Literature DB >> 28929285

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

Chelsea Lowther1,2, Gregory Costain3, Danielle A Baribeau4, Anne S Bassett5,6,7,8.   

Abstract

PURPOSE OF REVIEW: The purpose of this review is to summarize the role of genomic disorders in various psychiatric conditions and to highlight important recent advances in the field that are of potential clinical relevance. RECENT
FINDINGS: Genomic disorders are caused by large rare recurrent deletions and duplications at certain chromosomal "hotspots" (e.g., 22q11.2, 16p11.2, 15q11-q13, 1q21.1, 15q13.3) across the genome. Most overlap multiple genes, affect development, and are associated with variable cognitive and other neuropsychiatric expression. Although individually rare, genomic disorders collectively account for a significant minority of intellectual disability, autism spectrum disorder, and schizophrenia. Genome-wide chromosomal microarray analysis is capable of detecting all genomic disorders in a single test, offering the first opportunity for routine clinical genetic testing in psychiatric practice.

Entities:  

Keywords:  ADHD; Autism; CNV; Copy number variation; Genomic disorder; Schizophrenia

Mesh:

Year:  2017        PMID: 28929285     DOI: 10.1007/s11920-017-0831-5

Source DB:  PubMed          Journal:  Curr Psychiatry Rep        ISSN: 1523-3812            Impact factor:   5.285


  99 in total

Review 1.  Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Authors:  Anne S Bassett; Stephen W Scherer; Linda M Brzustowicz
Journal:  Am J Psychiatry       Date:  2010-05-03       Impact factor: 18.112

2.  Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.

Authors:  Andrew J Sharp; Sierra Hansen; Rebecca R Selzer; Ze Cheng; Regina Regan; Jane A Hurst; Helen Stewart; Sue M Price; Edward Blair; Raoul C Hennekam; Carrie A Fitzpatrick; Rick Segraves; Todd A Richmond; Cheryl Guiver; Donna G Albertson; Daniel Pinkel; Peggy S Eis; Stuart Schwartz; Samantha J L Knight; Evan E Eichler
Journal:  Nat Genet       Date:  2006-08-13       Impact factor: 38.330

3.  Parental expression is overvalued in the interpretation of rare inherited variants.

Authors:  Gregory Costain
Journal:  Eur J Hum Genet       Date:  2014-04-23       Impact factor: 4.246

4.  Response to clozapine in a clinically identifiable subtype of schizophrenia.

Authors:  Nancy J Butcher; Wai Lun Alan Fung; Laura Fitzpatrick; Alina Guna; Danielle M Andrade; Anthony E Lang; Eva W C Chow; Anne S Bassett
Journal:  Br J Psychiatry       Date:  2015-03-05       Impact factor: 9.319

5.  High frequencies of de novo CNVs in bipolar disorder and schizophrenia.

Authors:  Dheeraj Malhotra; Shane McCarthy; Jacob J Michaelson; Vladimir Vacic; Katherine E Burdick; Seungtai Yoon; Sven Cichon; Aiden Corvin; Sydney Gary; Elliot S Gershon; Michael Gill; Maria Karayiorgou; John R Kelsoe; Olga Krastoshevsky; Verena Krause; Ellen Leibenluft; Deborah L Levy; Vladimir Makarov; Abhishek Bhandari; Anil K Malhotra; Francis J McMahon; Markus M Nöthen; James B Potash; Marcella Rietschel; Thomas G Schulze; Jonathan Sebat
Journal:  Neuron       Date:  2011-12-22       Impact factor: 17.173

6.  Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.

Authors:  Abdul Noor; Anath C Lionel; Sarah Cohen-Woods; Narges Moghimi; James Rucker; Alanna Fennell; Bhooma Thiruvahindrapuram; Liana Kaufman; Bryan Degagne; John Wei; Sagar V Parikh; Pierandrea Muglia; Julia Forte; Stephen W Scherer; James L Kennedy; Wei Xu; Peter McGuffin; Anne Farmer; John Strauss; John B Vincent
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2014-04-03       Impact factor: 3.568

7.  Developmental trajectories for young children with 16p11.2 copy number variation.

Authors:  Raphael Bernier; Caitlin M Hudac; Qixuan Chen; Chubing Zeng; Arianne Stevens Wallace; Jennifer Gerdts; Rachel Earl; Jessica Peterson; Anne Wolken; Alana Peters; Ellen Hanson; Robin P Goin-Kochel; Stephen Kanne; LeeAnne Green Snyder; Wendy K Chung
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-03-27       Impact factor: 3.568

8.  Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.

