Claire Murphy
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Claire Murphy has a total of 131 co-authors. Here are the top co-authors by number of shared publications:
Aaron Jacobson
San Diego State University, San Diego, CA, USA
4 shared publicationsErin Green
San Diego State University/UC San Diego Joint Doctoral Program, San Diego, CA, USA
4 shared publicationsJacquelyn Szajer
SDSU/UCSD Joint Doctoral Program in Clinical Psychology,San Diego, California 92120,USA
3 shared publicationsLori Haase
San Diego State University/University of California San Diego Joint Doctoral Program in Clinical Psychology, CA, USA
3 shared publicationsConner Frank
SDSU/UC San Diego Joint Doctoral Program in Clinical Psychology San Diego California USA
2 shared publications- Conner Frank
SDSU/UCSD Joint Doctoral Program in Clinical Psychology, San Diego CA 92120 USA
2 shared publications
Latest Publications
- Open Access
- 2 December 2025
- Published by Elsevier in Brain Research
- Vol. 1872, 150084
Examining functional connectivity in metabolic syndrome and small vessel disease: A novel approach to understanding olfactory dysfunction and Alzheimer’s disease
- 2 December 2025
- Published by Elsevier in Brain Research
- Vol. 1872, 150084
Open AccessExamining functional connectivity in metabolic syndrome and small vessel disease: A novel approach to understanding olfactory dysfunction and Alzheimer’s disease
- Open Access
- 12 February 2025
- Published by Elsevier in Neurobiology of Aging
- Vol. 149, 44-53
Brain activation in older adults during odor identification is related to ApoE, t-tau/Aβ1–42, and hippocampal volume
- 12 February 2025
- Published by Elsevier in Neurobiology of Aging
- Vol. 149, 44-53
Open AccessBrain activation in older adults during odor identification is related to ApoE, t-tau/Aβ1–42, and hippocampal volume
- Open Access
- 18 May 2024
- Published by Oxford University Press (OUP) in Chemical Senses
- Vol. 49
Integrating the Patient’s Voice into the Research Agenda for Treatment of Chemosensory Disorders
World-wide some 658 million people were infected with COVID-19 and millions suffer from chemosensory impairment associated with long COVID. Current treatments for taste and smell disorders are limited. Involving patients has the potential to catalyze the dynamic exchange and development of new ideas and approaches to facilitate biomedical research and therapeutics. We assessed patients’ perceptions of the efficacy of treatments for chemosensory impairment using an online questionnaire completed by 5,815 people in the U.S. Logistic regression determined variables predictive of reported treatment efficacy for patients aged 18-24, 25-39, 40-60 and 60+ yrs. who were treated with nasal steroids, oral steroids, zinc, nasal rinse, smell training, theophylline, platelet rich plasma, and Omega 3. The most consistent predictor was age, with the majority of those 40-60 and 60+ reporting that nasal steroids, oral steroids, zinc, nasal rinse and smell training were only slightly effective or not effective at all. Many of these treatment strategies target regeneration and immune response, processes compromised by age. Only those under 40 reported more than slight efficacy of steroids or smell training. Findings emphasize the need to include patients of all ages in clinical trials. Older adults with olfactory impairment are at increased risk for Alzheimer’s disease (AD). We speculate that olfactory impairment associated with long COVID introduces the potential for a significant rise in AD. Long COVID-associated chemosensory impairment increases the urgency for translational and clinical research on novel treatment strategies. Suggestions for high priority areas for epidemiological, basic, and clinical research on chemosensory impairment follow.
