Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders-Reference-Cited by-同舟云学术

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Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders

Published:2018-03-25 Issue:5 Volume:78 Page:519-530
ISSN:1932-8451
Container-title:Developmental Neurobiology
language:en
Short-container-title:Devel Neurobio

Author:

Deshpande Aditi¹²³^ORCID,Weiss Lauren A.¹²³^ORCID

Affiliation:

1. Department of Psychiatry; University of California, San Francisco; San Francisco California 94143

2. Institute for Human Genetics, University of California, San Francisco; San Francisco California 94143

3. Weill Institute for Neurosciences, University of California, San Francisco; San Francisco California 94143

Funder

International Mental Health Research Organization

Simons Foundation

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Developmental Neuroscience

Reference90 articles.

1. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected];Alkuraya;Am J Hum Genet,2011

2. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans;Ardlie;Science (80-),2015

3. Mutations and modeling of the chromatin remodeler CHD8 define an emerging autism etiology;Barnard;Front Neurosci,2015

4. Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease;Bassett;Am J Psychiatry,2010

5. Developmental trajectories for young children with 16p11.2 copy number variation;Bernier;Am J Med Genet B Neuropsychiatr Genet,2017

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2. Experience of copy number variation sequencing applied in spontaneous abortion;BMC Medical Genomics;2024-01-08

3. Clinical application of single nucleotide polymorphism microarray analysis in pregnancy loss in Northwest China;Frontiers in Genetics;2023-12-14

4. Pathogenic recurrent copy number variants in 7,078 pregnancies via chromosomal microarray analysis;Journal of Perinatal Medicine;2023-12-12

5. Cell-type specific global reprogramming of the transcriptome and epigenome in induced neurons with the 16p11.2 neuropsychiatric CNVs;2023-08-04

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