Frontiers in Genetics

Original Research

Published on 07 Aug 2026

Confusion, communication, and consent: ELSI barriers to genomics-enhanced remediation in Alberta’s oil sands

in ELSI in Science and Genetics

Michelle Tilford-Shaw
Max Pospisil
Lori Bradford
Graham Strickert
Diane Dupont

Frontiers in Genetics

doi 10.3389/fgene.2026.1889489

170 views

Original Research

Published on 07 Aug 2026

Genetic associations and candidate functional genes linking depression and obesity: a multi-omics integrative study

in Behavioral and Psychiatric Genetics

Xingpei Li
Chunlin Chen
Huibing Li
Yiru He
Kailang Tang
Guanqiao Lai
Ziyang Yang
Wushu Chen
Huihui Yang

Frontiers in Genetics

doi 10.3389/fgene.2026.1855173

265 views

Review

Published on 07 Aug 2026

Chromatin remodeling and epigenetic regulation of mesenchymal stem/stromal cells in osteoarthritis

in Epigenetics and Genome Architecture

Mo Wu
Cenzhuo Sheng
Hanhao Zhang
Yuxin Chen
Tianyou Ma
Yirui Tong
Pengchao Xu
Peijian Tong
Hanting Xia

Frontiers in Genetics

doi 10.3389/fgene.2026.1877252

265 views

Original Research

Published on 07 Aug 2026

Next‐generation SNPs from lignin biosynthesis gene and transcription factors reveal a hidden teak (Tectona grandis L. f.) lineage: implications for plantation resilience and forest management

in Evolutionary, Population, and Conservation Genetics

Nuzhat Bano
Naseer Mohammad
Shamim Akhtar Ansari

Frontiers in Genetics

doi 10.3389/fgene.2026.1842536

203 views

Original Research

Accepted on 06 Aug 2026

Genome-wide identification of WOX transcription factors and functional characterization of WOX4 and WOX13 involved in cold stress response in Malus baccata

in Genomics of Plants and Plant-Associated Organisms

Tian Yanting
Hao Liu
Fei Wang
Lifang Yang
Xuhong Zhang
Huanyong Li
Xin Qi
Jing Guo

Frontiers in Genetics

Case Report

Accepted on 06 Aug 2026

Glycogen Storage Disease Type VII (Tarui Disease): a case report presenting a PFKM Variant Previously Described Only in Canine Models

in Genetics of Common and Rare Diseases

Mariapia Griffo
Nicola Molitierno
Laura Maria Napoli
Michela Ripolone
Simona Zanotti
Francesco Fortunato
Gabriele Tumminello
Maurizio Moggio
Marco Locatelli
Stefania Corti

Frontiers in Genetics

Editorial

Published on 06 Aug 2026

Editorial: Insights in RNA: 2025

in RNA

Hassan Dastsooz
Naoyuki Kataoka
Nicoletta Potenza

Frontiers in Genetics

doi 10.3389/fgene.2026.1947303

129 views

Case Report

Published on 06 Aug 2026

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family

in Genetics of Common and Rare Diseases

Qiong Pan
Yuefang Liu
Xueping Sun
Shoulian Lu
Lingling Li
Jiandong Shen

Frontiers in Genetics

doi 10.3389/fgene.2026.1850997

213 views

Original Research

Published on 06 Aug 2026

The complete chloroplast genome of Hedera helix (Araliaceae): comparative plastome analyses reveal divergence hotspots, selective constraints, and phylogenetic placement

in Genomics of Plants and Plant-Associated Organisms

Dujuan Zhan
Yaqi Fang
Hao Li
Chencheng Zheng
Jin Jiang
Jie Chen

Frontiers in Genetics

doi 10.3389/fgene.2026.1855347

201 views

Case Report

Accepted on 05 Aug 2026

Differential outcomes associated with the same pathogenic variant: long-term follow-up of a CHARGE syndrome case with a nonsense mutation c.6292C>T in the CHD gene

in Genetics of Common and Rare Diseases

Qiong-yu Wang
Jing-jing Huang
Fu-chun Wang
Jing-wei He

Frontiers in Genetics

Original Research

Published on 05 Aug 2026

Identification and prenatal diagnosis of a novel likely pathogenic ANOS1 variant in a large Chinese Kallmann syndrome family

in Genetics of Common and Rare Diseases

Xiulan Hao
Yanchou Ye
Mancheng Liu
Zhechao Zhang
Haofeng Ning
Xiaonan Wang
Fangchao Tao
Xiujing Huang
Jingran Du
Tian Li