Authors:  Dalila Pinto; Elsa Delaby; Daniele Merico; Mafalda Barbosa; Alison Merikangas; Lambertus Klei; Bhooma Thiruvahindrapuram; Xiao Xu; Robert Ziman; Zhuozhi Wang; Jacob A S Vorstman; Ann Thompson; Regina Regan; Marion Pilorge; Giovanna Pellecchia; Alistair T Pagnamenta; Bárbara Oliveira; Christian R Marshall; Tiago R Magalhaes; Jennifer K Lowe; Jennifer L Howe; Anthony J Griswold; John Gilbert; Eftichia Duketis; Beth A Dombroski; Maretha V De Jonge; Michael Cuccaro; Emily L Crawford; Catarina T Correia; Judith Conroy; Inês C Conceição; Andreas G Chiocchetti; Jillian P Casey; Guiqing Cai; Christelle Cabrol; Nadia Bolshakova; Elena Bacchelli; Richard Anney; Steven Gallinger; Michelle Cotterchio; Graham Casey; Lonnie Zwaigenbaum; Kerstin Wittemeyer; Kirsty Wing; Simon Wallace; Herman van Engeland; Ana Tryfon; Susanne Thomson; Latha Soorya; Bernadette Rogé; Wendy Roberts; Fritz Poustka; Susana Mouga; Nancy Minshew; L Alison McInnes; Susan G McGrew; Catherine Lord; Marion Leboyer; Ann S Le Couteur; Alexander Kolevzon; Patricia Jiménez González; Suma Jacob; Richard Holt; Stephen Guter; Jonathan Green; Andrew Green; Christopher Gillberg; Bridget A Fernandez; Frederico Duque; Richard Delorme; Geraldine Dawson; Pauline Chaste; Cátia Café; Sean Brennan; Thomas Bourgeron; Patrick F Bolton; Sven Bölte; Raphael Bernier; Gillian Baird; Anthony J Bailey; Evdokia Anagnostou; Joana Almeida; Ellen M Wijsman; Veronica J Vieland; Astrid M Vicente; Gerard D Schellenberg; Margaret Pericak-Vance; Andrew D Paterson; Jeremy R Parr; Guiomar Oliveira; John I Nurnberger; Anthony P Monaco; Elena Maestrini; Sabine M Klauck; Hakon Hakonarson; Jonathan L Haines; Daniel H Geschwind; Christine M Freitag; Susan E Folstein; Sean Ennis; Hilary Coon; Agatino Battaglia; Peter Szatmari; James S Sutcliffe; Joachim Hallmayer; Michael Gill; Edwin H Cook; Joseph D Buxbaum; Bernie Devlin; Louise Gallagher; Catalina Betancur; Stephen W Scherer
Journal:  Am J Hum Genet       Date:  2014-04-24       Impact factor: 11.025

9.  Refining analyses of copy number variation identifies specific genes associated with developmental delay.

Authors:  Bradley P Coe; Kali Witherspoon; Jill A Rosenfeld; Bregje W M van Bon; Anneke T Vulto-van Silfhout; Paolo Bosco; Kathryn L Friend; Carl Baker; Serafino Buono; Lisenka E L M Vissers; Janneke H Schuurs-Hoeijmakers; Alex Hoischen; Rolph Pfundt; Nik Krumm; Gemma L Carvill; Deana Li; David Amaral; Natasha Brown; Paul J Lockhart; Ingrid E Scheffer; Antonino Alberti; Marie Shaw; Rosa Pettinato; Raymond Tervo; Nicole de Leeuw; Margot R F Reijnders; Beth S Torchia; Hilde Peeters; Brian J O'Roak; Marco Fichera; Jayne Y Hehir-Kwa; Jay Shendure; Heather C Mefford; Eric Haan; Jozef Gécz; Bert B A de Vries; Corrado Romano; Evan E Eichler
Journal:  Nat Genet       Date:  2014-09-14       Impact factor: 38.330

10.  Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.

Authors:  Chelsea Lowther; Marsha Speevak; Christine M Armour; Elaine S Goh; Gail E Graham; Chumei Li; Susan Zeesman; Malgorzata J M Nowaczyk; Lee-Anne Schultz; Antonella Morra; Rob Nicolson; Peter Bikangaga; Dawa Samdup; Mostafa Zaazou; Kerry Boyd; Jack H Jung; Victoria Siu; Manjulata Rajguru; Sharan Goobie; Mark A Tarnopolsky; Chitra Prasad; Paul T Dick; Asmaa S Hussain; Margreet Walinga; Renske G Reijenga; Matthew Gazzellone; Anath C Lionel; Christian R Marshall; Stephen W Scherer; Dimitri J Stavropoulos; Elizabeth McCready; Anne S Bassett
Journal:  Genet Med       Date:  2016-05-19       Impact factor: 8.822

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  16 in total

1.  Blindness, Psychosis, and the Visual Construction of the World.

Authors:  Thomas A Pollak; Philip R Corlett
Journal:  Schizophr Bull       Date:  2020-12-01       Impact factor: 9.306

Review 2.  Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders.

Authors:  Patrick F Sullivan; Daniel H Geschwind
Journal:  Cell       Date:  2019-03-21       Impact factor: 41.582

3.  Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.

