeletal sites in females and males. | Q51229949 | ||
| Genome-wide scan identified QTLs underlying femoral neck cross-sectional geometry that are novel studied risk factors of osteoporosis. | Q51818216 | ||
| In vivo short-term precision of hip structure analysis variables in comparison with bone mineral density using paired dual-energy X-ray absorptiometry scans from multi-center clinical trials. | Q51974747 | ||
| Differential Genetic Effects of ESR1 Gene Polymorphisms on Osteoporosis Outcomes | Q57707723 | ||
| Mapping Quantitative Trait Loci for Cross-Sectional Geometry at the Femoral Neck | Q57779105 | ||
| Robust LOD scores for variance component-based linkage analysis | Q73132936 | ||
| Genome screen for quantitative trait loci underlying normal variation in femoral structure | Q73977325 | ||
| How to use ultrasound for risk assessment: a need for defining strategies | Q78137653 | ||
| Association of polymorphisms of the estrogen receptor alpha gene with bone mineral density and fracture risk in women: a meta-analysis | Q78465196 | ||
| Age, gender, and body mass effects on quantitative trait loci for bone mineral density: the Framingham Study | Q78756682 | ||
| MTHFR polymorphism and bone mineral density: meta-analysis of published studies | Q79370802 | ||
| Contribution of the LRP5 gene to normal variation in peak BMD in women | Q81199323 | ||
| Effects of teriparatide [rhPTH (1-34)] treatment on structural geometry of the proximal femur in elderly osteoporotic women | Q81723253 | ||
| Femur strength index predicts hip fracture independent of bone density and hip axis length | Q82423589 | ||
| Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with variation in vertebral bone mass, vertebral bone size, and stature in whites | Q33201369 | ||
| Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. | Q33242615 | ||
| The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports | Q33300809 | ||
| Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass | Q33593844 | ||
| The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis | Q34569981 | ||
| Epidemiology and outcomes of osteoporotic fractures | Q34671295 | ||
| Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men | Q34803808 | ||
| Molecular and genetic mechanisms of osteoporosis: implication for treatment | Q35610360 | ||
| Genetic variation at the low-density lipoprotein receptor-related protein 5 (LRP5) locus modulates Wnt signaling and the relationship of physical activity with bone mineral density in men | Q35738927 | ||
| Proximal hip geometry is linked to several chromosomal regions: genome-wide linkage results from the Framingham Osteoporosis Study | Q35950352 | ||
| Nonreplication in genetic studies of complex diseases--lessons learned from studies of osteoporosis and tentative remedies | Q36061544 | ||
| Defining the phenotype in human genetic studies: forward genetics and reverse phenotyping | Q36090067 | ||
| Determinants of the success of whole-genome association testing | Q36298055 | ||
| Meta-analysis of how well measures of bone mineral density predict occurrence of osteoporotic fractures | Q36598613 | ||
| Two new single-nucleotide polymorphisms in the COL1A1 upstream regulatory region and their relationship to bone mineral density. | Q38291564 | ||
| In vitro functional assay of alleles and haplotypes of two COL1A1-promoter SNPs | Q38328368 | ||
| Genome screen for a combined bone phenotype using principal component analysis: the Framingham study | Q38518092 | ||
| Risk factors for longitudinal bone loss in elderly men and women: the Framingham Osteoporosis Study | Q38526454 | ||
| Genetic and environmental contributions to the association between quantitative ultrasound and bone mineral density measurements: a twin study | Q39474189 | ||
| The heritability of bone mineral density, ultrasound of the calcaneus and hip axis length: a study of postmenopausal twins | Q40943137 | ||
| Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study | Q44125439 | ||
| Mapping of quantitative ultrasound of the calcaneus bone to chromosome 1 by genome-wide linkage analysis | Q44178324 | ||
| Elderly cohort study subjects unable to return for follow-up have lower bone mass than those who can return | Q44441046 | ||
| Simple measurement of femoral geometry predicts hip fracture: the study of osteoporotic fractures | Q44631595 | ||
| Interactions of interleukin-6 promoter polymorphisms with dietary and lifestyle factors and their association with bone mass in men and women from the Framingham Osteoporosis Study | Q44789769 | ||
| Association of a common polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with bone phenotypes depends on plasma folate status | Q44812034 | ||
