Frontiers in Genetics

Original Research

Published on 13 Feb 2026

Delineating the trajectory of adult chronic diseases and healthcare use for 22q11.2 microdeletion in a general population context

in Genetics of Common and Rare Diseases

Sarah L. Malecki
Tracy Heung
Samantha Morais
Refik Saskin
Drew Wilton
Therese A. Stukel
Eyal Cohen
Amol A. Verma
Anne S. Bassett

Frontiers in Genetics

doi 10.3389/fgene.2026.1737027

458 views

Opinion

Published on 13 Feb 2026

Imagining an ethics for synthetic biology

in ELSI in Science and Genetics

Varsha Aravind Paleri
Kristien Hens

Frontiers in Genetics

doi 10.3389/fgene.2026.1746379

296 views

Mini Review

Published on 13 Feb 2026

Recent advances in the detection technologies for balanced chromosomal rearrangements

in Human and Medical Genomics

Meng Gao
Jun Ren
Shanling Liu

Frontiers in Genetics

doi 10.3389/fgene.2026.1763846

530 views

Brief Research Report

Published on 13 Feb 2026

Differential genome-wide association analysis of schizophrenia and post-traumatic stress disorder identifies opposing effects at the MAPT/CRHR1 locus

in Human and Medical Genomics

Zhong‐shan Cheng

Frontiers in Genetics

doi 10.3389/fgene.2026.1728494

181 views

Editorial

Published on 13 Feb 2026

Editorial: Advancements in AI for the analysis and interpretation of large-scale data by omics techniques

in Computational Genomics

Angelo Facchiano
Deborah Giordano
Dominik Heider

Frontiers in Genetics

doi 10.3389/fgene.2026.1784820

117 views

Mini Review

Accepted on 12 Feb 2026

Regulatory Roles of the circRNA–RBP Axis in Exercise-Induced Skeletal Muscle Remodeling: Mechanistic Controversies and Translational Illusions

in RNA

Junjie Liu
Yupeng Yang
Heming Chen
Mingming Liu
Zhujun Mao
Zheng Mi

Frontiers in Genetics

Original Research

Accepted on 12 Feb 2026

Mutant p53 and TP53 mutations in esophageal squamous cell carcinoma: consistency and diagnostic significance

in Cancer Genetics and Oncogenomics

Xueyu Zhuang
Na Lin
Yanjuan Xu

Frontiers in Genetics

Case Report

Accepted on 12 Feb 2026

Co-occurring DMD, GJA1, and Novel FYCO1 Variants in a Proband from a Consanguineous Oculodentodigital Dysplasia Family: A Rare Multilocus Case Report

in Genetics of Common and Rare Diseases

Kondyarpu Abhishek
Nitish Kumar Mohanta
Joseph John
Swarupa Panda
Amit Kumar Satpathy
Roma Rattan
Ramchander Venkat Puppala

Frontiers in Genetics

Review

Accepted on 12 Feb 2026

Molecular Mediators of Motion: RNA-RBP Networks in Exercise-Induced Osteoarthritis Protection

in RNA

Yupeng Yang
Xue Wang
Xuchang Zhou
Ying Li
Yinghao Shen
Zhujun Mao
Junjie Liu
Zheng Mi

Frontiers in Genetics

Review

Accepted on 12 Feb 2026

Exercise Stress and Tissue Remodeling: Advances in Exosome-Mediated RNA-RBP Networks in Musculoskeletal Injury Repair and Functional Recovery

in RNA

Junjie Liu
Heming Chen
Yupeng Yang
Zheheng Jia
Ying Li
Xintong Zhong
Huimei Jiang
Zhujun Mao
Zheng Mi

