J
Jon J. Camp
Researcher at Mayo Clinic
Publications - 95
Citations - 3754
Jon J. Camp is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Bone density & Osteoporosis. The author has an hindex of 25, co-authored 93 publications receiving 3461 citations. Previous affiliations of Jon J. Camp include University of Rochester.
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Journal ArticleDOI
Population-based study of age and sex differences in bone volumetric density, size, geometry, and structure at different skeletal sites.
B. Lawrence Riggs,L. Joseph Melton,Richard A. Robb,Jon J. Camp,Elizabeth J. Atkinson,James M. Peterson,Peggy A Rouleau,Cynthia H. McCollough,Mary L. Bouxsein,Sundeep Khosla +9 more
TL;DR: Over life, the cross‐sectional area of the vertebrae and proximal femur increased by ∼15% in both sexes, whereas vBMD at these sites decreased by 39–55% and 34–46%, respectively, with greater decreases in women than in men.
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A population-based assessment of rates of bone loss at multiple skeletal sites: evidence for substantial trabecular bone loss in young adult women and men.
B. Lawrence Riggs,L. Joseph Melton,Richard A. Robb,Jon J. Camp,Elizabeth J. Atkinson,Lisa J McDaniel,Shreyasee Amin,Peggy A Rouleau,Sundeep Khosla +8 more
TL;DR: Using QCT, a longitudinal, population‐based assessment of rates of bone loss over life at the distal radius, distal tibia, and lumbar spine found that Cortical bone loss began in perimenopause in women and later in life in men.
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Defects in Mitochondrial Dynamics and Metabolomic Signatures of Evolving Energetic Stress in Mouse Models of Familial Alzheimer's Disease
Eugenia Trushina,Emirhan Nemutlu,Song Zhang,Trace A. Christensen,Jon J. Camp,Janny Mesa,Ammar Siddiqui,Yasushi Tamura,Hiromi Sesaki,Thomas M. Wengenack,Petras P. Dzeja,Joseph F. Poduslo +11 more
TL;DR: Mutation-specific alterations in mitochondrial dynamics, morphology and function in FAD mice occurred prior to the onset of memory and neurological phenotype and before the formation of amyloid deposits, suggesting mitochondrial dysfunction is an underlying event in AD progression.
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Structural determinants of vertebral fracture risk.
L. Joseph Melton,B. Lawrence Riggs,Tony M. Keaveny,Sara J. Achenbach,Paul F. Hoffmann,Jon J. Camp,Peggy A Rouleau,Mary L. Bouxsein,Shreyasee Amin,Elizabeth J. Atkinson,Richard A. Robb,Sundeep Khosla +11 more
TL;DR: Vertebral fractures are more strongly associated with specific bone density, structure, and strength parameters than with areal BMD, but all of these variables are correlated.
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Relationship of Volumetric BMD and Structural Parameters at Different Skeletal Sites to Sex Steroid Levels in Men
Sundeep Khosla,L. Joseph Melton,Richard A. Robb,Jon J. Camp,Elizabeth J. Atkinson,Ann L. Oberg,Peggy A Rouleau,B. Lawrence Riggs +7 more
TL;DR: It is shown that the previously postulated “threshold” for skeletal estrogen deficiency was most evident at cortical sites, and associations between these bone mass/structural parameters and sex steroid levels were progressively stronger with age.