Brandner, S, McAleenan, A S J, Jones, H E, Kernohan, A, Robinson, T, Schmidt, L, Dawson, S, Kelly, C J, Leal, E S, Faulkner, C L, Palmer, A, Wragg, C, Jefferies, S, Vale, L, Higgins, J P T & Kurian, K M 2021, ' Diagnostic accuracy of 1p/19q codeletion tests in oligodendroglioma : a comprehensive meta-analysis based on a Cochrane Systematic Review ', Neuropathology and Applied Neurobiology . https://doi.org/10.1111/nan.12790
Brandner, S, McAleenan, A, Kelly, C, Spiga, F, Cheng, H-Y, Dawson, S, Schmidt, L, Faulkner, C, Wragg, C, Jefferies, S, Higgins, J P T & Kurian, K M 2021, ' MGMT promoter methylation testing to predict overall survival in people with glioblastoma treated with temozolomide : A comprehensive meta-analysis based on a Cochrane Systematic Review ', Neuro-oncology, vol. 23, no. 9, noab105, pp. 1457-1469 . https://doi.org/10.1093/neuonc/noab105 Neuro Oncol Neuro-Oncology
Cochrane Database Syst Rev Mcaleenan, A S J, Kelly, C J, Spiga, F, Kernohan, A, Cheng, H-Y, Dawson, S, Schmidt, L, Robinson, T, Brandner, S, Faulkner, C, Wragg, C, Jefferies, S, Howell, A E, Vale, L, Higgins, J P T & Kurian, K M 2021, ' Prognostic value of test(s) for O6-methylguanine–DNA methyltransferase (MGMT) promoter methylation for predicting overall survival in people with glioblastoma treated with temozolomide ', Cochrane Database of Systematic Reviews, vol. 2021, no. 3, CD013316 . https://doi.org/10.1002/14651858.CD013316.pub2
Ellis, H P, McInerney, C E, Schrimpf, D, Stupnikov, A, Wadsley, M, Wragg, C, White, P, Prise, K M, McArt, D G & Kurian, K M 2019, ' Clinically Actionable Insights into Initial and Matched Recurrent Glioblastomas to Inform Novel Treatment Approaches ', Journal of Oncology, vol. 2019, 4878547 . https://doi.org/10.1155/2019/4878547 Journal of Oncology, Vol 2019 (2019) Journal of Oncology McArt, D, Ellis, H P, McInerney, C, Schrimpf, D, Sahm, F, Stupnikov, A, Wadsley, M, Wragg, C, White, P, Prise, K, McArt, D & Kurian, K M 2019, ' Clinically Actionable Insights into Initial and Matched Recurrent Glioblastomas to Inform Novel Treatment Approaches ', Journal of Oncology . https://doi.org/10.1155/2019/4878547
Hausenloy, D J, Kharbanda, R K, Møller, U K, Ramlall, M, Aarøe, J, Butler, R, Bulluck, H, Clayton, T, Dana, A, Dodd, M, Engstrom, T, Evans, R, Lassen, J F, Christensen, E F, Garcia-Ruiz, J M, Gorog, D A, Hjort, J, Houghton, R F, Ibanez, B, Knight, R, Lippert, F K, Lønborg, J T, Maeng, M, Milasinovic, D, More, R, Nicholas, J M, Jensen, L O, Perkins, A, Radovanovic, N, Rakhit, R D, Ravkilde, J, Ryding, A D, Schmidt, M R, Riddervold, I S, Sørensen, H T, Stankovic, G, Varma, M, Webb, I, Terkelsen, C J, Greenwood, J P, Yellon, D M, Bøtker, H E & CONDI-2/ERIC-PPCI Investigators 2019, ' Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI) : a single-blind randomised controlled trial ', Lancet, vol. 394, no. 10207, pp. 1415-1424 . https://doi.org/10.1016/S0140-6736(19)32039-2 Repisalud Instituto de Salud Carlos III (ISCIII) CONDI-2/ERIC-PPCI Investigators 2019, ' Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI) : a single-blind randomised controlled trial ', Lancet, vol. 394, no. 10207, pp. 1415-1424 . https://doi.org/10.1016/S0140-6736(19)32039-2 Hausenloy, D J, Kharbanda, R K, Møller, U K, Ramlall, M, Aarøe, J, Butler, R, Bulluck, H, Clayton, T, Dana, A, Dodd, M, Engstrom, T, Evans, R, Lassen, J F, Christensen, E F, Garcia-Ruiz, J M, Gorog, D A, Hjort, J, Houghton, R F, Ibanez, B, Knight, R, Lippert, F K, Lønborg, J T, Maeng, M, Milasinovic, D, More, R, Nicholas, J M, Jensen, L O, Perkins, A, Radovanovic, N, Rakhit, R D, Ravkilde, J, Ryding, A D, Schmidt, M R, Sørensen, H T, CONDI-2/ERIC-PPCI Investigators, Junker, A, Madsen, M, Christiansen, E H, Jakobsen, L, Carstensen, S, Kristensen, S D, Sørensen, R, Jensen, S E, Aziz, A, Hansen, H S, Ellert, J, Veien, K, Pedersen, K E, Hansen, K N, Ahlehoff, O, Giebner, M & Andersen, H R 2019, ' Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI) : a single-blind randomised controlled trial ', The Lancet, vol. 394, no. 10207, pp. 1415-1424 . https://doi.org/10.1016/S0140-6736(19)32039-2 Hausenloy, D J, Kharbanda, R K, Møller, U