학술논문

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학술논문
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'학술논문' 에서의 검색결과 138건 | 목록 1~10

  • 1 .
    Mapping the human genetic architecture of COVID-19
    저자
    by Niemi, MEK; Karjalainen, J; Liao, RG; Neale, BM; Daly, M, et al. 
    소스
    NATURE
    Initiative, COVID H G & Dark, P 2021, ' Mapping the human genetic architecture of COVID-19. ', Nature, vol. 600, no. 7889, pp. 472-477 . https://doi.org/10.1038/s41586-021-03767-x
    Nature
    Nature, 600(7889), 472-477. Nature Publishing Group
    Nature, vol 600, iss 7889
    Nature, 600, 472-477. NATURE PORTFOLIO
    Digital.CSIC. Repositorio Institucional del CSIC
    instname
    Nature, Nature Publishing Group, In press, ⟨10.1038/s41586-021-03767-x⟩
    COVID-19 Host Genetics Initiative 2021, ' Mapping the human genetic architecture of COVID-19 ', Nature, vol. 600, no. 7889, pp. 472-477 . https://doi.org/10.1038/s41586-021-03767-x
    Nature, 2021, 600 (7889), pp.472-477. ⟨10.1038/s41586-021-03767-x⟩
    Nature, Vol. 600, no. ²7889, p. 472-477 (2021)
    472–477
    Nature, vol. 600, no. 7889, pp. 472-477
    r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
    Digibug. Repositorio Institucional de la Universidad de Granada
    Nature, 600. Nature Publishing Group
    Nature, 600, 472-477. Nature Publishing Group
    Niemi, M E K, Karjalainen, J, Liao, R G, Neale, B M, Daly, M, Ganna, A, Pathak, G A, Andrews, S J, Kanai, M, Veerapen, K, Fernandez-Cadenas, I, Schulte, E C, Striano, P, Marttila, M, Minica, C, Marouli, E, Karim, M A, Wendt, F R, Savage, J, Sloofman, L, Butler-Laporte, G, Kim, H-N, Kanoni, S, Okada, Y, Byun, J, Han, Y, Uddin, M J, Smith, G D, Willer, C J, Buxbaum, J D, Karjalainen, J, Mehtonen, J, Folkersen, L, Moltke, I, Hinney, A, Wang, C, Ellinghaus, D, Brunak, S, Castro, P, Guindo-Martinez, M, Lee, J Y, Loos, R J F, Zhao, J H, Sun, Y V, Wang, B, Parker, R, Garcia, S M, Smith, O, Davis, C, COVID-19 Host Genetics Initiative, 23andMe COVID-19 Team, Norwegian SARS-CoV-2 Study Grp, Humanitas COVID-19 Task Force, Humanitas Gavazzeni COVID-19 Task, FHoGID, RegCOVID, P-PredictUs, SeroCOVID, CRiPSI, Genes & Hlth Res Team & UCLA Hlth ATLAS Data Mart Working 2021, ' Mapping the human genetic architecture of COVID-19 ', Nature, vol. 600, pp. 472-477 . https://doi.org/10.1038/s41586-021-03767-x
    Nature (Lond.) 600 (2021): 472–+. doi:10.1038/s41586-021-03767-x
    info:cnr-pdr/source/autori:Mari E. K. Niemi; Juha Karjalainen; Rachel G. Liao; Benjamin M. Neale; Mark Daly; Andrea Ganna; COVID-19 Host Genetics Initiative and the GEN-COVID Multicenter Study (including Stella, Alessandra and Biscarini, Filippo)/titolo:Mapping the human genetic architecture of COVID-19/doi:10.1038%2Fs41586-021-03767-x/rivista:Nature (Lond.)/anno:2021/pagina_da:472/pagina_a:+/intervallo_pagine:472–+/volume:600
    Ganna, A & Davey Smith, G 2021, ' Mapping the human genetic architecture of COVID-19 ', Nature . https://doi.org/10.1038/s41586-021-03767-x
    Nature 600, 472-477 (2021)
    Baillie, J K, Wilson, J F, Bulteel, N, Hayward, C, Klaric, L, Porteous, D J, Russell, C D, Tenesa, A, Norman, L & Scott-Brown, J & Swann, O 2021, ' Mapping the human genetic architecture of COVID-19 ', Nature . https://doi.org/10.1038/s41586-021-03767-x
  • 7 .
