Frontiers in Genetics

Original Research

Published on 18 Mar 2025

Genetic diversity and population structure of non-descript cattle in South African smallholder systems

in Livestock Genomics

M. P. Ramoroka
M. D. MacNeil
F. W. C. Neser
S. F. Lashmar
M. L. Makgahlela

Frontiers in Genetics

doi 10.3389/fgene.2025.1535730

3,762 views
2 citations

Original Research

Published on 17 Mar 2025

Exploring the oncogenic role and prognostic value of CKS1B in human lung adenocarcinoma and squamous cell carcinoma

in Computational Genomics

Md. Solayman Hossain
Tariqul Islam Tusar
Nairita Ahsan Faruqui
Tanjim Ishraq Rahaman
Yasin Arafath Sharker
Shimran Saharia Santo
Abu Tayab Moin
Yusha Araf
Ibrahim Khalil Afif
Shoaib Saikat

Frontiers in Genetics

doi 10.3389/fgene.2025.1449466

2,474 views
4 citations

Technology and Code

Published on 17 Mar 2025

weIMPUTE: a user-friendly web-based genotype imputation platform

in Computational Genomics

Mingliang Li
Zhuo Li
Defu Liu
Qi Li
Xiaodong Hu
Jun Yu
Jian Lin
Chunguang Bi
Guanshi Ye
Helong Yu

Frontiers in Genetics

doi 10.3389/fgene.2025.1532464

2,276 views

Brief Research Report

Published on 17 Mar 2025

Structural characteristics of mitochondrial genome of Spirobo-lus walkeri (Spirobolida: Spirobolidae), and phylogenetic analysis of Diplopoda

in Evolutionary and Population Genetics

Wenwen Zhang
Shengjun Zhao
Lingna Li
Yingzhu Li
Hongyi Liu
Peng Cui

Frontiers in Genetics

doi 10.3389/fgene.2025.1566634

1,378 views

Case Report

Published on 14 Mar 2025

Case report: Novel homozygous ACVRL1 missense variant in a family with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension: findings suggest a hypomorphic allele

in Genetics of Common and Rare Diseases

Akash Mathavan
Akshay Mathavan
Urszula Krekora
Adityanarayan Rao
Marc S. Zumberg
Jeb Justice
Pinar Bayrak-Toydemir
Jamie McDonald
Ali Ataya

Frontiers in Genetics

doi 10.3389/fgene.2025.1554624

2,030 views

Review

Published on 13 Mar 2025

Discovery of therapeutic targets in cardiovascular diseases using high-throughput chromosome conformation capture (Hi-C)

in Human and Medical Genomics

Quan Zheng
Ying Liu
Minghao Guo
Xin Zhang
Qingbin Zhang
Xi-Yong Yu
Zhongxiao Lin

Frontiers in Genetics

doi 10.3389/fgene.2025.1515010

2,275 views

Correction

Published on 13 Mar 2025

Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene

in Genetics of Common and Rare Diseases

Lixue Ouyang
Fan Yang
Hongyu Duan
Chuan Wang

Frontiers in Genetics

doi 10.3389/fgene.2025.1589037

963 views

Original Research

Published on 13 Mar 2025

Evolutionary history and divergence times of Tettigoniidae (Orthoptera) inferred from mitochondrial phylogenomics

in Evolutionary and Population Genetics

Tianyou Zhao
Zhenbin Lin
Hailin Yang
Fan Song
Zhenyuan Xia
Weidong Huang

Frontiers in Genetics

doi 10.3389/fgene.2025.1495754

2,394 views
3 citations

Original Research

Published on 12 Mar 2025

A rare variation of ERCC8 gene cause Cockayne syndrome in a Chinese family

in Genetics of Aging

Fengjuan Ding
Fei Hou
Bowen Zhao
Hua Jin

Frontiers in Genetics

doi 10.3389/fgene.2025.1531832

1,692 views

Original Research

Published on 12 Mar 2025

CLMT: graph contrastive learning model for microbe-drug associations prediction with transformer

in Computational Genomics

Liqi Xiao
Junlong Wu
Liu Fan
Lei Wang
Xianyou Zhu

Frontiers in Genetics

doi 10.3389/fgene.2025.1535279

1,582 views

Case Report

Published on 12 Mar 2025

Prenatal diagnosis of intellectual disability, autosomal dominant 29 with a nonsense pathogenic variant in SETBP1: a case report and literature review

