Frontiers in Genetics

Case Report

Published on 12 Aug 2024

Fahr’s syndrome as the initial imaging characteristics of MELAS syndrome with a possible seizure activity and cardiac arrest: a case report

in Genetics of Common and Rare Diseases

Yan Zheng
Haohao Wu
Meng Zhang
Baogang Huang
Junsu Yang
Chuan Liu
Hanmin Wang
Kang Du

Frontiers in Genetics

doi 10.3389/fgene.2024.1393158

1,332 views
1 citation

Original Research

Published on 12 Aug 2024

Prognostic value of four immune-related genes in lower-grade gliomas: a biomarker discovery study

in Computational Genomics

Shuowen Wang
Zijun Wang
Zhuo Liu
Jianxin Wu

Frontiers in Genetics

doi 10.3389/fgene.2024.1403587

1,250 views

Review

Published on 12 Aug 2024

Acute intermittent porphyria: a disease with low penetrance and high heterogeneity

in Genetics of Common and Rare Diseases

Jia-Jia Lei
Shuang Li
Bai-Xue Dong
Jing Yang
Yi Ren

Frontiers in Genetics

doi 10.3389/fgene.2024.1374965

1,865 views
1 citation

Original Research

Published on 09 Aug 2024

Identification of candidate SNPs associated with embryo mortality and fertility traits in lactating Holstein cows

in Livestock Genomics

Carolina L. Gonzalez Berrios
Courtney F. Bowden
Hamad M. Saad
Jeanette V. Bishop
Hana Van Campen
Pablo Pinedo
Thomas R. Hansen
Milton G. Thomas

Frontiers in Genetics

doi 10.3389/fgene.2024.1409335

1,763 views

Original Research

Published on 09 Aug 2024

Nonalcoholic or metabolic-associated fatty liver disease and colorectal polyps: evidence from meta-analysis and two-sample Mendelian randomization

in Statistical Genetics and Methodology

Dong Zhai
Sumei Xu
Haoge Liu
Xiaojuan Tong

Frontiers in Genetics

doi 10.3389/fgene.2024.1422827

1,770 views

Original Research

Published on 09 Aug 2024

TF-EPI: an interpretable enhancer-promoter interaction detection method based on Transformer

in Computational Genomics

Bowen Liu
Weihang Zhang
Xin Zeng
Martin Loza
Sung-Joon Park
Kenta Nakai

Frontiers in Genetics

doi 10.3389/fgene.2024.1444459

1,859 views

Original Research

Published on 09 Aug 2024

Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndrome

in Genetics of Common and Rare Diseases

Jian-Hui Zhang
Jie Liu
Dan-Dan Ruan
Qian Chen
Jie Yang
Min Wu
Hong-Ping Yu
Li-Sheng Liao
Xiao-Ling Zheng
Jie-Wei Luo

Frontiers in Genetics

doi 10.3389/fgene.2024.1419154

1,257 views

Original Research

Published on 09 Aug 2024

Molecular and physiological responses of two quinoa genotypes to drought stress

in Genomics of Plants and the Phytoecosystem

Xiaolin Zhu
Wenyu Liu
Baoqiang Wang
Ling Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1439046

1,417 views
2 citations

Case Report

Published on 09 Aug 2024

Case Report: Whole exome sequencing identifies compound heterozygous variants in the TRAPPC9 gene in a child with developmental delay

in Genetics of Common and Rare Diseases

Bingxuan Yu
Jing Chen
Shuo Yang
He Wang
Yuanyuan Xiao
Shanling Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1415194

