Identification of NCAN as a candidate gene for developmental dyslexia-Reference-Cited by-同舟云学术

Identification of NCAN as a candidate gene for developmental dyslexia

Published:2017-08-24 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Einarsdottir Elisabet^ORCID,Peyrard-Janvid Myriam,Darki Fahimeh,Tuulari Jetro J.,Merisaari Harri^ORCID,Karlsson Linnea,Scheinin Noora M.,Saunavaara Jani,Parkkola Riitta,Kantojärvi Katri,Ämmälä Antti-Jussi,Yiu-Lin Yu Nancy^ORCID,Matsson Hans,Nopola-Hemmi Jaana,Karlsson Hasse,Paunio Tiina,Klingberg Torkel,Leinonen Eira,Kere Juha^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-10175-7.pdf

Reference62 articles.

1. Habib, M. & Giraud, K. Dyslexia. Handbook of clinical neurology 111, 229–235, doi: 10.1016/B978-0-444-52891-9.00023-3 (2013).

2. Anthoni, H., Sucheston, L. E. & Lewis, B. A. et al. The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language. Behavior genetics 42, 509–527, doi: 10.1007/s10519-012-9532-3 (2012).

3. Hannula-Jouppi, K., Kaminen-Ahola, N. & Taipale, M. et al. The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS genetics 1, e50, doi: 10.1371/journal.pgen.0010050 (2005).

4. Taipale, M., Kaminen, N. & Nopola-Hemmi, J. et al. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proceedings of the National Academy of Sciences of the United States of America 100, 11553–11558, doi: 10.1073/pnas.1833911100 (2003).

5. Hofmeister, W., Nilsson, D. & Topa, A. et al. CTNND2-a candidate gene for reading problems and mild intellectual disability. Journal of medical genetics 52, 111–122, doi: 10.1136/jmedgenet-2014-102757 (2015).

Cited by 16 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. Human‐specific insights into candidate genes and boosted discoveries of novel loci illuminate roles of neuroglia in reading disorders;Genes, Brain and Behavior;2024-05-16

2. Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay;European Journal of Medical Genetics;2023-01

3. The Role of Genetic Factors in Reading and its Development Across Languages and Writing Systems;Scientific Studies of Reading;2022-01-31

4. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family;Human Genetics;2021-06-02

5. The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder;Brain Sciences;2021-05-14