Frontiers in Genetics

Original Research

Published on 21 Aug 2026

Genome-wide cis-expression Quantitative Trait Loci (eQTL) and transcriptomic signals reveal distinct molecular regulation across correlated feed efficiency traits

in Livestock Genomics

Steffimol Rose Chacko Kaitholil
Mark H. Mooney
Omar Cristobal-Carballo
Sevda Hosseinzadeh
Faisal I. Rezwan
Aurélie Aubry
Masoud Shirali

Frontiers in Genetics

doi 10.3389/fgene.2026.1871055

456 views

Original Research

Published on 21 Aug 2026

Identification of NETs and inflammation-related prognostic genes in breast cancer and PCR experimental validation

in Cancer Genetics and Oncogenomics

Zhihong Xu
Qian Ma
Qihua Jiang
Wensong Wei
Dan Tao

Frontiers in Genetics

doi 10.3389/fgene.2026.1900298

242 views

Perspective

Accepted on 20 Aug 2026

From Prohibition to Integration: LLMs in Scientific Publishing

in ELSI in Science and Genetics

Boris Kirov
Aleksandar Marinchev
Slavil Peykov
Vassil Galabov

Frontiers in Genetics

Original Research

Accepted on 19 Aug 2026

Specimen Composition and Spatial Sampling Constrain Longitudinal Transcriptomic Inference in Glioblastoma

in Cancer Genetics and Oncogenomics

Hengrui Ding
Er Nie
Manyi Xie
Qiang Wang
Mingyan Yu
Te Li
Zhonglin Li

Frontiers in Genetics

Mini Review

Accepted on 19 Aug 2026

AI-Driven Genotype-Phenotype Modeling: A Framework Integrating Multi-Modal Single-Cell Genomics and Reverse Vaccinology for De Novo design of Multi-Epitope Cancer Vaccines

in Human and Medical Genomics

Mahabub Mallik
Sahid Afrid Mollick

Frontiers in Genetics

Case Report

Published on 19 Aug 2026

Amyotrophic lateral sclerosis -plus patient with an intermediate-length CACNA1A allele: a Case Report

in Genetics of Common and Rare Diseases

Xinyao Gao
Tingting Wang
Sihui Chen
Yuanzheng Ma
Qianqian Wei
Chunyu Li
Huifang Shang
Xueping Chen

Frontiers in Genetics

doi 10.3389/fgene.2026.1860828

356 views

Original Research

Accepted on 18 Aug 2026

Computational Prioritization of Candidate TCDD-Associated Targets in Retinoblastoma Using Network Toxicology and Transcriptomic Analysis

in Predictive Toxicology and Exposomics

Yingluan Wang
Qiang Hu
Zhan Cao
Dian Ye
Dawei Sun
Lijun Qu

Frontiers in Genetics

155 views

Original Research

Accepted on 18 Aug 2026

Loss of Lactate Dehydrogenase A disrupts R-loop homeostasis and induces DNA damage in breast cancer cells

in Epigenetics and Genome Architecture

Shangzhen Li
Cheng Xu
Shuling Chen
Guoping Yin
Dawei Yang

Frontiers in Genetics

Original Research

Accepted on 18 Aug 2026

Transcriptional Signatures of Respiratory Syncytial Virus (RSV) Infection Using Relaxed Magnitude Altitude Score with Hub-Centric Network Analysis (RMAS-HCNA)

in Computational Genomics

Mostafa Rezapour
David A. Ornelles
Stephen J. Walker
Colin E. Bishop
Sean V. Murphy
Metin Nafi Gurcan
Patrick M. McNutt
Anthony Atala