Frontiers in Genetics

doi 10.3389/fgene.2026.1870344

399 views

Original Research

Published on 05 Aug 2026

Risk factors and early warning scoring system for chronic postsurgical pain following video-assisted thoracoscopic surgery in elderly lung cancer patients: a retrospective cohort study

in Cancer Genetics and Oncogenomics

Degui Wang
Weichen Pan
Qinghua Shi
Yuhong Liu

Frontiers in Genetics

doi 10.3389/fgene.2026.1879530

442 views

Review

Published on 05 Aug 2026

From markers to mechanisms: a comprehensive review of major genes and quantitative trait loci shaping the modern sheep (Ovis aries)

in Livestock Genomics

Mostafa Ghaderi-Zefrehei
Effat Nasre Esfahani
Hassan Amini Pozveh
Mohammadreza Hashemi
Parisa Dolati
Sonia Zakizadeh
Maryam Montazeri
Mustafa Muhaghegh Dolatabady
Ikhide Godwin Imumorin
Mohammad Hossein Banabazi

Frontiers in Genetics

doi 10.3389/fgene.2026.1865980

458 views

Hypothesis and Theory

Accepted on 04 Aug 2026

Economic impact of biomarker-based aging interventions on healthcare costs and individual value

in Epigenetics and Genome Architecture

Federico Felizzi

Frontiers in Genetics

Review

Published on 04 Aug 2026

Fabry nephropathy as the clinical anchor for kidney-centered metabolic surveillance: linking genetic heterogeneity to early risk identification

in Human and Medical Genomics

Yanshu Xie
Jingzi Zhong

Frontiers in Genetics

doi 10.3389/fgene.2026.1905397

316 views

Original Research

Published on 04 Aug 2026

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction

in Genetics of Common and Rare Diseases

Wanna Ke
Xiaojun Wen
Zhanhui Ou
Xiaowu Fang
Junye Huo
Xiufeng Lin
Xubin Zhang
Zhiming Li

Frontiers in Genetics

doi 10.3389/fgene.2026.1832329

318 views

Original Research

Published on 04 Aug 2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes

in Genetics of Common and Rare Diseases

Yufeng Huang
Lingyue Huang
Lilin Hu
Li Tan
Peiwei Zhao
Sukun Luo
Ting Yu
Yanqiu Hu
Yuanzhi He
Hao Du

Frontiers in Genetics

doi 10.3389/fgene.2026.1876428

422 views

Original Research

Published on 04 Aug 2026

NSF gene variants cause developmental and epileptic encephalopathy 96: expanding genotype and phenotypic spectrum with prenatal-onset features

in Genetics of Common and Rare Diseases

Qi Yang
Zailong Qin
Jiao Li
Qiang Zhang
Xunzhao Zhou
Sheng Yi
Shujie Zhang
Weiliang Lu
Shang Yi
Sheng He

Frontiers in Genetics

doi 10.3389/fgene.2026.1882449

369 views

Original Research

Accepted on 03 Aug 2026

Perceptions of and Willingness to Participate in Genomics Research Among a U.S. Sample

in ELSI in Science and Genetics

Emerson Dusic
Devin Madden
Isabella E. Rios
Bo J. Hwang
Sima Rabinowitz
Michelle A. Ramos
David R. Pletta
Rodrigo Aguayo-Romero
Mitchell R. Lunn
Kellan Baker

Frontiers in Genetics

119 views

Brief Research Report

Accepted on 03 Aug 2026

Prevalence of migalastat-amenable variants in patients with Fabry disease from Brazil, Argentina, and Colombia: an observational study

in Genetics of Common and Rare Diseases

Juan Manuel POLITEI
Ana María Zarante Bahamón
Ana Maria Martins
Afrânio Souza De Melo
Marcelo Horacio de Sa Pereira
Andréia Loures-Vale
Biliana O. Veleva-Rotse
Eva Krusinska
Val Lengoc

