المؤلفون: Aj, Schork, Wk, Thompson, Pham P, Torkamani A, Jc, Roddey, Pf, Sullivan, Jr, Kelsoe, Donovan Mc, O., Furberg H, Tobacco and Genetics Consortium, Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium, Nj, Schork, Oa, Andreassen, Am, Dale, Absher D, Agudo A, Almgren P, Ardissino D, Tl, Assimes, Bandinelli S, Barzan L, Bencko V, Benhamou S, Ej, Benjamin, Bernardinelli L, Bis J, Boehnke M, Boerwinkle E, Di, Boomsma, Brennan P, Canova C, Castellsagué X, Chanock S, Chasman D, Di, Conway, Dackor J, Ej, Geus, Duan J, Elosua R, Everett B, Fabianova E, Ferrucci L, Foretova L, Sp, Fortmann, Franceschini N, Frayling T, Furberg C, Pv, Gejman, Groop L, Gu F, Guralnik J, Se, Hankinson, Haritunians T, Healy C, Hofman A, Holcátová I, Dj, Hunter, Sj, Hwang, Jp, Ioannidis, Iribarren C, Au, Jackson, Janout V, Kaprio J, Kim Y, Kjaerheim K, Jw, Knowles, Kraft P, Ladenvall C, Lagiou P, Lanthrop M, Lerman C, Df, Levinson, Levy D, Md, Li, Dy, Lin, Eh, Lips, Lissowska J, Lowry R, Lucas G, Tv, Macfarlane, Maes H, Pm, Mannucci, Mates D, Mauri F, Ja, Mcgovern, Jd, Mckay, McKnight B, Melander O, Pa, Merlini, Milaneschi Y, Kl, Mohlke, Donnell Cj, O., Pare G, Bw, Penninx, Perry J, Posthuma D, Sr, Preis, Psaty B, Quertermous T, Vs, Ramachandran, Richiardi L, Ridker P, Rose J, Rudnai P, Salomaa V, Ar, Sanders, Sm, Schwartz, Shi J, Jh, Smit, Hm, Stringham, Szeszenia-Dabrowska N, Tanaka T, Taylor K, Thacker E, Thornton L, Tiemeier H, Tuomilehto J, Ag, Uitterlinden, Cm, Duijn, Jm, Vink, Vogelzangs N, Bf, Voight, Walter S, Willemsen G, Zaridze D, Znaor A, Akil H, Anjorin A, Backlund L, Ja, Badner, Jd, Barchas, Tb, Barrett, Bass N, Bauer M, Bellivier F, Se, Bergen, Berrettini W, Blackwood D, Cs, Bloss, Breen G, Breuer R, We, Bunner, Burmeister M, Byerley W, Caesar S, Chambert K, Cichon S, St Clair D, Da, Collier, Corvin A, Wh, Coryell, Craddock N, Dw, Craig, Daly M, Day R, Degenhardt F, Djurovic S, Dudbridge F, Hj, Edenberg, Elkin A, Etain B, Ae, Farmer, Ma, Ferreira, Ferrier I, Flickinger M, Foroud T, Frank J, Fraser C, Frisén L, Es, Gershon, Gill M, Gordon-Smith K, Ek, Green, Ta, Greenwood, Grozeva D, Guan W, Gurling H, Ó, Gustafsson, Ml, Hamshere, Hautzinger M, Herms S, Hipolito M, Pa, Holmans, Cm, Hultman, Jamain S, Eg, Jones, Jones I, Jones L, Kandaswamy R, Jl, Kennedy, Gk, Kirov, Dl, Koller, Kwan P, Landén M, Langstrom N, Lathrop M, Lawrence J, Wb, Lawson, Leboyer M, Ph, Lee, Li J, Lichtenstein P, Lin D, Liu C, Fw, Lohoff, Lucae S, Pb, Mahon, Maier W, Ng, Martin, Mattheisen M, Matthews K, Mattingsdal