Frontiers in Genetics | Neurogenomics

Original Research

Published on 23 Sep 2024

Unveiling the role of IGF1R in autism spectrum disorder: a multi-omics approach to decipher common pathogenic mechanisms in the IGF signaling pathway

in Neurogenomics

Kang Yang
Tian Zhang
Ruize Niu
Liyang Zhao
Zhonghe Cheng
Jun Li
Lifang Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1483574

4,728 views
1 citation

Editorial

Published on 11 Sep 2024

Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases

in Neurogenomics

Muthukumar Karuppasamy
Martine Tetreault
Jessica Rosati

Frontiers in Genetics

doi 10.3389/fgene.2024.1481705

1,521 views

Case Report

Published on 21 Aug 2024

Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome

in Neurogenomics

Christine Anna Dambietz
Andrea Doescher
Michael Heming
Anja Schirmacher
Bernhard Schlüter
Andrea Schulte-Mecklenbeck
Christian Thomas
Heinz Wiendl
Gerd Meyer zu Hörste
Sarah Wiethoff

Frontiers in Genetics

doi 10.3389/fgene.2024.1421952

2,793 views
2 citations

Case Report

Published on 17 Jul 2024

Long-term clinical course of adult-onset refractory epilepsy in cardiofaciocutaneous syndrome with a pathogenic MAP2K1 variant: a case report

in Neurogenomics

Rie Tsuburaya-Suzuki
Sachiko Ohori
Kohei Hamanaka
Atsushi Fujita
Naomichi Matsumoto
Masako Kinoshita

Frontiers in Genetics

doi 10.3389/fgene.2024.1410979

3,034 views
2 citations

Original Research

Published on 19 Jun 2024

Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosis

in Neurogenomics

Kevin E. Glinton
Charul Gijavanekar
Abbhirami Rajagopal
Laura P. Mackay
Kirt A. Martin
Phillip L. Pearl
K. Michael Gibson
Theresa A. Wilson
V. Reid Sutton
Sarah H. Elsea

Frontiers in Genetics

doi 10.3389/fgene.2024.1405468

4,871 views
4 citations

Review

Published on 15 May 2024

Diagnostic efficacy of long non-coding RNAs in multiple sclerosis: a systematic review and meta-analysis

in Neurogenomics

Yongdong Wang
Jing Wang
Xinyin Zhang
Chengyan Xia
Zhiping Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1400387

2,566 views
2 citations

Editorial

Published on 10 May 2024

Editorial: Multifaceted genes in amyotrophic lateral sclerosis-frontotemporal dementia volume II

in Neurogenomics

Francesca Luisa Conforti
Alan Edward Renton
Henry Houlden

Frontiers in Genetics

doi 10.3389/fgene.2024.1420029

1,735 views

Original Research

Published on 16 Apr 2024

Meta-analysis of differential gene expression in lower motor neurons isolated by laser capture microdissection from post-mortem ALS spinal cords

in Neurogenomics

William R. Swindell

Frontiers in Genetics

doi 10.3389/fgene.2024.1385114

6,693 views
3 citations

Correction

Published on 10 Apr 2024

Corrigendum: Exploring the bi-directional relationship and shared genes between depression and stroke via NHANES and bioinformatic analysis

in Neurogenomics

Zhanghuan Yang
Maokun He
Qian Zhang
Shifu Li
Hua Chen
Di Liao

Frontiers in Genetics

doi 10.3389/fgene.2024.1405696

2,281 views
1 citation

Case Report

Published on 09 Apr 2024

Case report: Novel NUS1 variant in a Chinese patient with tremors and intellectual disability

in Neurogenomics

Ruolin Li
Jiayi Yang
Jinfeng Ma
Aimei Zhang
Hongfang Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1373448

2,854 views
8 citations

Case Report

Published on 06 Mar 2024

Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review

in Neurogenomics

Fengji Cui
Tuoya Wulan
Qian Zhang
Victor Wei Zhang
Yuhua Jiang

Frontiers in Genetics

doi 10.3389/fgene.2024.1371282

4,750 views
1 citation

Opinion

Published on 13 Feb 2024

Leveraging genetics to optimize rehabilitation outcomes after spinal cord injury: contemporary challenges and future opportunities

in Neurogenomics

Andrew Park
Ryan Solinsky

Frontiers in Genetics

doi 10.3389/fgene.2024.1350422

2,351 views

Case Report

Published on 16 Jan 2024

Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia

in Neurogenomics

Manal Alaamery
Salam Massadeh
Manar Aldarwish
Nour Albesher
Nora Aljawini
Othman Alahmed
Amna Kashgari
Christopher A. Walsh
Wafaa Eyaid

Frontiers in Genetics

doi 10.3389/fgene.2023.1294214

3,912 views
4 citations

Original Research

Published on 04 Jan 2024

Integration of multi-omics technologies for molecular diagnosis in ataxia patients

in Neurogenomics

Sebastien Audet
Valerie Triassi
Myriam Gelinas
Nab Legault-Cadieux
Vincent Ferraro
Antoine Duquette
Martine Tetreault

