Lisa M. James

Dr. Lisa M. James

Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN 55455, USA

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 April 2015 in Experimental Brain Research
Verified
Journal Article
Closed access
PDF file
LJLisa M. James
Lisa M. James
SASamantha L. Anders
Samantha L. Anders
CPCarly K. Peterson
Carly K. Peterson
BEBrian E. Engdahl
Brian E. Engdahl
RKRobert F. Krueger
Robert F. Krueger
AGApostolos P. Georgopoulos
Apostolos P. Georgopoulos

1 September 2018 in EBioMedicine
Verified
Journal Article
Open access
LJLisa M. James
Lisa M. James
SDStacy Dolan
Stacy Dolan
ALArthur C. Leuthold
Arthur C. Leuthold
BEBrian E. Engdahl
Brian E. Engdahl
AGAngeliki Georgopoulos
Angeliki Georgopoulos
AGApostolos P. Georgopoulos
Apostolos P. Georgopoulos
Age-related brain changes are well-documented and influenced by genetics. Extensive research links apolipoprotein E (apoE) to brain function, with the E4 allele serving as a risk factor for brain disease, including Alzheimer's disease, and the E2 allele conferring protection. Recent evidence also supports protective effects of another gene, human leukocyte antigen (HLA) DRB1*13, on brain disease and age-related brain atrophy in cognitively healthy adults. Here we investigated the effects of apoE and HLA DRB1*13 on brain function by examining changes in neural network properties with age in healthy adults. One hundred seventy-eight cognitively healthy women (28-99 y old) underwent a magnetoencephalography scan and provided a blood sample for genetic analysis. Age-related changes in neural network variability in genetic subgroups of DRB1*13 × apoE genotype combinations were assessed using linear regression of network variability against age. For individuals lacking a DRB1*13 allele and/or carrying an apoE4 allele, network variability increased significantly with age. In contrast, no such increase was observed in the presence of DRB1*13 and/or apoE2. These findings extend previous research documenting the protective effect of DRB1*13 on brain structure to include protection against age-related changes in brain function, and demonstrate similar protective effects on neural network variability for either DRB1*13 or apoE2. These protective effects could be due to reduction or elimination of factors known to disrupt brain function, including neuroinflammation and amyloid beta protein. U.S. Department of Veterans Affairs, and University of Minnesota.

3 February 2024 in Vaccines
Verified
Journal Article
Open access
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AGApostolos P. Georgopoulos
Apostolos P. Georgopoulos
LJLisa M. James
Lisa M. James
Vaccination against Bacillus anthracis is the best preventive measure against the development of deadly anthrax disease in the event of exposure to anthrax either as a bioweapon or in its naturally occurring form. Anthrax vaccines, however, have historically been plagued with controversy, particularly related to their safety. Fortunately, recent improvements in anthrax vaccines have been shown to confer protection with reduced short-term safety concerns, although questions about long-term safety remain. Here, we (a) review recent and ongoing advances in anthrax vaccine development, (b) emphasize the need for thorough characterization of current (and future) vaccines, (c) bring to focus the importance of host immunogenetics as the ultimate determinant of successful antibody production and protection, and (d) discuss the need for the systematic, active, and targeted monitoring of vaccine recipients for possible Chronic Multisymptom Illness (CMI).

12 April 2019 in Frontiers in Aging Neuroscience
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Journal Article
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LJLisa M. James
Lisa M. James
AGApostolos P. Georgopoulos
Apostolos P. Georgopoulos
Human Leukocyte Antigen as a Key Factor in Preventing Dementia and Associated Apolipoprotein E4 Risk

5 May 2022 in Journal of Immunological Sciences
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Journal Article
Open access
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AGApostolos P. Georgopoulos
Apostolos P. Georgopoulos
LJLisa M. James
Lisa M. James
Human leukocyte antigen (HLA) genes have been associated with susceptibility and protection against a number of cancers. Here we used an immunogenetic epidemiological approach to evaluate the overall influence of 127 HLA Class I and II alleles on 30 types of cancer. We found a preponderance of protective alleles (negatively correlated with cancer prevalences), especially for HLA Class I. Of the 30 cancers investigated, 13 were associated with mostly protective HLA effects whereas only 2 were associated with mostly susceptibility HLA alleles. Taken together, these findings highlight the broad influence of HLA on cancer and the complexity of HLA-cancer associations.­­

15 March 2017 in Experimental Brain Research
Verified
Journal Article
Closed access
PDF file
LJLisa M. James
Lisa M. James
BEBrian E. Engdahl
Brian E. Engdahl
AGApostolos P. Georgopoulos
Apostolos P. Georgopoulos