Frontiers in Genetics

Systematic Review

Published on 12 Jan 2026

Coffin–Lowry syndrome: a systematic review of RPS6KA3 confirmed cases and implications for diagnosis and counseling

in Genetics of Common and Rare Diseases

Sabyasachi Maity
Miranda Montion
Danielle Boothe
Mona Attarpour
Ivy Mageto
Simran Agarwal
Rujul Patel
Chloe Lark
Nemesis Cardona Valentin
Esther Quinones-Budel

Frontiers in Genetics

doi 10.3389/fgene.2025.1715229

1,745 views

Opinion

Published on 12 Jan 2026

Rethinking Parkinson’s disease genetics in the precision medicine era: why genomic diversity matters?

in Neurogenomics

Camilla Teixeira Pinheiro Gusmão
Giselli Scaini
Everton Ferreira de Souza
Rafael Antônio Vicente Lacerda
Matheus de Almeida Costa
Raja Mehanna
João Quevedo
Howard Lopes Ribeiro Junior

Frontiers in Genetics

doi 10.3389/fgene.2025.1750113

1,308 views

Original Research

Published on 12 Jan 2026

Identification of IGF2BP3 and CENPA as key regulators of immunophenotypes in renal clear cell carcinoma

in Cancer Genetics and Oncogenomics

Tianjie Zhu
Liying He
Shuai Li
Jingyuan Zhao

Frontiers in Genetics

doi 10.3389/fgene.2025.1749780

902 views

Mini Review

Published on 12 Jan 2026

Ribosome plasticity in glioblastoma: a multi-omics framework for future investigation

in Cancer Genetics and Oncogenomics

Dario Benelli
Christian Barbato
Carlo Cogoni

Frontiers in Genetics

doi 10.3389/fgene.2025.1756452

1,063 views
1 citation

Original Research

Published on 12 Jan 2026

Does adoption of superior Murrah buffalo germplasm pay off? evidence from a causal impact study in Haryana, India

in Livestock Genomics

Makarabbi Gururaj
S. Aiswarya
Chhotaray Supriya
Sanjay Kumar

Frontiers in Genetics

doi 10.3389/fgene.2025.1713072

1,242 views

Original Research

Published on 12 Jan 2026

FSFT6mA: a feature-synthesis fine-tuning framework for DNA 6mA site prediction

in Computational Genomics

Hong-Jin Yu
Ying Zhang
Dong-Jun Yu
Guansheng Zheng

Frontiers in Genetics

doi 10.3389/fgene.2025.1750223

757 views

Review

Published on 12 Jan 2026

Histone modifications and depression: epigenetic mechanisms, therapeutic targets, and translational outlook

in Epigenomics and Epigenetics

Liang-Zhen Lv
Zhao-Di Wang
Jia-jie Ren
Lu-Hao Li
Xian-bao Liu
Jia-li Li
Hui Zhu
Bei Jiang
Ya-peng Han
Xue-ming Zhou

Frontiers in Genetics

doi 10.3389/fgene.2025.1722453

1,203 views

Original Research

Published on 12 Jan 2026

Time-series transcriptomic analysis of flower tissue during heat stress in heat-resilient and heat-sensitive Brassica napus L.

in Genomics of Plants and Plant-Associated Organisms

Xiaojie Hu
Sheng Chen
Xiaoke Ping
Kadambot H. M. Siddique
Wallace A. Cowling

Frontiers in Genetics

doi 10.3389/fgene.2025.1736538

1,069 views

Original Research

Published on 09 Jan 2026

The value of quantitative fluorescence polymerase chain reaction for the products of conception in the era of copy number variation sequencing

in Cytogenomics

Shaozhe Yang
Hewei Zhang
Yongli Wang
Qingwei Zhang
Yongyong Wu
Xiuhong Fu
Rongxiang Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1750362

