Literature DB >> 35411108

Genetic origins of schizophrenia find common ground.

Conrad O Iyegbe, Paul F O'Reilly.   

Abstract

Entities:  

Keywords:  Genetics; Genomics; Schizophrenia

Mesh：

Year:  2022        PMID： 35411108     DOI： 10.1038/d41586-022-00773-5

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  9 in total

Review 1.  African genetic diversity and adaptation inform a precision medicine agenda.

Authors:  Luisa Pereira; Leon Mutesa; Paulina Tindana; Michèle Ramsay
Journal:  Nat Rev Genet       Date:  2021-01-11       Impact factor: 53.242

Review 2.  Rare and common variants: twenty arguments.

Authors:  Greg Gibson
Journal:  Nat Rev Genet       Date:  2012-01-18       Impact factor: 53.242

3.  Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia.

Authors:  Duncan S Palmer; Daniel P Howrigan; Sinéad B Chapman; Rolf Adolfsson; Nick Bass; Douglas Blackwood; Marco P M Boks; Chia-Yen Chen; Claire Churchhouse; Aiden P Corvin; Nicholas Craddock; David Curtis; Arianna Di Florio; Faith Dickerson; Nelson B Freimer; Fernando S Goes; Xiaoming Jia; Ian Jones; Lisa Jones; Lina Jonsson; Rene S Kahn; Mikael Landén; Adam E Locke; Andrew M McIntosh; Andrew McQuillin; Derek W Morris; Michael C O'Donovan; Roel A Ophoff; Michael J Owen; Nancy L Pedersen; Danielle Posthuma; Andreas Reif; Neil Risch; Catherine Schaefer; Laura Scott; Tarjinder Singh; Jordan W Smoller; Matthew Solomonson; David St Clair; Eli A Stahl; Annabel Vreeker; James T R Walters; Weiqing Wang; Nicholas A Watts; Robert Yolken; Peter P Zandi; Benjamin M Neale
Journal:  Nat Genet       Date:  2022-04-11       Impact factor: 41.307

4.  Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.

Authors:  Ditte Demontis; Raymond K Walters; Joanna Martin; Manuel Mattheisen; Thomas D Als; Esben Agerbo; Gísli Baldursson; Rich Belliveau; Jonas Bybjerg-Grauholm; Marie Bækvad-Hansen; Felecia Cerrato; Kimberly Chambert; Claire Churchhouse; Ashley Dumont; Nicholas Eriksson; Michael Gandal; Jacqueline I Goldstein; Katrina L Grasby; Jakob Grove; Olafur O Gudmundsson; Christine S Hansen; Mads Engel Hauberg; Mads V Hollegaard; Daniel P Howrigan; Hailiang Huang; Julian B Maller; Alicia R Martin; Nicholas G Martin; Jennifer Moran; Jonatan Pallesen; Duncan S Palmer; Carsten Bøcker Pedersen; Marianne Giørtz Pedersen; Timothy Poterba; Jesper Buchhave Poulsen; Stephan Ripke; Elise B Robinson; F Kyle Satterstrom; Hreinn Stefansson; Christine Stevens; Patrick Turley; G Bragi Walters; Hyejung Won; Margaret J Wright; Ole A Andreassen; Philip Asherson; Christie L Burton; Dorret I Boomsma; Bru Cormand; Søren Dalsgaard; Barbara Franke; Joel Gelernter; Daniel Geschwind; Hakon Hakonarson; Jan Haavik; Henry R Kranzler; Jonna Kuntsi; Kate Langley; Klaus-Peter Lesch; Christel Middeldorp; Andreas Reif; Luis Augusto Rohde; Panos Roussos; Russell Schachar; Pamela Sklar; Edmund J S Sonuga-Barke; Patrick F Sullivan; Anita Thapar; Joyce Y Tung; Irwin D Waldman; Sarah E Medland; Kari Stefansson; Merete Nordentoft; David M Hougaard; Thomas Werge; Ole Mors; Preben Bo Mortensen; Mark J Daly; Stephen V Faraone; Anders D Børglum; Benjamin M Neale
Journal:  Nat Genet       Date:  2018-11-26       Impact factor: 38.330

5.  Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.