Frontiers in Genetics

doi 10.3389/fgene.2023.1304711

5,782 views
5 citations

Case Report

Published on 13 Dec 2023

MYRF-related mild encephalopathy with reversible myelin vacuolization: a case report and literature review

in Neurogenomics

Shumei Yao
Xiufeng Mo
Changjiang Luo
Chuanqiang Qu

Frontiers in Genetics

doi 10.3389/fgene.2023.1284060

3,055 views
2 citations

Editorial

Published on 13 Oct 2023

Editorial: Brain cancer pathogenesis and data integration

in Neurogenomics

Andrea Comba
Xinzhong Li
Barbara Breznik

Frontiers in Genetics

doi 10.3389/fgene.2023.1298285

2,605 views
3 citations

Brief Research Report

Published on 29 Aug 2023

Transcriptional diversity of the oxytocin receptor in prairie voles: mechanistic implications for behavioral neuroscience and maternal physiology

in Neurogenomics

Joshua S. Danoff
Emma A. Page
Allison M. Perkeybile
William M. Kenkel
Jason R. Yee
Craig F. Ferris
C. Sue Carter
Jessica J. Connelly

Frontiers in Genetics

doi 10.3389/fgene.2023.1225197

4,762 views
3 citations

Editorial

Published on 07 Aug 2023

Editorial: Insights in neurogenomics: 2022

in Neurogenomics

Aayushi Gandhi
Sarah H. Elsea

Frontiers in Genetics

doi 10.3389/fgene.2023.1252582

2,737 views

Original Research

Published on 06 Jul 2023

Uncovering ferroptosis in Parkinson’s disease via bioinformatics and machine learning, and reversed deducing potential therapeutic natural products

in Neurogenomics

Peng Wang
Qi Chen
Zhuqian Tang
Liang Wang
Bizhen Gong
Min Li
Shaodan Li
Minghui Yang

Frontiers in Genetics

doi 10.3389/fgene.2023.1231707

8,543 views
13 citations

Case Report

Published on 04 Jul 2023

Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy

in Neurogenomics

Yan Hu
Mingwei Huang
Jialun Wen
Jian Gao
Weiwei Long
Yansheng Shen
Qi Zeng
Yan Chen
Tian Zhang
Jianxiang Liao

Frontiers in Genetics

doi 10.3389/fgene.2023.1224949

4,180 views
7 citations

Case Report

Published on 14 Jun 2023

Genotype-phenotype correlation of deletions and duplications of 4p: case reports and literature review

in Neurogenomics

Xuan Zhang
Hongjuan Lu
Hanran Yang
Yichen Ji
Huixin Liu
Wenjian Liu
Jiayi Li
Zhixian Yang
Wei Sun

Frontiers in Genetics

doi 10.3389/fgene.2023.1174314

6,354 views
3 citations

Editorial

Published on 02 Jun 2023

Editorial: Evolution in Neurogenomics

in Neurogenomics

Jiuyong Xie
Robert Friedman

Frontiers in Genetics

doi 10.3389/fgene.2023.1220750

3,630 views

Original Research

Published on 26 May 2023

Association between TRP channels and glutamatergic synapse gene polymorphisms and migraine and the comorbidities anxiety and depression in a Chinese population

in Neurogenomics

Mingxue Wang
Yujia Gu
Shuhan Meng
Lixin Kang
Jing Yang
Degang Sun
Yuxing Liu
Ze Wan
Yi Shan
Dongjie Xue

Frontiers in Genetics

doi 10.3389/fgene.2023.1158028

5,918 views
13 citations

Original Research

Published on 16 May 2023

Gene expression profiling reveals a role of immune system and inflammation in innate and stress-induced anxiety-like behavior

in Neurogenomics

Adrien Gigliotta
Kalevi Trontti
Juho Väänänen
Iiris Hovatta

Frontiers in Genetics

doi 10.3389/fgene.2023.1173376

5,012 views
1 citation

235 articles

articles

Unveiling the role of IGF1R in autism spectrum disorder: a multi-omics approach to decipher common pathogenic mechanisms in the IGF signaling pathway

Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases

Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome

Long-term clinical course of adult-onset refractory epilepsy in cardiofaciocutaneous syndrome with a pathogenic MAP2K1 variant: a case report

Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosis

Diagnostic efficacy of long non-coding RNAs in multiple sclerosis: a systematic review and meta-analysis

Editorial: Multifaceted genes in amyotrophic lateral sclerosis-frontotemporal dementia volume II

Meta-analysis of differential gene expression in lower motor neurons isolated by laser capture microdissection from post-mortem ALS spinal cords

Corrigendum: Exploring the bi-directional relationship and shared genes between depression and stroke via NHANES and bioinformatic analysis

Case report: Novel NUS1 variant in a Chinese patient with tremors and intellectual disability

Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review

Leveraging genetics to optimize rehabilitation outcomes after spinal cord injury: contemporary challenges and future opportunities

Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia

Integration of multi-omics technologies for molecular diagnosis in ataxia patients

MYRF-related mild encephalopathy with reversible myelin vacuolization: a case report and literature review

Editorial: Brain cancer pathogenesis and data integration

Transcriptional diversity of the oxytocin receptor in prairie voles: mechanistic implications for behavioral neuroscience and maternal physiology

Editorial: Insights in neurogenomics: 2022

Uncovering ferroptosis in Parkinson’s disease via bioinformatics and machine learning, and reversed deducing potential therapeutic natural products

Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy

Genotype-phenotype correlation of deletions and duplications of 4p: case reports and literature review

Editorial: Evolution in Neurogenomics

Association between TRP channels and glutamatergic synapse gene polymorphisms and migraine and the comorbidities anxiety and depression in a Chinese population

Gene expression profiling reveals a role of immune system and inflammation in innate and stress-induced anxiety-like behavior