| A multivariate family-based association test using generalized estimating equations: FBAT-GEE. | Q45289835 | ||
| Are effects of MTHFR (C677T) genotype on BMD confined to women with low folate and riboflavin intake? Analysis of food records from the Danish osteoporosis prevention study. | Q46390096 | ||
| Effect of hormone replacement, alendronate, or combination therapy on hip structural geometry: a 3-year, double-blind, placebo-controlled clinical trial | Q46628543 | ||
| A new SNP in a negative regulatory region of the CYP19A1 gene is associated with lumbar spine BMD in postmenopausal women. | Q46847666 | ||
| Structural effects of raloxifene on the proximal femur: results from the multiple outcomes of raloxifene evaluation trial | Q46878691 | ||
| Polymorphisms in the aromatase gene predict areal BMD as a result of affected cortical bone size: the GOOD study | Q46898256 | ||
| P433 | issue | Suppl 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genome-wide association study | Q1098876 |
| P304 | page(s) | S14 | |
| P577 | publication date | 2007-01-01 | |
| P1433 | published in | BMC Medical Genetics | Q15759918 |
| P1476 | title | Genome-wide association with bone mass and geometry in the Framingham Heart Study | |
| P478 | volume | 8 | |
| 8 Suppl 1 |
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| Q57707706 | A Haplotype-Based Analysis of theLRP5Gene in Relation to Osteoporosis Phenotypes in Spanish Postmenopausal Women |
| Q34243817 | A Polymorphism in a gene encoding Perilipin 4 is associated with height but not with bone measures in individuals from the Framingham Osteoporosis Study |
| Q35744015 | A SNP in steroid receptor coactivator-1 disrupts a GSK3β phosphorylation site and is associated with altered tamoxifen response in bone |
| Q33987585 | A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro |
| Q35871212 | A functional haplotype in EIF2AK3, an ER stress sensor, is associated with lower bone mineral density |
| Q33716853 | A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women |
| Q58803790 | A genome-wide association study of energy intake and expenditure |
| Q21090760 | A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao) |
| Q30498219 | A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study |
| Q64084429 | Advanced Genetic Approaches in Discovery and Characterization of Genes Involved With Osteoporosis in Mouse and Human |
| Q30435869 | An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits |
| Q30437488 | An integrative genetics approach to identify candidate genes regulating BMD: combining linkage, gene expression, and association |
| Q27027555 | Arguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric genetics |
| Q28727687 | Assessment of gene-by-sex interaction effect on bone mineral density |
| Q36322116 | Assessment of osteoarthritis candidate genes in a meta-analysis of nine genome-wide association studies |
| Q35817451 | Association Study between the FTCDNL1 (FONG) and Susceptibility to Osteoporosis |
| Q33618811 | Association between secreted phosphoprotein-1 (SPP1) polymorphisms and low bone mineral density in women |
| Q57096416 | Association between the methylenetetrahydrofolate reductase c.677C>T polymorphism and bone mineral density: an updated meta-analysis |
| Q36010818 | Association of CDX1 binding site of periostin gene with bone mineral density and vertebral fracture risk. |
| Q36736449 | Association of DXA-derived bone mineral density and fat mass with African ancestry |
| Q45939130 | Association of ER-alpha gene polymorphism with metabolic phenotypes in Chinese Hans. |
| Q53809374 | Association of ESR1 and C6orf97 gene polymorphism with osteoporosis in postmenopausal women. |
| Q33645915 | Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. |
| Q36681939 | Association of the MTHFR C677T polymorphism and bone mineral density in postmenopausal women: a meta-analysis |
| Q34072806 | Association study of polymorphisms in the SOST gene region and parameters of bone strength and body composition in both young and elderly men: data from the Odense Androgen Study |
| Q44944631 | Bone mineral density and genetic markers involved in three connected pathways (focal adhesion, actin cytoskeleton regulation and cell cycle): the CUMAGAS-BMD information system |
| Q37185215 | Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study. |
| Q34539676 | Chapter 13: Mining electronic health records in the genomics era. |
| Q27014915 | Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed |
| Q33743947 | Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture |
| Q34055825 | Common genetic variants are associated with accelerated bone mineral density loss after hematopoietic cell transplantation |
| Q24599843 | Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women |
