Frontiers in Genetics

Original Research

Published on 13 Sep 2024

Role of telomere dysfunction and immune infiltration in idiopathic pulmonary fibrosis: new insights from bioinformatics analysis

in Computational Genomics

Chenkun Fu
Xin Tian
Shuang Wu
Xiaojuan Chu
Yiju Cheng
Xiao Wu
Wengting Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1447296

1,768 views
1 citation

Original Research

Published on 13 Sep 2024

Low prevalence of HIV in the northern Cameroon: contribution of some AIDS restriction genes and potential implications for gene therapy

in Genetics of Common and Rare Diseases

Patrice Djataou
Marceline Djuidje Ngounoue
Carine Nguefeu Nkenfou-Tchinda
Marie Nicole Ngoufack
Elise Elong
Aline Tiga
Clifford Muluh
Joelle Kadji Kameni
Moussa Djaouda
Alexis Ndjolo

Frontiers in Genetics

doi 10.3389/fgene.2024.1447971

1,087 views

Original Research

Published on 13 Sep 2024

Causal relationship between reproductive factors and female bone density: a univariate and multivariate mendelian randomization study

in Applied Genetic Epidemiology

Xiaojing Lin
Yaqi Zuo
Hongbo Hu
Jie Zhou

Frontiers in Genetics

doi 10.3389/fgene.2024.1393106

1,090 views

Editorial

Published on 12 Sep 2024

Editorial: Genomics of pathogens and vectors

in Applied Genetic Epidemiology

Gabriel Luz Wallau
Augusto Simoes-Barbosa
Túlio de Lima Campos

Frontiers in Genetics

doi 10.3389/fgene.2024.1483676

624 views

Case Report

Published on 12 Sep 2024

Case report: Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency in newborns

in Genetics of Common and Rare Diseases

Patryk Lipiński
Katarzyna Wójcicka-Kowalczyk
Anna Bogdańska
Ewa Ehmke
Magdalena Pajdowska
Katarzyna Skrzypek
Agnieszka Charzewska
Dorota Hoffman-Zacharska

Frontiers in Genetics

doi 10.3389/fgene.2024.1464556

1,057 views
1 citation

Retraction

Published on 11 Sep 2024

Retraction: Oncological effects and prognostic value of AMAP1 in gastric cancer

in Cancer Genetics

Frontiers Editorial Office

Frontiers in Genetics

doi 10.3389/fgene.2024.1491856

516 views

Case Report

Published on 11 Sep 2024

Case report: Unveiling genetic and phenotypic variability in Nonketotic hyperglycinemia: an atypical early onset case associated with a novel GLRX5 variant

in Genetics of Common and Rare Diseases

Victor Marin
Louis Lebreton
Claire Guibet
Samir Mesli
Isabelle Redonnet-Vernhet
Mathurin Dexant
Delphine Lamireau
Sandrine Roche
Margaux Gaschignard
Jean Delmas

Frontiers in Genetics

doi 10.3389/fgene.2024.1432272

1,135 views

Editorial

Published on 11 Sep 2024

Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases

in Neurogenomics

Muthukumar Karuppasamy
Martine Tetreault
Jessica Rosati

Frontiers in Genetics

doi 10.3389/fgene.2024.1481705

566 views

Original Research

Published on 11 Sep 2024

Ninein, a candidate gene for ethanol anxiolysis, shows complex exon-specific expression and alternative splicing differences between C57BL/6J and DBA/2J mice

in Pharmacogenetics and Pharmacogenomics

E. R. Gnatowski
J. L. Jurmain
M. G. Dozmorov
J. T. Wolstenholme
M. F. Miles

Frontiers in Genetics

doi 10.3389/fgene.2024.1455616

866 views

Systematic Review

Published on 11 Sep 2024

Association between haptoglobin polymorphism and coronary artery disease: a meta-analysis

in Applied Genetic Epidemiology

Jiao Wang
Xiaokai Zhou
Yue Su
Dongjian Chai
Yaoyao Ruan
Jinhua Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1434975