M, Ka, Mcghee, McGuffin P, Mg, Mcinnis, McIntosh A, McKinney R, Aw, Mclean, Fj, Mcmahon, McQuillin A, Meier S, Melle I, Meng F, Pb, Mitchell, Gw, Montgomery, Moran J, Morken G, Dw, Morris, Moskvina V, Muglia P, Tw, Mühleisen, Wj, Muir, Müller-Myhsok B, Rm, Myers, Cm, Nievergelt, Nikolov I, Nimgaonkar V, Mm, Nöthen, Ji, Nurnberger, Ea, Nwulia, O'Dushlaine C, Osby U, Óskarsson H, Mj, Owen, Petursson H, Bs, Pickard, Porgeirsson P, Jb, Potash, Propping P, Sm, Purcell, Quinn E, Raychaudhuri S, Rice J, Rietschel M, Ruderfer D, Schalling M, Af, Schatzberg, Wa, Scheftner, Pr, Schofield, Tg, Schulze, Schumacher J, Mm, Schwarz, Scolnick E, Lj, Scott, Pd, Shilling, Sigurdsson E, Sklar P, En, Smith, Stefansson H, Stefansson K, Steffens M, Steinberg S, Strauss J, Strohmaier J, Szelinger S, Rc, Thompson, Tozzi F, Treutlein J, Jb, Vincent, Sj, Watson, Tf, Wienker, Williamson R, Sh, Witt, Wright A, Xu W, Ah, Young, Pp, Zandi, Zhang P, Zöllner S, Agartz I, Albus M, Alexander M, Rl, Amdur, Amin F, Bitter I, Dw, Black, Ad, Børglum, Ma, Brown, Bruggeman R, Ng, Buccola, Wf, Byerley, Cahn W, Rm, Cantor, Vj, Carr, Sv, Catts, Choudhury K, Cloninger C, Cormican P, Pa, Danoy, Datta S, DeHert M, Demontis D, Dikeos D, Donnelly P, Donohoe G, Duong L, Dwyer S, Fanous A, Fink-Jensen A, Freedman R, Nb, Freimer, Friedl M, Georgieva L, Giegling I, Glenthøj B, Godard S, Golimbet V, de Haan L, Hansen M, Hansen T, Am, Hartmann, Fa, Henskens, Dm, Hougaard, Ingason A, Av, Jablensky, Kd, Jakobsen, Jay M, Eg, Jönsson, Jürgens G, Rs, Kahn, Mc, Keller, Ks, Kendler, Kenis G, Kenny E, Konnerth H, Konte B, Krabbendam L, Krasucki R, Vk, Lasseter, Laurent C, Lencz T, Lerer F, Ky, Liang, Ja, Lieberman, Dh, Linszen, Lönnqvist J, Cm, Loughland, Aw, Maclean, Bs, Maher, Ak, Malhotra, Mallet J, Malloy P, Jj, Mcgrath, McLean DE, Pt, Michie, Milanova V, Mors O, Pb, Mortensen, Bj, Mowry, Myin-Germeys I, Neale B, Da, Nertney, Nestadt G, Nielsen J, Nordentoft M, Norton N, O'Neill F, Olincy A, Olsen L, Ra, Ophoff, Tf, Ørntoft, van Os J, Pantelis C, Papadimitriou G, Cn, Pato, Mt, Pato, Peltonen L, Pickard B, Op, Pietiläinen, Pimm J, Ae, Pulver, Puri V, Digby Quested, Hb, Rasmussen, Jm, Réthelyi, Ribble R, Bp, Riley, Rossin L, Ruggeri M, Rujescu D, Schall U, Sg, Schwab, Rj, Scott, Jm, Silverman, Cc, Spencer, Strange A, Strengman E, Stroup T, Suvisaari J, Terenius L, Thirumalai S, Timm S, Toncheva D, Tosato S, Ej, Den Oord, Veldink J, Pm, Visscher, Walsh D, Ag, Wang, Werge T, Wiersma D, Db, Wildenauer, Hj, Williams, Nm, Williams, van Winkel R, Wormley B.