Frontiers in Genetics

Original Research

Accepted on 03 Aug 2026

Investigation of factors affecting egg breakage resistance in laying hens using data mining and machine learning methods

in Statistical Genetics and Methodology

Şenol Çelik
Turgay Şengül
Ömer Şengül

Frontiers in Genetics

Original Research

Accepted on 03 Aug 2026

Clinical Implementation of Next Generation Sequencing in Tertiary Health System: The Rijeka Retrospective Study

in Human and Medical Genomics

Nina Pereza
Sanja Dević Pavlić
Tea Mladenić
Željka Hrupački
Dorotea Vukelić Drašković
Luca Lovrecic
Aleš Maver
JADRANKA VRANEKOVIĆ
Iva Bilić Čače
Igor Prpic

Frontiers in Genetics

Mini Review

Accepted on 03 Aug 2026

Homeostatic Conflict as a Driver for Brain Aging

in Genetics of Aging

Cristian A Wulkop-Gil
Michael Petrascheck

Frontiers in Genetics

Case Report

Accepted on 03 Aug 2026

Persistent Isolated Hyperhomocysteinemia in an Adolescent with Celiac Disease and Homozygous MTHFR c.665C>T Polymorphism: A Multifactorial Disturbance of One-Carbon Metabolism

in Genomics of Nutrition and Metabolism

Zainab Al Masseri
Michal Inbar Feigenberg
Nicole Martin
Dawn Cordeiro
Laura Guilder
Christian Marshall

Frontiers in Genetics

17,031 articles

articles

Confusion, communication, and consent: ELSI barriers to genomics-enhanced remediation in Alberta’s oil sands

Genetic associations and candidate functional genes linking depression and obesity: a multi-omics integrative study

Chromatin remodeling and epigenetic regulation of mesenchymal stem/stromal cells in osteoarthritis

Next‐generation SNPs from lignin biosynthesis gene and transcription factors reveal a hidden teak (Tectona grandis L. f.) lineage: implications for plantation resilience and forest management

Genome-wide identification of WOX transcription factors and functional characterization of WOX4 and WOX13 involved in cold stress response in Malus baccata

Glycogen Storage Disease Type VII (Tarui Disease): a case report presenting a PFKM Variant Previously Described Only in Canine Models

Editorial: Insights in RNA: 2025

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family

The complete chloroplast genome of Hedera helix (Araliaceae): comparative plastome analyses reveal divergence hotspots, selective constraints, and phylogenetic placement

Differential outcomes associated with the same pathogenic variant: long-term follow-up of a CHARGE syndrome case with a nonsense mutation c.6292C>T in the CHD gene

Identification and prenatal diagnosis of a novel likely pathogenic ANOS1 variant in a large Chinese Kallmann syndrome family

Risk factors and early warning scoring system for chronic postsurgical pain following video-assisted thoracoscopic surgery in elderly lung cancer patients: a retrospective cohort study

From markers to mechanisms: a comprehensive review of major genes and quantitative trait loci shaping the modern sheep (Ovis aries)

Economic impact of biomarker-based aging interventions on healthcare costs and individual value

Fabry nephropathy as the clinical anchor for kidney-centered metabolic surveillance: linking genetic heterogeneity to early risk identification

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes

NSF gene variants cause developmental and epileptic encephalopathy 96: expanding genotype and phenotypic spectrum with prenatal-onset features

Perceptions of and Willingness to Participate in Genomics Research Among a U.S. Sample

Prevalence of migalastat-amenable variants in patients with Fabry disease from Brazil, Argentina, and Colombia: an observational study

Investigation of factors affecting egg breakage resistance in laying hens using data mining and machine learning methods

Clinical Implementation of Next Generation Sequencing in Tertiary Health System: The Rijeka Retrospective Study

Homeostatic Conflict as a Driver for Brain Aging

Persistent Isolated Hyperhomocysteinemia in an Adolescent with Celiac Disease and Homozygous MTHFR c.665C>T Polymorphism: A Multifactorial Disturbance of One-Carbon Metabolism