Frontiers in Genetics | Genetics of Common and Rare Diseases

Brief Research Report

Published on 12 Aug 2024

Four novel variants identified in the ACADVL gene causing very-long-chain acyl-coenzyme A dehydrogenase deficiency in four unrelated Chinese families

in Genetics of Common and Rare Diseases

Lulu Li
Yue Tang
Jinqi Zhao
Lifei Gong
Nan Yang
Shunan Wang
Haihe Yang
Yuanyuan Kong

Frontiers in Genetics

doi 10.3389/fgene.2024.1433160

2,257 views

Case Report

Published on 12 Aug 2024

Fahr’s syndrome as the initial imaging characteristics of MELAS syndrome with a possible seizure activity and cardiac arrest: a case report

in Genetics of Common and Rare Diseases

Yan Zheng
Haohao Wu
Meng Zhang
Baogang Huang
Junsu Yang
Chuan Liu
Hanmin Wang
Kang Du

Frontiers in Genetics

doi 10.3389/fgene.2024.1393158

1,754 views
1 citation

Case Report

Published on 12 Aug 2024

Case report: A novel mutation of the CAPN3 gene in a Chinese family with limb-girdle muscular dystrophy type 2A

in Genetics of Common and Rare Diseases

Wanjun Feng
Yanyan Cao
Ruolin Ren
Xiaohui Yang
Chunyan Cao
Hongwei Jiang
Ganqin Du

Frontiers in Genetics

doi 10.3389/fgene.2024.1410727

1,767 views

Review

Published on 12 Aug 2024

Acute intermittent porphyria: a disease with low penetrance and high heterogeneity

in Genetics of Common and Rare Diseases

Jia-Jia Lei
Shuang Li
Bai-Xue Dong
Jing Yang
Yi Ren

Frontiers in Genetics

doi 10.3389/fgene.2024.1374965

2,844 views
1 citation

Original Research

Published on 09 Aug 2024

Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndrome

in Genetics of Common and Rare Diseases

Jian-Hui Zhang
Jie Liu
Dan-Dan Ruan
Qian Chen
Jie Yang
Min Wu
Hong-Ping Yu
Li-Sheng Liao
Xiao-Ling Zheng
Jie-Wei Luo

Frontiers in Genetics

doi 10.3389/fgene.2024.1419154

1,548 views

Case Report

Published on 09 Aug 2024

Case Report: Whole exome sequencing identifies compound heterozygous variants in the TRAPPC9 gene in a child with developmental delay

in Genetics of Common and Rare Diseases

Bingxuan Yu
Jing Chen
Shuo Yang
He Wang
Yuanyuan Xiao
Shanling Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1415194

1,426 views

Original Research

Published on 08 Aug 2024

Using preimplantation genetic testing for monogenic disease for preventing citrullinemia type 1 transmission

in Genetics of Common and Rare Diseases

Zubo Wu
Tao Liang
Yi Liu
Xiaofang Ding
Defeng Shu

Frontiers in Genetics

doi 10.3389/fgene.2024.1389461

1,206 views

Mini Review

Published on 08 Aug 2024

The role of primary cilia in congenital heart defect-associated neurological impairments

in Genetics of Common and Rare Diseases

Nemanja Sarić
Nobuyuki Ishibashi

Frontiers in Genetics

doi 10.3389/fgene.2024.1460228

1,741 views
1 citation

Original Research

Published on 06 Aug 2024

Genetic testing and human leukocyte antigen in patients with hypertrophic cardiomyopathy and connective tissue diseases

in Genetics of Common and Rare Diseases

Daigo Hiraya
Nobuyuki Murakoshi
Miyako Igarashi
DongZhu Xu
Tomoko Ishizu

Frontiers in Genetics

doi 10.3389/fgene.2024.1432670

1,470 views

Review

Published on 02 Aug 2024

Molecular mechanisms and genetic factors contributing to the developmental dysplasia of the hip

in Genetics of Common and Rare Diseases

Xiaoming Zhao
Shuai Liu
Zhonghua Yang
Yong Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1413500

2,888 views
2 citations

Case Report

Published on 02 Aug 2024

Case report: Comprehensive exploration of a novel PFKM mutation in glycogen storage disease Type VII

in Genetics of Common and Rare Diseases

Ying Chen
Xinyu Wang
Na Ji
Qi Fang
Xin Chang
Meirong Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1422908

1,753 views

Original Research

Published on 01 Aug 2024

Authentication and validation of key genes in the treatment of atopic dermatitis with Runfuzhiyang powder: combined RNA-seq, bioinformatics analysis, and experimental research

in Genetics of Common and Rare Diseases

Yan Lin
Guangyi Xiong
Xiansong Xia
Zhiping Yin
Xuhui Zou
Xu Zhang
Chenghao Zhang
Jianzhou Ye

Frontiers in Genetics

doi 10.3389/fgene.2024.1335093

2,211 views

Original Research

Published on 31 Jul 2024

Predicting novel biomarkers for early diagnosis and dynamic severity monitoring of human ulcerative colitis

in Genetics of Common and Rare Diseases

Yu Chen
Li Chen
Sheng Huang
Li Yang
Li Wang
Feiyun Yang
Jinxiu Huang
Xiuliang Ding

Frontiers in Genetics

doi 10.3389/fgene.2024.1429482

2,205 views
2 citations

Brief Research Report

Published on 30 Jul 2024

SMN1 c.5C>G (p.Ala2Gly) missense variant, a challenging molecular SMA diagnosis associated with mild disease, preserves SMN nuclear gems in patient-specific fibroblasts

in Genetics of Common and Rare Diseases

Sara L. Cook
Christian Stout
Lindsey Kirkeby
Noemi Vidal-Folch
Devin Oglesbee
Linda Hasadsri
Duygu Selcen
Margherita Milone
Daniel Anderson
Nathan P. Staff

Frontiers in Genetics

doi 10.3389/fgene.2024.1406819

1,982 views
2 citations

Case Report

Published on 30 Jul 2024

Novel de novo SPAST mutation in a Han Chinese SPG4 patient: a case report

in Genetics of Common and Rare Diseases

Yu-Han Xu
Bao-Yu Yuan
Jia-Le Ji
Di Wu
Hong Zhou
Yi-Jing Guo

Frontiers in Genetics

doi 10.3389/fgene.2024.1410381

1,127 views

Systematic Review

Published on 29 Jul 2024

The prevalence, diagnostic accuracy and genotype-phenotype correlation of GNAS mutations in fibrous dysplasia: a meta-analysis

in Genetics of Common and Rare Diseases

Ao-Bo Zhang
Jian-Yun Zhang
Jiang Xue
Zhen-Chao Wu
Zhi-Xiu Xu
Li-Sha Sun
Tie-Jun Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1377716

1,973 views
3 citations