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

684 views

Original Research

Accepted on 15 Jul 2024

Genetic characterization of cashmere goat (Capra hircus) populations in Mongolia

in Livestock Genomics

Sergelen Baldan
Johann Sölkner
Kahsa Tadel Gebre
Gábor Mészáros
Richard Crooijmans
Kathiravan Periasamy
Rudolf Pichler
Bayarjargal Manaljav
Narantuya Baatar
Myagmarsuren Purevdorj

Frontiers in Genetics

doi 10.3389/fgene.2024.1421529

195 views

Original Research

Published on 15 Jul 2024

MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity

in Human and Medical Genomics

Zhen Li
Runqing Ma
Meijiao Ma
Xue Xiao
Xiaolong Qi
Hongjuan Ma
Xunlun Sheng
Weining Rong

Frontiers in Genetics

doi 10.3389/fgene.2024.1407361

506 views

Original Research

Published on 15 Jul 2024

MGPPI: multiscale graph neural networks for explainable protein–protein interaction prediction

in Computational Genomics

Shiwei Zhao
Zhenyu Cui
Gonglei Zhang
Yanlong Gong
Lingtao Su

Frontiers in Genetics

doi 10.3389/fgene.2024.1440448

740 views

Original Research

Published on 15 Jul 2024

Using metabolic abnormalities of carriers in the neonatal period to evaluate the pathogenicity of variants of uncertain significance in methylmalonic acidemia

in Statistical Genetics and Methodology

Dongfan Xiao
Congcong Shi
Yinchun Zhang
Sitao Li
Yuhao Ye
Guilong Yuan
Taohan Miu
Haiyan Ma
Shiguang Diao
Chaoyun Su

Frontiers in Genetics

doi 10.3389/fgene.2024.1403913

447 views

Original Research

Published on 15 Jul 2024

Screening and the analysis of genotypic and phenotypic characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Fujian province, China

in Applied Genetic Epidemiology

Jinfu Zhou
Yinglin Zeng
Jianping Tang
Shihong Chen
Guilin Li
Xiaolong Qiu
Peiran Zhao
Ting Huang
Jinying Luo
Na Lin

Frontiers in Genetics

doi 10.3389/fgene.2024.1422214

503 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

869 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

650 views

Original Research

Published on 12 Jul 2024

Stromal cell-expressed malignant gene patterns contribute to the progression of squamous cell carcinomas across different sites

in Cancer Genetics and Oncogenomics

Kaiyan Qi
Guangqi Li
Yuanjun Jiang
Xuexin Tan
Qiao Qiao

Frontiers in Genetics

doi 10.3389/fgene.2024.1342306

804 views

Original Research

Published on 12 Jul 2024

A cross-tissue transcriptome-wide association study identifies new susceptibility genes for frailty

in Genetics of Aging

Daoyi Lin
Shuyan Wu
Wangyu Li
Peng Ye
Xuan Pan
Ting Zheng
Fei Gao

Frontiers in Genetics

doi 10.3389/fgene.2024.1404456

777 views

Original Research

Published on 12 Jul 2024

Identifying selection signatures for immune response and resilience to Aleutian disease in mink using genotype data

in Livestock Genomics

Guoyu Hu
Duy Ngoc Do
Ghader Manafiazar
Alyson A. Kelvin
Mehdi Sargolzaei
Graham Plastow
Zhiquan Wang
Pourya Davoudi
Younes Miar

Frontiers in Genetics

doi 10.3389/fgene.2024.1370891

665 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

659 views

Original Research

Published on 11 Jul 2024

Methylation of SSTR4 promoter region in multiple mental health disorders

in Behavioral and Psychiatric Genetics

Rongrong Zhao
Huihui Shi
Yanqiu Wang
Shuaiyu Zheng
Yahui Xu

Frontiers in Genetics

doi 10.3389/fgene.2024.1431769

481 views

Original Research

Published on 11 Jul 2024

Genome-wide identification and drought stress-induced expression analysis of the NHX gene family in potato

in Genomics of Plants and the Phytoecosystem

Ji Yihong
Liu Zhen
Liu Chang
Shao Ziying
Zhang Ning
Suo Meiqing
Liu Yuhui
Wang Lei

Frontiers in Genetics

doi 10.3389/fgene.2024.1396375

661 views

Original Research

Published on 11 Jul 2024

Mendelian randomization of stroke risk after total hip and knee replacements

in Applied Genetic Epidemiology

Liang Pang
Zhihui Zheng
Pingping Su
Zhouhengte Xu
Yirui Chen
Zhicheng Liao
Pengcheng Jia
Xiuling Zhang
Cunxian Lv

Frontiers in Genetics

doi 10.3389/fgene.2024.1435124

719 views

Original Research

Published on 11 Jul 2024

Cross-species single-cell landscapes identify the pathogenic gene characteristics of inherited retinal diseases

in Computational Genomics

Hualei Hu
Fei Liu
Pan Gao
Yuwen Huang
Danna Jia
Jamas Reilly
Xiang Chen
Yunqiao Han
Kui Sun
Jiong Luo

Frontiers in Genetics

doi 10.3389/fgene.2024.1409016

918 views

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Articles

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

Genetic characterization of cashmere goat (Capra hircus) populations in Mongolia

MFRP variations cause nanophthalmos in five Chinese families with distinct phenotypic diversity

MGPPI: multiscale graph neural networks for explainable protein–protein interaction prediction

Using metabolic abnormalities of carriers in the neonatal period to evaluate the pathogenicity of variants of uncertain significance in methylmalonic acidemia

Screening and the analysis of genotypic and phenotypic characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Fujian province, China

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

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

Stromal cell-expressed malignant gene patterns contribute to the progression of squamous cell carcinomas across different sites

A cross-tissue transcriptome-wide association study identifies new susceptibility genes for frailty

Identifying selection signatures for immune response and resilience to Aleutian disease in mink using genotype data

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

Methylation of SSTR4 promoter region in multiple mental health disorders

Genome-wide identification and drought stress-induced expression analysis of the NHX gene family in potato

Mendelian randomization of stroke risk after total hip and knee replacements

Cross-species single-cell landscapes identify the pathogenic gene characteristics of inherited retinal diseases