Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

Published:2019-02-11 Issue:1 Volume:9 Page:
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Gialluisi Alessandro^ORCID,Andlauer Till F. M.^ORCID,Mirza-Schreiber Nazanin,Moll Kristina,Becker Jessica,Hoffmann Per^ORCID,Ludwig Kerstin U.^ORCID,Czamara Darina^ORCID,St Pourcain Beate^ORCID,Brandler William,Honbolygó Ferenc,Tóth Dénes,Csépe Valéria,Huguet Guillaume,Morris Andrew P.,Hulslander Jacqueline,Willcutt Erik G.,DeFries John C.,Olson Richard K.,Smith Shelley D.,Pennington Bruce F.,Vaessen Anniek,Maurer Urs,Lyytinen Heikki,Peyrard-Janvid Myriam,Leppänen Paavo H. T.,Brandeis Daniel,Bonte Milene,Stein John F.^ORCID,Talcott Joel B.^ORCID,Fauchereau Fabien,Wilcke Arndt,Francks Clyde,Bourgeron Thomas,Monaco Anthony P.,Ramus Franck^ORCID,Landerl Karin,Kere Juha^ORCID,Scerri Thomas S.,Paracchini Silvia^ORCID,Fisher Simon E.^ORCID,Schumacher Johannes,Nöthen Markus M.,Müller-Myhsok Bertram,Schulte-Körne Gerd

Funder

Max-Planck-Gesellschaft

Wellcome Trust

Agence Nationale de la Recherche

European Commission

Royal Society

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health

Link

http://www.nature.com/articles/s41398-019-0402-0.pdf

Reference118 articles.

1. Mascheretti, S. et al. Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms. Transl. Psychiatry 7, e987 (2017).

2. Margari, L. et al. Neuropsychopathological comorbidities in learning disorders. Bmc. Neurol. 13, 198 (2013).

3. Raskind, W. H., Peter, B., Richards, T., Eckert, M. M. & Berninger, V. W. The genetics of reading disabilities: From phenotypes to candidate genes. Front. Psychol. 3, 1–20 (2013).

4. Willcutt, E. G. et al. Etiology and neuropsychology of comorbidity between RD and ADHD: The case for multiple-deficit models. Cortex 46, 1345–1361 (2010).

5. Davis, C. J. et al. Etiology of reading difficulties and rapid naming: the Colorado twin study of reading disability. Behav. Genet. 31, 625–635 (2001).

Cited by 84 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. Alterations in neural activation in the ventral frontoparietal network during complex magnocellular stimuli in developmental dyslexia associated with READ1 deletion;Behavioral and Brain Functions;2024-06-26

2. Interaction between Risk Single-Nucleotide Polymorphisms of Developmental Dyslexia and Parental Education on Reading Ability: Evidence for Differential Susceptibility Theory;Behavioral Sciences;2024-06-19

3. The Emotional Impact of Family Involvement during Homework in Children with Neurodevelopmental Disorders: A Systematic Review;Children;2024-06-10

4. Continuity and change of genetic and environmental influences on reading and reading-related neurocognitive skills: A systematic review of longitudinal twin studies;Neuroscience & Biobehavioral Reviews;2024-04

5. Unraveling individual differences in learning potential: A dynamic framework for the case of reading development;Developmental Cognitive Neuroscience;2024-04

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3