- 18 May 2024
- Published by Oxford University Press (OUP) in Chemical Senses
- Vol. 49
Open AccessIntegrating the Patient’s Voice into the Research Agenda for Treatment of Chemosensory Disorders
World-wide some 658 million people were infected with COVID-19 and millions suffer from chemosensory impairment associated with long COVID. Current treatments for taste and smell disorders are limited. Involving patients has the potential to catalyze the dynamic exchange and development of new ideas and approaches to facilitate biomedical research and therapeutics. We assessed patients’ perceptions of the efficacy of treatments for chemosensory impairment using an online questionnaire completed by 5,815 people in the U.S. Logistic regression determined variables predictive of reported treatment efficacy for patients aged 18-24, 25-39, 40-60 and 60+ yrs. who were treated with nasal steroids, oral steroids, zinc, nasal rinse, smell training, theophylline, platelet rich plasma, and Omega 3. The most consistent predictor was age, with the majority of those 40-60 and 60+ reporting that nasal steroids, oral steroids, zinc, nasal rinse and smell training were only slightly effective or not effective at all. Many of these treatment strategies target regeneration and immune response, processes compromised by age. Only those under 40 reported more than slight efficacy of steroids or smell training. Findings emphasize the need to include patients of all ages in clinical trials. Older adults with olfactory impairment are at increased risk for Alzheimer’s disease (AD). We speculate that olfactory impairment associated with long COVID introduces the potential for a significant rise in AD. Long COVID-associated chemosensory impairment increases the urgency for translational and clinical research on novel treatment strategies. Suggestions for high priority areas for epidemiological, basic, and clinical research on chemosensory impairment follow.
- Open Access
- 3 May 2024
- Published by Wiley in Brain and Behavior
- Vol. 14 (5) , e3524
The effect of the apolipoprotein E ε4 allele and olfactory function on odor identification networks
Introduction: The combination of apolipoprotein E ε4 (ApoE ε4) status, odor identification, and odor familiarity predicts conversion to mild cognitive impairment (MCI) and Alzheimer's disease (AD).Methods: To further understand olfactory disturbances and AD risk, ApoE ε4 carrier (mean age 76.38 ± 5.21) and ε4 non‐carrier (mean age 76.8 ± 3.35) adults were given odor familiarity and identification tests and performed an odor identification task during fMRI scanning. Five task‐related functional networks were detected using independent components analysis. Main and interaction effects of mean odor familiarity ratings, odor identification scores, and ε4 status on network activation and task‐modulation of network functional connectivity (FC) during correct and incorrect odor identification (hits and misses), controlling for age and sex, were explored using multiple linear regression.Results: Findings suggested that sensory‐olfactory network activation was positively associated with odor identification scores in ε4 carriers with intact odor familiarity. The FC of sensory‐olfactory, multisensory‐semantic integration, and occipitoparietal networks was altered in ε4 carriers with poorer odor familiarity and identification. In ε4 carriers with poorer familiarity, connectivity between superior frontal areas and the sensory‐olfactory network was negatively associated with odor identification scores.Conclusions: The results contribute to the clarification of the neurocognitive structure of odor identification processing and suggest that poorer odor familiarity and identification in ε4 carriers may signal multi‐network dysfunction. Odor familiarity and identification assessment in ε4 carriers may contribute to the predictive value of risk for MCI and AD due to the breakdown of sensory‐cognitive network integration. Additional research on olfactory processing in those at risk for AD is warranted.
- 3 May 2024
- Published by Wiley in Brain and Behavior
- Vol. 14 (5) , e3524
Open AccessThe effect of the apolipoprotein E ε4 allele and olfactory function on odor identification networks
Introduction: The combination of apolipoprotein E ε4 (ApoE ε4) status, odor identification, and odor familiarity predicts conversion to mild cognitive impairment (MCI) and Alzheimer's disease (AD).Methods: To further understand olfactory disturbances and AD risk, ApoE ε4 carrier (mean age 76.38 ± 5.21) and ε4 non‐carrier (mean age 76.8 ± 3.35) adults were given odor familiarity and identification tests and performed an odor identification task during fMRI scanning. Five task‐related functional networks were detected using independent components analysis. Main and interaction effects of mean odor familiarity ratings, odor identification scores, and ε4 status on network activation and task‐modulation of network functional connectivity (FC) during correct and incorrect odor identification (hits and misses), controlling for age and sex, were explored using multiple linear regression.Results: Findings suggested that sensory‐olfactory network activation was positively associated with odor identification scores in ε4 carriers with intact odor familiarity. The FC of sensory‐olfactory, multisensory‐semantic integration, and occipitoparietal networks was altered in ε4 carriers with poorer odor familiarity and identification. In ε4 carriers with poorer familiarity, connectivity between superior frontal areas and the sensory‐olfactory network was negatively associated with odor identification scores.Conclusions: The results contribute to the clarification of the neurocognitive structure of odor identification processing and suggest that poorer odor familiarity and identification in ε4 carriers may signal multi‐network dysfunction. Odor familiarity and identification assessment in ε4 carriers may contribute to the predictive value of risk for MCI and AD due to the breakdown of sensory‐cognitive network integration. Additional research on olfactory processing in those at risk for AD is warranted.
