Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Al Eissa, Mariam"'
Autor:
Al Eissa MM; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Fiorentino A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.; Current address: Institute of Opthalmology, University College London, London, UK., Sharp SI; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., O'Brien NL; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Wolfe K; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Giaroli G; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Curtis D; University College London Genetics Institute, University College London, London, UK., Bass NJ; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., McQuillin A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.
Publikováno v:
Annals of human genetics [Ann Hum Genet] 2018 Mar; Vol. 82 (2), pp. 88-92. Date of Electronic Publication: 2017 Nov 17.
Autor:
Leonenko G; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK., Richards AL; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK., Walters JT; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK., Pocklington A; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK., Chambert K; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts., Al Eissa MM; Division of Psychiatry, Molecular Psychiatry Laboratory, University College London, London, UK., Sharp SI; Division of Psychiatry, Molecular Psychiatry Laboratory, University College London, London, UK., O'Brien NL; Division of Psychiatry, Molecular Psychiatry Laboratory, University College London, London, UK., Curtis D; UCL Genetics Institute, UCL, London, UK., Bass NJ; Division of Psychiatry, Molecular Psychiatry Laboratory, University College London, London, UK., McQuillin A; Division of Psychiatry, Molecular Psychiatry Laboratory, University College London, London, UK., Hultman C; Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden., Moran JL; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts., McCarroll SA; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.; Department of Genetics, Harvard Medical School, Boston, Massachusetts., Sklar P; Icahn School of Medicine at Mount Sinai, New York, New York., Neale BM; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.; Analytical and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts., Holmans PA; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK., Owen MJ; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK., Sullivan PF; Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.; Departments of Genetics and Psychiatry, University of North Carolina, Chapel Hill, North Carolina., O'Donovan MC; Division of Psychological Medicine and Clinical Neurosciences, MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, UK.
Publikováno v:
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] 2017 Oct; Vol. 174 (7), pp. 724-731. Date of Electronic Publication: 2017 Jul 18.
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Autor:
Singh, Tarjinder, Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D, Bass, Nicholas, Bigdeli, Tim B, Breen, Gerome, Bromet, Evelyn J, Buckley, Peter F, Bunney, William E, Bybjerg-Grauholm, Jonas, Byerley, William F, Chapman, Sinéad B, Chen, Wei J, Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M, DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A, Eskelinen, Saana, Fanous, Ayman H, Faraone, Stephen V, Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B, Gage, Diane, Gagliano Taliun, Sarah A, Ganna, Andrea, Genovese, Giulio, Glahn, David C, Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O, Holi, Matti, Hougaard, David M, Howrigan, Daniel P, Huang, Hailiang, Hwu, Hai-Gwo, Kahn, René S, Kang, Hyun Min, Karczewski, Konrad J, Kirov, George, Knowles, James A, Lee, Francis S, Lehrer, Douglas S, Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R, McCarroll, Steven A, McIntosh, Andrew M, Medeiros, Helena, Milani, Lili, Morley, Christopher P, Morris, Derek W, Mortensen, Preben Bo, Myers, Richard M, Nordentoft, Merete, O'Brien, Niamh L, Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H, Palmer, Duncan S, Paunio, Tiina, Quested, Digby, Rapaport, Mark H, Rees, Elliott, Rollins, Brandi, Satterstrom, F Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J, Sharp, Sally I, Sklar, Pamela, Smoller, Jordan W, Sobell, Janet L, Solomonson, Matthew, Stahl, Eli A, Stevens, Christine R, Suvisaari, Jaana, Tiao, Grace, Watson, Stanley J, Watts, Nicholas A, Blackwood, Douglas H, Børglum, Anders D, Cohen, Bruce M, Corvin, Aiden P, Esko, Tõnu, Freimer, Nelson B, Glatt, Stephen J, Hultman, Christina M, McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N, Pato, Michele T, Pulver, Ann E, St Clair, David
Publikováno v:
Nature, vol 604, iss 7906
Rare coding variation has historically provided the most direct connections between gene function and disease pathogenesis. By meta-analysing the whole exomes of 24,248 schizophrenia cases and 97,322 controls, we implicate ultra-rare coding variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::c1ad4cf630d3438bd954dc42fd8e4ecd
https://escholarship.org/uc/item/71f867t4
https://escholarship.org/uc/item/71f867t4