Frontiers in Genetics | Genetics of Common and Rare Diseases

Original Research

Published on 16 Jul 2024

Identification of the CDH18 gene associated with age-related macular degeneration using weighted gene co-expression network analysis

in Genetics of Common and Rare Diseases

Guina Liu
Mingqi Tan
Rui Liu
Xuejin Lu
Xiaoshuang Jiang
Yunpeng Bai
Zhigang Guo
Fang Lu

Frontiers in Genetics

doi 10.3389/fgene.2024.1378340

3,221 views

Original Research

Published on 15 Jul 2024

Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family

in Genetics of Common and Rare Diseases

Xinhe Fang
Meijiao Ma
Weining Rong
Yuan-Yuan Lian
Xueli Wu
Yongying Gao
Hui-Ping Li
Xunlun Sheng

Frontiers in Genetics

doi 10.3389/fgene.2024.1417584

4,165 views

Case Report

Published on 12 Jul 2024

Case report: A novel compound heterozygous variant in the COL4A3 gene was identified in a patient with autosomal recessive Alport syndrome

in Genetics of Common and Rare Diseases

Sha Chen
Yufeng Zhang
Jinjin He
Dingwei Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1426806

2,127 views

Case Report

Published on 11 Jul 2024

Case report: Two novel compound heterozygous variant of SLC12A3 gene in a gitelman syndrome family and literature review

in Genetics of Common and Rare Diseases

Xiaochen Ji
Nan Zhao
Haixia Liu
Yutong Wu
Lichao Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1391015

2,440 views

Original Research

Published on 10 Jul 2024

Novel pathogenic variants of DNAH5 associated with clinical and genetic spectra of primary ciliary dyskinesia in an Arab population

in Genetics of Common and Rare Diseases

Dalal A. Al-Mutairi
Basel H. Alsabah
Petra Pennekamp
Heymut Omran

Frontiers in Genetics

doi 10.3389/fgene.2024.1396797

2,704 views
1 citation

Original Research

Published on 10 Jul 2024

Identification and functional characteristics of a novel splicing heterozygote variant of COL2A1 associated with Stickler syndrome type I

in Genetics of Common and Rare Diseases

Yujing Gong
Weijian Zhu
Mianmian Zhu
Dan Chen
Sunke Wu
Sisi Hu
Yi Luo
Yiyi Jiang
Ting Zhu
Dan Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1308737

1,946 views

Original Research

Published on 10 Jul 2024

Novel genotypes and phenotypes in Snijders Blok-Campeau syndrome caused by CHD3 mutations

in Genetics of Common and Rare Diseases

Yuanyuan Gao
Pei Wang
Mengying Chen
Kexin Pang
Yifan Sun
Bixia Zheng
Taisong Li
Hongmei Zhang
Min Zhu

Frontiers in Genetics

doi 10.3389/fgene.2024.1347933

3,541 views
1 citation

Correction

Published on 10 Jul 2024

Corrigendum: Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017–2022

in Genetics of Common and Rare Diseases

Dongjuan Wang
Juan Zhang
Rui Yang
Dayong Zhang
Ming Wang
Chaowen Yu
Jingli Yang
Wenxia Huang
Shan Liu
Shi Tang

Frontiers in Genetics

doi 10.3389/fgene.2024.1449534

961 views

Original Research

Published on 10 Jul 2024

Identification of shared genetic risks underlying metabolic syndrome and its related traits in the Korean population

in Genetics of Common and Rare Diseases

Jun Young Kim
Yoon Shin Cho

Frontiers in Genetics

doi 10.3389/fgene.2024.1417262

2,593 views
5 citations

Editorial

Published on 26 Jun 2024

Editorial: Neuronal ceroid lipofuscinosis: molecular genetics and epigenetics

in Genetics of Common and Rare Diseases

Paschalis Nicolaou

Frontiers in Genetics

doi 10.3389/fgene.2024.1430703

1,648 views
1 citation

Correction

Published on 25 Jun 2024

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

in Genetics of Common and Rare Diseases

Rahma Mkaouar
Zied Riahi
Jihene Marrakchi
Nessrine Mezzi
Lilia Romdhane
Maroua Boujemaa
Hamza Dallali
Marwa Sayeb
Saida Lahbib
Hajer Jaouadi

Frontiers in Genetics

doi 10.3389/fgene.2024.1437233

1,290 views

Original Research

Published on 24 Jun 2024

Application of whole exome sequencing in carrier screening for high-risk families without probands

in Genetics of Common and Rare Diseases

Qinlin Huang
Zhongjie Wang
Yanling Teng
Wen Zhang
Juan Wen
Huimin Zhu
Desheng Liang
Lingqian Wu
Zhuo Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1415811

2,894 views
1 citation

Original Research

Published on 20 Jun 2024

How does the age of control individuals hinder the identification of target genes for Huntington’s disease?

in Genetics of Common and Rare Diseases

João Rafael Dias Pinto
Benedito Faustinoni Neto
Joyce Macedo Sanches Fernandes
Irina Kerkis
Rodrigo Pinheiro Araldi

Frontiers in Genetics

doi 10.3389/fgene.2024.1377237

1,694 views
3 citations

Editorial

Published on 20 Jun 2024

Editorial: Inborn errors of carbohydrate metabolism

in Genetics of Common and Rare Diseases

Iván Martínez-Duncker
Ida Vanessa Doederlein-Schwartz
Melania Abreu-González
José Elías García-Ortiz

Frontiers in Genetics

doi 10.3389/fgene.2024.1430414

2,543 views

Original Research

Published on 20 Jun 2024

ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans

in Genetics of Common and Rare Diseases

Guangyi Cao
Lina Yu
Junshun Fang
Ruixin Shi
Huijun Li
Feifei Lu
Xiaoyue Shen
Xiangyu Zhu
Shanshan Wang
Na Kong

Frontiers in Genetics

doi 10.3389/fgene.2024.1407202

1,983 views
1 citation

Original Research

Published on 17 Jun 2024

Deciphering the pathogenic role of rare RAF1 heterozygous missense mutation in the late-presenting DDH

in Genetics of Common and Rare Diseases

Yuzhao Liu
Xuesong Fan
Kun Qian
Changshun Wu
Laibo Zhang
Lin Yuan
Zhentao Man
Shuai Wu
Ping Li
Xianquan Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1375736

2,400 views