DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder

Author:

Rooney Kathleen,van der Laan LiselotORCID,Trajkova Slavica,Haghshenas Sadegheh,Relator Raissa,Lauffer Peter,Vos Niels,Levy Michael A.,Brunetti-Pierri Nicola,Terrone Gaetano,Mignot Cyril,Keren Boris,de Villemeur Thierry B.,Volker-Touw Catharina M.L.,Verbeek Nienke,van der Smagt Jasper J.,Oegema Renske,Brusco Alfredo,Ferrero Giovanni B.,Misra-Isrie Mala,Hochstenbach Ron,Alders Mariëlle,Mannens Marcel M.A.M.,Sadikovic BekimORCID,van Haelst Mieke M.,Henneman Peter

Funder

Ontario Genomics Institute

Ministero dell’Istruzione, dell’Università e della Ricerca

Genome Canada

Government of Canada

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference46 articles.

1. Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability;Bramswig;Hum Genet,2017

2. Expanding the phenotype of HNRNPU-related neurodevelopmental disorder with emphasis on seizure phenotype and review of literature;Taylor;Am J Med Genet A,2022

3. Molecular basis for the specific and multivariant recognitions of RNA substrates by human hnRNP A2/B1;Wu;Nat Commun,2018

4. HnRNP Q Has a suppressive role in the translation of mouse Cryptochrome1;Lim;PLoS One,2016

5. The hnRNP family: insights into their role in health and disease;Geuens;Hum Genet,2016

Cited by 12 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

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