Frontiers in Genetics

Review

Published on 23 Jan 2025

Genetic ancestry and the colonial legacies of race in genomics: a cross-disciplinary dialogue

in ELSI in Science and Genetics

Ernesto Schwartz-Marin
Tayyaba Jiwani
Sarah Abel
Yulia Egorova
Amade M’charek
Diogo Meyer
Andrés Moreno Estrada
Katharina Schramm
Peter Wade
Michel Naslavsky

Frontiers in Genetics

doi 10.3389/fgene.2024.1523406

4,579 views
2 citations

Original Research

Published on 22 Jan 2025

In silico design of an epitope-based vaccine ensemble for fasliolopsiasis

in Computational Genomics

Ruchishree Konhar
Kanhu Charan Das
Aiboklang Nongrum
Rohan Raj Samal
Shailesh Kumar Sarangi
Devendra Kumar Biswal

Frontiers in Genetics

doi 10.3389/fgene.2024.1451853

2,874 views
2 citations

Original Research

Published on 22 Jan 2025

DEmiRNA-mRNA regulatory network reveals miR‐122-5p as a regulatory factor of arginine metabolism in necrotizing enterocolitis

in RNA

Zhili Ding
Ting Guo
Qiang Tang
Yaqiang Hong
Zhibao Lv
Li Lu
Wenjun Zhuang

Frontiers in Genetics

doi 10.3389/fgene.2024.1480431

2,678 views
1 citation

Original Research

Published on 22 Jan 2025

Machine learning potential predictor of idiopathic pulmonary fibrosis

in Computational Genomics

Chenchun Ding
Quan Liao
Renjie Zuo
Shichao Zhang
Zhenzhen Guo
Junjie He
Ziwei Ye
Weibin Chen
Sunkui Ke

Frontiers in Genetics

doi 10.3389/fgene.2024.1464471

4,391 views

Correction

Published on 21 Jan 2025

Corrigendum: Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing

in Genomic Assay Technology

Ranran Zhang
Yu Tan
Li Wang
Hui Jian
Jing Zhu
Yuanyuan Xiao
Mengyu Tan
Jiaming Xue
Fan Yang
Weibo Liang

Frontiers in Genetics

doi 10.3389/fgene.2025.1553186

1,567 views

Original Research

Published on 21 Jan 2025

Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy

in Genetics of Common and Rare Diseases

Huafang Zou
Qian Zhang
Jianxiang Liao
Dongfang Zou
Zhanqi Hu
Bing Li
Li Chen
Jialun Wen
Xia Zhao
Victor Wei Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1496411

4,103 views
6 citations

Original Research

Published on 20 Jan 2025

Mutation in the COL2A1 gene is associated with acetabular dysplasia

in Genetics of Common and Rare Diseases

Miaomiao Xin
Xin Guan
Jiangfei Yang
Yi Li
Zhentao Man
Hongsheng Sun
Min Fu

Frontiers in Genetics

doi 10.3389/fgene.2024.1521412

3,020 views

Case Report

Published on 20 Jan 2025

Tell me y: anticipation of sex discrepancies in cell-free DNA testing due to maternal genetic abnormalities: a case report

in Human and Medical Genomics

Nuria Balaguer
Emilia Mateu-Brull
Jose Antonio Martínez-Conejero
Ana Cervero
Roser Navarro
Jorge Jiménez-Almazán
Miguel Milán

Frontiers in Genetics

doi 10.3389/fgene.2024.1502287

2,793 views

Case Report

Published on 20 Jan 2025

Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report

in Genetics of Common and Rare Diseases

Mingyue Zhuang
Yonglong Xu
Shiyi Zhong
Ziyuan Tian
Qingwu Liu
Dingquan Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1491870

4,172 views

Original Research

Published on 20 Jan 2025

Therapeutic target genes and regulatory networks of gallic acid in cervical cancer

in Cancer Genetics and Oncogenomics

Zhixi You
Ye Lei
Yongkang Yang
Zhihui Zhou
Xu Chao
Keyi Ju
Songyi Wang
Yuanyuan Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1508869