K, Ramlall, M, Aarøe, J, Butler, R, Bulluck, H, Clayton, T, Dana, A, Dodd, M, Engstrom, T, Evans, R, Lassen, J F, Christensen, E F, Garcia-Ruiz, J M, Gorog, D A, Hjort, J, Houghton, R F, Ibanez, B, Knight, R, Lippert, F K, Lønborg, J T, Maeng, M, Milasinovic, D, More, R, Nicholas, J M, Jensen, L O, Perkins, A, Radovanovic, N, Rakhit, R D, Ravkilde, J, Ryding, A D, Schmidt, M R, Riddervold, I S, Sørensen, H T, Stankovic, G, Varma, M, Webb, I, Terkelsen, C J, Greenwood, J P, Yellon, D M, Bøtker, H E, CONDI-2/ERIC-PPCI Investigators, Villadsen, A B, Raungaard, B, Thuesen, L, Christiansen, M K, Freeman, P, Jensen, S E & Skov, C S 2019, ' Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI) : a single-blind randomised controlled trial ', Lancet, vol. 394, no. 10207, pp. 1415-1424 . https://doi.org/10.1016/S0140-6736(19)32039-2
Cochrane Database Syst Rev McAleenan, A, Jones, H E, Kernohan, A, Faulkner, C L, Palmer, A, Dawson, S, Wragg, C, Jefferies, S, Brandner, S, Vale, L, Higgins, J P T & Kurian, K M 2022, ' Diagnostic test accuracy and cost-effectiveness of tests for codeletion of chromosomal arms 1p and 19q in people with glioma ', Cochrane Database of Systematic Reviews, vol. 2022, no. 3, CD013387 . https://doi.org/10.1002/14651858.CD013387.pub2
American Journal of Human Genetics, 104(6), 1210. Cell Press American Journal of Human Genetics, 104, 6, pp. 1210-1222 American Journal of Human Genetics American Journal of Human Genetics, 2019, 104 (6), pp.1210-1222. ⟨10.1016/j.ajhg.2019.03.021⟩ American Journal of Human Genetics, Elsevier (Cell Press), 2019, 104 (6), pp.1210-1222. ⟨10.1016/j.ajhg.2019.03.021⟩ American journal of human genetics, 104(6), 1210-1222. Cell Press American Journal of Human Genetics, 104, 1210-1222 O'Donnell-Luria, A H, Pais, L S, Faundes, V, Wood, J C, Sveden, A, Luria, V, Abou Jamra, R, Accogli, A, Amburgey, K, Anderlid, B M, Azzarello-Burri, S, Basinger, A A, Bianchini, C, Bird, L M, Buchert, R, Carre, W, Ceulemans, S, Charles, P, Cox, H, Culliton, L, Currò, A, Deciphering Developmental Disorders (DDD) Study, Demurger, F, Dowling, J J, Duban-Bedu, B, Dubourg, C, Eiset, S E, Escobar, L F, Ferrarini, A, Haack, T B, Hashim, M, Heide, S, Helbig, K L, Helbig, I, Heredia, R, Héron, D, Isidor, B, Jonasson, A R, Joset, P, Keren, B, Kok, F, Kroes, H, Lavillaureix, A, Lu, X, Maass, S, Maegawa, G H B, Marcelis, C M, Mark, P, Masruha, M, McLaughlin, H, McWalter, K, Melchinger, E, Mercimek-Andrews, S, Nava, C, Pendziwiat, M, Person, R, Ramelli, G P, Ramos, L, Rauch, A, Reavey, C, Renieri, A, Rieß, A, Sanchez-Valle, A, Sattar, S, Saunders, C, Schwarz, N, Smol, T, Srour, M, Steindl, K, Syrbe, S, Taylor, J C, Telegrafi, A, Thiffault, I, Trauner, D, van der Linden Jr., H, van Koningsbruggen, S, Vilard, L, Vogel, I, Vogt, J, Weber, Y G, Wentzensen, I, Widjaja, E, Zak, J, Baxter, S, Banka, S & Rodan, L H 2019, ' Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy ', American Journal of Human Genetics, vol. 104, no. 6, pp. 1210-1222 . https://doi.org/10.1016/j.ajhg.2019.03.021
Cochrane Database Syst Rev McAleenan, A, Howell, A, Kernohan, A, Faulkner, C L, Dawson, S, Wragg, C, Jefferies, S, Brandner, S, Vale, L, Higgins, J P T & Kurian, K M 2019, ' Prognostic value of test(S) for O 6-methylguanine-DNA methyltransferase (MGMT) promoter methylation for predicting overall survival in people with glioblastoma treated with temozolomide ', Cochrane Database of Systematic Reviews, vol. 2019, no. 4, CD013316 . https://doi.org/10.1002/14651858.CD013316
Gorman, K M, Meyer, E, Grozeva, D, Spinelli, E, McTague, A, Sanchis-Juan, A, Carss, K J, Bryant, E, Reich, A, Schneider, A L, Pressler, R M, Simpson, M A, Debelle, G D, Wassmer, E, Morton, J, Sieciechowicz, D, Jan-Kamsteeg, E, Paciorkowski, A R, King, M D, Cross, J H, Poduri, A, Mefford, H C, Scheffer, I E, Haack, T B, McCullagh, G, Deciphering Developmental Disorders Study, NIHR BioResource, UK10K Consortium, Millichap, J J, Carvill, G L, Clayton-Smith, J, Maher, E R, Raymond, F L & Kurian, M A 2019, ' Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia ', American journal of human genetics, vol. 104, no. 5, pp. 948-956 . https://doi.org/10.1016/j.ajhg.2019.03.005 American journal of human genetics, 104(5), 948-956. Cell Press