Frontiers in Genetics

Editorial

Published on 19 Mar 2025

Editorial: Functional study of novel VUS (variant of uncertain significance) mutations in single-gene inherited disease

in Statistical Genetics and Methodology

Guohua Yang
Hua Zhong
Huiliang Wen
Yiping Shen

Frontiers in Genetics

doi 10.3389/fgene.2025.1578736

2,580 views

Original Research

Published on 19 Mar 2025

Multi-tissue transcriptomic characterization of endogenous retrovirus-derived transcripts in Capra hircus

in Livestock Genomics

Ming-Di Li
Hu-Rong Li
Shao-Hui Ye

Frontiers in Genetics

doi 10.3389/fgene.2025.1544330

1,859 views

Original Research

Published on 19 Mar 2025

Exploring the complex population structure and admixture of four local Hungarian sheep breeds

in Livestock Genomics

Johanna Ramírez-Díaz
Tania Bobbo
Bernt Guldbrandtsen
Anna A. Schönherz
Paolo Cozzi
Szilvia Kusza
Goutam Sahana
Alessandra Stella
Arianna Manunza

Frontiers in Genetics

doi 10.3389/fgene.2025.1507315

4,140 views
2 citations

Mini Review

Published on 19 Mar 2025

Congenital heart disease presentations in the 15q11.2 microdeletion syndrome

in Genetics of Common and Rare Diseases

Claudia-Ioana Fifirig
Sabu Abraham
Bernard Keavney
Kathryn E. Hentges

Frontiers in Genetics

doi 10.3389/fgene.2025.1535732

4,907 views

Case Report

Published on 19 Mar 2025

Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3

in Genetics of Common and Rare Diseases

Jingqun Mai
Zhu Zhang
Bocheng Xu
Shanling Liu
He Wang
Hao Wang
Shuo Yang

Frontiers in Genetics

doi 10.3389/fgene.2025.1465527

1,670 views

Original Research

Published on 18 Mar 2025

Retrospective analysis of inflammatory biomarkers and prognosis in non-small cell lung cancer without adenocarcinoma in situ

in Cancer Genetics and Oncogenomics

Qing Zhao
Songping Cui
Bin Hu
Shuo Chen

Frontiers in Genetics

doi 10.3389/fgene.2025.1549602

1,470 views

Review

Published on 18 Mar 2025

Cotton under heat stress: a comprehensive review of molecular breeding, genomics, and multi-omics strategies

in Genomics of Plants and the Phytoecosystem

Tahira Luqman
Manzoor Hussain
Syed Riaz Ahmed
Iram Ijaz
Zahra Maryum
Sahar Nadeem
Zafran Khan
Sana Muhy Ud Din Khan
Mohammad Aslam
Yongming Liu

Frontiers in Genetics

doi 10.3389/fgene.2025.1553406

7,520 views
8 citations

Original Research

Published on 18 Mar 2025

Bioinformatics revealed biomarkers for diagnosis in kidney stones

in Genetics of Common and Rare Diseases

Ziqi He
Chao Song
Zhong Wang
Caitao Dong
Qinhong Jiang
Xi Yu
Guang Shan

Frontiers in Genetics

doi 10.3389/fgene.2025.1542840

3,388 views
1 citation

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

3,786 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

2,503 views
4 citations

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

1,384 views

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

2,290 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

2,039 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

2,289 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

2,423 views
3 citations

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

965 views

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

1,712 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

1,599 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

2,003 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

2,268 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

3,908 views
1 citation

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

1,875 views
4 citations

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

2,019 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

1,761 views
1 citation

16,444 articles

articles

Editorial: Functional study of novel VUS (variant of uncertain significance) mutations in single-gene inherited disease

Multi-tissue transcriptomic characterization of endogenous retrovirus-derived transcripts in Capra hircus

Exploring the complex population structure and admixture of four local Hungarian sheep breeds

Congenital heart disease presentations in the 15q11.2 microdeletion syndrome

Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3

Retrospective analysis of inflammatory biomarkers and prognosis in non-small cell lung cancer without adenocarcinoma in situ

Cotton under heat stress: a comprehensive review of molecular breeding, genomics, and multi-omics strategies

Bioinformatics revealed biomarkers for diagnosis in kidney stones

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

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

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

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)

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

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

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

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

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

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