% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Pardias:141087,
      author       = {Pardiñas, Antonio F and Holmans, Peter and Pocklington,
                      Andrew J and Escott-Price, Valentina and Ripke, Stephan and
                      Carrera, Noa and Legge, Sophie E and Bishop, Sophie and
                      Cameron, Darren and Hamshere, Marian L and Han, Jun and
                      Hubbard, Leon and Lynham, Amy and Mantripragada, Kiran and
                      Rees, Elliott and MacCabe, James H and McCarroll, Steven A
                      and Baune, Bernhard T and Breen, Gerome and Byrne, Enda M
                      and Dannlowski, Udo and Eley, Thalia C and Hayward, Caroline
                      and Martin, Nicholas G and McIntosh, Andrew M and Plomin,
                      Robert and Porteous, David J and Wray, Naomi R and
                      Caballero, Armando and Geschwind, Daniel H and Huckins,
                      Laura M and Ruderfer, Douglas M and Santiago, Enrique and
                      Sklar, Pamela and Stahl, Eli A and Won, Hyejung and Agerbo,
                      Esben and Als, Thomas D and Andreassen, Ole A and
                      Bækvad-Hansen, Marie and Mortensen, Preben Bo and Pedersen,
                      Carsten Bøcker and Børglum, Anders D and Bybjerg-Grauholm,
                      Jonas and Djurovic, Srdjan and Durmishi, Naser and Pedersen,
                      Marianne Giørtz and Golimbet, Vera and Grove, Jakob and
                      Hougaard, David M and Mattheisen, Manuel and Molden, Espen
                      and Mors, Ole and Nordentoft, Merete and
                      Pejovic-Milovancevic, Milica and Sigurdsson, Engilbert and
                      Silagadze, Teimuraz and Hansen, Christine Søholm and
                      Stefansson, Kari and Stefansson, Hreinn and Steinberg, Stacy
                      and Tosato, Sarah and Werge, Thomas and Consortium, GERAD1
                      and Consortium, CRESTAR and Collier, David A and Rujescu,
                      Dan and Kirov, George and Owen, Michael J and O'Donovan,
                      Michael C and Walters, James T R and Harold, Denise and
                      Sims, Rebecca and Gerrish, Amy and Chapman, Jade and
                      Escott-Price, Valentina and Abraham, Richard and
                      Hollingworth, Paul and Pahwa, Jaspreet and Denning, Nicola
                      and Thomas, Charlene and Taylor, Sarah and Powell, John and
                      Proitsi, Petroula and Lupton, Michelle and Lovestone, Simon
                      and Passmore, Peter and Craig, David and McGuinness,
                      Bernadette and Johnston, Janet and Todd, Stephen and Maier,
                      Wolfgang and Jessen, Frank and Heun, Reiner and Schurmann,
                      Britta and Ramirez, Alfredo and Becker, Tim and Herold,
                      Christine and Lacour, André and Drichel, Dmitriy and
                      Nothen, Markus and Goate, Alison and Cruchaga, Carlos and
                      Nowotny, Petra and Morris, John C and Mayo, Kevin and
                      Holmans, Peter and O'Donovan, Michael and Owen, Michael and
                      Williams, Julie and Achilla, Evanthia and Agerbo, Esben and
                      Barr, Cathy L and Böttger, Theresa Wimberly and Breen,
                      Gerome and Cohen, Dan and Collier, David A and Curran, Sarah
                      and Dempster, Emma and Dima, Danai and Sabes-Figuera, Ramon
                      and Flanagan, Robert J and Frangou, Sophia and Frank, Josef
                      and Gasse, Christiane and Gaughran, Fiona and Giegling, Ina
                      and Grove, Jakob and Hannon, Eilis and Hartmann, Annette M
                      and Heißerer, Barbara and Helthuis, Marinka and Horsdal,
                      Henriette Thisted and Ingimarsson, Oddur and Jollie, Karel
                      and Kennedy, James L and Köhler, Ole and Konte, Bettina and
                      Lang, Maren and Legge, Sophie E and Lewis, Cathryn and
                      MacCabe, James and Malhotra, Anil K and McCrone, Paul and
                      Meier, Sandra M and Mill, Jonathan and Mors, Ole and
                      Mortensen, Preben Bo and Nöthen, Markus M and O'Donovan,
                      Michael C and Owen, Michael J and Pardiñas, Antonio F and
                      Pedersen, Carsten B and Rietschel, Marcella and Rujescu, Dan
                      and Schwalber, Ameli and Sigurdsson, Engilbert and
                      Sørensen, Holger J and Spencer, Benjamin and Stefansson,
                      Hreinn and Støvring, Henrik and Strohmaier, Jana and
                      Sullivan, Patrick and Vassos, Evangelos and Verbelen, Moira
                      and Walters, James T R and Werge, Thomas},
      title        = {{C}ommon schizophrenia alleles are enriched in
                      mutation-intolerant genes and in regions under strong
                      background selection.},
      journal      = {Nature genetics},
      volume       = {50},
      number       = {3},
      issn         = {1061-4036},
      address      = {London},
      publisher    = {Macmillan Publishers Limited, part of Springer Nature},
      reportid     = {DZNE-2020-07409},
      pages        = {381-389},
      year         = {2018},
      abstract     = {Schizophrenia is a debilitating psychiatric condition often
                      associated with poor quality of life and decreased life
                      expectancy. Lack of progress in improving treatment outcomes
                      has been attributed to limited knowledge of the underlying
                      biology, although large-scale genomic studies have begun to
                      provide insights. We report a new genome-wide association
                      study of schizophrenia (11,260 cases and 24,542 controls),
                      and through meta-analysis with existing data we identify 50
                      novel associated loci and 145 loci in total. Through
                      integrating genomic fine-mapping with brain expression and
                      chromosome conformation data, we identify candidate causal
                      genes within 33 loci. We also show for the first time that
                      the common variant association signal is highly enriched
                      among genes that are under strong selective pressures. These
                      findings provide new insights into the biology and genetic
                      architecture of schizophrenia, highlight the importance of
                      mutation-intolerant genes and suggest a mechanism by which
                      common risk variants persist in the population.},
      keywords     = {Alleles / Case-Control Studies / Gene Frequency / Genes,
                      Lethal: genetics / Genetic Loci / Genetic Predisposition to
                      Disease / Genome-Wide Association Study / Humans /
                      Inheritance Patterns / Polymorphism, Single Nucleotide /
                      Schizophrenia: genetics / Selection, Genetic},
      cin          = {GenomMathematik / AG Roes},
      ddc          = {570},
      cid          = {I:(DE-2719)1013007 / I:(DE-2719)1610003},
      pnm          = {345 - Population Studies and Genetics (POF3-345) / 344 -
                      Clinical and Health Care Research (POF3-344)},
      pid          = {G:(DE-HGF)POF3-345 / G:(DE-HGF)POF3-344},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:29483656},
      pmc          = {pmc:PMC5918692},
      doi          = {10.1038/s41588-018-0059-2},
      url          = {https://pub.dzne.de/record/141087},
}