Frontiers in Genetics

Original Research

Accepted on 02 Oct 2026

Genome-wide diversity and Pinna rudis admixture reveal Thau Lagoon as a conservation reservoir for the collapsing fan mussel Pinna nobilis

in Evolutionary, Population, and Conservation Genetics

Mathieu Foulquié
Robert Bunet
Maite Vázquez Luis
Ioannis A. Giantsis
Fabio Scarpa
Daria Sanna
Elvira Alvarez Perez
Marco Casu
Jean-Marc Prévot
Nardo VICENTE

Frontiers in Genetics

Original Research

Accepted on 02 Oct 2026

CurvEdgeNet: Edge Feature Integration with Ricci Curvature for circRNA-Disease Association Prediction

in Computational Genomics

Wenjie Fan
Hao Liu
Xiaoyi Lv
Chen Chen
cheng chen
Yandan Xu

Frontiers in Genetics

Original Research

Accepted on 02 Oct 2026

Genetic prevalence of repeat expansion and other rare neurological disorders in the Quebec population

in Neurogenomics

Annelie De Mori
Marjorie Labrecque
Valérie Triassi
Sebastien Audet
Justin Pelletier
Abbe Lai
Roberta La Piana
Antoine Duquette
Claude Bhérer
Martine Tetreault

Frontiers in Genetics

Brief Research Report

Accepted on 02 Oct 2026

High-Resolution HLA Genetic Diversity in a Northeastern Mexican Clinical Cohort

in Immunogenetics

Jesús Antonio Ayala-Verdugo
José Carlos Jaime-Pérez
Sandra Iveth Mendoza-Ibarra
Carlos Octavio Cancela-Murrieta
Alondra Jetzany García-Valdez
Jorge Solis-Estrada
Rosario Salazar-Riojas
Andrés Gómez-De León
Perla Rocío Colunga-Pedraza
Olga Cantú-Rodríguez

Frontiers in Genetics

Original Research

Published on 02 Oct 2026

Longitudinal single-cell analysis identifies a chemotherapy-suppressed proliferative program associated with adverse prognosis in neuroblastoma

in Cancer Genetics and Oncogenomics

Aiguo Zhu
Jian Wang

Frontiers in Genetics

doi 10.3389/fgene.2026.1878093

278 views

Original Research

Published on 02 Oct 2026

Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs

in Evolutionary, Population, and Conservation Genetics

Litao Wu
Renhui Jiang
Xinyue Liu
Yinming Zhang

Frontiers in Genetics

doi 10.3389/fgene.2026.1931015

435 views

Original Research

Published on 02 Oct 2026

Clinical and genetic features, surgical management, and longitudinal follow-up in two children with progressive osseous heteroplasia

in Genetics of Common and Rare Diseases

Yuehan Yin
Binshan Zhao
Liying Sun
Wenyao Zhong
Dan Chen
Xiuli Zhao
Wen Tian

Frontiers in Genetics

doi 10.3389/fgene.2026.1883125

393 views

Case Report

Published on 02 Oct 2026

Endocardial thickening in dilated cardiomyopathy associated with FHL2 variant: a case report

in Human and Medical Genomics

Yana Wang
Lingfang Liang
Lingke Liu
Jiajia Ren
Xiaoxian Wang

Frontiers in Genetics

doi 10.3389/fgene.2026.1841224

332 views

Original Research

Accepted on 01 Oct 2026

Mechanism of the lncRNA-FGD5-AS1/miR-383-5p/SOCS3 Signaling Axis in Periodontitis

in Human and Medical Genomics

Ying Dai
Lan Ma
Guihong Xuan
Min Li

Frontiers in Genetics

Original Research

Published on 01 Oct 2026

A pilot genome-wide association study of ischemic heart disease with co-occurring arterial hypertension in a Kazakh cohort

in Human and Medical Genomics

Liliya Skvortsova
Kanagat Yergali
Assel Zhaxylykova
Mamura Begmanova
Almagul Mansharipova

