Literature DB >> 25156961

Targeted next-generation sequencing in the diagnosis of neurodevelopmental disorders.

N Okamoto1, F Miya2, T Tsunoda2, M Kato3, S Saitoh4, M Yamasaki5, A Shimizu6, C Torii7, Y Kanemura8,9, K Kosaki7.   

Abstract

We developed a next-generation sequencing (NGS) based mutation screening strategy for neurodevelopmental diseases. Using this system, we screened 284 genes in 40 patients. Several novel mutations were discovered. Patient 1 had a novel mutation in ACTB. Her dysmorphic feature was mild for Baraitser-Winter syndrome. Patient 2 had a truncating mutation of DYRK1A. She lacked microcephaly, which was previously assumed to be a constant feature of DYRK1A loss of function. Patient 3 had a novel mutation in GABRD gene. She showed Rett syndrome like features. Patient 4 was diagnosed with Noonan syndrome with PTPN11 mutation. He showed complete agenesis of corpus callosum. We have discussed these novel findings.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Baraitser-Winter syndrome; DYRK1A; GABRD; next-generation sequencing

Mesh:

Substances:

Year:  2014        PMID: 25156961     DOI: 10.1111/cge.12492

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  16 in total

1.  Could Dissimilar Phenotypic Effects of ACTB Missense Mutations Reflect the Actin Conformational Change? Two Novel Mutations and Literature Review.

Authors:  Anna Sandestig; Anna Green; Jon Jonasson; Hartmut Vogt; Johan Wahlström; Alexander Pepler; Katarina Ellnebo; Saskia Biskup; Margarita Stefanova
Journal:  Mol Syndromol       Date:  2018-08-09

2.  Exploration of Potential Ewing Sarcoma Drugs from FDA-Approved Pharmaceuticals through Computational Drug Repositioning, Pharmacogenomics, Molecular Docking, and MD Simulation Studies.

Authors:  Mubashir Hassan; Muhammad Yasir; Saba Shahzadi; Andrzej Kloczkowski
Journal:  ACS Omega       Date:  2022-06-01

3.  De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsy.

Authors:  Kameryn M Butler; Olivia A Moody; Elisabeth Schuler; Jason Coryell; John J Alexander; Andrew Jenkins; Andrew Escayg
Journal:  Brain       Date:  2018-08-01       Impact factor: 13.501

4.  Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.

Authors:  B W M van Bon; B P Coe; R Bernier; C Green; J Gerdts; K Witherspoon; T Kleefstra; M H Willemsen; R Kumar; P Bosco; M Fichera; D Li; D Amaral; F Cristofoli; H Peeters; E Haan; C Romano; H C Mefford; I Scheffer; J Gecz; B B A de Vries; E E Eichler
Journal:  Mol Psychiatry       Date:  2015-02-24       Impact factor: 15.992

5.  Ocular Phenotype Associated with DYRK1A Variants.

Authors:  Cécile Méjécase; Christopher M Way; Nicholas Owen; Mariya Moosajee
Journal:  Genes (Basel)       Date:  2021-02-05       Impact factor: 4.096

6.  A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations.

Authors:  Fuyuki Miya; Mitsuhiro Kato; Tadashi Shiohama; Nobuhiko Okamoto; Shinji Saitoh; Mami Yamasaki; Daichi Shigemizu; Tetsuo Abe; Takashi Morizono; Keith A Boroevich; Kenjiro Kosaki; Yonehiro Kanemura; Tatsuhiko Tsunoda
Journal:  Sci Rep       Date:  2015-03-19       Impact factor: 4.379

7.  Autism Linked to Increased Oncogene Mutations but Decreased Cancer Rate.

Authors:  Benjamin W Darbro; Rohini Singh; M Bridget Zimmerman; Vinit B Mahajan; Alexander G Bassuk
Journal:  PLoS One       Date:  2016-03-02       Impact factor: 3.240

Review 8.  Reviewing Evidence for the Relationship of EEG Abnormalities and RTT Phenotype Paralleled by Insights from Animal Studies.

Authors:  Kirill Smirnov; Tatiana Stroganova; Sophie Molholm; Olga Sysoeva
Journal:  Int J Mol Sci       Date:  2021-05-18       Impact factor: 5.923

Review 9.  The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome.

Authors:  Wendy Anne Gold; John Christodoulou
Journal:  Front Cell Neurosci       Date:  2015-07-14       Impact factor: 5.505

10.  Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.

Authors:  Mario Lucariello; Enrique Vidal; Silvia Vidal; Mauricio Saez; Laura Roa; Dori Huertas; Mercè Pineda; Esther Dalfó; Joaquin Dopazo; Paola Jurado; Judith Armstrong; Manel Esteller
Journal:  Hum Genet       Date:  2016-08-19       Impact factor: 4.132

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