المساهمون: Biological Psychology, Functional Genomics, Educational Neuroscience, Neuroscience Campus Amsterdam - Brain Mechanisms in Health & Disease, LEARN! - Social cognition and learning, Biophotonics and Medical Imaging, LEARN! - Brain, learning and development, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, EMGO+ - Mental Health, Neuroscience Campus Amsterdam - Brain Imaging Technology, LaserLaB - Biophotonics and Microscopy, ANS - Amsterdam Neuroscience, Adult Psychiatry, Psychiatry, Human genetics, Epidemiology and Data Science, NCA - Brain mechanisms in health and disease, NCA - Neurobiology of mental health, EMGO - Mental health, NCA - Brain imaging technology, Psychiatrie & Neuropsychologie, RS: MHeNs School for Mental Health and Neuroscience, Gibson, Greg, Germeys, Inez, van Winkel, Ruud, De Hert, Marc

المصدر: PLoS genetics, vol 9, iss 4
PLoS Genetics
Schork, AJ; Thompson, WK; Pham, P; Torkamani, A; Roddey, JC; Sullivan, PF; et al.(2013). All SNPs are not created equal: Genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genetics, 9(4). doi: 10.1371/journal.pgen.1003449. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/9xc7s4vr
Schork, A J, Thompson, W K, Pham, P, Torkamani, A, Roddey, J C, Sullivan, P F, Kelsoe, J, O'Donovan, M C, Furberg, H, Absher, D, Agudo, A, Almgren, P, Ardissino, D, Assimes, T L, Bandinelli, S, Barzan, L, Bencko, V, Benhamou, S, Benjamin, E J, Bernardinelli, L, Bis, J, Boehnke, M, Boerwinkle, E, Boomsma, D I, Brennan, P, Canova, C, Castellsagué, X, Chanock, S, Chasman, D I, Conway, D I, Dackor, J, de Geus, E J C, Duan, J, Elosua, R, Everett, B, Fabianova, E, Ferrucci, L, Foretova, L, Fortmann, S P, Franceschini, N, Frayling, T M, Furberg, C, Gejman, P V, Groop, L, Gu, F, Guralnik, J, Hankinson, S E, Haritunians, T, Healy, C, Hofman, A, Holcátová, I, Hunter, D J, Hwang, S J, Ioannidis, J P A, Iribarren, C, Jackson, A U, Janout, V, Kaprio, J, Kim, Y, Kjaerheim, K, Knowles, J W, Kraft, P, Ladenvall, C, Lagiou, P, Lanthrop, M, Lerman, C, Levinson, D F, Levy, D, Li, M D, Lin, D Y, Lips, E H, Lissowska, J, Lowry, R B, Lucas, G, Macfarlane, T V, Maes, H H M, Mannucci, P M, Mates, D, Mauri, F, McGovern, J A, McKay, J D, McKnight, B, Melander, O, Merlini, P A, Milaneschi, Y, Mohlke, K L, O'Donnell, C J, Pare, G, Penninx, B W J H, Perry, J R B, Posthuma, D, Preis, S R, Psaty, B, Quertermous, T, Ramachandran, V S, Richiardi, L, Ridker, P M, Rose, J, Rudnai, P, Salomaa, V, Sanders, A R, Schwartz, S M, Shi, J, Smit, J H, Stringham, H M, Szeszenia-Dabrowska, N, Tanaka, T, Taylor, K, Thacker, E E, Thornton, L, Tiemeier, H, Tuomilehto, J, Uitterlinden, A G, van Duijn, C M, Vink, J M, Vogelzangs, N, Voight, B F, Walter, S, Willemsen, G, Zaridze, D, Znaor, A, Akil, H, Anjorin, A, Backlund, L, Badner, J A, Barchas, J D, Barrett, T, Bass, N, Bauer, M, Bellivier, F, Bergen, S E, Berrettini, W, Blackwood, D, Bloss, C S, Breen, G, Breuer, R, Bunner, W E, Burmeister, M, Byerley, W F, Caesar, S, Chambert, K, Cichon, S, St Clair, D, Collier, D A, Corvin, A, Coryell, W H, Craddock, N, Craig, D W, Daly, M, Day, R, Degenhardt, F, Djurovic, S, Dudbridge, F, Edenberg, H J, Elkin, A, Etain, B, Farmer, A E, Ferreira, M A, Ferrier, I, Flickinger, M, Foroud, T, Frank, J, Fraser, C, Frisén, L, Gershon, E S, Gill, M, Gordon-Smith, K, Green, E K, Greenwood, T A, Grozeva, D, Guan, W, Gurling, H, Gustafsson, O, Hamshere, M L, Hautzinger, M, Herms, S, Hipolito, M, Holmans, P A, Hultman, C M, Jamain, S, Jones, E G, Jones, I, Jones, L, Kandaswamy, R, Kennedy, J