Frontiers in Genetics

doi 10.3389/fgene.2026.1927147

244 views

Case Report

Published on 01 Oct 2026

Case Report: McLeod syndrome caused by a nonsense variant c.484C > T (p.Gln162Ter) in the XK gene in a Chinese Han family

in Neurogenomics

Luochu Dong
Mange Liu
Ying Tan

Frontiers in Genetics

doi 10.3389/fgene.2026.1939479

301 views

Review

Published on 01 Oct 2026

M6A modification in lipid metabolism and related diseases

in Epigenetics and Genome Architecture

Zhiwen Hu
Didi Yuan
Xi Feng
Sai Hu

Frontiers in Genetics

doi 10.3389/fgene.2026.1890451

474 views

Original Research

Published on 01 Oct 2026

Burden of pathogenic variants in genes associated with medically actionable disease in the Slovenian population

in Genetics of Common and Rare Diseases

Urška Kotnik
Luca Lovrecic
Borut Peterlin

Frontiers in Genetics

doi 10.3389/fgene.2026.1847596

298 views

Mini Review

Published on 01 Oct 2026

From inherited susceptibility to tumor state: toward a stage-aware architecture for genomic risk stratification in prostate cancer

in Human and Medical Genomics

Ziheng Zheng
Xuechun Yang
Minqian Ou
Yuedong Chen
Deyong Gan

Frontiers in Genetics

doi 10.3389/fgene.2026.1969511

298 views

Original Research

Published on 01 Oct 2026

Exploring the potential targets and possible mechanisms of Shenqi Fuzheng Injection in the treatment of cancer-associated muscle wasting based on network pharmacology

in Genetics of Aging

Chen Liu
Ling Cheng
Wenfeng Ye
Lina Zhang

Frontiers in Genetics

doi 10.3389/fgene.2026.1876819

1,011 views

Original Research

Accepted on 30 Sep 2026

Genetically-proxied GLP1R agonism and cardiometabolic outcomes in East Asian Biobank Populations

in Applied Genetic Epidemiology

Alexander C Tinworth
Satoshi Koyama
Lazaros Belbasis
Elsa Valdes-Marquez
Kaoru Ito
Koichi Matsuda
Parag Gajendragadkar
Canqing Yu
Dianjianyi Sun
Pei Pei

Frontiers in Genetics

Original Research

Accepted on 30 Sep 2026

Genotype Distribution and Identification of Rare Variants in α/β-Thalassemia in Chengdu: Including the First Report of HBA1:c.300+48C>G

in Genetics of Common and Rare Diseases

Xiaohua Liu

Frontiers in Genetics

Original Research

Accepted on 30 Sep 2026

Prediction of lncRNA–Cervical Cancer Associations Using a Multi-View Collaborative Variational Autoencoder with Knowledge Distillation Transfer Learning

in RNA

Min Yuan
Yanchuan Xiong
Xiariwana Abasi
Runmei Guo
Yandan Xu
Guzhalinuer Abulizi

Frontiers in Genetics

Original Research

Accepted on 30 Sep 2026

Genome-Wide Association Mapping Reveals Genetic Control of Root Architecture and Physiological Drought Responses in Maize

in Genomics of Plants and Plant-Associated Organisms

Nusrat-ul Islam
M. Ashraf Rather
Dr Zahoor Ahmed Dar
Parvaze Sofi
Mohd Altaf Wani
Gowhar Ali
Aflaq Hamid
Bhupender Kumar
Ajaz Ahmad Lone
Asif Bashir Shikari

