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Dr Beate St Pourcain

Latest publications

  • Grove, J, Ripke, S, Als, TD, Mattheisen, M, Walters, RK, Won, H, Pallesen, J, Agerbo, E, Andreassen, OA, Anney, R, Awashti, S, Belliveau, R, Bettella, F, Buxbaum, JD, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Christensen, JH, Churchhouse, C, Dellenvall, K, Demontis, D, De Rubeis, S, Devlin, B, Djurovic, S, Dumont, AL, Goldstein, JI, Hansen, CS, Hauberg, ME, Hollegaard, MV, Hope, S, Howrigan, DP, Huang, H, Hultman, CM, Klei, L, Maller, J, Martin, J, Pedersen, CB, Smith, GD, St Pourcain, B & others 2019, ‘Identification of common genetic risk variants for autism spectrum disorder’. Nature Genetics, vol 51., pp. 431-444
  • , , , Demontis, D, Walters, RK, Martin, J, Mattheisen, M, Als, TD, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, JI, Grasby, KL, Grove, J, Gudmundsson, OO, Hansen, CS, Hauberg, ME, Hollegaard, MV, Howrigan, DP, Huang, H, Maller, JB, Martin, AR, Martin, NG, Moran, J, Pallesen, J, Palmer, DS, Pedersen, CB, Pedersen, MG, Poterba, T, Poulsen, JB, Ripke, S, Robinson, EB & others 2019, ‘Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder’. Nature Genetics, vol 51., pp. 63-75
  • Gialluisi, A, Andlauer, TF, Mirza-Schreiber, N, Moll, K, Becker, J, Hoffmann, P, Ludwig, KU, Czamara, D, St Pourcain, B, Brandler, W, Honbolygó, F, Tóth, D, Csépe, V, Huguet, G, Morris, AP, Hulslander, J, Willcutt, EG, DeFries, JC, Olson, RK, Smith, SD, Pennington, BF, Vaessen, A, Maurer, U, Lyytinen, H, Peyrard-Janvid, M, Leppänen, PH, Brandeis, D, Bonte, M, Stein, JF, Talcott, JB, Fauchereau, F, Wilcke, A, Francks, C, Bourgeron, T, Monaco, AP, Ramus, F, Landerl, K, Kere, J, Scerri, TS, Paracchini, S & others 2019, ‘Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia’. Translational Psychiatry, vol 9.
  • Gunz, P, Tilot, AK, Wittfeld, K, Teumer, A, Shapland, CY, van Erp, TG, Dannemann, M, Vernot, B, Neubauer, S, Guadalupe, T, Fernández, G, Brunner, HG, Enard, W, Fallon, J, Hosten, N, Völker, U, Profico, A, Di Vincenzo, F, Manzi, G, Kelso, J, St. Pourcain, B, Hublin, JJ, Franke, B, Pääbo, S, Macciardi, F, Grabe, HJ & Fisher, SE, 2019, ‘Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity’. Current Biology, vol 29., pp. 120-127.e5
  • Haworth, S, Shapland, CY, Hayward, C, Prins, BP, Felix, JF, Medina-Gomez, C, Rivadeneira, F, Wang, C, Ahluwalia, TS, Vrijheid, M, Guxens, M, Sunyer, J, Tachmazidou, I, Walter, K, Iotchkova, V, Jackson, A, Cleal, L, Huffmann, J, Min, JL, Sass, L, Timmers, PR, , Al Turki, S, Anderson, CA, Boustred, C, Curran, S, Day, IN, Evans, DM, Gaunt, TR, Kemp, JP, Lawson, D, Northstone, K, Paternoster, L, Ring, S, Shihab, HA, Shin, SY, Soranzo, N, Tian, J, Tobin, MD, Wain, LV & others 2019, ‘Low-frequency variation in TP53 has large effects on head circumference and intracranial volume’. Nature Communications, vol 10.
  • Howe, LJMS, Lawson, DJ, Davies, NM, St Pourcain, MUB, Lewis, SJ, Smith, GD & Hemani, G, 2019, ‘Genetic evidence for assortative mating on alcohol consumption in the UK Biobank’. Nature Communications.
  • Middeldorp, CM, Felix, JF, Mahajan, A, , , McCarthy, MI, Evans, D, Freathy, R, Lawlor, D, St Pourcain, B, Richmond, R, Sørensen, TIA, Taylor, M, Timpson, N, Tyrrell, J, Uitterlinden, AG, Smith, GD, Kemp, J, Paternoster, L & Granell, R, 2019, ‘The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) Consortia: design, results and future prospects’. European Journal of Epidemiology, vol 34., pp. 279-300
  • Howe, L, Richardson, T, Arathimos, R, Alvizi, L, Passos-Bueno, MR, Stanier, P, Nohr, EA, Ludwig, K, Mangold, E, Knapp, M, Stergiakouli, E, St Pourcain, B, Smith, GD, Sandy, J, Relton, C, Lewis, S, Hemani, G & Sharp, G, 2019, ‘Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate’. Epigenomics, vol 11., pp. 133-145
  • , Verhoef, E, Demontis, D, Burgess, S, Shapland, CY, Dale, PS, Okbay, A, Neale, BM, Faraone, SV, Stergiakouli, E, Smith, GD, Fisher, SE, Børglum, AD, St Pourcain, B, Agerbo, E, Als, TD, Bækved-Hansen, M, Belliveau, R, Børglum, AD, Bybjerg-Grauholm, J, Cerrato, F, Chambert, K, Churchhouse, C, Dalsgaard, S, Daly, MJ, Demontis, D, Dumont, A, Goldstein, J, Grove, J, Hansen, CS, Hauberg, ME, Hollegaard, MV, Hougaard, DM, Howrigan, DP, Huang, H, Maller, J, Martin, AR, Martin, J, Mattheisen, M, Moran, J & others 2019, ‘Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language’. Translational Psychiatry, vol 9., pp. 35
  • , , , Tedja, MS, Wojciechowski, R, Hysi, PG, Eriksson, N, Furlotte, NA, Verhoeven, VJ, Iglesias, AI, Meester-Smoor, MA, Tompson, SW, Fan, Q, Khawaja, AP, Cheng, CY, Höhn, R, Yamashiro, K, Wenocur, A, Grazal, C, Haller, T, Metspalu, A, Wedenoja, J, Jonas, JB, Wang, YX, Xie, J, Mitchell, P, Foster, PJ, Klein, BE, Klein, R, Paterson, AD, Hosseini, SM, Shah, RL, Williams, C, Teo, YY, Tham, YC, Gupta, P, Zhao, W, Shi, Y, Saw, WY, Tai, ES & others 2018, ‘Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error’. Nature Genetics, vol 50., pp. 834-848

View complete publications list in the University of Bristol publications system