L, Kirov, G K, Koller, D L, Kwan, P, Landén, M, Langstrom, N, Lathrop, M, Lawrence, J, Lawson, W B, Leboyer, M, Lee, P H, Li, J, Lichtenstein, P, Lin, D, Liu, C, Lohoff, F W, Lucae, S, Mahon, P B, Maier, W, Martin, N G, Mattheisen, M, Matthews, K, Mattingsdal, M, McGhee, K A, McGuffin, P, McInnis, M G, McIntosh, A, McKinney, R, McLean, A W, McMahon, F J, McQuillin, A, Meier, S, Melle, I, Meng, F, Mitchell, P B, Montgomery, G W, Moran, J, Morken, G, Morris, D W, Moskvina, V, Muglia, P, Mühleisen, T W, Muir, W J, Müller-Myhsok, B, Myers, R M, Nievergelt, C M, Nikolov, I, Nimgaonkar, V L, Nöthen, M M, Nurnberger, J I, Nwulia, E A, O'Dushlaine, C, Osby, U, Óskarsson, H, Owen, M J, Petursson, H, Pickard, B S, Porgeirsson, P, Potash, J B, Propping, P, Purcell, S M, Quinn, E, Raychaudhuri, S, Rice, J, Rietschel, M, Ruderfer, D, Schalling, M, Schatzberg, A F, Scheftner, W A, Schofield, P R, Schulze, T G, Schumacher, J, Schwarz, M M, Scolnick, E, Scott, L J, Shilling, P D, Sigurdsson, E, Sklar, P, Smith, E N, Stefansson, H, Stefansson, K, Steffens, M, Steinberg, S, Strauss, J, Strohmaier, J, Szelinger, S, Thompson, R C, Tozzi, F, Treutlein, J, Vincent, J B, Watson, S J, Wienker, T F, Williamson, R, Witt, S H, Wright, A, Xu, W, Young, A H, Zandi, P P, Zhang, P, Zöllner, S, Agartz, I, Albus, M, Alexander, M, Amdur, R L, Amin, F, Bitter, I, Black, D W, Børglum, A D, Brown, M A, Bruggeman, R, Buccola, N G, Cahn, W, Cantor, R M, Carr, V J, Catts, S V, Choudhury, K, Cloninger, C R, Cormican, P, Danoy, P A, Datta, S, DeHert, M, Demontis, D, Dikeos, D, Donnelly, P, Donohoe, G, Duong, L, Dwyer, S, Fanous, A, Fink-Jensen, A, Freedman, R, Freimer, N B, Friedl, M, Georgieva, L, Giegling, I, Glenthoj, B, Godard, S, Golimbet, V, de Haan, L, Hansen, M, Hansen, T, Hartmann, A M, Henskens, F A, Hougaard, D M, Ingason, A, Jablensky, A V, Jakobsen, K D, Jay, M, Jönsson, E G, Jürgens, G, Kahn, R S, Keller, M C, Kendler, K S, Kenis, G, Kenny, E, Konnerth, H, Konte, B, Krabbendam, L, Krasucki, R, Lasseter, V K, Laurent, C, Lencz, T, Lerer, F B, Liang, K Y, Lieberman, J A, Linszen, D H, Lönnqvist, J, Loughland, C M, Maclean, A W, Maher, B S, Malhotra, A K, Mallet, J, Malloy, P, McGrath, J J, McLean, D E, Michie, P T, Milanova, V, Mors, O, Mortensen, P B, Mowry, B J, Myin-Germeys, I, Neale, B, Nertney, D A, Nestadt, G, Nielsen, J, Nordentoft, M, Norton, N, O'Neill, F, Olincy, A, Olsen, L, Ophoff, R A, Orntoft, T F, van Os, J, Pantelis, C, Papadimitriou, G, Pato, C N, Peltonen, L, Pickard, B, Pietilainen, O P, Pimm, J, Pulver, A E, Puri, V, Quested, D, Rasmussen, H B, Rethelyi, J M, Ribble, R, Riley, B P, Rossin, L, Ruggeri, M, Rujescu, D, Schall, U, Schwab, S G, Scott, R J, Silverman, J M, Spencer, C C, Strange, A, Strengman, E, Stroup, T S, Suvisaari, J, Terenius, L, Thirumalai, S, Timm, S, Toncheva, D, Tosato, S, van den Oord, E J, Veldink, J, Visscher, P M, Walsh, D, Wang, A G, Werge, T, Wiersma, D, Wildenauer, D B, Williams, H J, Williams, N M, van Winkel, R, Wormley, B, Zammit, S, Schork, N J, Andreassen, O A & Dale, A M 2013, ' All SNPs are not created equal: Genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs ', PLoS Genetics, vol. 9, no. 4, e1003449, pp. e1003449 . https://doi.org/10.1371/journal.pgen.1003449
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PLoS Genetics, Vol 9, Iss 4, p e1003449 (2013)
PLoS Genetics, 9(4):e1003449. Public Library of Science
PLoS genetics, 9(4). Public Library of Science
Plos Genetics, 9(4):e1003449. Public Library of Science

