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Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 19, 2009
Association of CYP1B1 haplotypes and breast cancer risk in Caucasian womenYifan Huang, Amy Trentham-Dietz, Montserrat García-Closas, et al.
Current Eye Research|April 19, 2024
Longitudinal Evaluation of the Distribution of Intraretinal Hyper-Reflective Foci in Eyes with Intermediate Age-Related Macular DegenerationAditya Verma, Muneeswar G Nittala, Giulia Corradetti, et al.
The Journal of Surgical Research|August 23, 2024
Predictive Energy Equations Inaccurately Estimate Metabolic Demands of Older Adult Trauma PatientsKrista L Haines, Julie Walsh, Trevor Sytsma, et al.
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
Spatial Distribution of Missense Variants within Complement Proteins Associates with Age Related Macular DegenerationMichelle Grunin, Sarah de Jong, Ellen L Palmer, et al.
Ophthalmology|December 11, 2007
Peripheral reticular pigmentary change is associated with complement factor H polymorphism (Y402H) in age-related macular degenerationR Keith Shuler, Silke Schmidt, Paul Gallins, et al.
The New England Journal of Medicine|May 16, 1991
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneityT Siddique, D A Figlewicz, M A Pericak-Vance, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1993
Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humansP Gregor, R H Reeves, E W Jabs, et al.
American Journal of Human Genetics|August 1, 1992
Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease casesR E Tanzi, G Vaula, D M Romano, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Examination of association to autism of common genetic variationin genes related to dopamineB M Anderson, N Schnetz-Boutaud, J Bartlett, et al.
Archives of Neurology|November 1, 1992
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
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