Vicki E. Maltby

John Hunter Hospital — Australia

Medicine · Health Sciences

17h-index843citations73works0.82yr avg
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Research Topics

Multiple Sclerosis Research Studies(26), Epigenetics and DNA Methylation(16), Reproductive System and Pregnancy(9), Immune responses and vaccinations(8), MicroRNA in disease regulation(7)

Publications73 total

Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
Genome Medicine·2025· 1 citedOpen Access
Epstein–Barr Virus, Lower Vitamin D, Low Sun Exposure, and <i> <scp>HLA</scp> ‐ <scp>DRB1</scp> *1501 </i> Risk Variant Share Common Epigenetic Pathways Leading to Multiple Sclerosis Onset
Annals of Neurology·2025· 2 citedOpen Access
Menopause Impact on Multiple Sclerosis Disability Progression
JAMA Neurology·2025· 3 citedOpen Access
A neuro-metabolic MRI evaluation of the impact that dietary improvement has on MS: A pilot study
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition·2025
Impact of genetic susceptibility on Multiple Sclerosis immune methylome
Lirias·2025
COVID-19 Vaccine Boosters in People With Multiple Sclerosis
Neurology Neuroimmunology & Neuroinflammation·2025Open Access
Additional file 2 of Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
Figshare·2025Open Access
Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
Figshare·2025Open Access
Additional file 1 of Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
Figshare·2025Open Access
Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
UWA Profiles and Research Repository (University of Western Australia)·2025Open Access
Additional file 1 of Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
Figshare·2025Open Access
Additional file 2 of Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
UWA Profiles and Research Repository (University of Western Australia)·2025Open Access
Multiparametric MRI neuroimaging signatures predict cognitive decline in Multiple Sclerosis: a 5-year longitudinal study
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition·2024
Longitudinal epidemiology of multiple sclerosis over 60 years in Newcastle, Australia: 1961 to 2021
Multiple Sclerosis and Related Disorders·2024· 2 citedOpen Access
CLADIN- CLADribine and INnate immune response in multiple sclerosis – A phase IV prospective study
Clinical Immunology·2024· 4 cited
Investigation of Genomic Mimicry and Multimorbidity in Multiple Sclerosis Using Exome Sequencing
SSRN Electronic Journal·2024Open Access
Multi-modal neuroimaging signatures predict cognitive decline in multiple sclerosis: A 5-year longitudinal study
Multiple Sclerosis and Related Disorders·2023· 12 cited
A longitudinal analysis of brain volume changes in myelin oligodendrocyte glycoprotein antibody‐associated disease
Journal of Neuroimaging·2023· 6 citedOpen Access
Dairy and gluten in disease activity in multiple sclerosis
Multiple Sclerosis Journal - Experimental Translational and Clinical·2023· 4 citedOpen Access
Are we there yet? The holy grail: A biomarker for Multiple Sclerosis
Multiple Sclerosis and Related Disorders·2023
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Frequent Co-authors

Jeannette Lechner‐Scott(38), Rod A. Lea(30), Rodney J. Scott(21), Vilija Jokubaitis(15), Helmut Butzkueven(14), Bruce Taylor(10), Trevor J. Kilpatrick(10), Lotti Tajouri(9), Anneke van der Walt(9), Alexandre Xavier(9), Katherine Sanders(7), Maria Pia Campagna(7), Tomáš Kalinčík(6), Kira Groen(6), Mark Slee(6), Allan G. Kermode(6), Simon Broadley(6), Miles C. Benton(5), Anne‐Louise Ponsonby(5), Sean M. Burnard(4)