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Publications

The BLSA has generated hundreds of scientific papers and made major contributions to our understanding of aging and the aging process. On this page, you can explore BLSA publications from 1982 to the present.

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2015

Association between saccular function and gait speed: data from the Baltimore Longitudinal Study of Aging.
Otol Neurotol. 2015.

Layman AJ, et al. 36(2):260-6. doi: 10.1097/MAO.0000000000000544.
Association Between Visuospatial Ability and Vestibular Function in the Baltimore Longitudinal Study of Aging.
J Am Geriatr Soc. 2015.

Bigelow RT, et al. 63(9):1837-44. doi: 10.1111/jgs.13609.
Changes in Aβ biomarkers and associations with APOE genotype in 2 longitudinal cohorts.
Neurobiol Aging. 2015.

Resnick SM, et al. 36(8):2333-9. doi: 10.1016/j.neurobiolaging.2015.04.001.
Demographic and clinical variables affecting mid- to late-life trajectories of plasma ceramide and dihydroceramide species.
Aging Cell. 2015.

Mielke MM, et al. 14(6):1014-23. doi: 10.1111/acel.12369.
Detection of a novel, integrative aging process suggests complex physiological integration.
PLoS One. 2015.

Cohen AA, et al. 10(3):e0116489. doi: 10.1371/journal.pone.0116489.
Energy Metabolism and the Burden of Multimorbidity in Older Adults: Results From the Baltimore Longitudinal Study of Aging.
J Gerontol A Biol Sci Med Sci. 2015.

Fabbri E, et al. 70(11):1297-303. doi: 10.1093/gerona/glu209.
Epidemiology of vestibular evoked myogenic potentials: Data from the Baltimore Longitudinal Study of Aging.
Clin Neurophysiol. 2015.

Li C, et al. 126(11):2207-15. doi: 10.1016/j.clinph.2015.01.008.
Epidemiology of vestibulo-ocular reflex function: data from the Baltimore Longitudinal Study of Aging.
Otol Neurotol. 2015.

Li C, et al. 36(2):267-72. doi: 10.1097/MAO.0000000000000610.
Factors affecting longitudinal trajectories of plasma sphingomyelins: the Baltimore Longitudinal Study of Aging.
Aging Cell. 2015.

Mielke MM, et al. 14(1):112-21. doi: 10.1111/acel.12275.
FTO genotype and aging: pleiotropic longitudinal effects on adiposity, brain function, impulsivity and diet.
Mol Psychiatry. 2015.

Chuang YF, et al. 20(1):133-39. doi: 10.1038/mp.2014.49.
Gait characteristics associated with walking speed decline in older adults: results from the Baltimore Longitudinal Study of Aging.
Arch Gerontol Geriatr. 2015.

Jerome GJ, et al. 60(2):239-43. doi: 10.1016/j.archger.2015.01.007.
Gait energetic efficiency in older adults with and without knee pain: results from the Baltimore Longitudinal Study of Aging.
Age (Dordr). 2015.

Ko SU, et al. 37(1):9754. doi: 10.1007/s11357-015-9754-4.
Generalized multilevel function-on- scalar regression and principal component analysis.
Biometrics. 2015.

Goldsmith J, et al. 71(2):344-53. doi: 10.1111/biom.12278.
Greater cortical thinning in normal older adults predicts later cognitive impairment.
Neurobiol Aging. 2015.

Pacheco J, et al. 36(2):903-8. doi: 10.1016/j.neurobiolaging.2014.08.031.
Hyperglycemia predicts persistently lower muscle strength with aging.
Diabetes Care. 2015.

Kalyani RR, et al. 38(1):82-90. doi: 10.2337/dc14-1166.
Intra-individual lap time variation of the 400-m walk, an early mobility indicator of executive function decline in high-functioning older adults?
Age (Dordr). 2015.

Tian Q, et al. 37(6):115. doi: 10.1007/s11357-015-9855-0.
Lap time variation and executive function in older adults: the Baltimore Longitudinal Study of Aging.
Age Ageing. 2015.

Tian Q, et al. 44(5):796-800. doi: 10.1093/ageing/afv076.
Quantifying the lifetime circadian rhythm of physical activity: a covariate- dependent functional approach.
Biostatistics. 2015.

Xiao L, et al. 16(2):352-67. doi: 10.1093/biostatistics/kxu045.
Region of interest correction factors improve reliability of diffusion imaging measures within and across scanners and field strengths.
Neuroimage. 2015.

Venkatraman VK, et al. 119:406-16. doi: 10.1016/j.neuroimage.2015.06.078.
Renal function and long-term decline in cognitive function: the Baltimore Longitudinal Study of Aging.
Am J Nephrol. 2015.

Seliger SL, et al. 41(4-5):305-12. doi: 10.1159/000430922.
Sex-specific age associations of ankle proprioception test performance in older adults: results from the Baltimore Longitudinal Study of Aging.
Age Ageing. 2015.

Ko SU, et al. 44(3):485-90. doi: 10.1093/ageing/afv005.
Sex-specific differences in progressive glucose intolerance and hip geometry: the Baltimore Longitudinal Study of Aging.
Osteoporos Int. 2015.

Moseley KF, et al. 26(5):1555-62. doi: 10.1007/s00198-015-3027-z.
Statistical distance as a measure of physiological dysregulation is largely robust to variation in its biomarker composition.
PLoS One. 2015.

Cohen AA, et al. 10(4):e0122541. doi: 10.1371/journal.pone.0122541.
The Pittsburgh Fatigability scale for older adults: development and validation.
J Am Geriatr Soc. 2015.

Glynn NW, et al. 63(1):130-5. doi: 10.1111/jgs.13191.
Thyroid Hormone Therapy and Risk of Thyrotoxicosis in Community-Resident Older Adults: Findings from the Baltimore Longitudinal Study of Aging.
Thyroid. 2015.

Mammen JS, et al. 25(9):979-86. doi: 10.1089/thy.2015.0180.
Validation of Nutrient Intake Estimates Derived Using a Semi-Quantitative FFQ against 3 Day Diet Records in the Baltimore Longitudinal Study of Aging.
J Nutr Health Aging. 2015.

Talegawkar SA, et al. 19(10):994-1002. doi: 10.1007/s12603-015-0518-8.
Vitamin D deficiency and airflow limitation in the Baltimore Longitudinal Study of Ageing.
Eur J Clin Invest. 2015.

Moberg M, et al. 45(9):955-63. doi: 10.1111/eci.12498.
Newer (2016)
Older (2014)
Page Last Updated:  
April 5, 2022

The BLSA is conducted by the Intramural Research Program of the National Institute on Aging (NIA), part of the National Institutes of Health at the U.S. Department of Health and Human Services.

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