Original Research

Published on 16 May 2024

The NM_033380.2 transcript of the COL4A5 gene contains a variable splice site c.4822–10T>C, which has been identified as a causative factor for Alport syndrome

in Genetics of Common and Rare Diseases

Lei Liang
Haotian Wu
Jianrong Zhao

Frontiers in Genetics

doi 10.3389/fgene.2024.1330525

665 views

Original Research

Published on 16 May 2024

A panel based on three-miRNAs as diagnostic biomarker for prostate cancer

in RNA

Siwei Chen
Chong Lu
Shengjie Lin
Chen Sun
Zhenyu Wen
Zhenjian Ge
Wenkang Chen
Yingqi Li
Pengwu Zhang
Yutong Wu

Frontiers in Genetics

doi 10.3389/fgene.2024.1371441

1,027 views

Original Research

Published on 16 May 2024

Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities: case report and literature review

in Genetics of Common and Rare Diseases

Wei Zhang
Muhammad Tariq
Bhaskar Roy
Juan Shen
Ayaz Khan
Naveed Altaf Malik
Sijie He
Shahid Mahmood Baig
Xiaodong Fang
Jianguo Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1351710

1,153 views

Original Research

Published on 16 May 2024

A novel homozygous RSPH4A variant in a family with primary ciliary dyskinesia and literature review

in Genetics of Common and Rare Diseases

Chenling Shen
Yilin Shen
Weiyi Huang
Andi Zhang
Tianyuan Zou
Dongye Guo
Hao Wang
Jichang Wu
Haixia Hu
Mingliang Xiang

Frontiers in Genetics

doi 10.3389/fgene.2024.1364476

953 views

Original Research

Published on 15 May 2024

Genome-wide identification analysis in wild-type Solanum pinnatisectum reveals some genes defending against Phytophthora infestans

in Genomics of Plants and the Phytoecosystem

Chunxiu Shen
Qineng Lu
Di Yang
Xueru Zhang
Xinping Huang
Rungen Li
Zhiqun Que
Na Chen

Frontiers in Genetics

doi 10.3389/fgene.2024.1379784

1,057 views

Original Research

Published on 15 May 2024

Identifying potential drug targets for varicose veins through integration of GWAS and eQTL summary data

in Human and Medical Genomics

Yu Cui
Mengting Hu
He Zhou
Jiarui Guo
Qijia Wang
Zaihua Xu
Liyun Chen
Wancong Zhang
Shijie Tang

Frontiers in Genetics

doi 10.3389/fgene.2024.1385293

1,972 views
1 citation

Original Research

Published on 15 May 2024

Translation, validation, and comparison of genetic knowledge scales in Greek and German

in Genetics of Common and Rare Diseases

Florian Melchior
Konrad Beyreuther
Birgit Teichmann

Frontiers in Genetics

doi 10.3389/fgene.2024.1350308

1,047 views

Brief Research Report

Published on 15 May 2024

Application of whole exome sequencing in the diagnosis of muscular disorders: a study of Taiwanese pediatric patients

in Genetics of Common and Rare Diseases

Chung-Lin Lee
Chih-Kuang Chuang
Huei-Ching Chiu
Ya-Hui Chang
Yuan-Rong Tu
Yun-Ting Lo
Hsiang-Yu Lin
Shuan-Pei Lin

Frontiers in Genetics

doi 10.3389/fgene.2024.1365729

1,330 views

Original Research

Published on 15 May 2024

Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry

in Applied Genetic Epidemiology

Jean-Tristan Brandenburg
Wenlong Carl Chen
Palwende Romuald Boua
Melanie A. Govender
Godfred Agongo
Lisa K. Micklesfield
Hermann Sorgho
Stephen Tollman
Gershim Asiki
Felistas Mashinya

Frontiers in Genetics

doi 10.3389/fgene.2024.1372042

1,737 views

Original Research

Published on 15 May 2024

Genotype-based “virtual” metabolomics in a clinical biobank identifies novel metabolite-disease associations

in Applied Genetic Epidemiology

Minoo Bagheri
Andrei Bombin
Mingjian Shi
Venkatesh L. Murthy
Ravi Shah
Jonathan D. Mosley
Jane F. Ferguson

