Items where authors include "Dixit, A."

Article

Masoud, S., Wong, K., Pitcher, D. et al. (268 more authors) (2025) Quantifying association of early proteinuria and estimated glomerular filtration rate changes with long-term kidney failure in C3 glomerulopathy and immune-complex membranous proliferative glomerulonephritis using the United Kingdom RaDaR Registry. Kidney International. ISSN 0085-2538

Masoud, S., Wong, K., Pitcher, D. et al. (269 more authors) (2025) Quantifying association of early proteinuria and estimated glomerular filtration rate changes with long-term kidney failure in C3 glomerulopathy and immune-complex membranous proliferative glomerulonephritis using the United Kingdom RaDaR Registry. Kidney International. ISSN 0085-2538 (In Press)

Woods, E. orcid.org/0000-0003-2349-2688, Holmes, N., Denommé‐Pichon, A.S. orcid.org/0000-0002-8986-8222 et al. (14 more authors) (2025) An international ASXL3 natural history study: deep phenotypic analyses including detailed reports of a milder phenotype, novel associations, and clinical recommendations. American Journal of Medical Genetics Part A. e64157. ISSN 1552-4825

Anza-Ramirez, C., Miranda, J.J., Armocida, B. et al. (1444 more authors) (2025) Characterising acute and chronic care needs: insights from the Global Burden of Disease Study 2019. Nature Communications, 16. 4235. ISSN 2041-1723

Bhattacharyay, S., van Leeuwen, F.D., Beqiri, E. et al. (257 more authors) (2025) TILTomorrow today: dynamic factors predicting changes in intracranial pressure treatment intensity after traumatic brain injury. Scientific Reports, 15 (1). 95. ISSN 2045-2322

Copeland, H., Low, K.J., Wynn, S.L. et al. (89 more authors) (2024) Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders. Genetics in Medicine Open, 2. 101864. ISSN 2949-7744

Wong, K., Pitcher, D., Braddon, F. et al. (299 more authors) (2024) Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort. Kidney International Reports, 9 (7). pp. 2067-2083. ISSN 2468-0249

Wong, K., Pitcher, D., Braddon, F. et al. (299 more authors) (2024) Description and cross-sectional analyses of 25,880 adults and children in the UK National Registry of rare kidney diseases cohort. Kidney International Reports, 9 (7). pp. 2067-2083. ISSN 2468-0249

Schumacher, A.E., Kyu, H.H., Aali, A. et al. (1833 more authors) (2024) Global age-sex-specific mortality, life expectancy, and population estimates in 204 countries and territories and 811 subnational locations, 1950–2021, and the impact of the COVID-19 pandemic: a comprehensive demographic analysis for the Global Burden of Disease Study 2021. The Lancet, 403 (10440). pp. 1989-2056. ISSN 0140-6736

Wong, K., Pitcher, D., Braddon, F. et al. (294 more authors) (2024) Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort. The Lancet, 403 (10433). pp. 1279-1289. ISSN 0140-6736

Wong, K., Pitcher, D., Braddon, F. et al. (294 more authors) (2024) Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort. The Lancet, 403 (10433). pp. 1279-1289. ISSN 0140-6736

Boutan, C. orcid.org/0000-0002-1470-1946, Carosi, G. orcid.org/0000-0003-0130-6979, Rosenberg, L.J. orcid.org/0000-0003-0686-0485 et al. (23 more authors) (2023) Axions beyond gen 2. International Journal of Modern Physics A, 38 (33 & 34). 2330012. ISSN 0217-751X

Dawson, J., Engineer, N.D., Cramer, S.C. et al. (19 more authors) (2023) Vagus nerve stimulation paired with rehabilitation for upper limb motor impairment and function after chronic ischemic stroke: subgroup analysis of the randomized, blinded, pivotal, VNS-REHAB device trial. Neurorehabilitation and Neural Repair, 37 (6). pp. 367-373. ISSN 1545-9683

