نتائج البحث - "Chris C. A. Spencer"

المساهمون: Perceptual and Cognitive Neuroscience (PCN), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Clinical Cognitive Neuropsychiatry Research Program (CCNP), Stem Cell Aging Leukemia and Lymphoma (SALL), Psychiatrie & Neuropsychologie, RS: MHeNs - R2 - Mental Health, MUMC+: Hersen en Zenuw Centrum (3), MUMC+: MA Psychiatrie (3), Complex Trait Genetics, Amsterdam Neuroscience - Complex Trait Genetics, APH - Mental Health, ANS - Complex Trait Genetics, Adult Psychiatry, Other departments, Marshall, Christian R, Howrigan, Daniel P, Merico, Daniele, Thiruvahindrapuram, Bhooma, Lee, S Hong, Sebat, Jonathan, Psychosis Endophenotypes International Consortium, CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium, CNV, Schizophrenia Working Grp, Psychosis Endophenotypes, Rehabilitation Medicine, Child and Adolescent Psychiatry / Psychology

المصدر: Nature Genetics, 49(1), 27-35. Nature Publishing Group
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Marshall, Christian R; Howrigan, Daniel P; Merico, Daniele; Thiruvahindrapuram, Bhooma; Wu, Wenting; Greer, Douglas S; et al.(2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.. Nature genetics, 49(1), 27-35. doi: 10.1038/ng.3725. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/7jq1c9p6
Nature genetics, 49(1), 27-35. Nature Publishing Group
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fajarado, K V F, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W, Cloninger, C R, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Posthuma, D & Psychosis Endophenotypes International Consortium 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fuentes Fajarado, K V, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W, Cloninger, C R, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, J J, Curtis, D, Davidson, M, Davis, K L, Degenhardt, F, Del Favero, J, DeLisi, L E, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, A H, Farh, K H, Farrell, M S, Frank, J, Franke, L, Freedman, R, Freimer, N B, Friedman, J I, Forstner, A J, Fromer, M, Genovese, G, Georgieva, L, Gershon, E S, Giegling, I, Giusti-Rodríguez, P, Godard, S, Goldstein, J I, Gratten, J, De Haan, L, Hamshere, M L, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, A M, Henskens, F A, Herms, S, Hirschhorn, J N, Hoffmann, P, Hofman, A, Huang, H, Ikeda, M, Joa, I, Kähler, A K, Kahn, R S, Kalaydjieva, L, Karjalainen, J, Kavanagh, D, Keller, M C, Kelly, B J, Kennedy, J L, Kim, Y, Knowles, J A, Konte, B, Laurent, C, Lee, P, Lee, S H, Legge, S E, Lerer, B, Levy, D L, Liang, K Y, Lieberman, J, Lönnqvist, J, Loughland, C M, Magnusson, P K E, Maher, B S, Maier, W, Mallet, J, Mattheisen, M, Mattingsdal, M, McCarley, R W, McDonald, C, McIntosh, A M, Meier, S, Meijer, C J, Melle, I, Mesholam-Gately, R I, Metspalu, A, Michie, P T, Milani, L, Milanova, V, Mokrab, Y, Morris, D W, Müller-Myhsok, B, Murphy, K C, Murray, R M, Myin-Germeys, I, Nenadic, I, Nertney, D A, Nestadt, G, Nicodemus, K K, Nisenbaum, L, Nordin, A, O'Callaghan, E, O'Dushlaine, C, Oh, S Y, Olincy, A, Olsen, L, O'Neill, F A, Van Os, J, Pantelis, C, Papadimitriou, G N, Parkhomenko, E, Pato, M T, Paunio, T, Perkins, D O, Pers, T H, Pietiläinen, O, Pimm, J, Pocklington, A J, Powell, J, Price, A, Pulver, A E, Purcell, S M, Quested, D, Rasmussen, H B, Reichenberg, A, Reimers, M A, Richards, A L, Roffman, J L, Roussos, P, Ruderfer, D M, Salomaa, V, Sanders, A R, Savitz, A, Schall, U, Schulze, T G, Schwab, S G, Scolnick, E M, Scott, R J, Seidman, L J, Shi, J, Silverman, J M, Smoller, J W, Söderman, E, Spencer, C C A, Stahl, E A, Strengman, E, Strohmaier, J, Stroup, T S, Suvisaari, J, Svrakic, D M, Szatkiewicz, J P, Thirumalai, S, Tooney, P A, Veijola, J, Visscher, P M, Waddington, J, Walsh, D, Webb, B T, Weiser, M, Wildenauer, D B, Williams, N M, Williams, S, Witt, S H, Wolen, A R, Wormley, B K, Wray, N R, Wu, J Q, Zai, C C, Adolfsson, R, Andreassen, O A, Blackwood, D H R, Bramon, E, Buxbaum, J D, Cichon, S, Collier, D A, Corvin, A, Daly, M J, Darvasi, A, Domenici, E, Esko, T, Gejman, P V, Gill, M, Gurling, H, Hultman, C M, Iwata, N, Jablensky, A V, Jönsson, E G, Kendler, K S, Kirov, G, Knight, J, Levinson, D F, Li, Q S, McCarroll, S A, McQuillin, A, Moran, J L, Mowry, B J, Nöthen, M M, Ophoff, R A, Owen, M J, Palotie, A, Pato, C N, Petryshen, T L, Posthuma, D, Rietschel, M, Riley, B P, Rujescu, D, Sklar, P, St Clair, D, Walters, J T R, Werge, T, Sullivan, P F, O'Donovan, M C, Scherer, S W, Neale, B M & Sebat, J 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
NATURE GENETICS
Nature genetics
Marshall, C R, Howrigan, D P, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, D S, Antaki, D, Shetty, A, Holmans, P A, Pinto, D, Gujral, M, Brandler, W M, Malhotra, D, Wang, Z, Fajarado, K V F, Maile, M S, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, S-A, Belliveau, R A, Bergen, S E, Bertalan, M, Bevilacqua, E, Bigdeli, T B, Black, D W, Bruggeman, R, Buccola, N G, Buckner, R L, Bulik-Sullivan, B K, Byerley, W F, Cahn, W, Cai, G, Cairns, M J, Campion, D, Cantor, R M, Carr, V J, Carrera, N, Catts, S V, Chambert, K D, Cheng, W-T, Cloninger, C R, Cohen, D J, Cormican, P, McIntosh, A & Nicodemus, K & Blackwood, D H R 2017, ' Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects ', Nature Genetics, vol. 49, no. 1, pp. 27-35 . https://doi.org/10.1038/ng.3725
Nature Genetics

