Fellows’ Publications

Fasham, J., Leslie, J.S., Harrison, J.W., et al. No association between SCN9A and monogenic human epilepsy disorders. PLOS. (2020).

Gormley, M., Dudding, T., Sanderson, E. et al. A multivariable Mendelian randomization analysis investigating smoking and alcohol consumption in oral and oropharyngeal cancer. Nat Commun 11, 6071 (2020).

Carnegie R, Zheng J, Sallis HM, et al. Mendelian randomisation for nutritional psychiatry. Lancet Psychiatry. 2020;7(2):208-216.

Clarke SLN, Robertson L, Rice GI, et al. Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype. Pediatr Rheumatol Online J. 2020;18(1):37. Published 2020 May 12.

Ambatipudi S, Sharp GC, Clarke SLN, et al. Assessing the Role of DNA Methylation-Derived Neutrophil-to-Lymphocyte Ratio in Rheumatoid Arthritis. J Immunol Res. 2018;2018:2624981. Published 2018 Aug 14.

Harrison, Judith R. et al. ‘From Polygenic Scores to Precision Medicine in Alzheimer’s Disease: A Systematic Review’. Journal of Alzheimer’s Disease 1 Jan. 2020 : 1271 – 1283.

Harrison, J.. Caseras X. Foley, S. et al. P.3.24 Structural magnetic resonance imaging markers are associated with Alzheimer’s disease pathway-specific polygenic scores. European Neuropsychopharmacology, 2019 29:2, PS697

Borna S, Drobek A, Kralova J, et al. Transmembrane adaptor protein WBP1L regulates CXCR4 signalling and murine haematopoiesis. J Cell Mol Med. 2020;24(2):1980-1992.

Jeffries AR, Maroofian R, Salter CG, et al. Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging. Genome Res. 2019;29(7):1057-1066.

Fasham, J. Arno, G. Lin, S. et al. Delineating the expanding phenotype associated with SCAPER gene mutation. American Journal of Medical Genetics 2019, Part A 179, 1665-1671

Gormley, M. Ali, S, French, K. et al “Where are they now?” A Survey of Former Oral Surgery Trainees. Oral Surgery, 2020, ISSN 1752-2471.

Hughes AE, Hayes MG, Egan AM et al. All thresholds of maternal hyperglycaemia from the WHO 2013 criteria for gestational diabetes identify women with a higher genetic risk for type 2 diabetes [version 1; peer review: awaiting peer review]. Wellcome Open Res 2020, 5:175

Petralia, C.C.T., Manivannan, S., Shastin, D. et al. Effect of Steroid Therapy on Risk of Subsequent Surgery for Neurologically Stable Chronic Subdural Hemorrhage—Retrospective Cohort Study and Literature Review. World Neurosurgery, 2020, 138, Pages e35-e41

Thomas NJ, Lynam AL, Hill AV, et al. Type 1 diabetes defined by severe insulin deficiency occurs after 30 years of age and is commonly treated as type 2 diabetes. Diabetologia. 2019 Jul;62(7):1167-1172.

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