Authors:  Xabier Calle Sánchez; Dorte Helenius; Jonas Bybjerg-Grauholm; Carsten Pedersen; David M Hougaard; Anders D Børglum; Merete Nordentoft; Ole Mors; Preben B Mortensen; Daniel H Geschwind; Simone Montalbano; Armin Raznahan; Wesley K Thompson; Andrés Ingason; Thomas Werge
Journal:  JAMA Psychiatry       Date:  2022-01-01       Impact factor: 21.596

4.  Deletion at 12q12 increases the risk of developmental delay and intellectual disability.

Authors:  Ying Weng; Xiaoping Luo; Ling Hou
Journal:  Ann Hum Genet       Date:  2018-08-29       Impact factor: 1.670

5.  Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Authors:  Gregory Costain; Susan Walker; Bob Argiropoulos; Danielle A Baribeau; Anne S Bassett; Erik Boot; Koen Devriendt; Barbara Kellam; Christian R Marshall; Aparna Prasad; Moises A Serrano; D James Stavropoulos; Hope Twede; Joris R Vermeesch; Jacob A S Vorstman; Stephen W Scherer
Journal:  J Neurodev Disord       Date:  2019-02-07       Impact factor: 4.025

6.  A large data resource of genomic copy number variation across neurodevelopmental disorders.

Authors:  Mehdi Zarrei; Christie L Burton; Worrawat Engchuan; Edwin J Young; Edward J Higginbotham; Jeffrey R MacDonald; Brett Trost; Ada J S Chan; Susan Walker; Sylvia Lamoureux; Tracy Heung; Bahareh A Mojarad; Barbara Kellam; Tara Paton; Muhammad Faheem; Karin Miron; Chao Lu; Ting Wang; Kozue Samler; Xiaolin Wang; Gregory Costain; Ny Hoang; Giovanna Pellecchia; John Wei; Rohan V Patel; Bhooma Thiruvahindrapuram; Maian Roifman; Daniele Merico; Tara Goodale; Irene Drmic; Marsha Speevak; Jennifer L Howe; Ryan K C Yuen; Janet A Buchanan; Jacob A S Vorstman; Christian R Marshall; Richard F Wintle; David R Rosenberg; Gregory L Hanna; Marc Woodbury-Smith; Cheryl Cytrynbaum; Lonnie Zwaigenbaum; Mayada Elsabbagh; Janine Flanagan; Bridget A Fernandez; Melissa T Carter; Peter Szatmari; Wendy Roberts; Jason Lerch; Xudong Liu; Rob Nicolson; Stelios Georgiades; Rosanna Weksberg; Paul D Arnold; Anne S Bassett; Jennifer Crosbie; Russell Schachar; Dimitri J Stavropoulos; Evdokia Anagnostou; Stephen W Scherer
Journal:  NPJ Genom Med       Date:  2019-10-07       Impact factor: 8.617

7.  Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder.

Authors:  Kristiina Tammimies; Danyang Li; Ielyzaveta Rabkina; Sofia Stamouli; Martin Becker; Veronika Nicolaou; Steve Berggren; Christina Coco; Torbjörn Falkmer; Ulf Jonsson; Nora Choque-Olsson; Sven Bölte
Journal:  Sci Rep       Date:  2019-07-08       Impact factor: 4.379

8.  Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.

Authors:  Danijela Krgovic; Nadja Kokalj Vokac; Andreja Zagorac; Hojka Gregoric Kumperscak
Journal:  Sci Rep       Date:  2018-06-21       Impact factor: 4.379

9.  Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.

Authors:  Olafur O Gudmundsson; G Bragi Walters; Andres Ingason; Stefan Johansson; Tetyana Zayats; Lavinia Athanasiu; Ida Elken Sonderby; Omar Gustafsson; Muhammad S Nawaz; Gudbjorn F Jonsson; Lina Jonsson; Per-Morten Knappskog; Ester Ingvarsdottir; Katrin Davidsdottir; Srdjan Djurovic; Gun Peggy Strømstad Knudsen; Ragna Bugge Askeland; Gyda S Haraldsdottir; Gisli Baldursson; Pall Magnusson; Engilbert Sigurdsson; Daniel F Gudbjartsson; Hreinn Stefansson; Ole A Andreassen; Jan Haavik; Ted Reichborn-Kjennerud; Kari Stefansson
Journal:  Transl Psychiatry       Date:  2019-10-17       Impact factor: 6.222

Review 10.  Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature.

Authors:  Martilias Farrell; Maya Lichtenstein; Matthew K Harner; James J Crowley; Dawn M Filmyer; Gabriel Lázaro-Muñoz; Tyler E Dietterich; Lisa M Bruno; Rita A Shaughnessy; Tamara F Biondi; Stephan Burkholder; Jane Donmoyer; Jonathan S Berg; Jin Szatkiewicz; Patrick F Sullivan; Richard C Josiassen
Journal:  Transl Psychiatry       Date:  2020-01-28       Impact factor: 6.222

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