Literature DB >> 33131714

Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders.

Phil H Lee1, Yen-Chen A Feng1, Jordan W Smoller2.   

Abstract

Genome-wide analyses of common and rare genetic variations have documented the heritability of major psychiatric disorders, established their highly polygenic genetic architecture, and identified hundreds of contributing variants. In recent years, these studies have illuminated another key feature of the genetic basis of psychiatric disorders: the important role and pervasive nature of pleiotropy. It is now clear that a substantial fraction of genetic influences on psychopathology transcend clinical diagnostic boundaries. In this review, we summarize evidence in psychiatry for pleiotropy at multiple levels of analysis: from overall genome-wide correlation to biological pathways and down to the level of individual loci. We examine underlying mechanisms of observed pleiotropy, including genetic effects on neurodevelopment, diverse actions of regulatory elements, mediated effects, and spurious associations of genomic variation with multiple phenotypes. We conclude with an exploration of the implications of pleiotropy for understanding the genetic basis of psychiatric disorders, informing nosology, and advancing the aims of precision psychiatry and genomic medicine.
Copyright © 2020 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cross-disorder; GWAS; Genetic correlation; Nosology; Pleiotropy; Precision psychiatry; Psychiatric genetics

Mesh:

Year:  2020        PMID: 33131714      PMCID: PMC7898275          DOI: 10.1016/j.biopsych.2020.09.026

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  108 in total

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2.  Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.

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3.  Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Authors:  Hunna J Watson; Zeynep Yilmaz; Laura M Thornton; Christopher Hübel; Jonathan R I Coleman; Héléna A Gaspar; Julien Bryois; Anke Hinney; Virpi M Leppä; Manuel Mattheisen; Sarah E Medland; Stephan Ripke; Shuyang Yao; Paola Giusti-Rodríguez; Ken B Hanscombe; Kirstin L Purves; Roger A H Adan; Lars Alfredsson; Tetsuya Ando; Ole A Andreassen; Jessica H Baker; Wade H Berrettini; Ilka Boehm; Claudette Boni; Vesna Boraska Perica; Katharina Buehren; Roland Burghardt; Matteo Cassina; Sven Cichon; Maurizio Clementi; Roger D Cone; Philippe Courtet; Scott Crow; James J Crowley; Unna N Danner; Oliver S P Davis; Martina de Zwaan; George Dedoussis; Daniela Degortes; Janiece E DeSocio; Danielle M Dick; Dimitris Dikeos; Christian Dina; Monika Dmitrzak-Weglarz; Elisa Docampo; Laramie E Duncan; Karin Egberts; Stefan Ehrlich; Geòrgia Escaramís; Tõnu Esko; Xavier Estivill; Anne Farmer; Angela Favaro; Fernando Fernández-Aranda; Manfred M Fichter; Krista Fischer; Manuel Föcker; Lenka Foretova; Andreas J Forstner; Monica Forzan; Christopher S Franklin; Steven Gallinger; Ina Giegling; Johanna Giuranna; Fragiskos Gonidakis; Philip Gorwood; Monica Gratacos Mayora; Sébastien Guillaume; Yiran Guo; Hakon Hakonarson; Konstantinos Hatzikotoulas; Joanna Hauser; Johannes Hebebrand; Sietske G Helder; Stefan Herms; Beate Herpertz-Dahlmann; Wolfgang Herzog; Laura M Huckins; James I Hudson; Hartmut Imgart; Hidetoshi Inoko; Vladimir Janout; Susana Jiménez-Murcia; Antonio Julià; Gursharan Kalsi; Deborah Kaminská; Jaakko Kaprio; Leila Karhunen; Andreas Karwautz; Martien J H Kas; James L Kennedy; Anna Keski-Rahkonen; Kirsty Kiezebrink; Youl-Ri Kim; Lars Klareskog; Kelly L Klump; Gun Peggy S Knudsen; Maria C La Via; Stephanie Le Hellard; Robert D Levitan; Dong Li; Lisa Lilenfeld; Bochao Danae Lin; Jolanta Lissowska; Jurjen Luykx; Pierre J Magistretti; Mario Maj; Katrin Mannik; Sara Marsal; Christian R Marshall; Morten Mattingsdal; Sara McDevitt; Peter McGuffin; Andres Metspalu; Ingrid Meulenbelt; Nadia Micali; Karen Mitchell; Alessio Maria Monteleone; Palmiero Monteleone; Melissa A Munn-Chernoff; Benedetta Nacmias; Marie Navratilova; Ioanna Ntalla; Julie K O'Toole; Roel A Ophoff; Leonid Padyukov; Aarno Palotie; Jacques Pantel; Hana Papezova; Dalila Pinto; Raquel Rabionet; Anu Raevuori; Nicolas Ramoz; Ted Reichborn-Kjennerud; Valdo Ricca; Samuli Ripatti; Franziska Ritschel; Marion Roberts; Alessandro Rotondo; Dan Rujescu; Filip Rybakowski; Paolo Santonastaso; André Scherag; Stephen W Scherer; Ulrike Schmidt; Nicholas J Schork; Alexandra Schosser; Jochen Seitz; Lenka Slachtova; P Eline Slagboom; Margarita C T Slof-Op 't Landt; Agnieszka Slopien; Sandro Sorbi; Beata Świątkowska; Jin P Szatkiewicz; Ioanna Tachmazidou; Elena Tenconi; Alfonso Tortorella; Federica Tozzi; Janet Treasure; Artemis Tsitsika; Marta Tyszkiewicz-Nwafor; Konstantinos Tziouvas; Annemarie A van Elburg; Eric F van Furth; Gudrun Wagner; Esther Walton; Elisabeth Widen; Eleftheria Zeggini; Stephanie Zerwas; Stephan Zipfel; Andrew W Bergen; Joseph M Boden; Harry Brandt; Steven Crawford; Katherine A Halmi; L John Horwood; Craig Johnson; Allan S Kaplan; Walter H Kaye; James E Mitchell; Catherine M Olsen; John F Pearson; Nancy L Pedersen; Michael Strober; Thomas Werge; David C Whiteman; D Blake Woodside; Garret D Stuber; Scott Gordon; Jakob Grove; Anjali K Henders; Anders Juréus; Katherine M Kirk; Janne T Larsen; Richard Parker; Liselotte Petersen; Jennifer Jordan; Martin Kennedy; Grant W Montgomery; Tracey D Wade; Andreas Birgegård; Paul Lichtenstein; Claes Norring; Mikael Landén; Nicholas G Martin; Preben Bo Mortensen; Patrick F Sullivan; Gerome Breen; Cynthia M Bulik
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8.  Rbfox1 Mediates Cell-type-Specific Splicing in Cortical Interneurons.

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9.  Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

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10.  An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome.

Authors:  Tom G Richardson; Sean Harrison; Gibran Hemani; George Davey Smith
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5.  Developmental disorders caused by haploinsufficiency of transcriptional regulators: a perspective based on cell fate determination.

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6.  Corticolimbic DCC gene co-expression networks as predictors of impulsivity in children.

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7.  Editorial: Decoding Brain Function Through Genetics.

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