Items where Author is "Gill, M."

2016

Direk, N. and Williams, S. and Smith, J. A. and Ripke, S. and Air, T. and Amare, A. T. and Amin, N. and Baune, B. T. and Bennett, D. A. and Blackwood, D. H. and Boomsma, D. and Breen, G. and Buttenschon, H. N. and Byrne, E. M. and Borglum, A. D. and Castelao, E. and Cichon, S. and Clarke, T. K. and Cornelis, M. C. and Dannlowski, U. and De Jager, P. L. and Demirkan, A. and Domenici, E. and van Duijn, C. M. and Dunn, E. C. and Eriksson, J. G. and Esko, T. and Faul, J. D. and Ferrucci, L. and Fornage, M. and de Geus, E. and Gill, M. and Gordon, S. D. and Grabe, H. J. and van Grootheest, G. and Hamilton, S. P. and Hartman, C. A. and Heath, A. C. and Hek, K. and Hofman, A. and Homuth, G. and Horn, C. and Jan Hottenga, J. and Kardia, S. L. and Kloiber, S. and Koenen, K. and Kutalik, Z. and Ladwig, K. H. and Lahti, J. and Levinson, D. F. and Lewis, C. M. and Lewis, G. and Li, Q. S. and Llewellyn, D. J. and Lucae, S. and Lunetta, K. L. and MacIntyre, D. J. and Madden, P. and Martin, N. G. and McIntosh, A. M. and Metspalu, A. and Milaneschi, Y. and Montgomery, G. W. and Mors, O. and Mosley, T. H. and Jr., and Murabito, J. M. and Muller-Myhsok, B. and Nothen, M. M. and Nyholt, D. R. and O'Donovan, M. C. and Penninx, B. W. and Pergadia, M. L. and Perlis, R. and Potash, J. B. and Preisig, M. and Purcell, S. M. and Quiroz, J. A. and Raikkonen, K. and Rice, J. P. and Rietschel, M. and Rivera, M. and Schulze, T. G. and Shi, J. and Shyn, S. and Sinnamon, G. C. and Smit, J. H. and Smoller, J. W. and Snieder, H. and Tanaka, T. and Tansey, K. E. and Teumer, A. and Uher, R. and Umbricht, D. and Van der Auwera, S. and Ware, E. B. and Weir, D. R. and Weissman, M. M. and Willemsen, G. and Yang, J. and Zhao, W. and Tiemeier, H. and Sullivan, P. F.. (2016) An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. Biological Psychiatry, 83 (5). pp. 322-329.