    Pan-cancer analysis of whole genomes
    저자
    by Campbell, P. J. a.; Abpemail, Author; Getz, G. b.; C, D; Eemail, Author, et al. 
    소스
    Nature, vol 578, iss 7793
    Semple, C 2020, ' Pan-cancer analysis of whole genomes ', Nature, vol. 578, no. 7793, pp. 82-93 . https://doi.org/10.1038/s41586-020-1969-6
    Nature, 578, 82-93. Nature Publishing Group
    The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Bristow, R, Hayes, S, Wedge, D & et al. 2020, ' Pan-cancer analysis of whole genomes ', Nature. https://doi.org/10.1038/s41586-020-1969-6
    ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Weischenfeldt, J L, Sidiropoulos, N, Brunak, S & Rodriguez Gonzalez, F G 2020, ' Pan-cancer analysis of whole genomes ', Nature, vol. 578, no. 7793, pp. 82-93 . https://doi.org/10.1038/s41586-020-1969-6
    Digital.CSIC. Repositorio Institucional del CSIC
    instname
    ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium, Collaborators (2020). Pan-cancer analysis of whole genomes. Nature, 578(7793), pp. 82-93. Springer Nature 10.1038/s41586-020-1969-6
    Nature (London), 578 (7793
    Nature
    Scopus
    RUO. Repositorio Institucional de la Universidad de Oviedo
    Nature, 578(7793), 82-93. Nature Publishing Group
    Nature, 578, 7793, pp. 82-93
    Nature, 578 (7793)
    NATURE
    Dipòsit Digital de Documents de la UAB
    Universitat Autònoma de Barcelona
    The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020, ' Pan-cancer analysis of whole genomes ', Nature, vol. 578, no. 7793, pp. 82-93 . https://doi.org/10.1038/s41586-020-1969-6
    Dipòsit Digital de la UB
    Universidad de Barcelona
    Nature, 578, 82-93
    RUO: Repositorio Institucional de la Universidad de Oviedo
    Universidad de Oviedo (UNIOVI)
    UPCommons. Portal del coneixement obert de la UPC
    Universitat Politècnica de Catalunya (UPC)
  • 7 .
    Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness
    저자
    by Bigdeli, T. B; Ripke, S; Bacanu, Sa; Lee, S. H; Wray, Nr, et al. 
    소스
    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 276-289. Wiley-Liss Inc.
    ISSUE=171B;STARTPAGE=276;ENDPAGE=289;ISSN=1552-4841;TITLE=American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
    American journal of medical genetics. Part B, Neuropsychiatric genetics, 171BB(2), 276-289. Wiley-Liss Inc.
    Bigdeli, T B, Ripke, S, Bacanu, S A, Lee, S H, Schizophrenia Working Group of the Psychiatric Genomics, U & Posthuma, D 2016, ' Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, no. 171B, 2, pp. 276-289 . https://doi.org/10.1002/ajmg.b.32402
    American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 171(2), 276-289. Wiley
    American journal of medical genetics: part B: neuropsychiatric genetics
  • 7 .
    Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
    저자
    by Gusev, A; Lee, Sh; SWE SCZ, Consortium; O'Dushlaine, Cgusev; Trynka, G, et al. 
