Pages that link to "Q30435869"
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The following pages link to An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits (Q30435869):
Displaying 50 items.
- A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao) (Q21090760) (← links)
- Blood pressure loci identified with a gene-centric array (Q24630508) (← links)
- Clinical review: Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed (Q27014915) (← links)
- Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders (Q28082561) (← links)
- Evaluation of European coeliac disease risk variants in a north Indian population (Q28395308) (← links)
- Assessment of gene-by-sex interaction effect on bone mineral density (Q28727687) (← links)
- Dissecting cis regulation of gene expression in human metabolic tissues (Q28740835) (← links)
- Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture (Q28943527) (← links)
- Bicc1 is a genetic determinant of osteoblastogenesis and bone mineral density (Q30412670) (← links)
- Systems genetics: a novel approach to dissect the genetic basis of osteoporosis (Q30417371) (← links)
- Genetic association for renal traits among participants of African ancestry reveals new loci for renal function (Q30430672) (← links)
- Genome-wide association of an integrated osteoporosis-related phenotype: is there evidence for pleiotropic genes? (Q30506045) (← links)
- Identification of genes for complex diseases using integrated analysis of multiple types of genomic data (Q30562778) (← links)
- A correlated meta-analysis strategy for data mining "OMIC" scans. (Q30591226) (← links)
- GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data (Q30656680) (← links)
- JOINT ANALYSIS OF SNP AND GENE EXPRESSION DATA IN GENETIC ASSOCIATION STUDIES OF COMPLEX DISEASES. (Q30800044) (← links)
- Pathways of aging: comparative analysis of gene signatures in replicative senescence and stress induced premature senescence (Q30835675) (← links)
- MODMatcher: multi-omics data matcher for integrative genomic analysis (Q30842672) (← links)
- Integrative modeling of multi-platform genomic data under the framework of mediation analysis (Q30860315) (← links)
- iGWAS: Integrative Genome-Wide Association Studies of Genetic and Genomic Data for Disease Susceptibility Using Mediation Analysis (Q30956245) (← links)
- A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women (Q33716853) (← links)
- Genome-wide Association Studies for Osteoporosis: A 2013 Update (Q33822065) (← links)
- Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese (Q33900611) (← links)
- Gene-gene interaction between RBMS3 and ZNF516 influences bone mineral density (Q34024831) (← links)
- A novel role for interferon regulatory factor 1 (IRF1) in regulation of bone metabolism (Q34122992) (← links)
- Integrating heterogeneous high-throughput data for meta-dimensional pharmacogenomics and disease-related studies (Q34132233) (← links)
- Genetic variants in the SOX6 gene are associated with bone mineral density in both Caucasian and Chinese populations. (Q34228801) (← links)
- MiR-133a in human circulating monocytes: a potential biomarker associated with postmenopausal osteoporosis (Q34233659) (← links)
- Stitching together multiple data dimensions reveals interacting metabolomic and transcriptomic networks that modulate cell regulation (Q34234879) (← links)
- Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture (Q34268288) (← links)
- This I believe: gaining new insights through integrating "old" data (Q34424939) (← links)
- Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women (Q34469229) (← links)
- Bone mineral density-associated polymorphisms are associated with obesity-related traits in Korean adults in a sex-dependent manner (Q34541541) (← links)
- Genetic analysis identifies DDR2 as a novel gene affecting bone mineral density and osteoporotic fractures in Chinese population (Q35057656) (← links)
- Variation in the MC4R gene is associated with bone phenotypes in elderly Swedish women (Q35091801) (← links)
- Distinct requirements for cranial ectoderm and mesenchyme-derived wnts in specification and differentiation of osteoblast and dermal progenitors (Q35105732) (← links)
- GWAS in a box: statistical and visual analytics of structured associations via GenAMap (Q35182767) (← links)
- Gene-based association analysis identified novel genes associated with bone mineral density (Q35219519) (← links)
- Bias due to two-stage residual-outcome regression analysis in genetic association studies (Q35445819) (← links)
- Fast eQTL Analysis for Twin Studies (Q35748666) (← links)
- Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma (Q35830945) (← links)
- Rap1A Regulates Osteoblastic Differentiation via the ERK and p38 Mediated Signaling (Q35849580) (← links)
- Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density (Q35878152) (← links)
- Expression-based genome-wide association study links the receptor CD44 in adipose tissue with type 2 diabetes (Q35935710) (← links)
- Update on Wnt signaling in bone cell biology and bone disease. (Q36083303) (← links)
- Impact of common variation in bone-related genes on type 2 diabetes and related traits (Q36109239) (← links)
- Wntless functions in mature osteoblasts to regulate bone mass (Q36170753) (← links)
- Functional relevance for associations between osteoporosis and genetic variants (Q36331891) (← links)
- Incorporating Information of microRNAs into Pathway Analysis in a Genome-Wide Association Study of Bipolar Disorder (Q36473277) (← links)
- Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures (Q36511060) (← links)