Frontiers in Genetics

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

2,525 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

3,326 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

2,917 views
2 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

1,784 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

2,463 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

3,547 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

1,709 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

3,729 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

2,525 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

2,138 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

2,098 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

4,606 views
5 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

3,490 views
3 citations

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

2,240 views

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

2,614 views
1 citation

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

3,260 views
1 citation

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

3,115 views

Original Research

Published on 09 Jan 2025

Circle-seq reveals that eccDNA may be a key blood biomarker for HBV-associated liver cancer

in Cancer Genetics and Oncogenomics

Xiao K. Ran
Xiao F. Zhao
Zhen W. Wei
Hua Z. Pang
Yan F. Tang
Rong Liu
Tie X. Wu
Xu D. Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1454153

3,509 views
1 citation

Original Research

Published on 09 Jan 2025

A family with normal sperm motility carrying a sY86 deletion in AZFa region and partial deletion in AZFc region

in Human and Medical Genomics

Yuhong Zhao
Weiwei Zhi
Dongsheng Xiong
Ningjing Li
Xinrong Du
Jiuzhi Zeng
Guohui Zhang
Weixin Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1519774

2,343 views

Brief Research Report

Published on 09 Jan 2025

Variability of PRDM9 in buffaloes

in Livestock Genomics

Luca Godoi Rocha Santana
Jackeline Santos Alves
Fabieli Loise Braga Feitosa
Victoria Camilla Parente Rocha
Humberto Tonhati
Raphael Bermal Costa
Gregório Miguel Ferreira de Camargo

Frontiers in Genetics

doi 10.3389/fgene.2024.1479287

1,553 views

Editorial

Published on 09 Jan 2025

Editorial: Pharmacogenetics of psychiatric disorders

in Behavioral and Psychiatric Genetics

Sarah Allegra
Silvia De Francia
Stefano Comità
Maria Grazia Morgese
Thomas M. Polasek

Frontiers in Genetics

doi 10.3389/fgene.2024.1523071

1,844 views

Original Research

Published on 09 Jan 2025

Single-cell RNA sequencing elucidates cellular plasticity in esophageal small cell carcinoma following chemotherapy treatment

in Cancer Genetics and Oncogenomics

Qinkai Zhang
Ziyu Gao
Ru Qiu
Jizhao Cao
Chunxiao Zhang
Wei Qin
Meiling Yang
Xinyue Wang
Ciqiu Yang
Jie Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1477705

2,468 views
4 citations

Original Research

Published on 08 Jan 2025

DLBWE-Cys: a deep-learning-based tool for identifying cysteine S-carboxyethylation sites using binary-weight encoding

in Epigenomics and Epigenetics

Zhengtao Luo
Qingyong Wang
Yingchun Xia
Xiaolei Zhu
Shuai Yang
Zhaochun Xu
Lichuan Gu

Frontiers in Genetics

doi 10.3389/fgene.2024.1464976

2,124 views
1 citation

Original Research

Published on 08 Jan 2025

Detection of inversion with breakpoints in ARSB causing MPS VI by whole-genome sequencing: lessons learned and best practices

in Genetics of Common and Rare Diseases

Yufeng Huang
Wenyue Deng
Hui Huang
Xiankai Zhang
Xiaohong Chen
Jian Ye
Sukun Luo
Ting Yu
Hui Yao
Hao Du

Frontiers in Genetics

doi 10.3389/fgene.2024.1452498

1,502 views

16,444 articles

articles

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

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

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

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

Circle-seq reveals that eccDNA may be a key blood biomarker for HBV-associated liver cancer

A family with normal sperm motility carrying a sY86 deletion in AZFa region and partial deletion in AZFc region

Variability of PRDM9 in buffaloes

Editorial: Pharmacogenetics of psychiatric disorders

Single-cell RNA sequencing elucidates cellular plasticity in esophageal small cell carcinoma following chemotherapy treatment

DLBWE-Cys: a deep-learning-based tool for identifying cysteine S-carboxyethylation sites using binary-weight encoding

Detection of inversion with breakpoints in ARSB causing MPS VI by whole-genome sequencing: lessons learned and best practices