مصطلحات موضوعية: 0301 basic medicine, Male, 16P11.2, Duplication, Autism, Rearrangement, Genome-wide association study, Copy number variant, Gene, Medical and Health Sciences, 0302 clinical medicine, DUPLICATIONS, Risk Factors, Gene duplication, Genotype, Disorder, Copy-number variation, Genetics, Genetics & Heredity, RISK, copy number variation, REARRANGEMENTS, Biological Sciences, 16p11.2, 3. Good health, Phenotype, Female, Risk, CNVS, Genetic Markers, genetic etiology, CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium, DNA Copy Number Variations, DISORDERS, CNV, Non-allelic homologous recombination, PHENOTYPES, Biology, 03 medical and health sciences, SDG 3 - Good Health and Well-being, genomics, Journal Article, Humans, Comparative Study, Genetic Predisposition to Disease, AUTISM, Psychosis Endophenotypes International Consortium, MUTATIONS, Case-control study, Odds ratio, R1, GENE, 030104 developmental biology, genetics research, Genetic marker, Genetic Loci, Case-Control Studies, Mutation, Schizophrenia, Human medicine, 030217 neurology & neurosurgery, Developmental Biology, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cba303cd36092c93e5255ed7f9f5934
https://hdl.handle.net/1765/108379

Find this article in full text from ProQuest

10

Author response: Interferon lambda 4 impacts the genetic diversity of hepatitis C virus

المؤلفون: Eleanor Barnes, Nicole Zitzmann, Vanessa M. Cowton, P Simmonds, John F. Dillon, Paolo Piazza, J McLauchlan, P Troke, Sharon J. Hutchinson, E Barnes, C Holmes, Peter Simmonds, Jonathan K. Ball, Chris C. A. Spencer, S Smith, Elihu Aranday-Cortes, Paul Klenerman, David Bonsall, C Gore, Emma Hudson, Natasha K. Martin, Salim I. Khakoo, G R Foster, Amy Trebes, John McLauchlan, William L. Irving, Christopher Holmes, E Hudson, Neil Guha, Jane A. McKeating, P Shaw, E Thomson, Siu Hin Lau, A Murray, Arvind H. Patel, R Halford, Tamyo Mbisa, Graham R. Foster, Graham S Cooke, Ana da Silva Filipe, Kosh Agarwal, W Irving, Peter Vickerman, Vattipally B. Sreenu, P Klenerman, E. Thomson, Alec Miners, Vincent Pedergnana, G Burgess, C Spencer, Camilla L. C. Ip, M. Azim Ansari, Connor G. G. Bamford, Rory Bowden

مصطلحات موضوعية: Genetic diversity, Hepatitis C virus, medicine, Interferon Lambda-4, Biology, medicine.disease_cause, Virology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a40bbf620cd5285d88dc68dd523b280f
https://doi.org/10.7554/elife.42463.027

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