WNT signaling in bone homeostasis and disease: from human mutations to treatments

R Baron, M Kneissel - Nature medicine, 2013 - nature.com
Low bone mass and strength lead to fragility fractures, for example, in elderly individuals
affected by osteoporosis or children with osteogenesis imperfecta. A decade ago, rare …

Osteoporosis–a current view of pharmacological prevention and treatment

S Das, JC Crockett - Drug design, development and therapy, 2013 - Taylor & Francis
Postmenopausal osteoporosis is the most common bone disease, associated with low bone
mineral density (BMD) and pathological fractures which lead to significant morbidity. It is …

Involvement of WNT/β-catenin signaling in the treatment of osteoporosis

M Rossini, D Gatti, S Adami - Calcified tissue international, 2013 - Springer
Osteoblast differentiation is predominantly regulated by the WNT/β-catenin signaling
(canonical WNT pathway), which, together with bone morphogenetic proteins, acts as the …

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

U Styrkarsdottir, G Thorleifsson, P Sulem… - Nature, 2013 - nature.com
Low bone mineral density (BMD) is used as a parameter of osteoporosis. Genome-wide
association studies of BMD have hitherto focused on BMD as a quantitative trait, yielding …

Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects

FMK Williams, AT Bansal, JB van Meurs… - Annals of the …, 2013 - ard.bmj.com
Objective Lumbar disc degeneration (LDD) is an important cause of low back pain, which is
a common and costly problem. LDD is characterised by disc space narrowing and …

Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure

L Paternoster, M Lorentzon, T Lehtimäki… - PLoS …, 2013 - journals.plos.org
Most previous genetic epidemiology studies within the field of osteoporosis have focused on
the genetics of the complex trait areal bone mineral density (aBMD), not being able to …

Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans

LC Jacobs, A Wollstein, O Lao, A Hofman, CC Klaver… - Human genetics, 2013 - Springer
Natural variation in human skin pigmentation is primarily due to genetic causes rooted in
recent evolutionary history. Genetic variants associated with human skin pigmentation …

Meta‐analysis of genome‐wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

DL Koller, HF Zheng, D Karasik… - Journal of Bone and …, 2013 - academic.oup.com
Previous genome‐wide association studies (GWAS) have identified common variants in
genes associated with variation in bone mineral density (BMD), although most have been …

Genetic studies on components of the Wnt signalling pathway and the severity of joint destruction in rheumatoid arthritis

DPC de Rooy, NG Yeremenko, AG Wilson… - Annals of the …, 2013 - ard.bmj.com
Background Progression of joint destruction in rheumatoid arthritis (RA) is partly heritable;
knowledge of genetic factors may increase our understanding of the mechanisms underlying …

Alzheimer's disease genes and cognition in the nondemented general population

BFJ Verhaaren, MW Vernooij, PJ Koudstaal… - Biological …, 2013 - Elsevier
BACKGROUND: Genome-wide association studies have established 11 genes for late-
onset Alzheimer's disease (AD). We investigated whether these genes jointly affect cognition …