654 views

Correction

Published on 09 Jan 2026

Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype

in Neurogenomics

Mingkai Yang
Yanfang Xiao
Chanjuan Chen
Zhou Chu
Guohong Hu

Frontiers in Genetics

doi 10.3389/fgene.2025.1769021

747 views

Mini Review

Published on 09 Jan 2026

Reconstructing developmental lineages: a retrospective approach using somatic mutations and variant allele frequency

in Computational Genomics

Mahnoor Sajjad
Seong Gyu Kwon

Frontiers in Genetics

doi 10.3389/fgene.2025.1761810

992 views

Original Research

Published on 09 Jan 2026

Retrospective analysis of non-invasive prenatal testing: a population study involving 19,835 participants in the Shaoyang area

in Genetics of Common and Rare Diseases

Muping Zhou
Hua Zhang
Jun Wen
Na Liu
Zhongchun Wu
Ting Lin
Mengyun Tang
Yan Huang
Ying Xiao
Hui Xie

Frontiers in Genetics

doi 10.3389/fgene.2025.1748107

927 views

Case Report

Published on 08 Jan 2026

Case Report: Dual pathogenic mechanism of a PRKG2 missense variant underlies an attenuated phenotype of acromesomelic dysplasia

in Human and Medical Genomics

Daria Akimova
Tatiana Markova
Maria Orlova
Vladimir Kenis
Mikhail Skoblov

Frontiers in Genetics

doi 10.3389/fgene.2025.1708985

957 views

Review

Published on 08 Jan 2026

Omics in mini-livestock: a genomic perspective on the future of sustainable food systems

in Livestock Genomics

Alexander Sode
Arindam Halder
Julia Metzger

Frontiers in Genetics

doi 10.3389/fgene.2025.1740301

2,118 views

Original Research

Published on 08 Jan 2026

Systematic analysis of anoikis-related genes identifies SRPX2-FAK/AKT-IL-6 axis in the progression and peritoneal metastasis of gastric cancer

in Cancer Genetics and Oncogenomics

Dong Hou
Jinhao Yu
Yequan Xie
Shengning Zhou
Jintao Zeng
Mingtao Liang
Fang Zheng
Jianan Tan
Fanghai Han

Frontiers in Genetics

doi 10.3389/fgene.2025.1736097

1,523 views

Case Report

Published on 08 Jan 2026

Case Report: Novel GLA mutation in a Chinese female with renal-predominant Fabry disease and cardiac hypertrophy

in Genetics of Common and Rare Diseases

Lanxin Li
Tianyu Chang
Xichen Li
Yinglu Hao
Min Deng
Yanping Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1664286

954 views

Methods

Published on 07 Jan 2026

Resilience and evolutionary insights in PPI networks: comparative analysis of node resilience and centrality measures

in Computational Genomics

Jiarui Zhang

Frontiers in Genetics

doi 10.3389/fgene.2025.1613475

786 views

Review

Published on 07 Jan 2026

Exploring the role and therapeutic potential of RNA N6-methyladenosine modification in abortion disease pathology: a comprehensive review

in Epigenomics and Epigenetics

Zhuo Chang
Lu-Hao Li
Liang-Zhen Lv
Zhao-Di Wang
Qing-yi Wang
Hui Zhu
Bei Jiang
Xue-Ming Zhou
Ya-Peng Han
Xue Pan

Frontiers in Genetics

doi 10.3389/fgene.2025.1720842

1,035 views

Original Research

Published on 07 Jan 2026

TPM1-p.E181K mutation suppresses CaMKII/HDAC4 signaling pathway leading to pediatric restrictive cardiomyopathy

in Genetics of Common and Rare Diseases

Jia Fu
Jing Zhang
Youxian Zhang
Dongming Sun
Kun Xia
Ruigeng Wang
Xiaoyuan Feng
Aiguo Zhai
Yufeng Huang
Xiaobin Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1654907

