Original Research

Published on 13 Aug 2024

Causal associations between severe COVID-19 and diseases of seven organs: a proteome-wide mendelian randomization study

in Applied Genetic Epidemiology

Yunhan Shen
Yi Zhang
Ye-yang Xu
Xinyi Li
Jiachen Wu
Hao Pei
Linyan Wang
Tiansheng Zhu

Frontiers in Genetics

doi 10.3389/fgene.2024.1421824

1,593 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

949 views

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

1,062 views

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

843 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

1,116 views

Original Research

Published on 12 Aug 2024

Prognostic value of four immune-related genes in lower-grade gliomas: a biomarker discovery study

in Computational Genomics

Shuowen Wang
Zijun Wang
Zhuo Liu
Jianxin Wu

Frontiers in Genetics

doi 10.3389/fgene.2024.1403587

978 views

Original Research

Published on 09 Aug 2024

Nonalcoholic or metabolic-associated fatty liver disease and colorectal polyps: evidence from meta-analysis and two-sample Mendelian randomization

in Statistical Genetics and Methodology

Dong Zhai
Sumei Xu
Haoge Liu
Xiaojuan Tong

Frontiers in Genetics

doi 10.3389/fgene.2024.1422827

1,400 views

Original Research

Published on 09 Aug 2024

Identification of candidate SNPs associated with embryo mortality and fertility traits in lactating Holstein cows

in Livestock Genomics

Carolina L. Gonzalez Berrios
Courtney F. Bowden
Hamad M. Saad
Jeanette V. Bishop
Hana Van Campen
Pablo Pinedo
Thomas R. Hansen
Milton G. Thomas

Frontiers in Genetics

doi 10.3389/fgene.2024.1409335

1,359 views

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

947 views

Original Research

Published on 09 Aug 2024

TF-EPI: an interpretable enhancer-promoter interaction detection method based on Transformer

in Computational Genomics

Bowen Liu
Weihang Zhang
Xin Zeng
Martin Loza
Sung-Joon Park
Kenta Nakai

Frontiers in Genetics

doi 10.3389/fgene.2024.1444459

1,298 views

Original Research

Published on 09 Aug 2024

Molecular and physiological responses of two quinoa genotypes to drought stress

in Genomics of Plants and the Phytoecosystem

Xiaolin Zhu
Wenyu Liu
Baoqiang Wang
Ling Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1439046

1,039 views
1 citation

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

748 views

Editorial

Published on 09 Aug 2024

Editorial: The intricate web of gastrointestinal virome, mycome and archaeome: implications for gastrointestinal diseases

in Human and Medical Genomics

Asrar Ahmad
Mohammad Ashfaq
Mudasir Rashid

Frontiers in Genetics

doi 10.3389/fgene.2024.1463350

667 views

Original Research

Published on 08 Aug 2024

GWAS-significant loci and severe COVID-19: analysis of associations, link with thromboinflammation syndrome, gene-gene, and gene-environmental interactions

in Human and Medical Genomics

Alexey Valerevich Loktionov
Ksenia Andreevna Kobzeva
Andrey Romanovich Karpenko
Vera Alexeevna Sergeeva
Yuriy Lvovich Orlov
Olga Yurievna Bushueva

Frontiers in Genetics

doi 10.3389/fgene.2024.1434681

1,129 views

Original Research

Published on 08 Aug 2024

Integrative analysis reveals novel insights into juvenile idiopathic arthritis pathogenesis and shared molecular pathways with associated traits

in Computational Genomics

N. Pudjihartono
D. Ho
J. M. O’Sullivan

Frontiers in Genetics

doi 10.3389/fgene.2024.1448363

1,891 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

708 views

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Articles

Causal associations between severe COVID-19 and diseases of seven organs: a proteome-wide mendelian randomization study

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

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

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

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

Prognostic value of four immune-related genes in lower-grade gliomas: a biomarker discovery study

Nonalcoholic or metabolic-associated fatty liver disease and colorectal polyps: evidence from meta-analysis and two-sample Mendelian randomization

Identification of candidate SNPs associated with embryo mortality and fertility traits in lactating Holstein cows

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

TF-EPI: an interpretable enhancer-promoter interaction detection method based on Transformer

Molecular and physiological responses of two quinoa genotypes to drought stress

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

Editorial: The intricate web of gastrointestinal virome, mycome and archaeome: implications for gastrointestinal diseases

GWAS-significant loci and severe COVID-19: analysis of associations, link with thromboinflammation syndrome, gene-gene, and gene-environmental interactions

Integrative analysis reveals novel insights into juvenile idiopathic arthritis pathogenesis and shared molecular pathways with associated traits

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