Scrutinizing the Genetic Underpinnings of Bone Strength

Medication-related fall incidents in an older, ambulant population: the B-PROOF study.

Drugs & aging·2014

Determinants of maternal pregnancy one-carbon metabolism and newborn human DNA methylation profiles.

Reproduction (Cambridge, England)·2014

Results of 2-year vitamin B treatment on cognitive performance: secondary data from an RCT.

Neurology·2014

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.

Nature communications·2014

The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels.

PloS one·2014

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.

Molecular psychiatry·2014

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

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

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

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

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Scrutinizing the Genetic Underpinnings of Bone Strength

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Medication-related fall incidents in an older, ambulant population: the B-PROOF study.

Determinants of maternal pregnancy one-carbon metabolism and newborn human DNA methylation profiles.

Results of 2-year vitamin B treatment on cognitive performance: secondary data from an RCT.

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.

The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels.

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.

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

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

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

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

Osteosarcopenia Revisited: From Mechanisms to Management.

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

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

Scrutinizing the Genetic Underpinnings of Bone Strength

Related Concept Videos

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