Literature DB >> 23582872

Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Matthew F Pescosolido1, Ece D Gamsiz, Shailender Nagpal, Eric M Morrow.   

Abstract

OBJECTIVE: The purpose of the present study was to discover the extent to which distinct DSM disorders share large, highly recurrent copy number variants (CNVs) as susceptibility factors. We also sought to identify gene mechanisms common to groups of diagnoses and/or specific to a given diagnosis based on associations with CNVs.
METHOD: Systematic review of 820 PubMed articles on autism spectrum disorder (ASD), intellectual disability (ID), schizophrenia, and epilepsy produced 54 CNVs associated with one or several disorders. Pathway analysis on genes implicated by CNVs in different groupings was conducted.
RESULTS: The majority of CNVs were found in ID with the other disorders somewhat subsumed, yet certain CNVs were associated with isolated or groups of disorders. Based on genes implicated by CNVs, ID encompassed 96.8% of genes in ASD, 92.8% of genes in schizophrenia, and 100.0% of genes in epilepsy. Pathway analysis revealed that synapse processes were enriched in ASD, ID, and schizophrenia. Disease-specific processes were identified in ID (actin cytoskeleton processes), schizophrenia (ubiquitin-related processes), and ASD (synaptic vesicle transport and exocytosis).
CONCLUSIONS: Intellectual disability may arise from the broadest range of genetic pathways, and specific subsets of these pathways appear to be relevant to other disorders or combinations of these disorders. It is clear that statistically significant CNVs across disorders of cognitive development are highly enriched for biological processes related to the synapse. There are also disorder-specific processes that may aid in understanding the distinct presentations and pathophysiology of these disorders.
Copyright © 2013 American Academy of Child & Adolescent Psychiatry. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23582872      PMCID: PMC3774163          DOI: 10.1016/j.jaac.2013.01.003

Source DB:  PubMed          Journal:  J Am Acad Child Adolesc Psychiatry        ISSN: 0890-8567            Impact factor:   8.829


  79 in total

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Authors:  Eric M Morrow
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2010-11       Impact factor: 8.829

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Journal:  Am J Hum Genet       Date:  2012-04-12       Impact factor: 11.025

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

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Journal:  Neuron       Date:  2011-12-22       Impact factor: 17.173

4.  Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

Authors:  W Yan; L K Jacobsen; D M Krasnewich; X Y Guan; M C Lenane; S P Paul; H N Dalwadi; H Zhang; R T Long; S Kumra; B M Martin; P J Scambler; J M Trent; E Sidransky; E I Ginns; J L Rapoport
Journal:  Am J Med Genet       Date:  1998-02-07

5.  Rare chromosomal deletions and duplications increase risk of schizophrenia.

Authors: 
Journal:  Nature       Date:  2008-07-30       Impact factor: 49.962

6.  Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Authors:  Joseph T Glessner; Kai Wang; Guiqing Cai; Olena Korvatska; Cecilia E Kim; Shawn Wood; Haitao Zhang; Annette Estes; Camille W Brune; Jonathan P Bradfield; Marcin Imielinski; Edward C Frackelton; Jennifer Reichert; Emily L Crawford; Jeffrey Munson; Patrick M A Sleiman; Rosetta Chiavacci; Kiran Annaiah; Kelly Thomas; Cuiping Hou; Wendy Glaberson; James Flory; Frederick Otieno; Maria Garris; Latha Soorya; Lambertus Klei; Joseph Piven; Kacie J Meyer; Evdokia Anagnostou; Takeshi Sakurai; Rachel M Game; Danielle S Rudd; Danielle Zurawiecki; Christopher J McDougle; Lea K Davis; Judith Miller; David J Posey; Shana Michaels; Alexander Kolevzon; Jeremy M Silverman; Raphael Bernier; Susan E Levy; Robert T Schultz; Geraldine Dawson; Thomas Owley; William M McMahon; Thomas H Wassink; John A Sweeney; John I Nurnberger; Hilary Coon; James S Sutcliffe; Nancy J Minshew; Struan F A Grant; Maja Bucan; Edwin H Cook; Joseph D Buxbaum; Bernie Devlin; Gerard D Schellenberg; Hakon Hakonarson
Journal:  Nature       Date:  2009-04-28       Impact factor: 49.962

