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

847 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

660 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

679 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

582 views

Original Research

Published on 05 Sep 2024

Meta-analysis of set-based multiple phenotype association test based on GWAS summary statistics from different cohorts

in Statistical Genetics and Methodology

Lirong Zhu
Shuanglin Zhang
Qiuying Sha

Frontiers in Genetics

doi 10.3389/fgene.2024.1359591

613 views

Original Research

Published on 05 Sep 2024

Development and clinical validation of a novel detection kit for α-thalassemia in southern Chinese

in Genetics of Common and Rare Diseases

Yi-Yuan Ge
Jun Xie
Yu-Wei Liao
Long-Xu Xie
Li-Ye Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1457248

643 views

Original Research

Published on 05 Sep 2024

Parental genetic knowledge and attitudes toward childhood with genetic disorders

in Human and Medical Genomics

Maha Alotaibi

Frontiers in Genetics

doi 10.3389/fgene.2024.1434322

790 views

Correction

Published on 05 Sep 2024

Corrigendum: Genetic association of wool quality characteristics in United States Rambouillet sheep

in Livestock Genomics

Gabrielle M. Becker
Julia L. Woods
Christopher S. Schauer
Whit C. Stewart
Brenda M. Murdoch

Frontiers in Genetics

doi 10.3389/fgene.2024.1471185

370 views

Editorial

Published on 05 Sep 2024

Editorial: Methods in applied genetic epidemiology 2022

in Applied Genetic Epidemiology

Qi Guo
Christopher Neal Foley
Zhana Kuncheva

Frontiers in Genetics

doi 10.3389/fgene.2024.1469497

553 views

Editorial

Published on 05 Sep 2024

Editorial: Genetic regulation of reproduction traits in livestock species

in Livestock Genomics

M. M. D. Barbero
S. Lyu
F. Cendron
N. Song

Frontiers in Genetics

doi 10.3389/fgene.2024.1481463

520 views

Original Research

Published on 05 Sep 2024

The clinical utility of next generation sequencing in endometrial cancer: focusing on molecular subtyping and lynch syndrome

in Cancer Genetics and Oncogenomics

Yongzhen Guo
Guangwei Yan
Pei Zhang
Yixuan Liu
Chengquan Zhao
Xianxu Zeng

Frontiers in Genetics

doi 10.3389/fgene.2024.1440971

769 views

Mini Review

Published on 04 Sep 2024

Variation of tRNA modifications with and without intron dependency

in RNA

Sachiko Hayashi

Frontiers in Genetics

doi 10.3389/fgene.2024.1460902

1,200 views

Case Report

Published on 04 Sep 2024

Case report: A novel TLK2 variant with a neuropsychiatric phenotype from a Chinese family

in Genetics of Common and Rare Diseases

Hongmei Huang
Yue Qian
Chenlu Yang
Shijie Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1419027

589 views

Original Research

Published on 04 Sep 2024

mtPCDI: a machine learning-based prognostic model for prostate cancer recurrence

in Cancer Genetics and Oncogenomics

Guoliang Cheng
Junrong Xu
Honghua Wang
Jingzhao Chen
Liwei Huang
Zhi Rong Qian
Yong Fan

Frontiers in Genetics

doi 10.3389/fgene.2024.1430565

875 views

Original Research

Published on 04 Sep 2024

Genomic insight into COVID-19 severity in MAFLD patients: a single-center prospective cohort study

in Immunogenetics

Mykhailo Buchynskyi
Valentyn Oksenych
Iryna Kamyshna
Olena Budarna
Iryna Halabitska
Pavlo Petakh
Oleksandr Kamyshnyi

Frontiers in Genetics

doi 10.3389/fgene.2024.1460318

949 views

Original Research

Published on 04 Sep 2024

Identification and validation of diagnostic genes associated with neutrophil extracellular traps of type 2 diabetes mellitus

in Computational Genomics

Meifang He
Jin Niu
Haihua Cheng
Chaoying Guo

Frontiers in Genetics

doi 10.3389/fgene.2024.1373807

1,122 views

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Articles

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

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

Meta-analysis of set-based multiple phenotype association test based on GWAS summary statistics from different cohorts

Development and clinical validation of a novel detection kit for α-thalassemia in southern Chinese

Parental genetic knowledge and attitudes toward childhood with genetic disorders

Corrigendum: Genetic association of wool quality characteristics in United States Rambouillet sheep

Editorial: Methods in applied genetic epidemiology 2022

Editorial: Genetic regulation of reproduction traits in livestock species

The clinical utility of next generation sequencing in endometrial cancer: focusing on molecular subtyping and lynch syndrome

Variation of tRNA modifications with and without intron dependency

Case report: A novel TLK2 variant with a neuropsychiatric phenotype from a Chinese family

mtPCDI: a machine learning-based prognostic model for prostate cancer recurrence

Genomic insight into COVID-19 severity in MAFLD patients: a single-center prospective cohort study

Identification and validation of diagnostic genes associated with neutrophil extracellular traps of type 2 diabetes mellitus