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Marshall, CR, Marshall, CR, Howrigan, DP, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, DS, Antaki, D, Shetty, A, Holmans, PA et al (show 257 more authors) , Pinto, D, Gujral, M, Brandler, WM, Malhotra, D, Wang, Z, Fajarado, KVF, Maile, MS, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, SA, Jr, BRA, Bergen, SE, Ertalan, M, Bevilacqua, E, Bigdeli, TB, Black, DW, Bruggeman, R, Buccola, NG, Buckner, RL, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, MJ, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Cheng, W, Cloninger, CR, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, DeLisi, LE, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, AH, Farh, K-H, Farrell, MS, Frank, J, Franke, L, Freedman, R, Freimer, NB, Friedman, JI, Forstner, AJ, Fromer, M, Genovese, G, Georgieva, L, Gershon, ES, Giegling, I, Giusti-Rodriguez, P, Godard, S, Goldstein, JI, Gratten, J, de Haan, L, Hamshere, ML, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, AM, Henskens, FA, Herms, S, Hirschhorn, JN, Hoffinann, P, Hofman, A, Huang, H, Ikeda, M, Joa, I, Kahler, AK, Kahn, RS, Kalaydjieva, L, Karjalainen, J, Kavanagh, D, Keller, MC, Kelly, BJ, Kennedy, JL, Kim, Y, Knowles, JA, Konte, B, Laurent, C, Lee, P, Lee, SH, Legge, SE, Lerer, B, Levy, DL, Liang, K-Y, Lieberman, J, Lonnqvist, J, Loughland, CM, Magnusson, PKE, Maher, BS, Maier, W, Mallet, J, Mattheisen, M, Mattingsdal, M, McCarley, RW, McDonald, C, McIntosh, AM, Meier, S, Meijer, CJ, Melle, I, Mesholam-Gately, RI, Metspalu, A, Michie, PT, Milani, L, Milanova, V, Mokrab, Y, Morris, DW, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Murphy, KC, Murray, RM, Myin-Germeys, I, Nenadic, I, Nertney, DA, Nestadt, G, Nicodemus, KK, Nisenbaum, L, Nordin, A, O'Callaghan, E, O'Dushlaine, C, Oh, S-Y, Olincy, A, Olsen, L, O'Neill, FA, Van Os, J, Pantelis, C, Papadimitriou, GN, Parkhomenko, E, Pato, MT, Paunio, T, Perkins, DO, Pers, TH, Pietilainen, O, Pimm, J, Pocklington, AJ, Powell, J, Price, A, Pulver, AE, Purcell, SM, Quested, D, Rasmussen, HB, Reichenberg, A, Reimers, MA, Richards, AL, Roffman, JL, Roussos, P, Ruderfer, DM, Salomaa, V, Sanders, AR, Savitz, A, Schall, U, Schulze, TG, Schwab, SG, Scolnick, EM, Scott, RJ, Seidman, LJ, Shi, J, Silverman, JM, Smoller, JW, Soderman, E, Spencer, CCA, Stahl, EA, Strengman, E, Strohmaier, J, Stroup, TS, Suvisaari, J, Svrakic, DM, Szatkiewicz, JP, Thirumalai, S, Tooney, PA, Veijola, J, Visscher, PM, Waddington, J, Walsh, D, Webb, BT, Weiser, M, Wildenauer, DB, Williams, NM, Williams, S, Witt, SH, Wolen, AR, Wormley, BK, Wray, NR, Wu, JQ, Zai, CC, Adolfsson, R, Andreassen, OA, Blackwood, DHR, Bramon, E, Buxbaum, JD, Cichon, S, Collier, DA, Corvin, A, Daly, MJ, Darvasi, A, Domenici, E, Esko, T, Gejman, PV, Gill, M, Gurling, H, Hultman, CM, Iwata, N, Jablensky, AV, Jonsson, EG, Kendler, KS, Kirov, G, Knight, J, Levinson, DF, Li, QS, McCarroll, SA, McQuillin, A, Moran, JL, Mowry, BJ, Nothen, MM, Ophoff, RA, Owen, MJ, Palotie, A, Pato, CN, Petryshen, TL, Posthuma, D, Rietschel, M, Riley, BP, Rujescu, D, Sklar, P, St Clair, D, Walters, JTR, Werge, T, Siillivan, PF, O'Donovan, MC, Scherer, SW, Neale, BM, Sebat, J, CNV, , Grp, SW and Endophenotypes, P (2017) Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. NATURE GENETICS, 49 (1). pp. 27-35.