7.  Microduplications of 16p11.2 are associated with schizophrenia.

Authors:  Shane E McCarthy; Vladimir Makarov; George Kirov; Anjene M Addington; Jon McClellan; Seungtai Yoon; Diana O Perkins; Diane E Dickel; Mary Kusenda; Olga Krastoshevsky; Verena Krause; Ravinesh A Kumar; Detelina Grozeva; Dheeraj Malhotra; Tom Walsh; Elaine H Zackai; Paige Kaplan; Jaya Ganesh; Ian D Krantz; Nancy B Spinner; Patricia Roccanova; Abhishek Bhandari; Kevin Pavon; B Lakshmi; Anthony Leotta; Jude Kendall; Yoon-Ha Lee; Vladimir Vacic; Sydney Gary; Lilia M Iakoucheva; Timothy J Crow; Susan L Christian; Jeffrey A Lieberman; T Scott Stroup; Terho Lehtimäki; Kaija Puura; Chad Haldeman-Englert; Justin Pearl; Meredith Goodell; Virginia L Willour; Pamela Derosse; Jo Steele; Layla Kassem; Jessica Wolff; Nisha Chitkara; Francis J McMahon; Anil K Malhotra; James B Potash; Thomas G Schulze; Markus M Nöthen; Sven Cichon; Marcella Rietschel; Ellen Leibenluft; Vlad Kustanovich; Clara M Lajonchere; James S Sutcliffe; David Skuse; Michael Gill; Louise Gallagher; Nancy R Mendell; Nick Craddock; Michael J Owen; Michael C O'Donovan; Tamim H Shaikh; Ezra Susser; Lynn E Delisi; Patrick F Sullivan; Curtis K Deutsch; Judith Rapoport; Deborah L Levy; Mary-Claire King; Jonathan Sebat
Journal:  Nat Genet       Date:  2009-10-25       Impact factor: 38.330

8.  Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.

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Journal:  Am J Psychiatry       Date:  2011-02-15       Impact factor: 18.112

9.  Large recurrent microdeletions associated with schizophrenia.

Authors:  Hreinn Stefansson; Dan Rujescu; Sven Cichon; Olli P H Pietiläinen; Andres Ingason; Stacy Steinberg; Ragnheidur Fossdal; Engilbert Sigurdsson; Thordur Sigmundsson; Jacobine E Buizer-Voskamp; Thomas Hansen; Klaus D Jakobsen; Pierandrea Muglia; Clyde Francks; Paul M Matthews; Arnaldur Gylfason; Bjarni V Halldorsson; Daniel Gudbjartsson; Thorgeir E Thorgeirsson; Asgeir Sigurdsson; Adalbjorg Jonasdottir; Aslaug Jonasdottir; Asgeir Bjornsson; Sigurborg Mattiasdottir; Thorarinn Blondal; Magnus Haraldsson; Brynja B Magnusdottir; Ina Giegling; Hans-Jürgen Möller; Annette Hartmann; Kevin V Shianna; Dongliang Ge; Anna C Need; Caroline Crombie; Gillian Fraser; Nicholas Walker; Jouko Lonnqvist; Jaana Suvisaari; Annamarie Tuulio-Henriksson; Tiina Paunio; Timi Toulopoulou; Elvira Bramon; Marta Di Forti; Robin Murray; Mirella Ruggeri; Evangelos Vassos; Sarah Tosato; Muriel Walshe; Tao Li; Catalina Vasilescu; Thomas W Mühleisen; August G Wang; Henrik Ullum; Srdjan Djurovic; Ingrid Melle; Jes Olesen; Lambertus A Kiemeney; Barbara Franke; Chiara Sabatti; Nelson B Freimer; Jeffrey R Gulcher; Unnur Thorsteinsdottir; Augustine Kong; Ole A Andreassen; Roel A Ophoff; Alexander Georgi; Marcella Rietschel; Thomas Werge; Hannes Petursson; David B Goldstein; Markus M Nöthen; Leena Peltonen; David A Collier; David St Clair; Kari Stefansson
Journal:  Nature       Date:  2008-09-11       Impact factor: 49.962

10.  Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Authors:  Brian J O'Roak; Pelagia Deriziotis; Choli Lee; Laura Vives; Jerrod J Schwartz; Santhosh Girirajan; Emre Karakoc; Alexandra P Mackenzie; Sarah B Ng; Carl Baker; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Simon E Fisher; Jay Shendure; Evan E Eichler
Journal:  Nat Genet       Date:  2011-05-15       Impact factor: 38.330