- 1 October 2022
- Published by American Psychological Association (APA) in Neuropsychology
- Vol. 36 (7) , 651-663
Effects of language and acculturation on neurocognitive performance of Japanese Americans.
Despite significant work in African and Hispanic American populations, little information is available regarding performance of Japanese Americans on neuropsychological tests. The aim of this study was to examine the effects of dominant language and acculturation levels on the performance of Japanese Americans on selected neurocognitive tests. Based on their self-identified dominant language, 48 English-dominant speaking (ES) Japanese Americans (Mage = 64.48, SD = 10.52) and 52 Japanese-dominant speaking (JS) Japanese Americans (Mage = 60.17, SD = 11.15) were assessed on a neurocognitive battery. Significant differences in test performance were observed between the groups, with the JS group performing poorer on the measures of naming ability, verbal and olfactory learning/memory, and language, compared to the ES group. Levels of acculturation explained that group difference. The Brief Visuospatial Memory Test-Revised (BVMT-R) showed no group differences, suggesting lack of language proficiency and acculturation biases in this ethnic sample. Within the JS group, self-reported English proficiency and years of education obtained in Japan explained variance in addition to age, education, and gender, in performance on the Boston Naming Test and the Letter Fluency Test, respectively. The present study highlights the need for culturally sensitive evaluation in the neuropsychological assessment of this population. The variability in backgrounds contributed to the variability in performance between and within groups. Factors in addition to age and education, including the effects of primary language and acculturation, warrant consideration when evaluating the neuropsychological performance of Japanese Americans in research and clinical settings. (PsycInfo Database Record (c) 2022 APA, all rights reserved).
- 1 October 2022
- Published by American Psychological Association (APA) in Neuropsychology
- Vol. 36 (7) , 651-663
Effects of language and acculturation on neurocognitive performance of Japanese Americans.
Despite significant work in African and Hispanic American populations, little information is available regarding performance of Japanese Americans on neuropsychological tests. The aim of this study was to examine the effects of dominant language and acculturation levels on the performance of Japanese Americans on selected neurocognitive tests. Based on their self-identified dominant language, 48 English-dominant speaking (ES) Japanese Americans (Mage = 64.48, SD = 10.52) and 52 Japanese-dominant speaking (JS) Japanese Americans (Mage = 60.17, SD = 11.15) were assessed on a neurocognitive battery. Significant differences in test performance were observed between the groups, with the JS group performing poorer on the measures of naming ability, verbal and olfactory learning/memory, and language, compared to the ES group. Levels of acculturation explained that group difference. The Brief Visuospatial Memory Test-Revised (BVMT-R) showed no group differences, suggesting lack of language proficiency and acculturation biases in this ethnic sample. Within the JS group, self-reported English proficiency and years of education obtained in Japan explained variance in addition to age, education, and gender, in performance on the Boston Naming Test and the Letter Fluency Test, respectively. The present study highlights the need for culturally sensitive evaluation in the neuropsychological assessment of this population. The variability in backgrounds contributed to the variability in performance between and within groups. Factors in addition to age and education, including the effects of primary language and acculturation, warrant consideration when evaluating the neuropsychological performance of Japanese Americans in research and clinical settings. (PsycInfo Database Record (c) 2022 APA, all rights reserved).