746 views

Original Research

Published on 10 Sep 2024

BLESS: bagged logistic regression for biomarker identification

in Statistical Genetics and Methodology

Kyle Gardiner
Xuekui Zhang
Li Xing

Frontiers in Genetics

doi 10.3389/fgene.2024.1336891

906 views

Original Research

Published on 10 Sep 2024

Identification of two heterogeneous subtypes of hepatocellular carcinoma with distinct pathway activities and clinical outcomes based on gene set variation analysis

in Cancer Genetics and Oncogenomics

Zhipeng Jin
Xin Wang
Xue Zhang
Siqi Cheng
Yefu Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1441189

1,106 views

Editorial

Published on 10 Sep 2024

Editorial: Liquid biopsy and new omics technologies in vascular malformations

in Human and Medical Genomics

Massimo Vaghi
Elisa Frullanti
Maria Palmieri

Frontiers in Genetics

doi 10.3389/fgene.2024.1486606

499 views

Case Report

Published on 09 Sep 2024

Case report: Whole exome sequencing reveals a novel splicing variant of ANKRD17 gene in a Chinese male juvenile with developmental delay and transient tic disorder

in Genetics of Common and Rare Diseases

Jing Chen
Shuo Yang
He Wang
Hongjing Wang
Yuanyuan Xiao
Shanling Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1422469

963 views

Brief Research Report

Published on 09 Sep 2024

De novo and inherited micro-CNV at 16p13.11 in 21 Chinese patients with defective cardiac left-right patterning

in Genetics of Common and Rare Diseases

Kun Yu
Weicheng Chen
Yan Chen
Libing Shen
Boxuan Wu
Yuan Zhang
Xiangyu Zhou

Frontiers in Genetics

doi 10.3389/fgene.2024.1458953

1,074 views

Mini Review

Published on 09 Sep 2024

Harmonisation of the HLA tests for the diagnosis of coeliac disease: experiences from the Czech external proficiency testing program

in Immunogenetics

Milena Vrana
Jana Tajtlova
Frantisek Mrazek

Frontiers in Genetics

doi 10.3389/fgene.2024.1441769

782 views

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Articles

Role of telomere dysfunction and immune infiltration in idiopathic pulmonary fibrosis: new insights from bioinformatics analysis

Low prevalence of HIV in the northern Cameroon: contribution of some AIDS restriction genes and potential implications for gene therapy

Causal relationship between reproductive factors and female bone density: a univariate and multivariate mendelian randomization study

Editorial: Genomics of pathogens and vectors

Case report: Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency in newborns

Retraction: Oncological effects and prognostic value of AMAP1 in gastric cancer

Case report: Unveiling genetic and phenotypic variability in Nonketotic hyperglycinemia: an atypical early onset case associated with a novel GLRX5 variant

Editorial: Diagnosis, animal models and therapeutic interventions for neuromuscular diseases

Ninein, a candidate gene for ethanol anxiolysis, shows complex exon-specific expression and alternative splicing differences between C57BL/6J and DBA/2J mice

Association between haptoglobin polymorphism and coronary artery disease: a meta-analysis

BLESS: bagged logistic regression for biomarker identification

Identification of two heterogeneous subtypes of hepatocellular carcinoma with distinct pathway activities and clinical outcomes based on gene set variation analysis

Editorial: Liquid biopsy and new omics technologies in vascular malformations

Case report: Whole exome sequencing reveals a novel splicing variant of ANKRD17 gene in a Chinese male juvenile with developmental delay and transient tic disorder

De novo and inherited micro-CNV at 16p13.11 in 21 Chinese patients with defective cardiac left-right patterning

Harmonisation of the HLA tests for the diagnosis of coeliac disease: experiences from the Czech external proficiency testing program