    소스
    American journal of human genetics, 95(5), 535-552. Cell Press
    American Journal of Human Genetics, 95(5), 535-52. Cell Press
    Gusev, A, Lee, S H, Trynka, G, Finucane, H, Vilhjálmsson, B J, Xu, H, Zang, C, Ripke, S, Bulik-Sullivan, B, Stahl, E, Kähler, A K, Hultman, C M, Purcell, S M, McCarroll, S A, Daly, M, Pasaniuc, B, Sullivan, P F, Neale, B M, Wray, N R, Raychaudhuri, S, Price, A L & Schizophrenia Working Group of the Psychiatric Genomics Consortium (Manuel Mattheisen and Jakob Grove, members) 2014, ' Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases ', American Journal of Human Genetics, vol. 95, no. 5, pp. 535-52 . https://doi.org/10.1016/j.ajhg.2014.10.004
    Gusev, A, Lee, S H, Trynka, G, Finucane, H, Vilhjálmsson, B J, Xu, H, Zang, Z, Ripke, S, Bulik-Sullivan, B K, Stahl, E, Kähler, A K, Hultman, C M, Purcell, S M, McCarroll, S A, Daly, M, Pasaniuc, B, Sullivan, P F, Neale, B M, Wray, N R, Raychaudhuri, S & Price, A L 2014, ' Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. ', American Journal of Human Genetics, vol. 95, no. 5, pp. 535-552 . https://doi.org/10.1016/j.ajhg.2014.10.004
    The American Journal of Human Genetics
    ResearcherID
    American Journal of Human Genetics, 95(5), 535-552. Cell Press
  • 7 .
    Variability in Working Memory Performance Explained by Epistasis vs Polygenic Scores in the ZNF804A Pathway
    저자
    by Nicodemus, Kk; Hargreaves, A; Morris, D; Anney, R; Gill, M, et al. 
    소스
    Journal of the American Academy of Child and Adolescent Psychiatry, 71(7), 778-785. Elsevier Limited
    Nicodemus, K K, Hargreaves, A, Morris, D, Anney, R, Gill, M, Corvin, A, Donohoe, G & Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium 2014, ' Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway ', J A M A Psychiatry, vol. 71, no. 7, pp. 778-85 . https://doi.org/10.1001/jamapsychiatry.2014.528
    JAMA psychiatry, vol 71, iss 7
    Nicodemus, K K, Hargreaves, A, Morris, D, Anney, R, Gill, M, Corvin, A, Posthuma, D & Donohoe, G 2014, ' Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 71, no. 7, pp. 778-785 . https://doi.org/10.1001/jamapsychiatry.2014.528
    JAMA Psychiatry, 71(7), 778-785. American Medical Association
    JAMA psychiatry, 71(7), 778-785. American Medical Association
  • 7 .
    Landscape of somatic mutations in 560 breast cancer whole-genome sequences
    저자
    by John W.M. Martens; Sandrine Boyault; David Jones; Stefania Tommasi; Jeong-Yeon Lee, et al. 
    소스
    Nature, 534, 7605, pp. 47-67
    Nature
    Nature, Nature Publishing Group, 2016, 534 (7605), pp.47-54. ⟨10.1038/nature17676⟩
    Nature, 2016, 534 (7605), pp.47-54. ⟨10.1038/nature17676⟩
    Nature, 534, 47-54
    Nature, 534(7605), 47-+. Nature Publishing Group
    Nature, Nature Publishing Group, 2016, 534 (7605), pp.47-54. 〈10.1038/nature17676〉
    Nature, 534, 7605, pp. 47-54
    Nature, 534, 47-67
  • 7 .
    All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs
    저자
    by Aj, Schork; Wk, Thompson; Pham P; Torkamani A; Jc, Roddey, et al. 
    소스
    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
    BASE-Bielefeld Academic Search Engine
    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
  • 7 .
    Genetic schizophrenia risk variants jointly modulate total brain and white matter volume
    저자
    by Terwisscha van Scheltinga, Af; Bakker, Sc; van Haren, Ne; Derks, Em; Buizer Voskamp, Je, et al. 
    소스
    Biological psychiatry, 73(6), 525-531. Elsevier USA
    Biological Psychiatry
    Biological Psychiatry, 73(6), 525-531. Elsevier USA
    Biological Psychiatry, 73(6), 525-531. Elsevier Science
    Terwisscha van Scheltinga, A F, Bakker, S C, Haren, N E, Derks, E M, Buizer-Voskamp, J E, Boos, H B, Cahn, W, Hulshoff Pol, H E, Ripke, S, Ophoff, R A, Posthuma, D & Kahn, R S 2013, ' Genetic schizophrenia risk variants jointly modulate total brain and white matter volume ', Biological Psychiatry, vol. 73, no. 6, pp. 525-531 . https://doi.org/10.1016/j.biopsych.2012.08.017
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