Literature DB >> 20565924

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.

Richard Delorme1, Daniel Moreno-De-Luca, Aurélie Gennetier, Wolfgang Maier, Pauline Chaste, Rainald Mössner, Hans Jörgen Grabe, Stephan Ruhrmann, Peter Falkai, Marie-Christine Mouren, Marion Leboyer, Michael Wagner, Catalina Betancur.   

Abstract

BACKGROUND: Obsessive-compulsive disorder (OCD) is a clinically and etiologically heterogeneous syndrome. The high frequency of obsessive-compulsive symptoms reported in subjects with the 22q11.2 deletion syndrome (DiGeorge/velocardiofacial syndrome) or Prader-Willi syndrome (15q11-13 deletion of the paternally derived chromosome), suggests that gene dosage effects in these chromosomal regions could increase risk for OCD. Therefore, the aim of this study was to search for microrearrangements in these two regions in OCD patients.
METHODS: We screened the 15q11-13 and 22q11.2 chromosomal regions for genomic imbalances in 236 patients with OCD using multiplex ligation-dependent probe amplification (MLPA).
RESULTS: No deletions or duplications involving 15q11-13 or 22q11.2 were identified in our patients.
CONCLUSIONS: Our results suggest that deletions/duplications of chromosomes 15q11-13 and 22q11.2 are rare in OCD. Despite the negative findings in these two regions, the search for copy number variants in OCD using genome-wide array-based methods is a highly promising approach to identify genes of etiologic importance in the development of OCD.

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Year:  2010        PMID: 20565924      PMCID: PMC2909937          DOI: 10.1186/1471-2350-11-100

Source DB:  PubMed          Journal:  BMC Med Genet        ISSN: 1471-2350            Impact factor:   2.103


  41 in total

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Authors:  Annemieke J M H Verkerk; Carol A Mathews; Marijke Joosse; Bert H J Eussen; Peter Heutink; Ben A Oostra
Journal:  Genomics       Date:  2003-07       Impact factor: 5.736

3.  Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.

Authors:  Matthew W State; John M Greally; Adam Cuker; Peter N Bowers; Octavian Henegariu; Thomas M Morgan; Murat Gunel; Michael DiLuna; Robert A King; Carol Nelson; Abigail Donovan; George M Anderson; James F Leckman; Trevor Hawkins; David L Pauls; Richard P Lifton; David C Ward
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-07       Impact factor: 11.205

4.  Emergence of compulsive behavior and tantrums in children with Prader-Willi syndrome.

Authors:  A Dimitropoulos; I D Feurer; M G Butler; T Thompson
Journal:  Am J Ment Retard       Date:  2001-01

5.  Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.

Authors:  A E Pulver; G Nestadt; R Goldberg; R J Shprintzen; M Lamacz; P S Wolyniec; B Morrow; M Karayiorgou; S E Antonarakis; D Housman
Journal:  J Nerv Ment Dis       Date:  1994-08       Impact factor: 2.254

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Journal:  J Am Acad Child Psychiatry       Date:  1982-07

7.  Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

Authors:  D F Papolos; G L Faedda; S Veit; R Goldberg; B Morrow; R Kucherlapati; R J Shprintzen
Journal:  Am J Psychiatry       Date:  1996-12       Impact factor: 18.112

Review 8.  Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.

Authors:  Douglas C Bittel; Merlin G Butler
Journal:  Expert Rev Mol Med       Date:  2005-07-25       Impact factor: 5.600

Review 9.  Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.

Authors:  Lisa J Kobrynski; Kathleen E Sullivan
Journal:  Lancet       Date:  2007-10-20       Impact factor: 79.321

10.  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

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  8 in total

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

Review 2.  Genetics of obsessive-compulsive disorder and related disorders.

Authors:  Heidi A Browne; Shannon L Gair; Jeremiah M Scharf; Dorothy E Grice
Journal:  Psychiatr Clin North Am       Date:  2014-07-23

3.  High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder.

Authors:  Edna Grünblatt; Beatrice Oneda; Arif B Ekici; Juliane Ball; Julia Geissler; Steffen Uebe; Marcel Romanos; Anita Rauch; Susanne Walitza
Journal:  BMC Med Genomics       Date:  2017-11-28       Impact factor: 3.063

4.  Obsessive Compulsive Symptoms and Psychopathological Profile in Children and Adolescents with KBG syndrome.

Authors:  Paolo Alfieri; Francesco Demaria; Serena Licchelli; Ornella Santonastaso; Cristina Caciolo; Maria Cristina Digilio; Lorenzo Sinibaldi; Chiara Leoni; Maria Gnazzo; Marco Tartaglia; Patrizio Pasqualetti; Stefano Vicari
Journal:  Brain Sci       Date:  2019-11-07

5.  Mutation screening of the UBE3A gene in Chinese Han population with autism.

Authors:  Xue Zhao; Ran Zhang; Shunying Yu
Journal:  BMC Psychiatry       Date:  2020-12-11       Impact factor: 3.630

6.  An inherited small microdeletion at 15q13.3 in a patient with early-onset obsessive-compulsive disorder.

Authors:  Carolina Cappi; Ana Gabriela Hounie; Daniel B Mariani; Juliana Belo Diniz; Aderbal R T Silva; Viviane N S Reis; Ariane F Busso; Amanda Gonçalves Silva; Felipe Fidalgo; Silvia Regina Rogatto; Euripedes C Miguel; Ana C Krepischi; Helena Brentani
Journal:  PLoS One       Date:  2014-10-10       Impact factor: 3.240

7.  Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways.

Authors:  C Cappi; H Brentani; L Lima; S J Sanders; G Zai; B J Diniz; V N S Reis; A G Hounie; M Conceição do Rosário; D Mariani; G L Requena; R Puga; F L Souza-Duran; R G Shavitt; D L Pauls; E C Miguel; T V Fernandez
Journal:  Transl Psychiatry       Date:  2016-03-29       Impact factor: 6.222

8.  Defining Mental and Behavioural Disorders in Genetically Determined Neurodevelopmental Syndromes with Particular Reference to Prader-Willi Syndrome.

Authors:  Anthony J Holland; Lucie C S Aman; Joyce E Whittington
Journal:  Genes (Basel)       Date:  2019-12-09       Impact factor: 4.096

  8 in total

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