Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
出版年份 2011 全文链接
标题
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
作者
关键词
-
出版物
NATURE GENETICS
Volume 43, Issue 7, Pages 685-689
出版商
Springer Nature
发表日期
2011-05-30
DOI
10.1038/ng.845
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- LocusZoom: regional visualization of genome-wide association scan results
- (2010) R. J. Pruim et al. BIOINFORMATICS
- ProbABEL package for genome-wide association analysis of imputed data
- (2010) Yurii S Aulchenko et al. BMC BIOINFORMATICS
- The majority of the genetic risk for Paget’s disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes
- (2010) Pui Yan Jenny Chung et al. HUMAN GENETICS
- Frequency and characteristics of familial aggregation of paget's disease of bone
- (2010) A.A. Morales-Piga et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Familial aggregation of paget's disease of bone
- (2010) Ethel S. Siris et al. JOURNAL OF BONE AND MINERAL RESEARCH
- SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone
- (2010) Luigi Gennari et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Mutations ofSQSTM1are associated with severity and clinical outcome in paget disease of bone
- (2010) Micaela Rios Visconti et al. JOURNAL OF BONE AND MINERAL RESEARCH
- CCN family 2/connective tissue growth factor (CCN2/CTGF) promotes osteoclastogenesis via induction of and interaction with dendritic cell-specific transmembrane protein (DC-STAMP)
- (2010) Takashi Nishida et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Transcriptome genetics using second generation sequencing in a Caucasian population
- (2010) Stephen B. Montgomery et al. NATURE
- Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
- (2010) Omar M E Albagha et al. NATURE GENETICS
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
- (2010) Benjamin F Voight et al. NATURE GENETICS
- Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210
- (2010) Patrick Smits et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility
- (2010) Tanja Zeller et al. PLoS One
- Randomized trial of intensive bisphosphonate treatment versus symptomatic management in paget's disease of bone
- (2009) Anne L Langston et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
- (2009) Fernando Rivadeneira et al. NATURE GENETICS
- Genetic Epidemiology of Paget’s Disease of Bone in Italy: sequestosome1/p62 Gene Mutational Test and Haplotype Analysis at 5q35 in a Large Representative Series of Sporadic and Familial Italian Cases of Paget’s Disease of Bone
- (2008) Alberto Falchetti et al. CALCIFIED TISSUE INTERNATIONAL
- Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
- (2008) Itsik Pe'er et al. GENETIC EPIDEMIOLOGY
- Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin
- (2008) Hans Christian Hennies et al. NATURE GENETICS
- Mapping the Genetic Architecture of Gene Expression in Human Liver
- (2008) Eric E Schadt et al. PLOS BIOLOGY
- High-Resolution Mapping of Expression-QTLs Yields Insight into Human Gene Regulation
- (2008) Jean-Baptiste Veyrieras et al. PLoS Genetics
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