Demineralization–remineralization dynamics in teeth and bone by Abou Neel EA, Aljabo A, Strange A, Ibrahim S, Coathup M, Young AM, Bozec L, Mudera V

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A robust clustering algorithm for identifying problematic samples in genome-wide association studies by Bellenguez, C, Strange, A, Freeman, C, Wellcome Trust Case Control Consortium 2, Donnelly, P, Spencer, C

Deep learning for automatic segmentation of the nuclear envelope in electron microscopy data, trained with volunteer segmentations by Spiers, H, Songhurst, H, Nightingale, L, de Folter, J, Hutchings, R, Peddie, CJ, Weston, A, Strange, A, Hindmarsh, S, Lintott, CJ, Collinson, LM, Jones, ML

Self-supervised machine learning to characterise step counts from wrist-worn accelerometers in the UK Biobank by Small, SR, Chan, S, Walmsley, R, von Fritsch, L, Acquah, A, Mertes, G, Feakins, BG, Creagh, A, Strange, A, Matthews, CE, Clifton, DA, Price, AJ, Khalid, S, Bennett, D, Doherty, A

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus. by Blue Mountains Eye Study (BMES), Wellcome Trust Case Control Consortium 2 (WTCCC2), Strange, A, Bellenguez, C, Freeman, C, Pirinen, M, Su, Z, Band, G, Pearson, R, Vukcevic, D, Rautanen, A, Spencer, C, Donnelly, P

A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation by Bramon, E, Pirinen, M, Strange, A, Lin, K, Freeman, C, Bellenguez, C, Su, Z, Band, G, Pearson, R, Vukcevic, D, Langford, C, Deloukas, P, Hunt, S, Gray, E, Dronov, S, Potter, S, Tashakkori-Ghanbaria, A, Edkins, S, Bumpstead, S, Arranz, M, Bakker, S, Bender, S, Bruggeman, R, Cahn, W, Chandler, D

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. by Fakiola, M, Strange, A, Cordell, H, Miller, E, Pirinen, M, Su, Z, Mishra, A, Mehrotra, S, Monteiro, G, Band, G, Bellenguez, C, Dronov, S, Edkins, S, Freeman, C, Giannoulatou, E, Gray, E, Hunt, SE, Lacerda, H, Langford, C, Pearson, R, Pontes, N, Rai, M, Singh, S, Smith, L, Sousa, O

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. by Sawcer, S, Hellenthal, G, Pirinen, M, Spencer, C, Patsopoulos, N, Moutsianas, L, Dilthey, A, Su, Z, Freeman, C, Hunt, SE, Edkins, S, Gray, E, Booth, DR, Potter, S, Goris, A, Band, G, Oturai, AB, Strange, A, Saarela, J, Bellenguez, C, Fontaine, B, Gillman, M, Hemmer, B, Gwilliam, R, Zipp, F

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. by Zhou, K, Bellenguez, C, Spencer, C, Bennett, A, Coleman, R, Tavendale, R, Hawley, SA, Donnelly, L, Schofield, C, Groves, C, Burch, L, Carr, F, Strange, A, Freeman, C, Blackwell, J, Bramon, E, Brown, M, Casas, J, Corvin, A, Craddock, N, Deloukas, P, Dronov, S, Duncanson, A, Edkins, S, Gray, E

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke by Bellenguez, C, Bevan, S, Gschwendtner, A, Spencer, C, Burgess, A, Pirinen, M, Jackson, C, Traylor, M, Strange, A, Su, Z, Band, G, Syme, P, Malik, R, Pera, J, Bo, N, Lemmens, R, Freeman, C, Schanz, R, James, T, Poole, D, Murphy, L, Segal, H, Cortellini, L, Cheng, Y, Woo, D

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes by Zhou, K, Bellenguez, C, Spencer, C, Bennett, A, Coleman, R, Tavendale, R, Hawley, SA, Donnelly, L, Schofield, C, Groves, C, Burch, L, Carr, F, Strange, A, Freeman, C, Blackwell, J, Bramon, E, Brown, M, Casas, J, Corvin, A, Craddock, N, Deloukas, P, Dronov, S, Duncanson, A, Edkins, S, Gray, E

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. by Strange, A, Capon, F, Spencer, C, Knight, J, Weale, M, Allen, M, Barton, A, Band, G, Bellenguez, C, Bergboer, J, Blackwell, J, Bramon, E, Bumpstead, S, Casas, J, Cork, M, Corvin, A, Deloukas, P, Dilthey, A, Duncanson, A, Edkins, S, Estivill, X, Fitzgerald, O, Freeman, C, Giardina, E, Gray, E