2015

Lee, S. H. and Byrne, E. M. and Hultman, C. M. and Kahler, A. and Vinkhuyzen, A. A. and Ripke, S. and Andreassen, O. A. and Frisell, T. and Gusev, A. and Hu, X. and Karlsson, R. and Mantzioris, V. X. and McGrath, J. J. and Mehta, D. and Stahl, E. A. and Zhao, Q. and Kendler, K. S. and Sullivan, P. F. and Price, A. L. and O'Donovan, M. and Okada, Y. and Mowry, B. J. and Raychaudhuri, S. and Wray, N. R. and Schizophrenia Working Group of the Psychiatric Genomics, Consortium and Rheumatoid Arthritis Consortium, International and Schizophrenia Working Group of the Psychiatric Genomics Consorti, Authors and Byerley, W. and Cahn, W. and Cantor, R. M. and Cichon, S. and Cormican, P. and Curtis, D. and Djurovic, S. and Escott-Price, V. and Gejman, P. V. and Georgieva, L. and Giegling, I. and Hansen, T. F. and Ingason, A. and Kim, Y. and Konte, B. and Lee, P. H. and McIntosh, A. and McQuillin, A. and Morris, D. W. and Nothen, M. M. and O'Dushlaine, C. and Olincy, A. and Olsen, L. and Pato, C. N. and Pato, M. T. and Pickard, B. S. and Posthuma, D. and Rasmussen, H. B. and Rietschel, M. and Rujescu, D. and Schulze, T. G. and Silverman, J. M. and Thirumalai, S. and Werge, T. and Agartz, I. and Amin, F. and Azevedo, M. H. and Bass, N. and Black, D. W. and Blackwood, D. H. and Bruggeman, R. and Buccola, N. G. and Choudhury, K. and Cloninger, R. C. and Corvin, A. and Craddock, N. and Daly, M. J. and Datta, S. and Donohoe, G. J. and Duan, J. and Dudbridge, F. and Fanous, A. and Freedman, R. and Freimer, N. B. and Friedl, M. and Gill, M. and Gurling, H. and De Haan, L. and Hamshere, M. L. and Hartmann, A. M. and Holmans, P. A. and Kahn, R. S. and Keller, M. C. and Kenny, E. and Kirov, G. K. and Krabbendam, L. and Krasucki, R. and Lawrence, J. and Lencz, T. and Levinson, D. F. and Lieberman, J. A. and Lin, D. Y. and Linszen, D. H. and Magnusson, P. K. and Maier, W. and Malhotra, A. K. and Mattheisen, M. and Mattingsdal, M. and McCarroll, S. A. and Medeiros, H. and Melle, I. and Milanova, V. and Myin-Germeys, I. and Neale, B. M. and Ophoff, R. A. and Owen, M. J. and Pimm, J. and Purcell, S. M. and Puri, V. and Quested, D. J. and Rossin, L. and Ruderfer, D. and Sanders, A. R. and Shi, J. and Sklar, P. and St Clair, D. and Stroup, T. S. and Van Os, J. and Visscher, P. M. and Wiersma, D. and Zammit, S. and Rheumatoid Arthritis Consortium International, Authors and Bridges, S. L. and Jr., and Choi, H. K. and Coenen, M. J. and de Vries, N. and Dieud, P. and Greenberg, J. D. and Huizinga, T. W. and Padyukov, L. and Siminovitch, K. A. and Tak, P. P. and Worthington, J. and De Jager, P. L. and Denny, J. C. and Gregersen, P. K. and Klareskog, L. and Mariette, X. and Plenge, R. M. and van Laar, M. and van Riel, P.. (2015) New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology, 44 (5). pp. 1706-1721.

2014

Li, M. and Luo, X.-J. and Rietschel, M. and Lewis, C. M. and Mattheisen, M. and Müller-Myhsok, B. and Jamain, S. and Leboyer, M. and Landén, M. and Thompson, P. M. and Cichon, S. and Nöthen, M. M. and Schulze, T. G. and Sullivan, P. F. and Bergen, S. E. and Donohoe, G. and Morris, D. W. and Hargreaves, A. and Gill, M. and Corvin, A. and Hultman, C. and Toga, A. W. and Shi, L. and Lin, Q. and Shi, H. and Gan, L. and Meyer-Lindenberg, A. and Czamara, D. and Henry, C. and Etain, B. and Bis, J. C. and Ikram, M. A. and Fornage, M. and Debette, S. and Launer, L. J. and Seshadri, S. and Erk, S. and Walter, H. and Heinz, A. and Bellivier, F. and Stein, J. L. and Medland, S. E. and Arias Vasquez, A. and Hibar, D. P. and Franke, B. and Martin, N. G. and Wright, M. J. and MooDS Bipolar Consortium, and Swedish Bipolar Study Group, and Alzheimer's Disease Neuroimaging Initiative, and Enigma Consortium, and Charge Consortium, and Su, B.. (2014) Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4). pp. 452-461.

