Associated Papers
Identification of rare genetic variants in familial forms and unrelated cases of bisphosphonates-associated atypical femur fracture.
Michou L et al.
Joint Bone Spine, 2025
Assessing the contribution of genes involved in monogenic bone disorders to the etiology of atypical femoral fractures.
Garcia-Giralt N et al.
Human Genomics, 2024
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc4.xlsx › Supplementary_Table_4
Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients.
Zhou W et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2023
37076969 (PubMed )
Supplement: JBMR-38-896-s002.xlsx › S.Table3
On the association between Chiari malformation type 1, bone mineral density and bone related genes.
Martínez-Gil N et al.
Bone Reports, 2022
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