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: Levinson DF; Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, Calif., USA. dflev@stanford.edu, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM, Wormley B, Lasseter VK, Albus M, Godard-Bauché S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S, Dudbridge F, Holmans PA

مؤلفون مشاركون: Schizophrenia Psychiatric GWAS Consortium

المصدر: The American journal of psychiatry [Am J Psychiatry] 2012 Sep; Vol. 169 (9), pp. 963-73.

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

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

مواضيع طبية MeSH: Genetic Predisposition to Disease/*genetics , Genome-Wide Association Study/*statistics & numerical data , Schizophrenia/*genetics, Black People/genetics ; Case-Control Studies ; DNA Copy Number Variations/genetics ; Female ; Genome-Wide Association Study/methods ; Genotype ; Humans ; Male ; Pedigree ; Polymorphism, Single Nucleotide/genetics ; White People/genetics

المؤلفون: Cubells JF; Department of Human Genetics, Emory University School of Medicine, Atlanta 30322, GA, USA. jcubell@emory.edu, Sun X, Li W, Bonsall RW, McGrath JA, Avramopoulos D, Lasseter VK, Wolyniec PS, Tang YL, Mercer K, Pulver AE, Elston RC

المصدر: Human genetics [Hum Genet] 2011 Nov; Vol. 130 (5), pp. 635-43. Date of Electronic Publication: 2011 Apr 21.

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

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Linkage*, Dopamine beta-Hydroxylase/*genetics , Schizophrenia/*enzymology , Schizophrenia/*genetics, Chromosomes, Human, Pair 19/genetics ; Dopamine beta-Hydroxylase/blood ; Female ; Humans ; Lod Score ; Male ; Polymorphism, Single Nucleotide ; Schizophrenia/blood

المؤلفون: Fallin MD; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA., Lasseter VK, Liu Y, Avramopoulos D, McGrath J, Wolyniec PS, Nestadt G, Liang KY, Chen PL, Valle D, Pulver AE

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] 2011 Mar; Vol. 156 (2), pp. 188-97. Date of Electronic Publication: 2010 Dec 28.

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

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-485X (Electronic) Linking ISSN: 15524841 NLM ISO Abbreviation: Am J Med Genet B Neuropsychiatr Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Linkage* , Polymorphism, Single Nucleotide*, Intercellular Signaling Peptides and Proteins/*genetics , Nerve Tissue Proteins/*genetics , Schizophrenia/*genetics, Case-Control Studies ; Chromosomes, Human, Pair 8/genetics ; Family ; Female ; Humans ; Male ; Meta-Analysis as Topic ; Pedigree ; White People/genetics ; Young Adult

المؤلفون: Li Q; Department of Biostatistics, Bloomberg School of Public Health, Baltimore, Maryland 21205, USA., Fallin MD, Louis TA, Lasseter VK, McGrath JA, Avramopoulos D, Wolyniec PS, Valle D, Liang KY, Pulver AE, Ruczinski I

المصدر: Genetic epidemiology [Genet Epidemiol] 2010 Jul; Vol. 34 (5), pp. 396-406.

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

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8411723 Publication Model: Print Cited Medium: Internet ISSN: 1098-2272 (Electronic) Linking ISSN: 07410395 NLM ISO Abbreviation: Genet Epidemiol Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Jews* , Parents* , Polymorphism, Single Nucleotide*, Schizophrenia/*genetics, Alleles ; Female ; Genetic Testing ; Genotype ; Haplotypes ; Humans ; Logistic Models ; Male ; Models, Genetic ; Phenotype ; Schizophrenia/ethnology

المؤلفون: Ng MY; King's College London, Department of Medical and Molecular Genetics, London, UK., Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, Mowry BJ, Brzustowicz LM, Maziade M, Sklar P, Garver DL, Abecasis GR, Lerer B, Fallin MD, Gurling HM, Gejman PV, Lindholm E, Moises HW, Byerley W, Wijsman EM, Forabosco P, Tsuang MT, Hwu HG, Okazaki Y, Kendler KS, Wormley B, Fanous A, Walsh D, O'Neill FA, Peltonen L, Nestadt G, Lasseter VK, Liang KY, Papadimitriou GM, Dikeos DG, Schwab SG, Owen MJ, O'Donovan MC, Norton N, Hare E, Raventos H, Nicolini H, Albus M, Maier W, Nimgaonkar VL, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe RR, Silverman JM, Bassett AS, Roy MA, Mérette C, Pato CN, Pato MT, Roos JL, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders AR, Duan J, Jazin E, Myles-Worsley M, Karayiorgou M, Lewis CM

المصدر: Molecular psychiatry [Mol Psychiatry] 2009 Aug; Vol. 14 (8), pp. 774-85. Date of Electronic Publication: 2008 Dec 30.