Steinberg, S. and de Jong, S. and Mattheisen, M. and Costas, J. and Demontis, D. and Jamain, S. and Pietiläinen, O. P. H. and Lin, K. and Papiol, S. and Huttenlocher, J. and Sigurdsson, E. and Vassos, E. and Giegling, I. and Breuer, R. and Fraser, G. and Walker, N. and Melle, I. and Djurovic, S. and Agartz, I. and Tuulio-Henriksson, A. and Suvisaari, J. and Lönnqvist, J. and Paunio, T. and Olsen, L. and Hansen, T. and Ingason, A. and Pirinen, M. and Strengman, E. and Group, and Hougaard, D. M. and Ørntoft, T. and Didriksen, M. and Hollegaard, M. V. and Nordentoft, M. and Abramova, L. and Kaleda, V. and Arrojo, M. and Sanjuán, J. and Arango, C. and Etain, B. and Bellivier, F. and Méary, A. and Schürhoff, F. and Szoke, A. and Ribolsi, M. and Magni, V. and Siracusano, A. and Sperling, S. and Rossner, M. and Christiansen, C. and Kiemeney, L. A. and Franke, B. and van den Berg, L. H. and Veldink, J. and Curran, S. and Bolton, P. and Poot, M. and Staal, W. and Rehnstrom, K. and Kilpinen, H. and Freitag, C. M. and Meyer, J. and Magnusson, P. and Saemundsen, E. and Martsenkovsky, I. and Bikshaieva, I. and Martsenkovska, I. and Vashchenko, O. and Raleva, M. and Paketchieva, K. and Stefanovski, B. and Durmishi, N. and Pejovic Milovancevic, M. and Lecic Tosevski, D. and Silagadze, T. and Naneishvili, N. and Mikeladze, N. and Surguladze, S. and Vincent, J. B. and Farmer, A. and Mitchell, P. B. and Wright, A. and Schofield, P. R. and Fullerton, J. M. and Montgomery, G. W. and Martin, N. G. and Rubino, I. A. and van Winkel, R. and Kenis, G. and De Hert, M. and Réthelyi, J. M. and Bitter, I. and Terenius, L. and Jönsson, E. G. and Bakker, S. and van Os, J. and Jablensky, A. and Leboyer, M. and Bramon, E. and Powell, J. and Murray, R. and Corvin, A. and Gill, M. and Morris, D. and O'Neill, F. A. and Kendler, K. and Riley, B. and Wellcome Trust Case Control Consortium, and Craddock, N. and Owen, M. J. and O'Donovan, M. C. and Thorsteinsdottir, U. and Kong, A. and Ehrenreich, H. and Carracedo, A. and Golimbet, V. and Andreassen, O. A. and Børglum, A. D. and Mors, O. and Mortensen, P. B. and Werge, T. and Ophoff, R. A. and Nöthen, M. M. and Rietschel, M. and Cichon, S. and Ruggeri, M. and Tosato, S. and Palotie, A. and St Clair, D. and Rujescu, D. and Collier, D. A. and Stefansson, H. and Stefansson, K.. (2014) Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1). pp. 108-114.

Luo, X.-J. and Li, M. and Huang, L. and Steinberg, S. and Mattheisen, M. and Liang, G. and Donohoe, G. and Shi, Y. and Chen, C. and Yue, W. and Alkelai, A. and Lerer, B. and Li, Z. and Yi, Q. and Rietschel, M. and Cichon, S. and Collier, D. A. and Tosato, S. and Suvisaari, J. and Rujescu, Dan and Golimbet, V. and Silagadze, T. and Durmishi, N. and Milovancevic, M. P. and Stefansson, H. and Schulze, T. G. and Nöthen, M. M. and Chen, C. and Lyne, R. and Morris, D. W. and Gill, M. and Corvin, A. and Zhang, D. and Dong, Q. and Moyzis, R. K. and Stefansson, K. and Sigurdsson, E. and Hu, F. and MooDS SCZ Consortium, and Su, B. and Gan, L.. (2014) Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene. Molecular Psychiatry, 19 (7). pp. 774-783.

2013

Mota, N. R. and Bau, C. H. and Banaschewski, T. and Buitelaar, J. K. and Ebstein, R. P. and Franke, B. and Gill, M. and Kuntsi, J. and Manor, I. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. and Steinhausen, H. -C. and Faraone, S. V. and Asherson, P.. (2013) Association between DRD2/DRD4 interaction and conduct disorder : A potential developmental pathway to alcohol dependence. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 162, H. 6. pp. 546-549.

Bralten, J. and Franke, B. and Waldman, ID. and Rommelse, N. and Hartman, C. and Asherson, P. and Banaschewski, T. and Ebstein, RP. and Gill, M. and Miranda, A. and Oades, RD. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Osterlaan, J. and Sonuga-Barke, EJ. and Steinhausen, H. -C. and Faraone, SV. and Buitelaar, J. and Arias-Vásquez, A.. (2013) Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD. Journal of the American Academy of Child and Adolescent Psychiatry, 52 (11). pp. 1204-1212.

2010

Aebi, M. and Müller, U. C. and Asherson, P. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Eisenberg, J. and Gill, M. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Thompson, M. and Taylor, E. and Faraone, S. V. and Steinhausen, H.-C.. (2010) Predictability of oppositional defiant disorder and symptom dimensions in children and adolescents with ADHD combined type. Psychological medicine, Vol. 40, H. 12. pp. 2089-2100.

