Frontiers in Genetics

Original Research

Published on 25 Apr 2025

Correlation of tumor necrosis factor-α and interleukin-1 single-nucleotide polymorphisms with the risk of migraine development

in Neurogenomics

Guijiao Huang
Xin Dong
Xiaojiao Shao
Mengping Wu
Shan Gao
Yixuan Wang
Xinying Guan

Frontiers in Genetics

doi 10.3389/fgene.2025.1556498

1,661 views
2 citations

Original Research

Published on 25 Apr 2025

A rare germline mutation reverses the suppressive effect of GPC5 thereby promoting lung adenocarcinoma development and tumorigenesis

in Cancer Genetics and Oncogenomics

Zhifa Zheng
Lina Zhao
Sen Zhao
Zhihong Wu
Nan Wu

Frontiers in Genetics

doi 10.3389/fgene.2025.1582504

2,236 views

Original Research

Published on 25 Apr 2025

Relationship of VDR and VDBP gene polymorphisms with sepsis susceptibility and prognosis

in Genetics of Common and Rare Diseases

Chan Lian
Kangtai Ying
Haiyan Shao
Haiting Gu
Wenwei Mao

Frontiers in Genetics

doi 10.3389/fgene.2025.1590750

1,603 views

Perspective

Published on 25 Apr 2025

Emerging and evolving values in the changing landscape of genomics

in ELSI in Science and Genetics

Maria Siermann
Riya Mohan
Eline M. Bunnik
Anne Cambon-Thomsen
Ruth Chadwick
Martina C. Cornel
Johannes J. M. van Delden
Yann Joly
Fruzsina Molnár-Gábor
Maria Pilar Nicolás Jiménez

Frontiers in Genetics

doi 10.3389/fgene.2025.1566291

3,510 views
3 citations

Original Research

Published on 25 Apr 2025

Fetal karyotyping in adolescent pregnancies: a population-based cohort study on outcomes of invasive prenatal testing

in Human and Medical Genomics

Jakub Staniczek
Maisa Manasar-Dyrbuś
Patrycja Sodowska
Krzysztof Sodowski
Agata Włoch
Bartosz Czuba
Wojciech Cnota
Monika Paul-Samojedny
Agnieszka Kania
Henryka Sodowska

Frontiers in Genetics

doi 10.3389/fgene.2025.1581249

2,173 views

Case Report

Published on 25 Apr 2025

Prenatal diagnosis of a compound heterozygous variation in the FBXL4 gene by trio-WES and imaging monitoring: a case report

in Genetics of Common and Rare Diseases

Yujia Zhai
Jing Chen
Shuo Yang
He Wang
Yuanyuan Xiao
Shanling Liu

Frontiers in Genetics

doi 10.3389/fgene.2025.1539288

1,886 views

Review

Published on 25 Apr 2025

Mitochondrial microRNAs (mitomiRs) as emerging biomarkers and therapeutic targets for chronic human diseases

in RNA

Andrea Méndez-García
Marely Abigail García-Mendoza
Carmila Patricia Zárate-Peralta
Fernanda Valeria Flores-Perez
Luis Fernando Carmona-Ramirez
Surajit Pathak
Antara Banerjee
Asim K. Duttaroy
Sujay Paul

Frontiers in Genetics

doi 10.3389/fgene.2025.1555563

5,121 views
2 citations

Original Research

Published on 24 Apr 2025

Key gene screening and diagnostic model establishment for acute type a aortic dissection

in Computational Genomics

Yue Pan
Zhiming Yu
Xiaoyu Qian
Xuesong Zhang
Qun Xue
Weizhang Xiao

Frontiers in Genetics

doi 10.3389/fgene.2025.1586880

3,249 views

Original Research

Published on 24 Apr 2025

Genomic and health characteristics of crossbred dairy cattle in central Uganda

in Livestock Genomics

Enrique Sanchez-Molano
Robert Mukiibi
Valentina Riggio
Joel Ogwang
Leonard Kawule
Katali Benda
Peter Beine
Barend M. de Clare Bronsvoort
James Prendergast
Andrea B. Doeschl-Wilson

Frontiers in Genetics

doi 10.3389/fgene.2025.1567910

2,023 views
1 citation

Original Research

Published on 24 Apr 2025

Integration of bulk RNA-seq and scRNA-seq reveals transcriptomic signatures associated with deep vein thrombosis

in Computational Genomics

Bao-ze Pan
Ming-jun Jiang
Li-ming Deng
Jie Chen
Xian-peng Dai
Zi-xuan Wu
Zhi-he Deng
Dong-yang Luo
Yang-yi-jing Wang
Dan Ning