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1.  Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Authors:  Lauren M McGrath; Dongmei Yu; Christian Marshall; Lea K Davis; Bhooma Thiruvahindrapuram; Bingbin Li; Carolina Cappi; Gloria Gerber; Aaron Wolf; Frederick A Schroeder; Lisa Osiecki; Colm O'Dushlaine; Andrew Kirby; Cornelia Illmann; Stephen Haddad; Patience Gallagher; Jesen A Fagerness; Cathy L Barr; Laura Bellodi; Fortu Benarroch; O Joseph Bienvenu; Donald W Black; Michael H Bloch; Ruth D Bruun; Cathy L Budman; Beatriz Camarena; Danielle C Cath; Maria C Cavallini; Sylvain Chouinard; Vladimir Coric; Bernadette Cullen; Richard Delorme; Damiaan Denys; Eske M Derks; Yves Dion; Maria C Rosário; Valsama Eapen; Patrick Evans; Peter Falkai; Thomas V Fernandez; Helena Garrido; Daniel Geller; Hans J Grabe; Marco A Grados; Benjamin D Greenberg; Varda Gross-Tsur; Edna Grünblatt; Gary A Heiman; Sian M J Hemmings; Luis D Herrera; Ana G Hounie; Joseph Jankovic; James L Kennedy; Robert A King; Roger Kurlan; Nuria Lanzagorta; Marion Leboyer; James F Leckman; Leonhard Lennertz; Christine Lochner; Thomas L Lowe; Gholson J Lyon; Fabio Macciardi; Wolfgang Maier; James T McCracken; William McMahon; Dennis L Murphy; Allan L Naarden; Benjamin M Neale; Erika Nurmi; Andrew J Pakstis; Michele T Pato; Carlos N Pato; John Piacentini; Christopher Pittenger; Yehuda Pollak; Victor I Reus; Margaret A Richter; Mark Riddle; Mary M Robertson; David Rosenberg; Guy A Rouleau; Stephan Ruhrmann; Aline S Sampaio; Jack Samuels; Paul Sandor; Brooke Sheppard; Harvey S Singer; Jan H Smit; Dan J Stein; Jay A Tischfield; Homero Vallada; Jeremy Veenstra-VanderWeele; Susanne Walitza; Ying Wang; Jens R Wendland; Yin Yao Shugart; Euripedes C Miguel; Humberto Nicolini; Ben A Oostra; Rainald Moessner; Michael Wagner; Andres Ruiz-Linares; Peter Heutink; Gerald Nestadt; Nelson Freimer; Tracey Petryshen; Danielle Posthuma; Michael A Jenike; Nancy J Cox; Gregory L Hanna; Helena Brentani; Stephen W Scherer; Paul D Arnold; S Evelyn Stewart; Carol A Mathews; James A Knowles; Edwin H Cook; David L Pauls; Kai Wang; Jeremiah M Scharf
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2014-06-24       Impact factor: 8.829

2.  Genomic imbalances in pediatric patients with chronic kidney disease.

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3.  The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development.

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Journal:  Cell       Date:  2018-11-01       Impact factor: 41.582

Review 4.  Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms.

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Review 5.  Delivery of epilepsy care to adults with intellectual and developmental disabilities.

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6.  Pathway-wide association study identifies five shared pathways associated with schizophrenia in three ancestral distinct populations.

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7.  Familial risk of epilepsy: a population-based study.

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Journal:  Brain       Date:  2014-01-26       Impact factor: 13.501

8.  Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

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9.  Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Authors:  S H Witt; F Streit; M Jungkunz; J Frank; S Awasthi; C S Reinbold; J Treutlein; F Degenhardt; A J Forstner; S Heilmann-Heimbach; L Dietl; C E Schwarze; D Schendel; J Strohmaier; A Abdellaoui; R Adolfsson; T M Air; H Akil; M Alda; N Alliey-Rodriguez; O A Andreassen; G Babadjanova; N J Bass; M Bauer; B T Baune; F Bellivier; S Bergen; A Bethell; J M Biernacka; D H R Blackwood; M P Boks; D I Boomsma; A D Børglum; M Borrmann-Hassenbach; P Brennan; M Budde; H N Buttenschøn; E M Byrne; P Cervantes; T-K Clarke; N Craddock; C Cruceanu; D Curtis; P M Czerski; U Dannlowski; T Davis; E J C de Geus; A Di Florio; S Djurovic; E Domenici; H J Edenberg; B Etain; S B Fischer; L Forty; C Fraser; M A Frye; J M Fullerton; K Gade; E S Gershon; I Giegling; S D Gordon; K Gordon-Smith; H J Grabe; E K Green; T A Greenwood; M Grigoroiu-Serbanescu; J Guzman-Parra; L S Hall; M Hamshere; J Hauser; M Hautzinger; U Heilbronner; S Herms; S Hitturlingappa; P Hoffmann; P Holmans; J-J Hottenga; S Jamain; I Jones; L A Jones; A Juréus; R S Kahn; J Kammerer-Ciernioch; G Kirov; S Kittel-Schneider; S Kloiber; S V Knott; M Kogevinas; M Landén; M Leber; M Leboyer; Q S Li; J Lissowska; S Lucae; N G Martin; F Mayoral-Cleries; S L McElroy; A M McIntosh; J D McKay; A McQuillin; S E Medland; C M Middeldorp; Y Milaneschi; P B Mitchell; G W Montgomery; G Morken; O Mors; T W Mühleisen; B Müller-Myhsok; R M Myers; C M Nievergelt; J I Nurnberger; M C O'Donovan; L M O Loohuis; R Ophoff; L Oruc; M J Owen; S A Paciga; B W J H Penninx; A Perry; A Pfennig; J B Potash; M Preisig; A Reif; F Rivas; G A Rouleau; P R Schofield; T G Schulze; M Schwarz; L Scott; G C B Sinnamon; E A Stahl; J Strauss; G Turecki; S Van der Auwera; H Vedder; J B Vincent; G Willemsen; C C Witt; N R Wray; H S Xi; A Tadic; N Dahmen; B H Schott; S Cichon; M M Nöthen; S Ripke; A Mobascher; D Rujescu; K Lieb; S Roepke; C Schmahl; M Bohus; M Rietschel
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Review 10.  Genetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical Landscape.

Authors:  Brenda Finucane; Scott M Myers
Journal:  Curr Genet Med Rep       Date:  2016-06-24
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