Frontiers in Genetics

Brief Research Report

Accepted on 12 Feb 2026

Late Diagnosis and Effective Everolimus Treatment in a Familial Case of Tuberous Sclerosis Complex: A Case Report)

in Applied Genetic Epidemiology

Fang Dai
Yulian Duan
Bao-an Di
Qiang Feng
Jing Cui
Tao Lv

Frontiers in Genetics

Mini Review

Accepted on 12 Feb 2026

Long Noncoding RNAs in tumor stemness: Emerging Mechanisms and Therapeutic Opportunities

in Cancer Genetics and Oncogenomics

Eduardo M Reis
Daniela Sanchez Bassères

Frontiers in Genetics

Editorial

Accepted on 12 Feb 2026

Editorial: Advancements in Sequencing Technologies for Epigenomic and Transcriptomic Analysis: From Bulk to Single-Cell Resolution

in Computational Genomics

Laura Veschetti
Massimiliano Cocca
DAGO DOUGBA NOEL
Giovanni Malerba

Frontiers in Genetics

Perspective

Accepted on 12 Feb 2026

Modeling APOE, morbidity, and mortality: a reproducibility challenge for genetic epidemiology

in Applied Genetic Epidemiology

Erling Häggström Gunfridsson

Frontiers in Genetics

Original Research

Published on 12 Feb 2026

Structural pharmacogenomics of drug-associated SNPs in oral squamous cell carcinoma

in Pharmacogenetics and Pharmacogenomics

Punya Sunil
K. C. Ananth Kumar
A. I. Ananthakrishnan
Sebanti Gupta
Ranajit Das

Frontiers in Genetics

doi 10.3389/fgene.2026.1666142

236 views

Case Report

Published on 12 Feb 2026

Case Report: Recurrent stroke-like episodes triggered by high-altitude exposure in X-linked charcot-marie-tooth disease

in Neurogenomics

Jing Zhong
Tang Yang
Bo Wu
Shuai Jiang

Frontiers in Genetics

doi 10.3389/fgene.2026.1769172

139 views

Original Research

Published on 12 Feb 2026

Circ-104792/miR-133a/Bcl-xL influences the proliferation and function of human trophoblastic and decidual stromal cells involved in recurrent abortion disease

in Human and Medical Genomics

Wenjuan Ma
Yuan Ma
Hongli Zhu
Panpan Shi
Xiaochun Huang
Yang Yang

Frontiers in Genetics

doi 10.3389/fgene.2026.1707900

317 views

Systematic Review

Published on 12 Feb 2026

The impact of circulating tumor DNA on the prognosis of liver cancer and its predictive value: a meta analysis

in Cancer Genetics and Oncogenomics

Bing Wu
Shuhui Ke
Lingling Zhu
Rongrong Dong
Jinqian Luan

Frontiers in Genetics

doi 10.3389/fgene.2026.1767755

162 views

Original Research

Published on 12 Feb 2026

Genetic polymorphisms of the CDC27 gene are associated with susceptibility and outcomes of non-syndromic congenital heart disease: a bi-ethnic case–control study in Chinese populations

in Genetics of Common and Rare Diseases

Teng Yuan
Feng Zhu
Aikebai Aisan
Tunike Maheshati
Yunxia Li
Ren Tian
You Chen

Frontiers in Genetics

doi 10.3389/fgene.2026.1701812

185 views

Original Research

Accepted on 11 Feb 2026

Age at natural menopause, reproductive lifespan and Alzheimer's Disease in females: is APOE ε4 the missing link?

in Statistical Genetics and Methodology

Francesco Bruno
Patrizia Spadafora
Paolo Abondio
Antonio Qualtieri
Ersilia Paparazzo
Mirella Aurora Aceto
Ida Veltri
Selene De Benedittis
Beatrice Maria Greco
Annamaria Cerantonio