Hayter, M., Lee, A. orcid.org/0000-0003-1378-3123, Dixit, A. et al. (9 more authors) (2023) Experiences of domestic violence prevention interventions and gender equality promotion work: a qualitative study of Nirdhar Groups in rural India [version 1; peer review: awaiting peer review]. F1000Research, 12. 388. ISSN 2046-1402

Valluru, M.K. orcid.org/0000-0001-9156-866X, Chung, N.K.X., Gilchrist, M. et al. (6 more authors) (2023) A founder UMOD variant is a common cause of hereditary nephropathy in the British population. Journal of Medical Genetics, 60 (4). pp. 397-405. ISSN 0022-2593

Howe, E.I., Zeldovich, M., Andelic, N. et al. (263 more authors) (2022) Rehabilitation and outcomes after complicated vs uncomplicated mild TBI: results from the CENTER-TBI study. BMC Health Services Research, 22 (1). 1536. ISSN 1472-6963

Åkerlund, C.A.I., Holst, A., Stocchetti, N. et al. (255 more authors) (2022) Clustering identifies endotypes of traumatic brain injury in an intensive care cohort: a CENTER-TBI study. Critical Care, 26. 228. ISSN 1364-8535

Thomas, I., Dickens, A.M., Posti, J.P. orcid.org/0000-0002-5925-5193 et al. (252 more authors) (2022) Serum metabolome associated with severity of acute traumatic brain injury. Nature Communications, 13. 2545. ISSN 2041-1723

Gröschel, M.I., van den Boom, M., Dixit, A. et al. (5 more authors) (2022) Management of childhood MDR-TB in Europe and Central Asia : report of a Regional WHO meeting. International Journal of Tuberculosis and Lung Disease, 26 (5). pp. 433-440. ISSN 1027-3719

Citerio, G. orcid.org/0000-0002-5374-3161, Robba, C., Rebora, P. et al. (253 more authors) (2021) Management of arterial partial pressure of carbon dioxide in the first week after traumatic brain injury: results from the CENTER-TBI study. Intensive Care Medicine, 47. pp. 961-973. ISSN 0342-4642

Ercole, A., Dixit, A., Nelson, D.W. et al. (11 more authors) (2021) Imputation strategies for missing baseline neurological assessment covariates after traumatic brain injury: A CENTER-TBI study. PLoS ONE, 16 (8). e0253425. ISSN 1932-6203

Muir, K.W., Bulters, D., Willmot, M. et al. (11 more authors) (2020) Intracerebral implantation of human neural stem cells and motor recovery after stroke: multicentre prospective single-arm study (PISCES-2). Journal of Neurology, Neurosurgery & Psychiatry, 91 (4). pp. 396-401. ISSN 0022-3050

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836

Friend, R.M., Anwar, N.H., Dixit, A. et al. (7 more authors) (2016) Re-imagining Inclusive Urban Futures for Transformation. Current Opinion in Environmental Sustainability, 20. pp. 67-72. ISSN 1877-3435

Fitzgerald, T.W., Gerety, S.S., Jones, W.D. et al. (263 more authors) (2015) Large-scale discovery of novel genetic causes of developmental disorders. Nature, 519. pp. 223-228. ISSN 0028-0836

Proceedings Paper

Chung, N.K.X., Valluru, M., Butland, L. et al. (3 more authors) (2022) MO030 : Familial clustering of a rare UMOD variant in undiagnosed hereditary nephropathy suggests the presence of a common ancestral founder mutation. In: Nephrology Dialysis Transplantation. 59th ERA Congress, 19-22 May 2022, Paris, France (and virtual). Oxford University Press .

Preprint

Copeland, H., Low, K.J., Wynn, S. et al. (89 more authors) (2023) Large-scale evaluation of outcomes following a genetic diagnosis in children with severe developmental disorders. [Preprint] (Submitted)