Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry-Reference-Cited by-同舟云学术

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Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry

Published:2019-07-16 Issue:1 Volume:10 Page:
ISSN:2040-2392
Container-title:Molecular Autism
language:en
Short-container-title:Molecular Autism

Author:

Pollak Rebecca M., ,Murphy Melissa M.,Epstein Michael P.,Zwick Michael E.,Klaiman Cheryl,Saulnier Celine A.,Mulle Jennifer G.^ORCID

Funder

National Institute of Mental Health

National Institutes of Health

School of Medicine, Emory University

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1186/s13229-019-0281-5.pdf

Reference75 articles.

1. Stefansson H, Meyer-Lindenberg A, Steinberg S, Magnusdottir B, Morgen K, Arnarsdottir S, Bjornsdottir G, Walters GB, Jonsdottir GA, Doyle OM, et al. CNVs conferring risk of autism or schizophrenia affect cognition in controls. Nature. 2014;505:361–6.

2. Kendall KM, Rees E, Escott-Price V, Einon M, Thomas R, Hewitt J, O’Donovan MC, Owen MJ, Walters JTR, Kirov G. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK biobank subjects. Biol Psychiatry. 2017;82:103–10.

3. Willatt L, Cox J, Barber J, Cabanas ED, Collins A, Donnai D, FitzPatrick DR, Maher E, Martin H, Parnau J, et al. 3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome. Am J Hum Genet. 2005;77:154–60.

4. Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, et al. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication. Mol Cytogenet. 2008;1:8.

5. Glassford MR, Rosenfeld JA, Freedman AA, Zwick ME, Mulle JG. Unique Rare Chromosome Disorder Support G: Novel features of 3q29 deletion syndrome: results from the 3q29 registry. Am J Med Genet Part A. 2016;170A:999–1006.

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