Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications-Reference-Cited by-同舟云学术

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications

Published:2018-03-31 Issue:4 Volume:177 Page:397-405
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Wolfe Kate¹^ORCID,McQuillin Andrew¹,Alesi Viola²,Boudry Labis Elise³,Cutajar Peter⁴,Dallapiccola Bruno²,Dentici Maria Lisa²,Dieux-Coeslier Anne⁵⁶,Duban-Bedu Benedicte⁷,Duelund Hjortshøj Tina⁸,Goel Himanshu⁹¹⁰,Loddo Sara²,Morrogh Deborah¹¹,Mosca-Boidron Anne-Laure¹²,Novelli Antonio²,Olivier-Faivre Laurence¹³^ORCID,Parker Jennifer¹¹,Parker Michael J.¹⁴,Patch Christine¹⁵¹⁶,Pelling Anna L.¹⁷,Smol Thomas³⁶,Tümer Zeynep⁸,Vanakker Olivier¹⁸,van Haeringen Arie¹⁹,Vanlerberghe Clémence⁵⁶,Strydom Andre¹²⁰,Skuse David²¹,Bass Nick¹

Affiliation:

1. Molecular Psychiatry Laboratory, Division of Psychiatry; University College London; London United Kingdom

2. Medical Genetics Unit, Medical Genetics Laboratory; Bambino Gesù Pediatric Hospital, IRCCS; Rome Italy

3. Institut de génétique médicale, CHU Lille; Lille France

4. Nottinghamshire Healthcare NHS Foundation Trust; Nottingham United Kingdom

5. Service de génétique clinique, CHU Lille; Lille France

6. EA7364, RADEME, Université de Lille; Lille France

7. Centre de génétique chromosomique, Hopital Saint-Vincent de Paul; Lille France

8. Kennedy Center, Department of Clinical Genetics; Copenhagen University Hospital, Rigshospitalet; Copenhagen Denmark

9. Hunter Genetics; Waratah New South Wales Australia

10. University of Newcastle; Callaghan New South Wales Australia

11. North East Thames Regional Genetics Service Laboratory; London United Kingdom

12. Service de Cytogénétique, Plateau technique de Biologie; CHU Dijon France

13. Centre de référence Anomalies du développement et Syndromes malformatifs, FHU TRANSLAD; CHU Dijon France

14. Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Western Bank; Sheffield United Kingdom

15. King's College London, Florence Nightingale Faculty of Nursing and Midwifery; London United Kingdom

16. Genomics England, Dawson Hall, Charterhouse Square; London United Kingdom

17. Information Officer, Unique - The Rare Chromosome Disorder Support Group (www.rarechromo.org), The Stables, Station Road West; Oxted, Surrey United Kingdom

18. Center for Medical Genetics; Ghent University Hospital; Ghent Belgium

19. Department of Clinical Genetics; Leiden University Medical Center; Leiden The Netherlands

20. Department of Forensic and Neurodevelopmental Science; Institute of Psychiatry, Psychology and Neuroscience, Kings College London; London United Kingdom

21. Behavioural and Brain Sciences Unit; Institute of Child Health, University College London; London United Kingdom

Funder

Baily Thomas Charitable Fund

Medical Research Council

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference29 articles.

1. Transmitted cytogenetic abnormalities in patients with mental retardation: Pathogenic or normal variants?;Bisgaard;European Journal of Medical Genetics,2007

2. A copy number variation morbidity map of developmental delay;Cooper;Nature Genetics,2011

3. Adult neuropsychiatric expression and familial segregation of 2q13 duplications;Costain;American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics,2014