| Q33900611 | Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese |
| Q34539647 | Contribution of a common variant in the promoter of the 1-α-hydroxylase gene (CYP27B1) to fracture risk in the elderly |
| Q63951607 | Dissecting the Genetics of Osteoporosis using Systems Approaches |
| Q58034749 | Estrogen, exercise, and the skeleton |
| Q28748949 | European bone mineral density loci are also associated with BMD in East-Asian populations |
| Q37389487 | Family-based genome-wide association studies |
| Q38134247 | From genotype to phenotype in human atherosclerosis--recent findings |
| Q36331891 | Functional relevance for associations between osteoporosis and genetic variants |
| Q37223540 | Gene set analyses of genome-wide association studies on 49 quantitative traits measured in a single genetic epidemiology dataset |
| Q34314297 | Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study |
| Q34024831 | Gene-gene interaction between RBMS3 and ZNF516 influences bone mineral density |
| Q34170688 | Genetic Determinants of Osteoporosis: Common Bases to Cardiovascular Diseases? |
| Q37777644 | Genetic epidemiology of age-related osteoporosis and its clinical applications. |
| Q38079132 | Genetic profiling and individualized assessment of fracture risk |
| Q28756424 | Genetic studies in osteoporosis--the end of the beginning |
| Q35622181 | Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence |
| Q24289507 | Genetic variation in candidate osteoporosis genes, bone mineral density, and fracture risk: the study of osteoporotic fractures |
| Q38031141 | Genetics and the individualized prediction of fracture |
| Q37681343 | Genetics of osteoporosis: accelerating pace in gene identification and validation |
| Q37112051 | Genetics of pediatric bone strength |
| Q28732063 | Genetics of the musculoskeletal system: a pleiotropic approach |
| Q64077229 | Genome-scale Capture C promoter interactions implicate effector genes at GWAS loci for bone mineral density |
| Q35156251 | Genome-wide association study for femoral neck bone geometry |
| Q41232551 | Genome-wide association study of body mass index in subjects with alcohol dependence |
| Q24595779 | Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women |
| Q35934634 | Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density |
| Q37156061 | Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis |
| Q37591295 | Genome-wide linkage scan for quantitative trait loci underlying normal variation in heel bone ultrasound measures |
| Q55423209 | Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level. |
| Q28741604 | Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study |
| Q33930490 | Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition |
| Q35776279 | Genomewide pharmacogenetics of bisphosphonate-induced osteonecrosis of the jaw: the role of RBMS3 |
| Q56984164 | Genomic analyses of human European diversity at the southwestern edge: isolation, African influence and disease associations in the Canary Islands |
| Q35608491 | HDL cholesterol and bone mineral density: is there a genetic link? |
| Q33527154 | Haplotypes of intron 4 of the estrogen receptor alpha gene and hip fractures: a replication study in Caucasians |
| Q35592683 | High dimensional endophenotype ranking in the search for major depression risk genes |
| Q38371984 | How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports. |
| Q37402642 | How genomics has informed our understanding of the pathogenesis of osteoporosis |
| Q28741685 | How pleiotropic genetics of the musculoskeletal system can inform genomics and phenomics of aging |
| Q38968738 | How rare bone diseases have informed our knowledge of complex diseases |
| Q35156181 | IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study |
| Q38969228 | Identification and validation of genetic variants that influence transcription factor and cell signaling protein levels. |
| Q37618991 | Identification of a Copy Number Variation on Chromosome 20q13.12 Associated with Osteoporotic Fractures in the Korean Population |
| Q30450935 | Identification of a gene module associated with BMD through the integration of network analysis and genome-wide association data |
| Q35854005 | Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations |
| Q36269193 | Influence of vitamin D and estrogen receptor gene polymorphisms on calcium absorption: BsmI predicts a greater decrease during energy restriction |
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| Q34801273 | Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects |
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| Q35157827 | Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. |
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