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

بيانات الدورية: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Linkage* , Genetic Predisposition to Disease* , Genome-Wide Association Study*/methods, Chromosomes, Human/*genetics , Schizophrenia/*genetics, Female ; Genome, Human/genetics ; Humans ; Lod Score ; Male ; Pedigree

المؤلفون: Holmans PA; Department of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK., Riley B, Pulver AE, Owen MJ, Wildenauer DB, Gejman PV, Mowry BJ, Laurent C, Kendler KS, Nestadt G, Williams NM, Schwab SG, Sanders AR, Nertney D, Mallet J, Wormley B, Lasseter VK, O'Donovan MC, Duan J, Albus M, Alexander M, Godard S, Ribble R, Liang KY, Norton N, Maier W, Papadimitriou G, Walsh D, Jay M, O'Neill A, Lerer FB, Dikeos D, Crowe RR, Silverman JM, Levinson DF

المصدر: Molecular psychiatry [Mol Psychiatry] 2009 Aug; Vol. 14 (8), pp. 786-95. Date of Electronic Publication: 2009 Feb 17.

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

بيانات الدورية: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5578 (Electronic) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Linkage* , Genetic Predisposition to Disease* , Genome-Wide Association Study*, Schizophrenia/*genetics, Chromosomes, Human ; Genome, Human ; Humans ; Pedigree ; Polymorphism, Single Nucleotide

المؤلفون: McGrath JA; Department of Psychiatry, The Johns Hopkins University School of Medicine, 1820 Lancaster St, Ste 300, Baltimore, MD 21231, USA., Avramopoulos D, Lasseter VK, Wolyniec PS, Fallin MD, Liang KY, Nestadt G, Thornquist MH, Luke JR, Chen PL, Valle D, Pulver AE

المصدر: Archives of general psychiatry [Arch Gen Psychiatry] 2009 Jun; Vol. 66 (6), pp. 591-600.

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

بيانات الدورية: Publisher: American Medical Assn Country of Publication: United States NLM ID: 0372435 Publication Model: Print Cited Medium: Internet ISSN: 1538-3636 (Electronic) Linking ISSN: 0003990X NLM ISO Abbreviation: Arch Gen Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Phenotype* , Schizophrenic Psychology*, Psychotic Disorders/*genetics , Schizophrenia/*genetics, Adult ; Case-Control Studies ; Cross-Cultural Comparison ; Diagnostic and Statistical Manual of Mental Disorders ; Educational Status ; Female ; Genetic Variation ; Humans ; Jews/genetics ; Jews/psychology ; Male ; Middle Aged ; Principal Component Analysis ; Psychiatric Status Rating Scales/statistics & numerical data ; Psychometrics/statistics & numerical data ; Psychotic Disorders/diagnosis ; Psychotic Disorders/psychology ; Schizophrenia/diagnosis ; Social Adjustment

المؤلفون: Chen PL; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA., Avramopoulos D, Lasseter VK, McGrath JA, Fallin MD, Liang KY, Nestadt G, Feng N, Steel G, Cutting AS, Wolyniec P, Pulver AE, Valle D

المصدر: American journal of human genetics [Am J Hum Genet] 2009 Jan; Vol. 84 (1), pp. 21-34.

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 Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Linkage*, Chromosomes, Human, Pair 10/*genetics , Intracellular Signaling Peptides and Proteins/*genetics , Schizophrenia/*genetics, Chromosome Mapping ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Neuregulins ; Polymorphism, Single Nucleotide ; Young Adult

المؤلفون: Avramopoulos D; Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland 21231, USA., Lasseter VK, Fallin MD, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Pulver AE

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2007 Nov; Vol. 9 (11), pp. 745-51.

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

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 12* , Genetic Linkage* , Jews*, Bipolar Disorder/*genetics , Receptors, N-Methyl-D-Aspartate/*genetics, Bipolar Disorder/ethnology ; Chromosome Mapping ; Genetic Heterogeneity ; Humans