Frontiers in Genetics

Original Research

Published on 14 Aug 2024

Causal association between inflammatory bowel disease and acute pancreatitis: a two-sample bidirectional mendelian randomization study

in Statistical Genetics and Methodology

Cong Zhang
Xiujing Fan
Zhijun Li
Zongyi Hu
Chengcheng He
Shanping Wang
Mingsong Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1324893

2,909 views
4 citations

Original Research

Published on 14 Aug 2024

Novel PTPRQ variants associated with hearing loss in a Chinese family PTPRQ variants in Chinese hearing loss

in Applied Genetic Epidemiology

Yuan Hou
Yuanzhen Shi
Longyan Liu
Shihong Duan

Frontiers in Genetics

doi 10.3389/fgene.2024.1399760

2,440 views

Editorial

Published on 14 Aug 2024

Editorial: Synthetic biology and therapeutic applications of transfer RNA

in RNA

Dieter Söll
Patrick O’Donoghue
Ilka U. Heinemann

Frontiers in Genetics

doi 10.3389/fgene.2024.1468891

3,459 views

Case Report

Published on 13 Aug 2024

Asymmetric scapuloperoneal phenotype of MATR3-related distal myopathy: case series

in Genetics of Common and Rare Diseases

Aysylu Murtazina
Dmitrii Subbotin
Anna Kuchina
Olga Gilvanova
Daniil Degterev
Olga Shchagina
Tatiana Cherevatova
Maria Bulakh
Darya Sherstyukova
Oksana Ryzhkova

Frontiers in Genetics

doi 10.3389/fgene.2024.1414928

2,726 views

Case Report

Published on 13 Aug 2024

Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas

in Genetics of Common and Rare Diseases

Artem Borovikov
Andrey Marakhonov
Aysylu Murtazina
Kseniya Davydenko
Alexandra Filatova
Nailya Galeeva
Varvara Kadnikova
Natalya Ogorodova
Daria Gorodilova
Ilya Kanivets

Frontiers in Genetics

doi 10.3389/fgene.2024.1435493

2,085 views
1 citation

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

3,567 views
2 citations

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

2,751 views
2 citations

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

4,064 views
4 citations

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

3,435 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

2,385 views
4 citations

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

5,974 views
4 citations

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

3,529 views
1 citation

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

3,690 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

2,567 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

4,240 views
3 citations

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

3,387 views
7 citations

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

2,403 views
2 citations

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

1,832 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

4,847 views
5 citations

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

3,653 views
5 citations

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

2,370 views
1 citation

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

3,090 views
1 citation

Original Research

Published on 08 Aug 2024

Unveiling potential drug targets for lung squamous cell carcinoma through the integration of druggable genome and genome-wide association data

in Statistical Genetics and Methodology

Wenhua Wu
Zhengrui Chen
Haiteng Wen
Haiyun Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1431684

5,844 views
1 citation

Original Research

Published on 07 Aug 2024

Associations of genetically predicted iron status with 24 gastrointestinal diseases and gut microbiota: a Mendelian randomization study

in Nutritional Genomics

Tao Su
Xiang Peng
Ying Gan
Hongzhen Wu
Shulin Ma
Min Zhi
Yi Lu
Shixue Dai
Jiayin Yao

Frontiers in Genetics

doi 10.3389/fgene.2024.1406230

6,734 views
1 citation

16,560 articles

articles

Causal association between inflammatory bowel disease and acute pancreatitis: a two-sample bidirectional mendelian randomization study

Novel PTPRQ variants associated with hearing loss in a Chinese family PTPRQ variants in Chinese hearing loss

Editorial: Synthetic biology and therapeutic applications of transfer RNA

Asymmetric scapuloperoneal phenotype of MATR3-related distal myopathy: case series

Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas

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

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

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

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

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

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

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

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

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

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

Unveiling potential drug targets for lung squamous cell carcinoma through the integration of druggable genome and genome-wide association data

Associations of genetically predicted iron status with 24 gastrointestinal diseases and gut microbiota: a Mendelian randomization study