- Open Access
- 23 October 2021
- Published by MDPI AG in Brain Sciences
- Vol. 11 (11) , 1391
Olfactory Measures as Predictors of Conversion to Mild Cognitive Impairment and Alzheimer’s Disease
Background: Early biomarkers of prodromal Alzheimer’s disease (AD) are critical both to initiate interventions and to choose participants for clinical trials. Odor threshold, odor identification and odor familiarity are impaired in AD. Methods: We investigated the relative abilities of standard screening (MMSE) and olfactory measures to predict transitions from cognitively normal (CN) to mild cognitive impairment (MCI), from CN to AD, and MCI to AD. The archival sample of 497, from the UCSD ADRC, included participants who were CN, MCI, AD and converters to MCI or AD. Apoe ε4 status, a genetic risk factor, was available for 256 participants, 132 were ε4 carriers. A receiver operating characteristic curve (ROC) curve plots the trade-off between sensitivity and specificity. Area under the ROC curve (AUC) was used to determine diagnostic accuracy. Results: Different measures were better predictors at specific stages of disease risk; e.g., odor familiarity, odor identification and the combination showed higher predictive value for converting from MCI to AD in ε4 carriers than the MMSE. Combining odor familiarity and odor identification produced an AUC of 1.0 in ε4 carriers, MMSE alone was 0.58. Conclusions: Olfactory biomarkers show real promise as non-invasive indicators of prodromal AD. The results support the value of combining olfactory measures in assessment of risk for conversion to MCI and to AD.
- 23 October 2021
- Published by MDPI AG in Brain Sciences
- Vol. 11 (11) , 1391
Open AccessOlfactory Measures as Predictors of Conversion to Mild Cognitive Impairment and Alzheimer’s Disease
Background: Early biomarkers of prodromal Alzheimer’s disease (AD) are critical both to initiate interventions and to choose participants for clinical trials. Odor threshold, odor identification and odor familiarity are impaired in AD. Methods: We investigated the relative abilities of standard screening (MMSE) and olfactory measures to predict transitions from cognitively normal (CN) to mild cognitive impairment (MCI), from CN to AD, and MCI to AD. The archival sample of 497, from the UCSD ADRC, included participants who were CN, MCI, AD and converters to MCI or AD. Apoe ε4 status, a genetic risk factor, was available for 256 participants, 132 were ε4 carriers. A receiver operating characteristic curve (ROC) curve plots the trade-off between sensitivity and specificity. Area under the ROC curve (AUC) was used to determine diagnostic accuracy. Results: Different measures were better predictors at specific stages of disease risk; e.g., odor familiarity, odor identification and the combination showed higher predictive value for converting from MCI to AD in ε4 carriers than the MMSE. Combining odor familiarity and odor identification produced an AUC of 1.0 in ε4 carriers, MMSE alone was 0.58. Conclusions: Olfactory biomarkers show real promise as non-invasive indicators of prodromal AD. The results support the value of combining olfactory measures in assessment of risk for conversion to MCI and to AD.
- Open Access
- 6 May 2021
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 16 (5) , e0249348
Metabolic syndrome and cognitive performance across the adult lifespan
Metabolic Syndrome (MetS) is associated with increased rates of mortality and increased risk for developing dementia. Changes in brain structure and cognitive functioning have been reported within the literature. However, research examining cognitive performance in individuals with MetS is limited, inconclusive, and focuses primarily on older cohorts. As such, the effect of MetS on cognitive functioning earlier in the lifespan is unclear. This study aimed to investigate cognitive performance in young, middle-aged, and older adults with multiple metabolic and vascular risk factors in a sample of community dwelling participants (N = 128). Participants were administered a comprehensive neuropsychological battery and self-report measures. As expected, older adults performed more poorly than young and middle-aged adults across most assessments. Relative to controls, individuals with MetS reported greater hunger and disinhibited eating. MetS participants performed more poorly on Color-Word Interference: Inhibition. Additionally, when weight was accounted for, there was a significant relationship between MetS and select executive functioning tasks in middle-aged adults. These findings suggest that aspects of executive functioning may be impaired in MetS and could be further impacted by excess weight in middle-age. Future studies aimed at investigating potential causal relationships between metabolic and vascular risk factors, disinhibited eating, and executive dysfunction may provide insight into effective intervention targets to prevent MetS.