مصطلحات موضوعية: False discovery rate, Netherlands Twin Register (NTR), Cancer Research, Linkage disequilibrium, Genome-wide association study, Linkage Disequilibrium, 0302 clinical medicine, 2.1 Biological and endogenous factors, Aetiology, Genetics (clinical), Genetics, 0303 health sciences, Statistics, Genomics, Single Nucleotide, Genome Scans, Tobacco and Genetics Consortium, Functional Genomics, Phenotype, complex trait, Research Article, Bipolar Disorder Psychiatric Genomics Consortium, lcsh:QH426-470, SNP, Single-nucleotide polymorphism, Computational biology, Biostatistics, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, "genome-wide association study", Genome Analysis Tools, Clinical Research, Schizophrenia Psychiatric Genomics Consortium, Genome-Wide Association Studies, Humans, Genetic Predisposition to Disease, Statistical Methods, Polymorphism, Molecular Biology, Genetic Association Studies, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genetic association, Linkage (software), Human Genome, Computational Biology, Human Genetics, Heritability, R1, schizophrenia, lcsh:Genetics, Schizophrenia, Mathematics, 030217 neurology & neurosurgery, Genome-Wide Association Study, Developmental Biology

وصف الملف: application/pdf; Print-Electronic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dbecf9afc07529e710d6735ed9014c9
https://escholarship.org/uc/item/9xc7s4vr