in Genetics of Common and Rare Diseases

Zhuo Wei
Liying Yao
Lei Zhang
Shanshan Li
Meiyi Xu
Dan Wu
Wen Li
Ying Chang

Frontiers in Genetics

doi 10.3389/fgene.2025.1463485

1,994 views

Original Research

Published on 12 Mar 2025

Genetic determinism of cortisol levels in pig

in Livestock Genomics

Elena Terenina
Nathalie Iannuccelli
Yvon Billon
Katia Fève
Laure Gress
Darya Bazovkina
Pierre Mormede
Catherine Larzul

Frontiers in Genetics

doi 10.3389/fgene.2025.1461385

2,256 views
3 citations

Original Research

Published on 12 Mar 2025

Identification and validation of key biomarkers associated with immune and oxidative stress for preeclampsia by WGCNA and machine learning

in Computational Genomics

Tiantian Yu
Guiying Wang
Xia Xu
Jianying Yan

Frontiers in Genetics

doi 10.3389/fgene.2025.1500061

3,884 views
1 citation

Review

Published on 11 Mar 2025

Bibliometric analysis of case-control studies on the association between HLA alleles and multiple sclerosis in adults

in Applied Genetic Epidemiology

Enola Maer
Marjorie Maya Hubacher
Livia Livint Popa
Dana Marieta Fodor
Razvan Mircea Chereches
Dafin F. Muresanu
Vitalie Vacaras
Maria Chiriac
Horea Vladi Matei
Nicu Catalin Draghici

Frontiers in Genetics

doi 10.3389/fgene.2025.1524360

2,015 views

Editorial

Published on 11 Mar 2025

Editorial: Understanding molecular mechanisms to facilitate the development of biomarkers for therapeutic intervention in gastrointestinal diseases and sepsis

in Human and Medical Genomics

Dipak Kumar Sahoo
Romy M. Heilmann
Ashish Patel

Frontiers in Genetics

doi 10.3389/fgene.2025.1581299

1,865 views
4 citations

Brief Research Report

Published on 11 Mar 2025

Retrospective chart review of inherited and idiopathic dystonia

in Applied Genetic Epidemiology

A. Alakkas
H. Shinawi
J. A. Bajwa
O. Alsinaidi
A. Al-Hashim

Frontiers in Genetics

doi 10.3389/fgene.2025.1504744

1,768 views

Case Report

Published on 11 Mar 2025

A de novo TNNI3K variant aggravates the pathogenicity of DMD-associated early-onset cardiomyopathy: a case report

in Genetics of Common and Rare Diseases

Di Qie
Yang Zhai
Fan Yang
Yifei Li
Rong Xu

Frontiers in Genetics

doi 10.3389/fgene.2025.1525941

1,748 views
1 citation

Original Research

Published on 10 Mar 2025

Detection of a novel large fragment deletion in the alpha-globin gene cluster using the CNVplex technology

in Genetics of Common and Rare Diseases

Jianfei Xu
Liang Hu
Lijuan Wen
Xianzhen Cao
Hongyan Xu
Qi Luo
Yuhong Long
Tingyu Ji
Lifang Sun
Fengxiang Wei

Frontiers in Genetics

doi 10.3389/fgene.2025.1518392

1,916 views

Original Research

Published on 10 Mar 2025

Identification and validation of prognostic biomarkers related to tumor immune invasion in pancreatic cancer

in Cancer Genetics and Oncogenomics

Minxue Chen
Xinyuan Zhou
Yong Fan
Chen Wang

Frontiers in Genetics

doi 10.3389/fgene.2025.1556544

2,737 views

Original Research

Published on 10 Mar 2025

Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases

in Genetics of Common and Rare Diseases

Xuejun Ouyang
Dazhi Chi
Yu Zhang
Tian Yu
Qian Zhang
Lei Xu
Victor Wei Zhang
Bin Wang

