Genetics of fracture: challenges and opportunities

Effect of LED spectra on growth, physiology, and biochemical profiles of African marigold (Tagetes erecta L.).

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Clinical trial and real-world evidence of circulating tumor DNA monitoring to predict recurrence in patients with resected colorectal cancer.

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Genomic regions affecting perinatal and early life survival in dairy calves.

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Use of federated learning to develop an artificial intelligence model predicting usable blastocyst formation from pre-ICSI oocyte images.

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Imputation accuracy and carrier frequency of deleterious recessive defects in Australian dairy cattle.

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Clinical and technical factors in endoscopic skull base surgery associated with reconstructive success.

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Deciphering the development of synovial joints in the limbs: Recent discoveries and clinical implications.

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Lesion Expansion in Craniofacial Fibrous Dysplasia: Natural History and Indicators of Progression in the Frontal, Zygomatic, and Sphenoid Bones.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·2026

Genotype-First Characterization of Familial Hypocalciuric Hypercalcemia Type 1: Prevalence, Serum Calcium and Clinical Associations.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·2026

Identification of a novel small-molecule modulator targeting SNX10 to inhibit osteoclastic bone resorption.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·2026

Osteosarcopenia Revisited: From Mechanisms to Management.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·2026

Multimorbidity Double Burden: Elevated Refracture Risk Despite High Mortality Following Fractures - A Linked Cohort Study.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·2026

[Autism - Phenotypic variability].

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Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

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Genetics of fracture: challenges and opportunities

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Genetics of fracture: challenges and opportunities

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