المؤلفون: Marshall CR; Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada., Howrigan DP; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Merico D; Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada., Thiruvahindrapuram B; Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada., Wu W; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Greer DS; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Antaki D; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Shetty A; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Holmans PA; MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.; National Centre for Mental Health, Cardiff University, Cardiff, UK., Pinto D; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA.; Department of Genetics and Genomic Sciences, Seaver Autism Center, Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA., Gujral M; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Brandler WM; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Malhotra D; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA.; Neuroscience Discovery and Translational Area, Pharma Research and Early Development, F. Hoffmann-La Roche, Ltd, Basel, Switzerland., Wang Z; Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada., Fajarado KVF; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Maile MS; Beyster Center for Psychiatric Genomics, University of California, San Diego, La Jolla, California, USA.; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA., Ripke S; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Agartz I; NORMENT, KG Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Department of Psychiatry, Diakonhjemmet Hospital, Oslo, Norway.; Department of Clinical Neuroscience, Psychiatry Section, Karolinska Institutet, Stockholm, Sweden., Albus M; State Mental Hospital, Haar, Germany., Alexander M; Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, California, USA., Amin F; Department of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia, USA.; Department of Psychiatry and Behavioral Sciences, Atlanta Veterans Affairs Medical Center, Atlanta, Georgia, USA., Atkins J; School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, New South Wales, Australia.; Hunter Medical Research Institute, New Lambton, New South Wales, Australia., Bacanu SA; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, Virginia, USA., Belliveau RA Jr; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Bergen SE; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden., Bertalan M; Institute of Biological Psychiatry, Mental Health Centre Sct. Hans, Mental Health Services Copenhagen, Copenhagen, Denmark.; Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Denmark., Bevilacqua E; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Bigdeli TB; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, Virginia, USA., Black DW; Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA., Bruggeman R; Department of Psychiatry, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Buccola NG; School of Nursing, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA., Buckner RL; Center for Brain Science, Harvard University, Cambridge, Massachusetts, USA.; Department of Psychiatry, Massachusetts General Hospital, Boston, Massachusetts, USA.; Athinoula A. Martinos Center, Massachusetts General Hospital, Boston, Massachusetts, USA., Bulik-Sullivan B; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Byerley W; Department of Psychiatry, University of California at San Francisco, San Francisco, California, USA., Cahn W; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, the Netherlands., Cai G; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA.; Department of Human Genetics, Icahn School of Medicine at Mount Sinai, New York, New York, USA., Cairns MJ; School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, New South Wales, Australia.; Schizophrenia Research Institute, Sydney, New South Wales, Australia.; Priority Centre for Translational Neuroscience and Mental Health, University of Newcastle, Newcastle, New South Wales, Australia., Campion D; Centre Hospitalier du Rouvray and INSERM U1079, Faculty of Medicine, Rouen, France., Cantor RM; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA., Carr VJ; Schizophrenia Research Institute, Sydney, New South Wales, Australia.; School of Psychiatry, University of New South Wales, Sydney, New South Wales, Australia., Carrera N; MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Catts SV; Schizophrenia Research Institute, Sydney, New South Wales, Australia.; Department of Psychiatry, Royal Brisbane and Women's Hospital, University of Queensland, Brisbane, Queensland, Australia., Chambert KD; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Cheng W; Department of Computer Science, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Cloninger CR; Department of Psychiatry, Washington University, St. Louis, Missouri, USA., Cohen D; Department of Child and Adolescent Psychiatry, Assistance Publique-Hospitaux de Paris, Pierre and Marie Curie Faculty of Medicine and Institute for Intelligent Systems and Robotics, Paris, France., Cormican P; Neuropsychiatric Genetics Research Group, Department of Psychiatry, Trinity College Dublin, Dublin, Ireland., Craddock N; MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.; National Centre for Mental Health, Cardiff University, Cardiff, UK., Crespo-Facorro B; Instituto de Formación e Investigación Marqués de Valdecilla, University Hospital Marqués de Valdecilla, University of Cantabria, Santander, Spain.; Centro Investigación Biomédica en Red Salud Mental, Madrid, Spain., Crowley JJ; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Curtis D; Department of Psychological Medicine, Queen Mary University of London, London, UK.; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Davidson M; Department of Psychiatry, Sheba Medical Center, Tel Hashomer, Israel., Davis KL; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA., Degenhardt F; Institute of Human Genetics, University of Bonn, Bonn, Germany.; Department of Genomics, Life and Brain Center, Bonn, Germany., Del Favero J; Applied Molecular Genomics Unit, VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium., DeLisi LE; Virginia Boston Health Care System, Brockton, Massachusetts, USA.; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA., Dikeos D; First Department of Psychiatry, University of Athens Medical School, Athens, Greece., Dinan T; Department of Psychiatry, University College Cork, Cork, Ireland., Djurovic S; NORMENT, KG Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway., Donohoe G; Neuropsychiatric Genetics Research Group, Department of Psychiatry, Trinity College Dublin, Dublin, Ireland.; Cognitive Genetics and Therapy Group, School of Psychology and Discipline of Biochemistry, National University of Ireland Galway, Galway, Ireland., Drapeau E; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA., Duan J; Department of Psychiatry and Behavioral Sciences, NorthShore University HealthSystem, Evanston, Illinois, USA.; Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois, USA., Dudbridge F; Department of Non-Communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK., Eichhammer P; Department of Psychiatry, University of Regensburg, Regensburg, Germany., Eriksson J; Folkhälsan Research Center and Biomedicum Helsinki, Helsinki, Finland.; National Institute for Health and Welfare, Helsinki, Finland.; Department of General Practice, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland., Escott-Price V; MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK., Essioux L; Translational Technologies and Bioinformatics, Pharma Research and Early Development, F. 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مؤلفون مشاركون: Psychosis Endophenotypes International Consortium, CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium

المصدر: Nature genetics [Nat Genet] 2017 Jan; Vol. 49 (1), pp. 27-35. Date of Electronic Publication: 2016 Nov 21.

نوع المنشور: Comparative Study; Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study*, DNA Copy Number Variations/*genetics , Genetic Loci/*genetics , Genetic Markers/*genetics , Schizophrenia/*genetics, Case-Control Studies ; Female ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Risk Factors