Frontiers in Genetics

doi 10.3389/fgene.2025.1551879

3,623 views
1 citation

Original Research

Published on 24 Apr 2025

Genetic estimates and genome-wide association studies of antibody response in Tanzanian dairy cattle

in Livestock Genomics

Luis E. Hernandez-Castro
Elizabeth Anne Jessie Cook
Oswald Matika
Isaac Joseph Mengele
Shabani Kiyabo Motto
Shedrack Festo Bwatota
Bibiana Zirra-Shallangwa
Ricardo Pong-Wong
James Prendergast
Raphael Mrode

Frontiers in Genetics

doi 10.3389/fgene.2025.1497355

2,630 views

Methods

Published on 24 Apr 2025

MSI expresso: a software for determining MSI status and detecting MSI-related transcription events from RNA sequencing data

in Computational Genomics

Emmanuel Tubacher
Alexandre How-Kit
Mourad Sahbatou
Alex Duval
Victor Renault
Jean-François Deleuze

Frontiers in Genetics

doi 10.3389/fgene.2025.1523278

2,685 views

Original Research

Published on 23 Apr 2025

Complete mitochondrial genome of Ficus hirta and its comparative analysis

in Genomics of Plants and the Phytoecosystem

Wangdong Deng
Xinyi Cai

Frontiers in Genetics

doi 10.3389/fgene.2025.1530105

1,923 views

Editorial

Published on 23 Apr 2025

Editorial: Impact of heavy metal on aquatic life and human health

in Predictive Toxicology and Exposomics

Ahmed H. El-Sappah
Heba H. Abdel-Kader
Manzar Abbas
Sara Zafar
Jia Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1608524

2,628 views
1 citation

Case Report

Published on 22 Apr 2025

Case report: a case of hypoparathyroidism–sensorineural deafness–renal dysplasia syndrome

in Genetics of Common and Rare Diseases

Jinyan Yang
Yanjie Mei
Feifei Tang
Xinhong Guo
Yanhua Kong
Ying Deng

Frontiers in Genetics

doi 10.3389/fgene.2025.1501427

1,498 views

Review

Published on 22 Apr 2025

Regulatory mechanisms of m6A RNA methylation in esophageal cancer: a comprehensive review

in RNA

Long Wen
Jiang Fu
Zixu Wang
Rangping Xie
Shengjie Tang
Li Yu
Haining Zhou

Frontiers in Genetics

doi 10.3389/fgene.2025.1561799

2,921 views
1 citation

Original Research

Published on 22 Apr 2025

RNA-seq analysis reveals key genes associated with downregulation of APE1 in esophageal squamous cell carcinoma

in Cancer Genetics and Oncogenomics

Alan Chu
Xiao Liu
Shijia Liu
Mengxi Li
Rui Song
Lanlan Gan
Yongtai Wang
Zongwen Liu
Chen Sun

Frontiers in Genetics

doi 10.3389/fgene.2025.1549371

1,984 views

Original Research

Published on 22 Apr 2025

Novel ACAD8 variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and management

in Genetics of Common and Rare Diseases

Yilun Tao
Dong Han
Jianfang Li
Xiaoyun Li
Luna Hao
Wenxia Song
Lihong Wang
Xiaoze Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1532902

1,613 views

Original Research

Published on 17 Apr 2025

Identification of diagnostic biomarkers for fibromyalgia using gene expression analysis and machine learning

in Statistical Genetics and Methodology

Fuyu Zhao
Jianan Zhao
Yang Li
Chenyang Song
Yaxin Cheng
Yunshen Li
Shiya Wu
Bingheng He
Juan Jiao
Cen Chang

Frontiers in Genetics

doi 10.3389/fgene.2025.1535541

4,466 views
2 citations

Case Report

Published on 17 Apr 2025

CEBPA-associated familial acute myeloid leukemia mimicking Werner syndrome: a case report

in Genetics of Common and Rare Diseases

Tanguy Demaret
Damien Feret
Barbara Lambert
Delphine Pranger
Jean-Louis Dargent
Maria Dolores Martin Martinez
Antonio Renda
Isabelle Maystadt

