Items where authors include "Dixit, A."

Article

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

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

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

Dawson, J., Engineer, N.D., Cramer, S.C. et al. (19 more authors) (2022) 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. ISSN 1545-9683

Valluru, M.K. orcid.org/0000-0001-9156-866X, Chung, N.K.X., Gilchrist, M. et al. (6 more authors) (2022) A founder UMOD variant is a common cause of hereditary nephropathy in the British population. Journal of Medical Genetics. ISSN 0022-2593

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

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)