المؤلفون: Ripke S; 1] Analytical and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, USA. [2] Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA. [3]., O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O'Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT, Levinson DF, Gejman PV, Kendler KS, Laurent C, Mowry BJ, O'Donovan MC, Owen MJ, Pulver AE, Riley BP, Schwab SG, Wildenauer DB, Dudbridge F, Holmans P, Shi J, Albus M, Alexander M, Campion D, Cohen D, Dikeos D, Duan J, Eichhammer P, Godard S, Hansen M, Lerer FB, Liang KY, Maier W, Mallet J, Nertney DA, Nestadt G, Norton N, O'Neill FA, Papadimitriou GN, Ribble R, Sanders AR, Silverman JM, Walsh D, Williams NM, Wormley B, Arranz MJ, Bakker S, Bender S, Bramon E, Collier D, Crespo-Facorro B, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Lawrie S, Lewis CM, Lin K, Linszen DH, Mata I, McIntosh A, Murray RM, Ophoff RA, Powell J, Rujescu D, Van Os J, Walshe M, Weisbrod M, Wiersma D, Donnelly P, Barroso I, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin AP, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Spencer CC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson RD, Strange A, Su Z, Vukcevic D, Donnelly P, Langford C, Hunt SE, Edkins S, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Potter SC, Ravindrarajah R, Ricketts M, Tashakkori-Ghanbaria A, Waller MJ, Weston P, Widaa S, Whittaker P, Barroso I, Deloukas P, Mathew CG, Blackwell JM, Brown MA, Corvin AP, McCarthy MI, Spencer CC, Bramon E, Corvin AP, O'Donovan MC, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF

مؤلفون مشاركون: Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2

المصدر: Nature genetics [Nat Genet] 2013 Oct; Vol. 45 (10), pp. 1150-9. Date of Electronic Publication: 2013 Aug 25.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Genome-Wide Association Study*, Schizophrenia/*genetics, Case-Control Studies ; Female ; Humans ; Male ; Polymorphism, Single Nucleotide ; Sweden

المؤلفون: Holliday EG; correspondence and reprint requests to Prof. Mowry; bryan_mowry@qcmhr.uq.edu.au., Nyholt DR, Tirupati S, John S, Ramachandran P, Ramamurti M, Ramadoss AJ, Jeyagurunathan A, Kottiswaran S, Smith HJ, Filippich C, Nertney DA, Nancarrow DJ, Hayward NK, Watkins WS, Jorde LB, Thara R, Mowry BJ

المصدر: The American journal of psychiatry [Am J Psychiatry] 2009 Feb; Vol. 166 (2), pp. 206-15. Date of Electronic Publication: 2008 Oct 01.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0370512 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1535-7228 (Electronic) Linking ISSN: 0002953X NLM ISO Abbreviation: Am J Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Mapping*, Chromosomes, Human, Pair 1/*genetics , Schizophrenia/*genetics, Adult ; Alleles ; Consanguinity ; Cyclic Nucleotide Phosphodiesterases, Type 4/genetics ; Female ; Genotype ; Humans ; India ; Lod Score ; Male ; Microsatellite Repeats/genetics ; Middle Aged ; Polymorphism, Single Nucleotide/genetics ; Schizophrenia/diagnosis ; Schizophrenia/ethnology

المؤلفون: Sanders AR; Department of Psychiatry and Behavioural Sciences, Evanston Northwestern Healthcare Research Institute, Evanston, IL 60201-3137, USA., Duan J, Levinson DF, Shi J, He D, Hou C, Burrell GJ, Rice JP, Nertney DA, Olincy A, Rozic P, Vinogradov S, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Crowe RR, Cloninger CR, Martinez M, Gejman PV

المصدر: The American journal of psychiatry [Am J Psychiatry] 2008 Apr; Vol. 165 (4), pp. 497-506. Date of Electronic Publication: 2008 Jan 15.

نوع المنشور: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Psychiatric Association Country of Publication: United States NLM ID: 0370512 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-953X (Print) Linking ISSN: 0002953X NLM ISO Abbreviation: Am J Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Genotype*, Schizophrenia/*genetics , White People/*genetics, Adolescent ; Adult ; Catechol O-Methyltransferase/genetics ; Catechol O-Methyltransferase/metabolism ; Chromosome Mapping/statistics & numerical data ; Female ; Follow-Up Studies ; Genetic Predisposition to Disease/genetics ; Genetic Variation/genetics ; Haplotypes/genetics ; Humans ; Linkage Disequilibrium/genetics ; Male ; Polymorphism, Single Nucleotide ; Psychotic Disorders/genetics ; Psychotic Disorders/metabolism ; Quality Control ; Schizophrenia/metabolism

المؤلفون: Holliday EG; Queensland Centre for Mental Health Research, The Park, Centre for Mental Health, Wacol, Queensland, Australia. lizh@qcmhr.uq.edu.au, Handoko HY, James MR, McGrath JJ, Nertney DA, Tirupati S, Thara R, Levinson DF, Hayward NK, Mowry BJ, Nyholt DR

المصدر: Twin research and human genetics : the official journal of the International Society for Twin Studies [Twin Res Hum Genet] 2006 Aug; Vol. 9 (4), pp. 531-9.