Frontiers in Genetics

Mini Review

Accepted on 18 Aug 2026

Mechanisms for the formation and maintenance of microhabitat self-organization in the root system of orchid

in Genomics of Plants and Plant-Associated Organisms

Junyang Song
Xinying Hao
Jianfeng Chen
Shankang Wang

Frontiers in Genetics

Correction

Accepted on 18 Aug 2026

Correction: Editorial: Hepatocellular carcinoma: from bench to bedside

in Cancer Genetics and Oncogenomics

Evin Iscan
Aaron Balasingam Koenig
Xiaogang Wu

Frontiers in Genetics

Original Research

Published on 18 Aug 2026

Comprehensive analysis of SYTL4 differential expression and clinical implications in DLBCL

in Cancer Genetics and Oncogenomics

Yue Li
Qiqi Zhou

Frontiers in Genetics

doi 10.3389/fgene.2026.1908683

482 views

Opinion

Published on 18 Aug 2026

Repositioning candidate gene approaches in the post-GWAS era: a clinical perspective from psychiatric pharmacogenetics

in Pharmacogenetics and Pharmacogenomics

Milica Pjevac
Jurij Bon
Vita Dolžan

Frontiers in Genetics

doi 10.3389/fgene.2026.1828563

774 views

Original Research

Published on 18 Aug 2026

NLRP3 inflammasome pathway activation is associated with cardiac remodeling, gut microbiota dysbiosis, and dietary protein restriction in a rat heart failure model: an integrative exploratory analysis

in Human and Medical Genomics

Xiaopeng Li
Chen Yang
Mengmeng Nie
Yong Zhang

Frontiers in Genetics

doi 10.3389/fgene.2026.1852819

397 views

Systematic Review

Published on 18 Aug 2026

Diagnostic accuracy of cell-free DNA-based non-invasive prenatal testing for fetal aneuploidies: a systematic review

in Human and Medical Genomics

Sharif Alhajlah

Frontiers in Genetics

doi 10.3389/fgene.2026.1886738

800 views

Original Research

Accepted on 17 Aug 2026

Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion

in Genetics of Common and Rare Diseases

Jiao Tong
Xu Chen
Tao Wang
Shan Ma
Yali Zhao
Dongdong Shi
Xin Wang
Dongmei Yan

Frontiers in Genetics

100 views

Case Report

Accepted on 17 Aug 2026

Presymptomatic Risdiplam in Preterm Monozygotic Twins with Co-occurring Spinal Muscular Atrophy and Tuberous Sclerosis Complex

in Genetics of Common and Rare Diseases

Xiaofang zhang
Yanjuan Wang
Si-Xiu Li
Ping Liu
Wenguang Hu

Frontiers in Genetics

Case Report

Accepted on 17 Aug 2026

A Rare De Novo Contiguous 15q11.1-q13.3 Duplication with Tetrasomy (CN=4) and Adjacent Trisomy (CN=3) Associated with Severe Global Developmental Delay, Autism Spectrum Disorder, and Subclinical Epileptiform Discharges: A Case Report and Literature Review

in Genetics of Common and Rare Diseases

Xinyu Zhou
HongYan Xie
Haoyan Yu
Zhiyuan Zhang
Yangfan Qi
Kai Jiang
Shungzhu Lin

Frontiers in Genetics

Original Research

Accepted on 17 Aug 2026

Yield of Actionable Variants From High-Risk Cancer Gene Panel Testing in Guideline-Eligible and Ineligible Individuals

in Cancer Genetics and Oncogenomics

Sarah S. Lee
Jingwen Zhang
Sara L. Bristow
Susan Rojahn
Mia Mackall
Meenakshi Malhotra
Youbao Sha
Eileen Hoffman
Vivienne Souter
Minetta C Liu

Frontiers in Genetics

113 views

Original Research

Accepted on 17 Aug 2026

A methodological framework for developing bioinformatics databases: A case study on the Boesenbergia rotunda genome database

in Computational Genomics

Sarinder Kaur Dhillon
Wai Shi Pang
Chee How Teo
V R Naresh Mutha
Jennifer Ann Harikrishna

Frontiers in Genetics

Original Research

Accepted on 17 Aug 2026

The Expressions and m⁶A Methylation Modification Patterns of mRNAs and lncRNAs in Major Depressive Disorder

in Epigenetics and Genome Architecture

Liang Liu
Zhaonan Yang
Kunru Tan
Shuhao Xu
Jia Xu
Jinbao Niu
Xiuxian Yang

Frontiers in Genetics

Case Report

Accepted on 17 Aug 2026

Adult presentation of SLC29A3-related disorder spectrum with marked hypogammaglobulinemia due to a recurrent homozygous pathogenic variant (G437R): a case report

in Genetics of Common and Rare Diseases

Mohammad Ameen Ishqair
Abbas K. H. Masalma
Mohanad Saleh
Fawaz Awad
ALiaa Khalili
Anas Ameen Ishqair
Somaya Salah
Abed-Rahman N. Saleh