Frontiers in Genetics

doi 10.3389/fgene.2025.1526077

2,018 views

Original Research

Published on 07 Mar 2025

Tetrahymena thermophila glutathione-S-transferase superfamily: an eco-paralogs gene network differentially responding to various environmental abiotic stressors and an update on this gene family in ciliates

in Predictive Toxicology and Exposomics

Ruth Ortega
Ana Martin-González
Juan-Carlos Gutiérrez

Frontiers in Genetics

doi 10.3389/fgene.2025.1538168

2,193 views

Case Report

Published on 07 Mar 2025

Case Report: Area of focus clinical presentation and KMT2D gene mutation at the c.15535C>T site in a case of Kabuki syndrome

in Genetics of Common and Rare Diseases

Wen Li
Mengjie Lin
Jinwei Dao
Li Shi
Wei Yi
Jia Lei
Yaxian Song
Jiaolou Dong
Meiwei Zhao
Yushan Xu

Frontiers in Genetics

doi 10.3389/fgene.2025.1523228

2,664 views

Case Report

Published on 06 Mar 2025

Case report: Clinicopathological characteristics of SASH1 mutation-related dyschromatosis: a rethinking of the classification of dyschromatosis

in Genetics of Common and Rare Diseases

Tingmei Wang
Dong Li
Yunhua Deng

Frontiers in Genetics

doi 10.3389/fgene.2025.1414129

1,377 views

Case Report

Published on 06 Mar 2025

Case report: Severe arrhythmogenic cardiomyopathy in a young girl with compound heterozygous DSG2 and MYBPC3 variants with a 6-year follow-up

in Human and Medical Genomics

Ryotaro Hashizume
Hiroshi Imai
Hiroyuki Ohashi
Hirofumi Sawada
Noriko Yodoya
Ryuji Okamoto
Kaoru Dohi
Chika Kasai
Takahito Kitajima
Takumi Fujiwara

Frontiers in Genetics

doi 10.3389/fgene.2025.1545561

2,719 views
1 citation

16,436 articles

articles

Genetic diversity and population structure of non-descript cattle in South African smallholder systems

Exploring the oncogenic role and prognostic value of CKS1B in human lung adenocarcinoma and squamous cell carcinoma

weIMPUTE: a user-friendly web-based genotype imputation platform

Structural characteristics of mitochondrial genome of Spirobo-lus walkeri (Spirobolida: Spirobolidae), and phylogenetic analysis of Diplopoda

Case report: Novel homozygous ACVRL1 missense variant in a family with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension: findings suggest a hypomorphic allele

Discovery of therapeutic targets in cardiovascular diseases using high-throughput chromosome conformation capture (Hi-C)

Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene

Evolutionary history and divergence times of Tettigoniidae (Orthoptera) inferred from mitochondrial phylogenomics

A rare variation of ERCC8 gene cause Cockayne syndrome in a Chinese family

CLMT: graph contrastive learning model for microbe-drug associations prediction with transformer

Prenatal diagnosis of intellectual disability, autosomal dominant 29 with a nonsense pathogenic variant in SETBP1: a case report and literature review

Genetic determinism of cortisol levels in pig

Identification and validation of key biomarkers associated with immune and oxidative stress for preeclampsia by WGCNA and machine learning

Bibliometric analysis of case-control studies on the association between HLA alleles and multiple sclerosis in adults

Editorial: Understanding molecular mechanisms to facilitate the development of biomarkers for therapeutic intervention in gastrointestinal diseases and sepsis

Retrospective chart review of inherited and idiopathic dystonia

A de novo TNNI3K variant aggravates the pathogenicity of DMD-associated early-onset cardiomyopathy: a case report

Detection of a novel large fragment deletion in the alpha-globin gene cluster using the CNVplex technology

Identification and validation of prognostic biomarkers related to tumor immune invasion in pancreatic cancer

Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseases

Tetrahymena thermophila glutathione-S-transferase superfamily: an eco-paralogs gene network differentially responding to various environmental abiotic stressors and an update on this gene family in ciliates

Case Report: Area of focus clinical presentation and KMT2D gene mutation at the c.15535C>T site in a case of Kabuki syndrome

Case report: Clinicopathological characteristics of SASH1 mutation-related dyschromatosis: a rethinking of the classification of dyschromatosis

Case report: Severe arrhythmogenic cardiomyopathy in a young girl with compound heterozygous DSG2 and MYBPC3 variants with a 6-year follow-up