3,105 views
3 citations

Brief Research Report

Published on 20 Jan 2025

Comprehensive analysis of the circRNA expression profile and circRNA-miRNA-mRNA network in pelvic organ prolapse

in RNA

Qian Wang
Zuoxi He
Lisha Ding
Yuqing Liu
Xiaoli Zhang
Tao Wang
Xiaoyu Niu

Frontiers in Genetics

doi 10.3389/fgene.2024.1527223

1,987 views

Case Report

Published on 17 Jan 2025

Case Report: A 3’ splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child

in Neurogenomics

Dandan Shi
Nannan Li
Caifang Fan
Qiang Luo

Frontiers in Genetics

doi 10.3389/fgene.2024.1508922

2,708 views

Brief Research Report

Published on 17 Jan 2025

Updates on the molecular spectrum of MEFV variants in lebanese patients with Familial Mediterranean Fever

in Genetics of Common and Rare Diseases

Rudy Feghali
José-Noel Ibrahim
Nabiha Salem
Romy Moussallem
Ghina Hijazi
Charbel Attieh
Tony Yammine
Alain Chebly

Frontiers in Genetics

doi 10.3389/fgene.2024.1506656

3,954 views
7 citations

Original Research

Published on 15 Jan 2025

Classical and machine learning tools for identifying yellow-seeded Brassica napus by fusion of hyperspectral features

in Genomics of Plants and the Phytoecosystem

Fan Liu
Fang Wang
Zaiqi Zhang
Liang Cao
Jinran Wu
You-Gan Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1518205

1,876 views
3 citations

Original Research

Published on 15 Jan 2025

Exploring prognosis and therapeutic strategies for HBV-HCC patients based on disulfidptosis-related genes

in Computational Genomics

Chuankuo Zhang
Xing Zhang
Shengjie Dai
Wenjun Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1522484

3,979 views

Original Research

Published on 15 Jan 2025

Increased cardiac macrophages in Sorbs2-deficient hearts: revealing a potential role for macrophage in responding to embryonic myocardial abnormalities

in Genetics of Common and Rare Diseases

Beibei Hu
Xiangyang Liu
Shanshan Xiong
Qin Gong
Junjie Yang
Hongjun Shi
Min Zhang
Fei Liang
Zhen Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1525931

2,724 views

Case Report

Published on 15 Jan 2025

Case Report: Novel ADA2 variants cause atypical adenosine deaminase 2 deficiency

in Genetics of Common and Rare Diseases

Haishao Yu
Shuangzhu Lin
Lin Li
Jiayi Li
Qiandui Chen
Yuheng Wu
Yangfan Qi
Wanqi Wang
Xingzhi Chang
Jie Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1478581

2,345 views
1 citation

Original Research

Published on 15 Jan 2025

Identification of key miRNAs and target genes in extracellular vesicles derived from low-intensity pulsed ultrasound-treated stem cells

in Stem Cell Research

Xin Yin
Jialian Yi
Fugang Mao
Qisheng Tang
Xinyu Zhang
Xiaoyu Yang
Hongqing Xie
Linping Wang
Shuifen Sun
Xin Yu

Frontiers in Genetics

doi 10.3389/fgene.2024.1407671

2,361 views

Original Research

Published on 14 Jan 2025

Integrating single-cell RNA-seq and bulk RNA-seq to explore prognostic value and immune landscapes of methionine metabolism-related signature in breast cancer

in Cancer Genetics and Oncogenomics

Yanxian Gao
Ziyu Feng
Hailong Zhao
Xinghai Liu
Muyu Zhu
Xiafei Yu
Xiaoan Liu
Xian Wu
Jing Tao