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke by Bellenguez, C, Bevan, S, Gschwendtner, A, Spencer, C, Burgess, A, Pirinen, M, Jackson, C, Traylor, M, Strange, A, Su, Z, Band, G, Syme, P, Malik, R, Pera, J, Bo, N, Bo, N, Lemmens, R, Lemmens, R, Freeman, C, Schanz, R, James, T, Poole, D, Murphy, L, Segal, H, Cortellini, L

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. by Bellenguez, C, Bevan, S, Gschwendtner, A, Spencer, C, Burgess, A, Pirinen, M, Jackson, C, Traylor, M, Strange, A, Su, Z, Band, G, Syme, P, Malik, R, Pera, J, Norrving, B, Lemmens, R, Freeman, C, Schanz, R, James, T, Poole, D, Murphy, L, Segal, H, Cortellini, L, Cheng, Y, Woo, D

Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia by Strange, A, Riley, B, Spencer, C, Morris, D, Pirinen, M, O'Dushlaine, C, Su, Z, Maher, B, Freeman, C, Cormican, P, Bellenguez, C, Kenny, E, Band, G, Wormley, B, Donohoe, G, Dilthey, A, Moutsianas, L, Quinn, E, Edkins, S, Judge, R, Coleman, K, Hunt, S, Tropea, D, Roche, S, Cummings, L

A genome-wide asociation study identifies new psoriasis susceptibility loci and an interaction betwEn HLA-C and ERAP1 by Strange, A, Capon, F, Spencer, C, Knight, J, Weale, M, Allen, M, Barton, A, Band, G, Bellenguez, C, Bergboer, J, BlackweL, J, Bramon, E, Bumpstead, S, Casas, J, Cork, M, Corvin, A, Deloukas, P, Dilthey, A, Duncanson, A, Edkins, S, EstiviL, X, Fitzgerald, O, FrEman, C, Giardina, E, Gray, E

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. by Morris, D, Pearson, R, Cormican, P, Kenny, E, O'Dushlaine, C, Perreault, L, Giannoulatou, E, Tropea, D, Maher, B, Wormley, B, Kelleher, E, Fahey, C, Molinos, I, Bellini, S, Pirinen, M, Strange, A, Freeman, C, Thiselton, D, Elves, R, Regan, R, Ennis, S, Dinan, T, McDonald, C, Murphy, K, O'Callaghan, E

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus by Su, Z, Gay, L, Strange, A, Palles, C, Palles, C, Band, G, Whiteman, D, Lescai, F, Langford, C, Nanji, M, Edkins, S, Van Der Winkel, A, Levine, D, Sasieni, P, Bellenguez, C, Howarth, K, Freeman, C, Trudgill, N, Tucker, A, Pirinen, M, Peppelenbosch, M, Van Der Laan, L, Kuipers, E, Drenth, J, Peters, W

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. by Su, Z, Gay, L, Strange, A, Palles, C, Band, G, Whiteman, D, Lescai, F, Langford, C, Nanji, M, Edkins, S, van der Winkel, A, Levine, D, Sasieni, P, Bellenguez, C, Howarth, K, Freeman, C, Trudgill, N, Tucker, A, Pirinen, M, Peppelenbosch, M, van der Laan, L, Kuipers, E, Drenth, J, Peters, W, Reynolds, J

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. by Spencer, C, Plagnol, V, Strange, A, Gardner, M, Paisan-Ruiz, C, Band, G, Barker, R, Bellenguez, C, Bhatia, K, Blackburn, H, Blackwell, J, Bramon, E, Brown, M, Brown, M, Burn, D, Casas, J, Chinnery, P, Clarke, C, Corvin, A, Craddock, N, Deloukas, P, Edkins, S, Evans, J, Freeman, C, Gray, E, Hardy, J, Hudson, G, Hunt, S, Jankowski, J, Langford, C, Lees, A, Markus, H, Mathew, C, McCarthy, M, Morrison, K, Palmer, C, Pearson, J, Peltonen, L, Pirinen, M, Plomin, R, Potter, S, Rautanen, A, Sawcer, S, Su, Z, Trembath, R, Viswanathan, A, Williams, N, Morris, H, Donnelly, P, Wood, N