Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of <i>LRFN5</i> Expression-Reference-Cited by-同舟云学术

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Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression

Published:2010 Issue:1 Volume:1 Page:46-57
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

de Bruijn D.R.H.,van Dijk A.H.A.,Pfundt R.,Hoischen A.,Merkx G.F.M.,Gradek G.A.,Lybæk H.,Stray-Pedersen A.,Brunner H.G.,Houge G.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 36 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2024-06-04

2. Two polygenic mouse models of major depressive disorders identify TMEM161B as a potential biomarker of disease in humans;Neuropsychopharmacology;2024-02-07

3. A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome;Scientific Reports;2023-08-10

4. LRFN5 and OLFM4 as novel potential biomarkers for major depressive disorder: a pilot study;Translational Psychiatry;2023-06-06

5. A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome;2023-03-27

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