Frontiers in Genetics

doi 10.3389/fgene.2024.1521269

5,063 views
6 citations

Original Research

Published on 13 Jan 2025

Improving prenatal diagnosis with combined karyotyping, CNV-seq and QF-PCR: a comprehensive analysis of chromosomal abnormalities in high-risk pregnancies

in Cytogenomics

Jia-pei Liu
Shan-Bing Wang
Li Luo
Ya-mei Guo

Frontiers in Genetics

doi 10.3389/fgene.2024.1517270

3,937 views
3 citations

Clinical Trial

Published on 13 Jan 2025

Genetic variation in patent foramen ovale: a case-control genome-wide association study

in Genetics of Common and Rare Diseases

Bosi Dong
Yajiao Li
Fandi Ai
Jia Geng
Ting Tang
Wan Peng
Yusha Tang
Hui Wang
Zixuan Tian
Fengxiao Bu

Frontiers in Genetics

doi 10.3389/fgene.2024.1523304

2,996 views
1 citation

Original Research

Published on 13 Jan 2025

Uncovering somatic mosaic variants of PIK3CA-related overgrowth disorders – three cases with different clinical presentations

in Human and Medical Genomics

M. Tooming
P. Mertsina
T. Kahre
R. Teek
I. Vainumäe
S. Lilles
M. H. Wojcik
P. Ilves
K. Õunap

Frontiers in Genetics

doi 10.3389/fgene.2024.1484651

2,549 views

Original Research

Published on 10 Jan 2025

Depression-related innate immune genes and pan-cancer gene analysis and validation

in Cancer Genetics and Oncogenomics

Yakun Yang
Wei Han
Xiaoyu Zhang
Hao Yuan
Ran Wang
Jia Yang
Cuixia An
Dongyang Huang

Frontiers in Genetics

doi 10.3389/fgene.2024.1521238

3,619 views
2 citations

Original Research

Published on 10 Jan 2025

Comprehensive analysis of ferroptosis-related genes reveals potential therapeutic targets in osteoporosis patients: a computational analysis and in vitro experiments

in Human and Medical Genomics

Sihui Chen
Yi Jiang
Guoqin Xie
Peng Wu
Jinyu Zhu

Frontiers in Genetics

doi 10.3389/fgene.2024.1522809

3,392 views

16,548 articles

articles

Genetic ancestry and the colonial legacies of race in genomics: a cross-disciplinary dialogue

In silico design of an epitope-based vaccine ensemble for fasliolopsiasis

DEmiRNA-mRNA regulatory network reveals miR‐122-5p as a regulatory factor of arginine metabolism in necrotizing enterocolitis

Machine learning potential predictor of idiopathic pulmonary fibrosis

Corrigendum: Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing

Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy

Mutation in the COL2A1 gene is associated with acetabular dysplasia

Tell me y: anticipation of sex discrepancies in cell-free DNA testing due to maternal genetic abnormalities: a case report

Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report

Therapeutic target genes and regulatory networks of gallic acid in cervical cancer

Comprehensive analysis of the circRNA expression profile and circRNA-miRNA-mRNA network in pelvic organ prolapse

Case Report: A 3’ splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child

Updates on the molecular spectrum of MEFV variants in lebanese patients with Familial Mediterranean Fever

Classical and machine learning tools for identifying yellow-seeded Brassica napus by fusion of hyperspectral features

Exploring prognosis and therapeutic strategies for HBV-HCC patients based on disulfidptosis-related genes

Increased cardiac macrophages in Sorbs2-deficient hearts: revealing a potential role for macrophage in responding to embryonic myocardial abnormalities

Case Report: Novel ADA2 variants cause atypical adenosine deaminase 2 deficiency

Identification of key miRNAs and target genes in extracellular vesicles derived from low-intensity pulsed ultrasound-treated stem cells

Integrating single-cell RNA-seq and bulk RNA-seq to explore prognostic value and immune landscapes of methionine metabolism-related signature in breast cancer

Improving prenatal diagnosis with combined karyotyping, CNV-seq and QF-PCR: a comprehensive analysis of chromosomal abnormalities in high-risk pregnancies

Genetic variation in patent foramen ovale: a case-control genome-wide association study

Uncovering somatic mosaic variants of PIK3CA-related overgrowth disorders – three cases with different clinical presentations

Depression-related innate immune genes and pan-cancer gene analysis and validation

Comprehensive analysis of ferroptosis-related genes reveals potential therapeutic targets in osteoporosis patients: a computational analysis and in vitro experiments