943 views

Editorial

Published on 09 Aug 2024

Editorial: The intricate web of gastrointestinal virome, mycome and archaeome: implications for gastrointestinal diseases

in Human and Medical Genomics

Asrar Ahmad
Mohammad Ashfaq
Mudasir Rashid

Frontiers in Genetics

doi 10.3389/fgene.2024.1463350

851 views

Original Research

Published on 08 Aug 2024

Integrative analysis reveals novel insights into juvenile idiopathic arthritis pathogenesis and shared molecular pathways with associated traits

in Computational Genomics

N. Pudjihartono
D. Ho
J. M. O’Sullivan

Frontiers in Genetics

doi 10.3389/fgene.2024.1448363

2,400 views

Original Research

Published on 08 Aug 2024

GWAS-significant loci and severe COVID-19: analysis of associations, link with thromboinflammation syndrome, gene-gene, and gene-environmental interactions

in Human and Medical Genomics

Alexey Valerevich Loktionov
Ksenia Andreevna Kobzeva
Andrey Romanovich Karpenko
Vera Alexeevna Sergeeva
Yuriy Lvovich Orlov
Olga Yurievna Bushueva

Frontiers in Genetics

doi 10.3389/fgene.2024.1434681

1,454 views
1 citation

Original Research

Published on 08 Aug 2024

Using preimplantation genetic testing for monogenic disease for preventing citrullinemia type 1 transmission

in Genetics of Common and Rare Diseases

Zubo Wu
Tao Liang
Yi Liu
Xiaofang Ding
Defeng Shu

Frontiers in Genetics

doi 10.3389/fgene.2024.1389461

947 views

Mini Review

Published on 08 Aug 2024

The role of primary cilia in congenital heart defect-associated neurological impairments

in Genetics of Common and Rare Diseases

Nemanja Sarić
Nobuyuki Ishibashi

Frontiers in Genetics

doi 10.3389/fgene.2024.1460228

1,261 views

Original Research

Published on 08 Aug 2024

Unveiling potential drug targets for lung squamous cell carcinoma through the integration of druggable genome and genome-wide association data

in Statistical Genetics and Methodology

Wenhua Wu
Zhengrui Chen
Haiteng Wen
Haiyun Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1431684

3,197 views
1 citation

Original Research

Published on 07 Aug 2024

Associations of genetically predicted iron status with 24 gastrointestinal diseases and gut microbiota: a Mendelian randomization study

in Nutritional Genomics

Tao Su
Xiang Peng
Ying Gan
Hongzhen Wu
Shulin Ma
Min Zhi
Yi Lu
Shixue Dai
Jiayin Yao

Frontiers in Genetics

doi 10.3389/fgene.2024.1406230

2,675 views

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Articles

Fahr’s syndrome as the initial imaging characteristics of MELAS syndrome with a possible seizure activity and cardiac arrest: a case report

Prognostic value of four immune-related genes in lower-grade gliomas: a biomarker discovery study

Acute intermittent porphyria: a disease with low penetrance and high heterogeneity

Identification of candidate SNPs associated with embryo mortality and fertility traits in lactating Holstein cows

Nonalcoholic or metabolic-associated fatty liver disease and colorectal polyps: evidence from meta-analysis and two-sample Mendelian randomization

TF-EPI: an interpretable enhancer-promoter interaction detection method based on Transformer

Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndrome

Molecular and physiological responses of two quinoa genotypes to drought stress

Case Report: Whole exome sequencing identifies compound heterozygous variants in the TRAPPC9 gene in a child with developmental delay

Editorial: The intricate web of gastrointestinal virome, mycome and archaeome: implications for gastrointestinal diseases

Integrative analysis reveals novel insights into juvenile idiopathic arthritis pathogenesis and shared molecular pathways with associated traits

GWAS-significant loci and severe COVID-19: analysis of associations, link with thromboinflammation syndrome, gene-gene, and gene-environmental interactions

Using preimplantation genetic testing for monogenic disease for preventing citrullinemia type 1 transmission

The role of primary cilia in congenital heart defect-associated neurological impairments

Unveiling potential drug targets for lung squamous cell carcinoma through the integration of druggable genome and genome-wide association data

Associations of genetically predicted iron status with 24 gastrointestinal diseases and gut microbiota: a Mendelian randomization study