Authors:  Niamh Mullins; Andreas J Forstner; Kevin S O'Connell; Brandon Coombes; Jonathan R I Coleman; Zhen Qiao; Thomas D Als; Tim B Bigdeli; Sigrid Børte; Julien Bryois; Alexander W Charney; Ole Kristian Drange; Michael J Gandal; Saskia P Hagenaars; Masashi Ikeda; Nolan Kamitaki; Minsoo Kim; Kristi Krebs; Georgia Panagiotaropoulou; Brian M Schilder; Laura G Sloofman; Stacy Steinberg; Vassily Trubetskoy; Bendik S Winsvold; Hong-Hee Won; Liliya Abramova; Kristina Adorjan; Esben Agerbo; Mariam Al Eissa; Diego Albani; Ney Alliey-Rodriguez; Adebayo Anjorin; Verneri Antilla; Anastasia Antoniou; Swapnil Awasthi; Ji Hyun Baek; Marie Bækvad-Hansen; Nicholas Bass; Michael Bauer; Eva C Beins; Sarah E Bergen; Armin Birner; Carsten Bøcker Pedersen; Erlend Bøen; Marco P Boks; Rosa Bosch; Murielle Brum; Ben M Brumpton; Nathalie Brunkhorst-Kanaan; Monika Budde; Jonas Bybjerg-Grauholm; William Byerley; Murray Cairns; Miquel Casas; Pablo Cervantes; Toni-Kim Clarke; Cristiana Cruceanu; Alfredo Cuellar-Barboza; Julie Cunningham; David Curtis; Piotr M Czerski; Anders M Dale; Nina Dalkner; Friederike S David; Franziska Degenhardt; Srdjan Djurovic; Amanda L Dobbyn; Athanassios Douzenis; Torbjørn Elvsåshagen; Valentina Escott-Price; I Nicol Ferrier; Alessia Fiorentino; Tatiana M Foroud; Liz Forty; Josef Frank; Oleksandr Frei; Nelson B Freimer; Louise Frisén; Katrin Gade; Julie Garnham; Joel Gelernter; Marianne Giørtz Pedersen; Ian R Gizer; Scott D Gordon; Katherine Gordon-Smith; Tiffany A Greenwood; Jakob Grove; José Guzman-Parra; Kyooseob Ha; Magnus Haraldsson; Martin Hautzinger; Urs Heilbronner; Dennis Hellgren; Stefan Herms; Per Hoffmann; Peter A Holmans; Laura Huckins; Stéphane Jamain; Jessica S Johnson; Janos L Kalman; Yoichiro Kamatani; James L Kennedy; Sarah Kittel-Schneider; James A Knowles; Manolis Kogevinas; Maria Koromina; Thorsten M Kranz; Henry R Kranzler; Michiaki Kubo; Ralph Kupka; Steven A Kushner; Catharina Lavebratt; Jacob Lawrence; Markus Leber; Heon-Jeong Lee; Phil H Lee; Shawn E Levy; Catrin Lewis; Calwing Liao; Susanne Lucae; Martin Lundberg; Donald J MacIntyre; Sigurdur H Magnusson; Wolfgang Maier; Adam Maihofer; Dolores Malaspina; Eirini Maratou; Lina Martinsson; Manuel Mattheisen; Steven A McCarroll; Nathaniel W McGregor; Peter McGuffin; James D McKay; Helena Medeiros; Sarah E Medland; Vincent Millischer; Grant W Montgomery; Jennifer L Moran; Derek W Morris; Thomas W Mühleisen; Niamh O'Brien; Claire O'Donovan; Loes M Olde Loohuis; Lilijana Oruc; Sergi Papiol; Antonio F Pardiñas; Amy Perry; Andrea Pfennig; Evgenia Porichi; James B Potash; Digby Quested; Towfique Raj; Mark H Rapaport; J Raymond DePaulo; Eline J Regeer; John P Rice; Fabio Rivas; Margarita Rivera; Julian Roth; Panos