Musculoskeletal research has been enriched in the past ten years with a great wealth of new discoveries arising from genome wide association studies (GWAS). In addition to the novel factors identified by GWAS, the advent of whole-genome and whole-exome sequencing efforts in family based studies has also identified new genes and pathways. However, the function and the mechanisms by which such genes influence clinical traits remain largely unknown. There is imperative need to bring multidisciplinary expertise together that will allow translating these genomic discoveries into useful clinical applications with the potential of improving patient care. Therefore "GEnomics of MusculoSkeletal traits TranslatiOnal NEtwork" (GEMSTONE) aims to set th...
Osteoarthritis is the most common musculoskeletal disease and the leading cause of disability global...
Functional genomics is a challenging new way to address a complex disease like osteoarthritis on a m...
The discovery that sclerostin is the defective protein underlying the rare heritable bone mass disor...
Musculoskeletal research has been enriched in the past ten years with a great wealth of new discover...
Musculoskeletal research has been enriched in the past ten years with a great wealth of new discover...
The availability of large human datasets for genome-wide association studies (GWAS) and the advancem...
The availability of large human datasets for genome-wide association studies (GWAS) and the advancem...
The development of high‐throughput genotyping technologies and large biobank collections, complement...
A synoptic overview of scientific methods applied in bone and associated research fields across spec...
Copyright © 2021 Foessl, Bassett, Bjørnerem, Busse, Calado, Chavassieux, Christou, Douni, Fiedler, F...
The complex nature and polygenic determination of most bone disorders require new approaches to sear...
A synoptic overview of scientific methods applied in bone and associated research fields across spec...
A synoptic overview of scientific methods applied in bone and associated research fields across spec...
An ultimate goal of genetic research is to understand the connection between genotype and phenotype ...
Osteoarthritis is the most common musculoskeletal disease and the leading cause of disability global...
Osteoarthritis is the most common musculoskeletal disease and the leading cause of disability global...
Functional genomics is a challenging new way to address a complex disease like osteoarthritis on a m...
The discovery that sclerostin is the defective protein underlying the rare heritable bone mass disor...
Musculoskeletal research has been enriched in the past ten years with a great wealth of new discover...
Musculoskeletal research has been enriched in the past ten years with a great wealth of new discover...
The availability of large human datasets for genome-wide association studies (GWAS) and the advancem...
The availability of large human datasets for genome-wide association studies (GWAS) and the advancem...
The development of high‐throughput genotyping technologies and large biobank collections, complement...
A synoptic overview of scientific methods applied in bone and associated research fields across spec...
Copyright © 2021 Foessl, Bassett, Bjørnerem, Busse, Calado, Chavassieux, Christou, Douni, Fiedler, F...
The complex nature and polygenic determination of most bone disorders require new approaches to sear...
A synoptic overview of scientific methods applied in bone and associated research fields across spec...
A synoptic overview of scientific methods applied in bone and associated research fields across spec...
An ultimate goal of genetic research is to understand the connection between genotype and phenotype ...
Osteoarthritis is the most common musculoskeletal disease and the leading cause of disability global...
Osteoarthritis is the most common musculoskeletal disease and the leading cause of disability global...
Functional genomics is a challenging new way to address a complex disease like osteoarthritis on a m...
The discovery that sclerostin is the defective protein underlying the rare heritable bone mass disor...