1,007 views

Original Research

Published on 07 Jan 2026

DDA-bench: a manually curated database for benchmarking datasets and baseline performance values in predicting drug-disease associations

in Computational Genomics

Han Xing
Yongjian Zhao

Frontiers in Genetics

doi 10.3389/fgene.2025.1755600

797 views

Original Research

Published on 07 Jan 2026

(Not) “just your nature”. Diagnostic journeys of adults with neurofibromatosis type 1 in Poland

in ELSI in Science and Genetics

Katarzyna Kowal
Jan Domaradzki

Frontiers in Genetics

doi 10.3389/fgene.2025.1713304

1,142 views

Case Report

Published on 07 Jan 2026

Case Report: Myoclonic and tremulous movements associated with COQ8A-related coenzyme Q10 deficiency type 4

in Genetics of Common and Rare Diseases

Di Wang
Guojian Zhang
Xiaojing Fang
Fang Liu
Li Wang

Frontiers in Genetics

doi 10.3389/fgene.2025.1682085

982 views

Original Research

Published on 07 Jan 2026

Salmonella enterica serovar Typhimurium-induced alterations in inflammatory chemokine mRNA expressions and hemato-biochemical variations in three different strains of chicken

in Livestock Genomics

Shabir Mir
Nazir A. Ganai
Syed M. Ahmad
Ishraq Hussain
Gowhar G. Sheikh
Nusrat Nabi
Hassan A. Rudayni
Ahmed A. Allam

Frontiers in Genetics

doi 10.3389/fgene.2025.1645142

1,033 views
1 citation

Original Research

Published on 07 Jan 2026

Biobanking as a research accelerator: the perspectives of medical students and interns at a saudi university

in ELSI in Science and Genetics

Leena AbuOmar
Mariam M. Al Eissa
Hani Tamim
Sadeq Abu-Dawas
Ahmed Yaqinuddin
Khaled Alkattan

Frontiers in Genetics

doi 10.3389/fgene.2025.1687927

1,065 views

16,587 articles

articles

Coffin–Lowry syndrome: a systematic review of RPS6KA3 confirmed cases and implications for diagnosis and counseling

Rethinking Parkinson’s disease genetics in the precision medicine era: why genomic diversity matters?

Identification of IGF2BP3 and CENPA as key regulators of immunophenotypes in renal clear cell carcinoma

Ribosome plasticity in glioblastoma: a multi-omics framework for future investigation

Does adoption of superior Murrah buffalo germplasm pay off? evidence from a causal impact study in Haryana, India

FSFT6mA: a feature-synthesis fine-tuning framework for DNA 6mA site prediction

Histone modifications and depression: epigenetic mechanisms, therapeutic targets, and translational outlook

Time-series transcriptomic analysis of flower tissue during heat stress in heat-resilient and heat-sensitive Brassica napus L.

The value of quantitative fluorescence polymerase chain reaction for the products of conception in the era of copy number variation sequencing

Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype

Reconstructing developmental lineages: a retrospective approach using somatic mutations and variant allele frequency

Retrospective analysis of non-invasive prenatal testing: a population study involving 19,835 participants in the Shaoyang area

Case Report: Dual pathogenic mechanism of a PRKG2 missense variant underlies an attenuated phenotype of acromesomelic dysplasia

Omics in mini-livestock: a genomic perspective on the future of sustainable food systems

Systematic analysis of anoikis-related genes identifies SRPX2-FAK/AKT-IL-6 axis in the progression and peritoneal metastasis of gastric cancer

Case Report: Novel GLA mutation in a Chinese female with renal-predominant Fabry disease and cardiac hypertrophy

Resilience and evolutionary insights in PPI networks: comparative analysis of node resilience and centrality measures

Exploring the role and therapeutic potential of RNA N6-methyladenosine modification in abortion disease pathology: a comprehensive review

TPM1-p.E181K mutation suppresses CaMKII/HDAC4 signaling pathway leading to pediatric restrictive cardiomyopathy

DDA-bench: a manually curated database for benchmarking datasets and baseline performance values in predicting drug-disease associations

(Not) “just your nature”. Diagnostic journeys of adults with neurofibromatosis type 1 in Poland

Case Report: Myoclonic and tremulous movements associated with COQ8A-related coenzyme Q10 deficiency type 4

Salmonella enterica serovar Typhimurium-induced alterations in inflammatory chemokine mRNA expressions and hemato-biochemical variations in three different strains of chicken

Biobanking as a research accelerator: the perspectives of medical students and interns at a saudi university