Roussos; Douglas M Ruderfer; Cristina Sánchez-Mora; Eva C Schulte; Fanny Senner; Sally Sharp; Paul D Shilling; Engilbert Sigurdsson; Lea Sirignano; Claire Slaney; Olav B Smeland; Daniel J Smith; Janet L Sobell; Christine Søholm Hansen; Maria Soler Artigas; Anne T Spijker; Dan J Stein; John S Strauss; Beata Świątkowska; Chikashi Terao; Thorgeir E Thorgeirsson; Claudio Toma; Paul Tooney; Evangelia-Eirini Tsermpini; Marquis P Vawter; Helmut Vedder; James T R Walters; Stephanie H Witt; Simon Xi; Wei Xu; Jessica Mei Kay Yang; Allan H Young; Hannah Young; Peter P Zandi; Hang Zhou; Lea Zillich; Rolf Adolfsson; Ingrid Agartz; Martin Alda; Lars Alfredsson; Gulja Babadjanova; Lena Backlund; Bernhard T Baune; Frank Bellivier; Susanne Bengesser; Wade H Berrettini; Douglas H R Blackwood; Michael Boehnke; Anders D Børglum; Gerome Breen; Vaughan J Carr; Stanley Catts; Aiden Corvin; Nicholas Craddock; Udo Dannlowski; Dimitris Dikeos; Tõnu Esko; Bruno Etain; Panagiotis Ferentinos; Mark Frye; Janice M Fullerton; Micha Gawlik; Elliot S Gershon; Fernando S Goes; Melissa J Green; Maria Grigoroiu-Serbanescu; Joanna Hauser; Frans Henskens; Jan Hillert; Kyung Sue Hong; David M Hougaard; Christina M Hultman; Kristian Hveem; Nakao Iwata; Assen V Jablensky; Ian Jones; Lisa A Jones; René S Kahn; John R Kelsoe; George Kirov; Mikael Landén; Marion Leboyer; Cathryn M Lewis; Qingqin S Li; Jolanta Lissowska; Christine Lochner; Carmel Loughland; Nicholas G Martin; Carol A Mathews; Fermin Mayoral; Susan L McElroy; Andrew M McIntosh; Francis J McMahon; Ingrid Melle; Patricia Michie; Lili Milani; Philip B Mitchell; Gunnar Morken; Ole Mors; Preben Bo Mortensen; Bryan Mowry; Bertram Müller-Myhsok; Richard M Myers; Benjamin M Neale; Caroline M Nievergelt; Merete Nordentoft; Markus M Nöthen; Michael C O'Donovan; Ketil J Oedegaard; Tomas Olsson; Michael J Owen; Sara A Paciga; Chris Pantelis; Carlos Pato; Michele T Pato; George P Patrinos; Roy H Perlis; Danielle Posthuma; Josep Antoni Ramos-Quiroga; Andreas Reif; Eva Z Reininghaus; Marta Ribasés; Marcella Rietschel; Stephan Ripke; Guy A Rouleau; Takeo Saito; Ulrich Schall; Martin Schalling; Peter R Schofield; Thomas G Schulze; Laura J Scott; Rodney J Scott; Alessandro Serretti; Cynthia Shannon Weickert; Jordan W Smoller; Hreinn Stefansson; Kari Stefansson; Eystein Stordal; Fabian Streit; Patrick F Sullivan; Gustavo Turecki; Arne E Vaaler; Eduard Vieta; John B Vincent; Irwin D Waldman; Thomas W Weickert; Thomas Werge; Naomi R Wray; John-Anker Zwart; Joanna M Biernacka; John I Nurnberger; Sven Cichon; Howard J Edenberg; Eli A Stahl; Andrew McQuillin; Arianna Di Florio; Roel A Ophoff; Ole A Andreassen
Journal:  Nat Genet       Date:  2021-05-17       Impact factor: 38.330