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Schormair, B, Zhao, C, Bell, S, Tilch, E, Salminen, AV, Putz, B, Dauvilliers, Y, Stefani, A, Hogl, B, Poewe, W et al (show 89 more authors) , Kemlink, D, Sonka, K, Bachmann, CG, Paulus, W, Trenkwalder, C, Oertel, WH, Hornyak, M, Teder-Laving, M, Metspalu, A, Hadjigeorgiou, GM, Polo, O, Fietze, I, Ross, OA, Wszolek, Z, Butterworth, AS, Soranzo, N, Ouwehand, WH, Roberts, DJ, Danesh, J, Allen, RP, Earley, CJ, Ondo, WG, Xiong, L, Montplaisir, J, Gan-Or, Z, Perola, M, Vodicka, P, Dina, C, Franke, A, Tittmann, L, Stewart, AFR, Shah, SH, Gieger, C, Peters, A, Rouleau, GA, Berger, K, Oexle, K, Di Angelantonio, E, Hinds, DA, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Winkelmann, J, Balkau, B, Ducimetiere, P, Eschwege, E, Ranciere, F, Alhenc-Gelas, F, Gallois, Y, Girault, A, Fumeron, F, Marre, M, Roussel, R, Bonnet, F, Bonnefond, A, Cauchi, S, Froguel, P, Cogneau, J, Born, C, Caces, E, Cailleau, M, Lantieri, O, Moreau, JG, Rakotozafy, F, Tichet, J, Vol, S, Agee, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Hinds, DA, Hromatka, BS, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Northover, CA, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Tung, JY, Vacic, V and Wilson, CH (2017) Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. Lancet Neurol, 16 (11). pp. 898-907.

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Gormley, P, Anttila, V, Winsvold, BS, Palta, P, Esko, T, Pers, TH, Farh, KH, Cuenca-Leon, E, Muona, M, Furlotte, NA et al (show 67 more authors) , Kurth, T, Ingason, A, McMahon, G, Ligthart, L, Terwindt, GM, Kallela, M, Freilinger, TM, Ran, C, Gordon, SG, Stam, AH, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, HHH, Lehtimäki, T, Sarin, AP, Wedenoja, J, Hinds, DA, Buring, JE, Schürks, M, Ridker, PM, Hrafnsdottir, MG, Stefansson, H, Ring, SM, Hottenga, JJ, Penninx, BWJH, Färkkilä, M, Artto, V, Kaunisto, M, Vepsäläinen, S, Malik, R, Heath, AC, Madden, PAF, Martin, NG, Montgomery, GW, Kurki, MI, Kals, M, Mägi, R, Pärn, K, Hämäläinen, E, Huang, H, Byrnes, AE, Franke, L, Huang, J, Stergiakouli, E, Lee, PH, Sandor, C, Webber, C, Cader, Z, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Schreiber, S, Meitinger, T, Eriksson, JG, Salomaa, V, Heikkilä, K, Loehrer, E, Uitterlinden, AG, Hofman, A, Van Duijn, CM, Cherkas, L, Pedersen, LM, Stubhaug, A, Nielsen, CS, Männikkö, M, Mihailov, E and Milani, L (2016) Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, 48 (8). pp. 856-866.

Care, A ORCID: 0000-0003-2131-0406, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Olearo, E, Todros, T, Caradeux, J, Goya, M, Palacio, M, Carreras, E and Alfirevic, Z ORCID: 0000-0001-9276-518X (2019) Should phenotype of previous preterm birth influence management of women with short cervix in subsequent pregnancy? Comparison of vaginal progesterone and Arabin pessary. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 53 (4). pp. 529-534.

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Goodfellow, L ORCID: 0000-0002-8111-5007, Verwijs, MC, Care, A ORCID: 0000-0003-2131-0406, Sharp, A ORCID: 0000-0003-3396-7464, Ivandic, J, Poljak, B, Roberts, D, Bronowski, C ORCID: 0000-0001-8089-4021, Gill, AC, Darby, AC ORCID: 0000-0002-3786-6209 et al (show 4 more authors) , Alfirevic, A ORCID: 0000-0002-2801-9817, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Alfirevic, Z and van de Wijgert, JHHM ORCID: 0000-0003-2728-4560 (2021) Vaginal bacterial load in the second trimester is associated with early preterm birth recurrence: a nested case-control study. BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 128 (13). pp. 2061-2072.