Frontiers in Genetics

Original Research

Accepted on 17 Aug 2026

Missingness-aware machine learning using routine laboratory data for distinguishing hepatitis from cirrhosis

in Computational Genomics

Yang Qin
Xueri Hu
Tinjun Zhang
Qirong Zhu
Chengxing Yin
Zhihui Ren
Jiayi Feng
Cangjie Xue
Juanjuan Kang
Fengjun Liu

Frontiers in Genetics

Original Research

Accepted on 17 Aug 2026

Integrating Single-Cell Multi-Omics for Precision Radiotherapy Stratification in Hypopharyngeal Squamous Cell Carcinoma

in Cancer Genetics and Oncogenomics

Weishi Zhang
Mei Yao

Frontiers in Genetics

17,064 articles

articles

Genome-wide cis-expression Quantitative Trait Loci (eQTL) and transcriptomic signals reveal distinct molecular regulation across correlated feed efficiency traits

Identification of NETs and inflammation-related prognostic genes in breast cancer and PCR experimental validation

From Prohibition to Integration: LLMs in Scientific Publishing

Specimen Composition and Spatial Sampling Constrain Longitudinal Transcriptomic Inference in Glioblastoma

AI-Driven Genotype-Phenotype Modeling: A Framework Integrating Multi-Modal Single-Cell Genomics and Reverse Vaccinology for De Novo design of Multi-Epitope Cancer Vaccines

Amyotrophic lateral sclerosis -plus patient with an intermediate-length CACNA1A allele: a Case Report

Computational Prioritization of Candidate TCDD-Associated Targets in Retinoblastoma Using Network Toxicology and Transcriptomic Analysis

Loss of Lactate Dehydrogenase A disrupts R-loop homeostasis and induces DNA damage in breast cancer cells

Transcriptional Signatures of Respiratory Syncytial Virus (RSV) Infection Using Relaxed Magnitude Altitude Score with Hub-Centric Network Analysis (RMAS-HCNA)

Mechanisms for the formation and maintenance of microhabitat self-organization in the root system of orchid

Correction: Editorial: Hepatocellular carcinoma: from bench to bedside

Comprehensive analysis of SYTL4 differential expression and clinical implications in DLBCL

Repositioning candidate gene approaches in the post-GWAS era: a clinical perspective from psychiatric pharmacogenetics

NLRP3 inflammasome pathway activation is associated with cardiac remodeling, gut microbiota dysbiosis, and dietary protein restriction in a rat heart failure model: an integrative exploratory analysis

Diagnostic accuracy of cell-free DNA-based non-invasive prenatal testing for fetal aneuploidies: a systematic review

Genotype-phenotypic correlation in a Chinese patient with isolated lissencephaly sequence caused by 17p13.3p13.2 chromosomal microdeletion

Presymptomatic Risdiplam in Preterm Monozygotic Twins with Co-occurring Spinal Muscular Atrophy and Tuberous Sclerosis Complex

A Rare De Novo Contiguous 15q11.1-q13.3 Duplication with Tetrasomy (CN=4) and Adjacent Trisomy (CN=3) Associated with Severe Global Developmental Delay, Autism Spectrum Disorder, and Subclinical Epileptiform Discharges: A Case Report and Literature Review

Yield of Actionable Variants From High-Risk Cancer Gene Panel Testing in Guideline-Eligible and Ineligible Individuals

A methodological framework for developing bioinformatics databases: A case study on the Boesenbergia rotunda genome database

The Expressions and m⁶A Methylation Modification Patterns of mRNAs and lncRNAs in Major Depressive Disorder

Adult presentation of SLC29A3-related disorder spectrum with marked hypogammaglobulinemia due to a recurrent homozygous pathogenic variant (G437R): a case report

Missingness-aware machine learning using routine laboratory data for distinguishing hepatitis from cirrhosis

Integrating Single-Cell Multi-Omics for Precision Radiotherapy Stratification in Hypopharyngeal Squamous Cell Carcinoma