نوع المنشور: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Cambridge University Press Country of Publication: England NLM ID: 101244624 Publication Model: Print Cited Medium: Print ISSN: 1832-4274 (Print) Linking ISSN: 18324274 NLM ISO Abbreviation: Twin Res Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Alleles* , Genetic Predisposition to Disease* , Linkage Disequilibrium* , Polymorphism, Single Nucleotide*, Carrier Proteins/*genetics , Schizophrenia/*genetics, Australia ; Case-Control Studies ; Dysbindin ; Dystrophin-Associated Proteins ; Female ; Haplotypes ; Humans ; India ; Male ; Risk Factors ; White People

المؤلفون: Suarez BK; Department of Psychiatry and Genetics, Washington University, St. Louis, MO, USA., Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV

المصدر: American journal of human genetics [Am J Hum Genet] 2006 Feb; Vol. 78 (2), pp. 315-33. Date of Electronic Publication: 2006 Jan 03.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease*, Chromosomes, Human, Pair 11/*genetics , Chromosomes, Human, Pair 8/*genetics , Schizophrenia/*genetics, Adolescent ; Adult ; Black or African American/genetics ; Chromosome Mapping ; Female ; Genetic Linkage ; Genome, Human ; Humans ; Male ; Nerve Tissue Proteins/genetics ; Neuregulin-1 ; Pedigree ; White People/genetics

المؤلفون: Handoko HY; Queensland Centre for Mental Health Research, The Park, Centre for Mental Health, Wacol, QLD, Australia., Nyholt DR, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ

المصدر: Molecular psychiatry [Mol Psychiatry] 2005 Jun; Vol. 10 (6), pp. 589-97.

نوع المنشور: Clinical Trial; Controlled Clinical Trial; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print ISSN: 1359-4184 (Print) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Catechol O-Methyltransferase/*genetics , Chromosomes, Human, Pair 22/*genetics , Linkage Disequilibrium/*genetics , Polymorphism, Single Nucleotide/*genetics , Schizophrenia/*enzymology , Schizophrenia/*genetics, Amino Acid Substitution/genetics ; Australia ; Family ; Female ; Genetic Predisposition to Disease/genetics ; Humans ; Male ; Pedigree ; Risk Factors ; White People/genetics

المؤلفون: Mowry BJ; Queensland Centre for Mental Health Research, The Park -- Centre for Mental Health, Wacol, Queensland, Australia. bryan_mowry@qcsr.uq.edu.au, Holmans PA, Pulver AE, Gejman PV, Riley B, Williams NM, Laurent C, Schwab SG, Wildenauer DB, Bauché S, Owen MJ, Wormley B, Sanders AR, Nestadt G, Liang KY, Duan J, Ribble R, Norton N, Soubigou S, Maier W, Ewen-White KR, DeMarchi N, Carpenter B, Walsh D, Williams H, Jay M, Albus M, Nertney DA, Papadimitriou G, O'Neill A, O'Donovan MC, Deleuze JF, Lerer FB, Dikeos D, Kendler KS, Mallet J, Silverman JM, Crowe RR, Levinson DF

المصدر: Molecular psychiatry [Mol Psychiatry] 2004 Aug; Vol. 9 (8), pp. 784-95.

نوع المنشور: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print ISSN: 1359-4184 (Print) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 22/*genetics , Schizophrenia/*genetics, Chromosome Mapping ; Genetic Markers ; Genetic Predisposition to Disease ; Humans

المؤلفون: Handoko HY; Queensland Centre for Schizophrenia Research, The Park, Centre for Mental Health, Wacol, Queensland, Australia., Nancarrow DJ, Hayward NK, Ohaeri JU, Aghanwa H, McGrath JJ, Levinson DF, Johns C, Walters MK, Nertney DA, Srinivasan TN, Thara R, Mowry BJ

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2003 Aug 15; Vol. 121B (1), pp. 1-6.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print Cited Medium: Print ISSN: 1552-4841 (Print) Linking ISSN: 15524841 NLM ISO Abbreviation: Am J Med Genet B Neuropsychiatr Genet Subsets: MEDLINE

مواضيع طبية MeSH: Haplotypes*, Schizophrenia/*genetics , Tumor Necrosis Factor-alpha/*genetics, Australia ; Fiji ; Humans ; Promoter Regions, Genetic