Frontiers in Genetics

Review

Accepted on 11 Feb 2026

Multiscale Computational Genomics in Wilson Disease: From Atomic Dynamics to Clinical Prediction

in Computational Genomics

Moujun Luan
Qingkai Xue
Yujie Cao
Gangli Cheng
Xingxing Huo

Frontiers in Genetics

Brief Research Report

Published on 11 Feb 2026

Genomic innovation in precision oncology: integrated CRISPR-TTP bioengineering architecture for Ewing Sarcoma (version 4.0 – complete architectural specification)

in Cancer Genetics and Oncogenomics

Alexey Mikhailovich Burlai

Frontiers in Genetics

doi 10.3389/fgene.2026.1727708

556 views

Original Research

Published on 11 Feb 2026

Identification of programmed cell death and mitochondria correlated biomarkers for Kawasaki disease by integrated bioinformatics and machine-learning algorithms with RT-qPCR verification

in Computational Genomics

Tengyang Wang
Chengyi Wang
Yiwei Chen
Xiaofeng Guo

Frontiers in Genetics

doi 10.3389/fgene.2026.1677146

363 views

Original Research

Accepted on 10 Feb 2026

Clinical and Genetic Features of Hereditary Transthyretin Amyloidosis with Polyneuropathy in China: Insights from Case Analysis and Literature Review

in Genetics of Common and Rare Diseases

Xiaoyang Yuan
Yajun Lv
Xue Wang
Bing Han
Bingchuan Xie

Frontiers in Genetics

16,571 articles

articles

Delineating the trajectory of adult chronic diseases and healthcare use for 22q11.2 microdeletion in a general population context

Imagining an ethics for synthetic biology

Recent advances in the detection technologies for balanced chromosomal rearrangements

Differential genome-wide association analysis of schizophrenia and post-traumatic stress disorder identifies opposing effects at the MAPT/CRHR1 locus

Editorial: Advancements in AI for the analysis and interpretation of large-scale data by omics techniques

Regulatory Roles of the circRNA–RBP Axis in Exercise-Induced Skeletal Muscle Remodeling: Mechanistic Controversies and Translational Illusions

Mutant p53 and TP53 mutations in esophageal squamous cell carcinoma: consistency and diagnostic significance

Co-occurring DMD, GJA1, and Novel FYCO1 Variants in a Proband from a Consanguineous Oculodentodigital Dysplasia Family: A Rare Multilocus Case Report

Molecular Mediators of Motion: RNA-RBP Networks in Exercise-Induced Osteoarthritis Protection

Exercise Stress and Tissue Remodeling: Advances in Exosome-Mediated RNA-RBP Networks in Musculoskeletal Injury Repair and Functional Recovery

Late Diagnosis and Effective Everolimus Treatment in a Familial Case of Tuberous Sclerosis Complex: A Case Report)

Long Noncoding RNAs in tumor stemness: Emerging Mechanisms and Therapeutic Opportunities

Editorial: Advancements in Sequencing Technologies for Epigenomic and Transcriptomic Analysis: From Bulk to Single-Cell Resolution

Modeling APOE, morbidity, and mortality: a reproducibility challenge for genetic epidemiology

Structural pharmacogenomics of drug-associated SNPs in oral squamous cell carcinoma

Case Report: Recurrent stroke-like episodes triggered by high-altitude exposure in X-linked charcot-marie-tooth disease

Circ-104792/miR-133a/Bcl-xL influences the proliferation and function of human trophoblastic and decidual stromal cells involved in recurrent abortion disease

The impact of circulating tumor DNA on the prognosis of liver cancer and its predictive value: a meta analysis

Genetic polymorphisms of the CDC27 gene are associated with susceptibility and outcomes of non-syndromic congenital heart disease: a bi-ethnic case–control study in Chinese populations

Age at natural menopause, reproductive lifespan and Alzheimer's Disease in females: is APOE ε4 the missing link?

Multiscale Computational Genomics in Wilson Disease: From Atomic Dynamics to Clinical Prediction

Genomic innovation in precision oncology: integrated CRISPR-TTP bioengineering architecture for Ewing Sarcoma (version 4.0 – complete architectural specification)

Identification of programmed cell death and mitochondria correlated biomarkers for Kawasaki disease by integrated bioinformatics and machine-learning algorithms with RT-qPCR verification

Clinical and Genetic Features of Hereditary Transthyretin Amyloidosis with Polyneuropathy in China: Insights from Case Analysis and Literature Review