Frontiers in Genetics

doi 10.3389/fgene.2025.1575651

2,063 views

Original Research

Published on 17 Apr 2025

Identification of a novel homozygous SLC13A5 nonstop mutation in a Chinese family with epileptic encephalopathy and developmental delay

in Genetics of Common and Rare Diseases

Hua He
Lijuan Long
Manling Tang
Qiang Xu
Shengwu Duan
Ge Chen
Yan Zhao
Qiongfang Wu
Jia Chen

Frontiers in Genetics

doi 10.3389/fgene.2025.1474390

1,790 views

Original Research

Published on 17 Apr 2025

Correlation between gene polymorphisms and perioperative analgesia in patients undergoing gynecological surgery

in Pharmacogenetics and Pharmacogenomics

Meng Cai
Xiaofeng Lei
Lin Gan
Jing Li
Jin Yu

Frontiers in Genetics

doi 10.3389/fgene.2025.1509042

1,634 views

Case Report

Published on 17 Apr 2025

Estrogen-secreting testicular tumors in 46,XY female patients with 17α-hydroxylase/17,20-lyase deficiency: two unusual case reports and a review of the literature

in Genetics of Common and Rare Diseases

Julio Americo Pereira Batatinha
Mirian Yumie Nishi
Rafael Loch Batista
José Antônio Diniz Faria Júnior
Maria Helena Palma Sircili
Francisco Tibor Denes
Maria Jimena Chafloque Mesia
Laura da Silva Salvanini
Elaine Maria Frade Costa
Filomena Marino Carvalho

Frontiers in Genetics

doi 10.3389/fgene.2025.1508792

2,129 views
1 citation

Original Research

Published on 16 Apr 2025

The potential crosstalk genes and molecular mechanisms between systemic lupus erythematosus and periodontitis

in Computational Genomics

Kai Zhao
Xiaolong Li
Qingmiao Zhu
Mengyu Zhu
Jinge Huang
Ting Zhao

Frontiers in Genetics

doi 10.3389/fgene.2025.1527713

2,975 views
1 citation

16,438 articles

articles

Correlation of tumor necrosis factor-α and interleukin-1 single-nucleotide polymorphisms with the risk of migraine development

A rare germline mutation reverses the suppressive effect of GPC5 thereby promoting lung adenocarcinoma development and tumorigenesis

Relationship of VDR and VDBP gene polymorphisms with sepsis susceptibility and prognosis

Emerging and evolving values in the changing landscape of genomics

Fetal karyotyping in adolescent pregnancies: a population-based cohort study on outcomes of invasive prenatal testing

Prenatal diagnosis of a compound heterozygous variation in the FBXL4 gene by trio-WES and imaging monitoring: a case report

Mitochondrial microRNAs (mitomiRs) as emerging biomarkers and therapeutic targets for chronic human diseases

Key gene screening and diagnostic model establishment for acute type a aortic dissection

Genomic and health characteristics of crossbred dairy cattle in central Uganda

Integration of bulk RNA-seq and scRNA-seq reveals transcriptomic signatures associated with deep vein thrombosis

Genetic estimates and genome-wide association studies of antibody response in Tanzanian dairy cattle

MSI expresso: a software for determining MSI status and detecting MSI-related transcription events from RNA sequencing data

Complete mitochondrial genome of Ficus hirta and its comparative analysis

Editorial: Impact of heavy metal on aquatic life and human health

Case report: a case of hypoparathyroidism–sensorineural deafness–renal dysplasia syndrome

Regulatory mechanisms of m6A RNA methylation in esophageal cancer: a comprehensive review

RNA-seq analysis reveals key genes associated with downregulation of APE1 in esophageal squamous cell carcinoma

Novel ACAD8 variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and management

Identification of diagnostic biomarkers for fibromyalgia using gene expression analysis and machine learning

CEBPA-associated familial acute myeloid leukemia mimicking Werner syndrome: a case report

Identification of a novel homozygous SLC13A5 nonstop mutation in a Chinese family with epileptic encephalopathy and developmental delay

Correlation between gene polymorphisms and perioperative analgesia in patients undergoing gynecological surgery

Estrogen-secreting testicular tumors in 46,XY female patients with 17α-hydroxylase/17,20-lyase deficiency: two unusual case reports and a review of the literature

The potential crosstalk genes and molecular mechanisms between systemic lupus erythematosus and periodontitis