6.  Neuropsychiatric Genetics of African Populations-Psychosis (NeuroGAP-Psychosis): a case-control study protocol and GWAS in Ethiopia, Kenya, South Africa and Uganda.

Authors:  Anne Stevenson; Dickens Akena; Rocky E Stroud; Lukoye Atwoli; Megan M Campbell; Lori B Chibnik; Edith Kwobah; Symon M Kariuki; Alicia R Martin; Victoria de Menil; Charles R J C Newton; Goodman Sibeko; Dan J Stein; Solomon Teferra; Zukiswa Zingela; Karestan C Koenen
Journal:  BMJ Open       Date:  2019-02-19       Impact factor: 2.692

7.  Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

Authors:  Tarjinder Singh; Mitja I Kurki; David Curtis; Shaun M Purcell; Lucy Crooks; Jeremy McRae; Jaana Suvisaari; Himanshu Chheda; Douglas Blackwood; Gerome Breen; Olli Pietiläinen; Sebastian S Gerety; Muhammad Ayub; Moira Blyth; Trevor Cole; David Collier; Eve L Coomber; Nick Craddock; Mark J Daly; John Danesh; Marta DiForti; Alison Foster; Nelson B Freimer; Daniel Geschwind; Mandy Johnstone; Shelagh Joss; Georg Kirov; Jarmo Körkkö; Outi Kuismin; Peter Holmans; Christina M Hultman; Conrad Iyegbe; Jouko Lönnqvist; Minna Männikkö; Steve A McCarroll; Peter McGuffin; Andrew M McIntosh; Andrew McQuillin; Jukka S Moilanen; Carmel Moore; Robin M Murray; Ruth Newbury-Ecob; Willem Ouwehand; Tiina Paunio; Elena Prigmore; Elliott Rees; David Roberts; Jennifer Sambrook; Pamela Sklar; David St Clair; Juha Veijola; James T R Walters; Hywel Williams; Patrick F Sullivan; Matthew E Hurles; Michael C O'Donovan; Aarno Palotie; Michael J Owen; Jeffrey C Barrett
Journal:  Nat Neurosci       Date:  2016-03-14       Impact factor: 24.884

8.  Evidence for 28 genetic disorders discovered by combining healthcare and research data.

Authors:  Joanna Kaplanis; Kaitlin E Samocha; Laurens Wiel; Zhancheng Zhang; Kevin J Arvai; Ruth Y Eberhardt; Giuseppe Gallone; Stefan H Lelieveld; Hilary C Martin; Jeremy F McRae; Patrick J Short; Rebecca I Torene; Elke de Boer; Petr Danecek; Eugene J Gardner; Ni Huang; Jenny Lord; Iñigo Martincorena; Rolph Pfundt; Margot R F Reijnders; Alison Yeung; Helger G Yntema; Lisenka E L M Vissers; Jane Juusola; Caroline F Wright; Han G Brunner; Helen V Firth; David R FitzPatrick; Jeffrey C Barrett; Matthew E Hurles; Christian Gilissen; Kyle Retterer
Journal:  Nature       Date:  2020-10-14       Impact factor: 49.962
  9 in total
  3 in total

1.  Abnormal levels of mitochondrial Ca2+ channel proteins in plasma neuron-derived extracellular vesicles of early schizophrenia.

Authors:  Edward J Goetzl; Vinod H Srihari; Maja Mustapic; Dimitrios Kapogiannis; George R Heninger
Journal:  FASEB J       Date:  2022-08       Impact factor: 5.834

Review 2.  Estimating the number of diseases - the concept of rare, ultra-rare, and hyper-rare.

Authors:  C I Edvard Smith; Peter Bergman; Daniel W Hagey
Journal:  iScience       Date:  2022-07-01

3.  Widespread cortical thinning, excessive glutamate and impaired linguistic functioning in schizophrenia: A cluster analytic approach.

Authors:  Liangbing Liang; Angélica M Silva; Peter Jeon; Sabrina D Ford; Michael MacKinley; Jean Théberge; Lena Palaniyappan
Journal:  Front Hum Neurosci       Date:  2022-08-05       Impact factor: 3.473
  3 in total

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