Frontiers in Genetics

Original Research

Accepted on 30 Sep 2026

Inherited Metabolic Diseases Mimicking Hereditary Spastic Paraplegia: A Cohort of ten Egyptian patients

in Genetics of Common and Rare Diseases

Ola Ali Khalifa
Tarek Mohamed Youssef
Radwa Gamal Mahmoud

Frontiers in Genetics

Review

Accepted on 30 Sep 2026

More than one and less than many: Research and Care in Pediatric First-in-Human Cell and Gene Therapy Clinical Trials

in ELSI in Science and Genetics

Stanislav Birko
Ma'n H. Zawati

Frontiers in Genetics

Original Research

Published on 30 Sep 2026

From ISO 9001:2015 to ISO 20387:2018: a proposed implementation roadmap for biobanks

in ELSI in Science and Genetics

Michael Zuniga
Denis Marino
Gabriele Hartl
Berthold Huppertz
Zisis Kozlakidis
Karine Sargsyan

Frontiers in Genetics

doi 10.3389/fgene.2026.1953941

858 views

Original Research

Published on 30 Sep 2026

Bioinformatic prediction, qCLASH, and AlphaFold3 reveal non-overlapping layers of the miR-214-3p–mRNA interactome

in RNA

Jia Yao
Bingqiao Huang
Chenyu Chang
Ziqi Lin
Jinyue Lei
Weifeng Zhu
Mo Lisha
Tielong Xu

Frontiers in Genetics

doi 10.3389/fgene.2026.1924314

353 views

Case Report

Accepted on 29 Sep 2026

Prenatal diagnosis of congenital knee dislocation caused by BICD2 gene variant

in Genetics of Common and Rare Diseases

xiaohua ge
wencong li
hong wei
Meijuan Liu

Frontiers in Genetics

17,204 articles

articles

Genome-wide diversity and Pinna rudis admixture reveal Thau Lagoon as a conservation reservoir for the collapsing fan mussel Pinna nobilis

CurvEdgeNet: Edge Feature Integration with Ricci Curvature for circRNA-Disease Association Prediction

Genetic prevalence of repeat expansion and other rare neurological disorders in the Quebec population

High-Resolution HLA Genetic Diversity in a Northeastern Mexican Clinical Cohort

Longitudinal single-cell analysis identifies a chemotherapy-suppressed proliferative program associated with adverse prognosis in neuroblastoma

Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs

Clinical and genetic features, surgical management, and longitudinal follow-up in two children with progressive osseous heteroplasia

Endocardial thickening in dilated cardiomyopathy associated with FHL2 variant: a case report

Mechanism of the lncRNA-FGD5-AS1/miR-383-5p/SOCS3 Signaling Axis in Periodontitis

A pilot genome-wide association study of ischemic heart disease with co-occurring arterial hypertension in a Kazakh cohort

Case Report: McLeod syndrome caused by a nonsense variant c.484C > T (p.Gln162Ter) in the XK gene in a Chinese Han family

M6A modification in lipid metabolism and related diseases

Burden of pathogenic variants in genes associated with medically actionable disease in the Slovenian population

From inherited susceptibility to tumor state: toward a stage-aware architecture for genomic risk stratification in prostate cancer

Exploring the potential targets and possible mechanisms of Shenqi Fuzheng Injection in the treatment of cancer-associated muscle wasting based on network pharmacology

Genetically-proxied GLP1R agonism and cardiometabolic outcomes in East Asian Biobank Populations

Genotype Distribution and Identification of Rare Variants in α/β-Thalassemia in Chengdu: Including the First Report of HBA1:c.300+48C>G

Prediction of lncRNA–Cervical Cancer Associations Using a Multi-View Collaborative Variational Autoencoder with Knowledge Distillation Transfer Learning

Genome-Wide Association Mapping Reveals Genetic Control of Root Architecture and Physiological Drought Responses in Maize

Inherited Metabolic Diseases Mimicking Hereditary Spastic Paraplegia: A Cohort of ten Egyptian patients

More than one and less than many: Research and Care in Pediatric First-in-Human Cell and Gene Therapy Clinical Trials

From ISO 9001:2015 to ISO 20387:2018: a proposed implementation roadmap for biobanks

Bioinformatic prediction, qCLASH, and AlphaFold3 reveal non-overlapping layers of the miR-214-3p–mRNA interactome

Prenatal diagnosis of congenital knee dislocation caused by BICD2 gene variant