- 6 May 2021
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 16 (5) , e0249348
Open AccessMetabolic syndrome and cognitive performance across the adult lifespan
Metabolic Syndrome (MetS) is associated with increased rates of mortality and increased risk for developing dementia. Changes in brain structure and cognitive functioning have been reported within the literature. However, research examining cognitive performance in individuals with MetS is limited, inconclusive, and focuses primarily on older cohorts. As such, the effect of MetS on cognitive functioning earlier in the lifespan is unclear. This study aimed to investigate cognitive performance in young, middle-aged, and older adults with multiple metabolic and vascular risk factors in a sample of community dwelling participants (N = 128). Participants were administered a comprehensive neuropsychological battery and self-report measures. As expected, older adults performed more poorly than young and middle-aged adults across most assessments. Relative to controls, individuals with MetS reported greater hunger and disinhibited eating. MetS participants performed more poorly on Color-Word Interference: Inhibition. Additionally, when weight was accounted for, there was a significant relationship between MetS and select executive functioning tasks in middle-aged adults. These findings suggest that aspects of executive functioning may be impaired in MetS and could be further impacted by excess weight in middle-age. Future studies aimed at investigating potential causal relationships between metabolic and vascular risk factors, disinhibited eating, and executive dysfunction may provide insight into effective intervention targets to prevent MetS.
- 1 January 2021
- Published by Springer Nature
- p. 145-158
Olfactory Impairment and Neurodegenerative Disorders
- 1 January 2021
- Published by Springer Nature
- p. 145-158
Olfactory Impairment and Neurodegenerative Disorders
- Open Access
- 1 September 2020
- Published by Elsevier in Neurobiology of Aging
- Vol. 93, 25-34
Older, non-demented apolipoprotein ε4 carrier males show hyperactivation and structural differences in odor memory regions: a blood-oxygen-level-dependent and structural magnetic resonance imaging study
- 1 September 2020
- Published by Elsevier in Neurobiology of Aging
- Vol. 93, 25-34
Open AccessOlder, non-demented apolipoprotein ε4 carrier males show hyperactivation and structural differences in odor memory regions: a blood-oxygen-level-dependent and structural magnetic resonance imaging study
- Open Access
- 24 March 2020
- Published by Frontiers Media SA in Frontiers in Neuroscience
- Vol. 14, 173
The Brief Form of the California Odor Learning Test 3
This study explored whether a Brief Form of the California Odor Learning Test 3 (COLT), an olfactory analog of the newly released Brief Form of the California Verbal Learning Test (CVLT 3), could retain the ability of the COLT to detect odor memory dysfunctions observed in normal aging. 52 participants, 28 young (18–30 years old) and 24 old (65 years of age and older), were administered the Brief Forms of the CVLT 3 and the COLT 3. Results indicated poorer performance in immediate and delayed odor recall in older than in younger adults. Poorer odor recognition memory performance in older adults than in younger adults was detected. This study suggests that the Brief Form of the COLT can detect differential odor learning and memory between young and older adults. Thus, the current brief test holds promise as a measure that can be incorporated into studies that demand a brief, non-invasive test capable of detecting impairment in olfactory function.
- 24 March 2020
- Published by Frontiers Media SA in Frontiers in Neuroscience
- Vol. 14, 173
Open AccessThe Brief Form of the California Odor Learning Test 3
This study explored whether a Brief Form of the California Odor Learning Test 3 (COLT), an olfactory analog of the newly released Brief Form of the California Verbal Learning Test (CVLT 3), could retain the ability of the COLT to detect odor memory dysfunctions observed in normal aging. 52 participants, 28 young (18–30 years old) and 24 old (65 years of age and older), were administered the Brief Forms of the CVLT 3 and the COLT 3. Results indicated poorer performance in immediate and delayed odor recall in older than in younger adults. Poorer odor recognition memory performance in older adults than in younger adults was detected. This study suggests that the Brief Form of the COLT can detect differential odor learning and memory between young and older adults. Thus, the current brief test holds promise as a measure that can be incorporated into studies that demand a brief, non-invasive test capable of detecting impairment in olfactory function.