Wood, A. C. and Rijsdijk, F. and Johnson, K. A. and Andreou, P. and Albrecht, B. and Arias-Vasquez, A. and Buitelaar, J. K. and McLoughlin, G. and Rommelse, N. N. J. and Sergeant, J. A. and Sonuga-Barke, E. J. S. and Uebel, H. and van der Meere, J. J. and Banaschewski, T. and Gill, M. and Manor, I. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Steinhausen, H. C. and Faraone, S. V. and Asherson, P. and Kuntsi, J.. (2010) The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ. Psychological medicine, Vol. 41, H. 4. pp. 861-871.

2009

Hawi, Z. and Kent, L. and Hill, M. and Anney, R. J. L. and Brookes, K. J. and Barry, E. and Franke, B. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Faraone, S. V. and Asherson, P. and Gill, M.. (2009) ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 150B, H. 1. pp. 97-102.

2008

Asherson, P. and Zhou, K. and Anney, R. J. L. and Franke, B. and Buitelaar, J. and Ebstein, R. and Gill, M. and Altink, M. and Arnold, R. and Boer, F. and Brookes, K. and Buschgens, C. and Butler, L. and Cambell, D. and Chen, W. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Johansson, L. and Lubetzki, I. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Neale, B. and Rijsdijk, F. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Xu, X. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V.. (2008) A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13 (5). pp. 514-521.

Brookes, K. J. and Xu, X. and Anney, R. and Franke, B. and Zhou, K. and Chen, Wai and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Eisenberg, J. and Gill, M. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and Asherson, P.. (2008) Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1519-1523.

Christiansen, H. and Chen, W. and Oades, R. D. and Asherson, P. and Taylor, E. A. and Lasky-Su, J. and Zhou, K. and Banaschewski, T. and Buschgens, C. and Franke, B. and Gabriels, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Psychogiou, L. and Rommelse, N. N. J. and Uebel, H. and Buitelaar, J. and Ebstein, R. P. and Eisenberg, J. and Gill, M. and Miranda, A. and Mulas, F. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. S. and Steinhausen, H.-C. and Thompson, M. and Faraone, S. V.. (2008) Co-transmission of conduct problems with attention-deficit/hyperactivity disorder : familial evidence for a distinct disorder. Journal of neural transmission, Vol. 115, No. 2. pp. 163-175.

Brookes, K. J. and Neale, B. and Xu, X. and Thapar, A. and Gill, M. and Langley, K. and Hawi, Z. and Mill, J. and Taylor, E. and Franke, B. and Chen, W. and Ebstein, R. and Buitelaar, J. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H. C. and Faraone, S. V. and Asherson, P.. (2008) Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 147B (1). pp. 94-99.

Xu, X. and Duman, E. A. and Aysimi, E. and Anney, R. and Brookes, K. and Franke, B. and Zhou, K. and Buschgens, C. and Chen, W. and Christiansen, H. and Eisenberg, J. and Gabriëls, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Rommelse, N. and Thompson, M. and Uebel, H. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Gill, M. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and Asherson, P.. (2008) No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1306-1309.

Xu, X. and Hawi, Z. and Brookes, K. J. and Anney, R. and Bellgrove, M. and Franke, B. and Barry, E. and Chen, W. and Kuntsi, J. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Fitzgerald, M. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Faraone, S. V. and Gill, M. and Asherson, P.. (2008) Replication of a rare protective allele in the noradrenaline transporter gene and ADHD. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1564-1567.

2006

Brookes, K. and Xu, X. and Chen, W. and Zhou, K. and Neale, B. and Lowe, N. and Anney, R. and Aneey, R. and Franke, B. and Gill, M. and Ebstein, R. and Buitelaar, J. and Sham, P. and Campbell, D. and Knight, J. and Andreou, P. and Altink, M. and Arnold, R. and Boer, F. and Buschgens, C. and Butler, L. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Korn-Lubetzki, I. and Johansson, L. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Craig, I. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Kuntsi, J. and Manor, I. and McGuffin, P. and Miranda, A. and Oades, R. D. and Plomin, R. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V. and Asherson, P.. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11 (10). pp. 934-953.