Frontiers in Genetics

doi 10.3389/fgene.2024.1392622

1,461 views

Review

Published on 15 May 2024

Diagnostic efficacy of long non-coding RNAs in multiple sclerosis: a systematic review and meta-analysis

in Neurogenomics

Yongdong Wang
Jing Wang
Xinyin Zhang
Chengyan Xia
Zhiping Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1400387

799 views

Original Research

Published on 14 May 2024

Integrated analysis of muscle transcriptome, miRNA, and proteome of Chinese indigenous breed Ningxiang pig in three developmental stages

in Livestock Genomics

Wenwu Chen
Yu Xiao
Fang Yang
Sui Liufu
Yan Gong
Zhi Li
Shuo Zhang
Shengguo Tang
Biao Li
Haiming Ma

Frontiers in Genetics

doi 10.3389/fgene.2024.1393834

990 views

Original Research

Published on 14 May 2024

Genetic evidence reveals a causal relationship between rheumatoid arthritis and interstitial lung disease

in Immunogenetics

Rong Zhao
Yi-Wen Zhang
Jin-Cheng Guo
Jun Qiao
Shan Song
Ting-Ting Zhang
He-Yi Zhang
Sheng-Xiao Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1395315

1,659 views

Original Research

Published on 14 May 2024

Comprehensive analysis of differential long non-coding RNA and messenger RNA expression in cholelithiasis using high-throughput sequencing and bioinformatics

in RNA

Yanbo Sun
Conghui Xu
Jing Luo
Shumin Li
Shi Chen
Yunyun Cen
Pengyuan Xu

Frontiers in Genetics

doi 10.3389/fgene.2024.1375019

1,008 views

Original Research

Published on 14 May 2024

A whole-exome sequencing study of patent foramen ovale: investigating genetic variants and their association with cardiovascular disorders

in Genetics of Common and Rare Diseases

Xinyi Li
Lingling Xie
Jin Dai
Xinbin Zhou
Tingting Chen
Wei Mao

Frontiers in Genetics

doi 10.3389/fgene.2024.1405307

1,104 views

Original Research

Published on 13 May 2024

Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart disease

in Genetics of Common and Rare Diseases

Laura B. Oehlman
Alexander R. Opotowsky
Kathryn N. Weaver
Nicole M. Brown
Cara L. Barnett
Erin M. Miller
Hua He
Amy R. Shikany

Frontiers in Genetics

doi 10.3389/fgene.2024.1398887

805 views

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Articles

The NM_033380.2 transcript of the COL4A5 gene contains a variable splice site c.4822–10T>C, which has been identified as a causative factor for Alport syndrome

A panel based on three-miRNAs as diagnostic biomarker for prostate cancer

Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities: case report and literature review

A novel homozygous RSPH4A variant in a family with primary ciliary dyskinesia and literature review

Genome-wide identification analysis in wild-type Solanum pinnatisectum reveals some genes defending against Phytophthora infestans

Identifying potential drug targets for varicose veins through integration of GWAS and eQTL summary data

Translation, validation, and comparison of genetic knowledge scales in Greek and German

Application of whole exome sequencing in the diagnosis of muscular disorders: a study of Taiwanese pediatric patients

Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry

Genotype-based “virtual” metabolomics in a clinical biobank identifies novel metabolite-disease associations

Diagnostic efficacy of long non-coding RNAs in multiple sclerosis: a systematic review and meta-analysis

Integrated analysis of muscle transcriptome, miRNA, and proteome of Chinese indigenous breed Ningxiang pig in three developmental stages

Genetic evidence reveals a causal relationship between rheumatoid arthritis and interstitial lung disease

Comprehensive analysis of differential long non-coding RNA and messenger RNA expression in cholelithiasis using high-throughput sequencing and bioinformatics

A whole-exome sequencing study of patent foramen ovale: investigating genetic variants and their association with cardiovascular disorders

Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart disease