Frontiers in Genetics

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

2,964 views
4 citations

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

2,639 views
5 citations

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

2,964 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

5,599 views
1 citation

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

2,798 views
16 citations

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

5,186 views
1 citation

Original Research

Published on 04 Sep 2024

Exploring the causal link among statin drugs and the osteoarthritis risk based on Mendelian randomization research

in Statistical Genetics and Methodology

Wenjie Chen
Zhi Sun
Xinhai Xiong
Haitao Tan
Junhao Hu
Chenrui Liu
Cheng Chen

Frontiers in Genetics

doi 10.3389/fgene.2024.1390387

3,577 views
6 citations

Original Research

Published on 03 Sep 2024

Construction of circRNA-mediated ceRNA network and immunoassay for investigating pathogenesis of COPD

in Cancer Genetics and Oncogenomics

Ting Yang
Wenya Xu
Jie Zhao
Jie Chen
Siguang Li
Lingsang Lin
Yi Zhong
Zehua Yang
Tian Xie
Yipeng Ding

Frontiers in Genetics

doi 10.3389/fgene.2024.1402856

2,504 views

Review

Published on 03 Sep 2024

A comprehensive review of artificial intelligence for pharmacology research

in Computational Genomics

Bing Li
Kan Tan
Angelyn R. Lao
Haiying Wang
Huiru Zheng
Le Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1450529

10,519 views
6 citations

Mini Review

Published on 03 Sep 2024

Advances in stem cell therapy for diabetic foot

in Stem Cell Research

Yinfeng Xia
Ping Wu
Hong Chen
Zhiyong Chen

Frontiers in Genetics

doi 10.3389/fgene.2024.1427205

7,130 views
11 citations

Original Research

Published on 02 Sep 2024

Lipids, lipid-lowering drugs and lateral epicondylitis of the humerus: a drug-targeted Mendelian randomization study

in Statistical Genetics and Methodology

Meng-Meng Liu
Xiang Chen
Xiao-Hang Bao
Bao-Hua Huang

Frontiers in Genetics

doi 10.3389/fgene.2024.1437712

2,732 views

Original Research

Published on 02 Sep 2024

Evidence of survival bias in the association between APOE-Є4 and age at ischemic stroke onset

in Genetics of Aging

Joanna von Berg
Patrick F. McArdle
Paavo Häppölä
Jeffrey Haessler
Charles Kooperberg
Robin Lemmens
Alessandro Pezzini
Vincent Thijs
Sara L. Pulit
Steven J. Kittner

Frontiers in Genetics

doi 10.3389/fgene.2024.1392061

3,002 views

Original Research

Published on 02 Sep 2024

Elucidating the role of hepatic enzymes in spontaneous abortion: a Mendelian randomization approach

in Statistical Genetics and Methodology

Yingping Zhu
Zhenghong Li
Xingfang Liu
Chengping Wen

Frontiers in Genetics

doi 10.3389/fgene.2024.1336728

3,061 views

Case Report

Published on 02 Sep 2024

Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3

in Genetics of Common and Rare Diseases

Wang Li
Zhongliang Li
Junhui Fu
Kaili Xu
Daoqi Mei
Xiaona Wang
Taisong Li
Xilong Du

Frontiers in Genetics

doi 10.3389/fgene.2024.1382275

2,710 views
1 citation

Review

Published on 30 Aug 2024

Nutrigenomic underpinnings of intestinal stem cells in inflammatory bowel disease and colorectal cancer development

in Human and Medical Genomics

Jennifer Ho
Nicholas Puoplo
Namrata Pokharel
Aanya Hirdaramani
Aylin C. Hanyaloglu
Chia-Wei Cheng

Frontiers in Genetics

doi 10.3389/fgene.2024.1349717

5,131 views
4 citations

Data Report

Published on 30 Aug 2024

Genome assembly, characterization, and mining of biosynthetic gene clusters (BGCs) from Chlorogloeopsis sp. ULAP02 isolated from Mt. Ulap, Itogon, Benguet, Philippines

in Genomics of Plants and the Phytoecosystem

Libertine Rose S. Sanchez
Danica Pearl M. Untiveros
Maria Theresa T. Tengco
Ernelea P. Cao

Frontiers in Genetics

doi 10.3389/fgene.2024.1422274

2,680 views

Correction

Published on 30 Aug 2024

Corrigendum: Evidence for a genetic contribution to the ossification of spinal ligaments in ossification of posterior longitudinal ligament and diffuse idiopathic skeletal hyperostosis: a narrative review

in Genetics of Common and Rare Diseases

Ana Rita Couto
Bruna Parreira
Deborah M. Power
Luís Pinheiro
João Madruga Dias
Irina Novofastovski
Iris Eshed
Piercarlo Sarzi-Puttini
Nicola Pappone
Fabiola Atzeni

Frontiers in Genetics

doi 10.3389/fgene.2024.1477788

1,626 views

Data Report

Published on 30 Aug 2024

Genome of Methylomonas sp. AM2-LC, representing a methanotrophic bacterial species isolated from water column of a boreal, oxygen-stratified lake

in Evolutionary and Population Genetics

Antti J. Rissanen
Rahul Mangayil
Ramita Khanongnuch

Frontiers in Genetics

doi 10.3389/fgene.2024.1440435

2,553 views

Mini Review

Published on 30 Aug 2024

Human sulfotransferase SULT2B1 physiological role and the impact of genetic polymorphism on enzyme activity and pathological conditions

in Pharmacogenetics and Pharmacogenomics

Fatemah A. Alherz

Frontiers in Genetics

doi 10.3389/fgene.2024.1464243

3,732 views
10 citations

Original Research

Published on 30 Aug 2024

Identification and expression analysis of bZIP transcription factors in Setaria italica in response to dehydration stress

in Genomics of Plants and the Phytoecosystem

Xuefei Yang
Changyong Gao
Yaqian Hu
Qianru Ma
Zejun Li
Jing Wang
Zhaoqun Li
Li Zhang
Dongming Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1466486

1,787 views
2 citations

Original Research

Published on 30 Aug 2024

Causal role of gut microbiota, serum metabolites, immunophenotypes in myocarditis: a mendelian randomization study

in Statistical Genetics and Methodology

Kaiyuan Li
Peng Liu
Xiuqi Wang
Zhipeng Zheng
Miao Liu
Jun Ye
Li Zhu

Frontiers in Genetics

doi 10.3389/fgene.2024.1382502

2,570 views
2 citations

Original Research

Published on 30 Aug 2024

Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing

in Behavioral and Psychiatric Genetics

Yuka Shiota
Tomoaki Nishiyama
Shigeru Yokoyama
Yuko Yoshimura
Chiaki Hasegawa
Sanae Tanaka
Sumie Iwasaki
Mitsuru Kikuchi

Frontiers in Genetics

doi 10.3389/fgene.2024.1352480

8,587 views
6 citations

Original Research

Published on 30 Aug 2024

Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

in Genetics of Common and Rare Diseases

Jamil Amjad Hashmi
Muhammad Latif
Reham M. Balahmar
Muhammad Zeeshan Ali
Fatima Alfadhli
Muzammil Ahmad Khan
Sulman Basit

Frontiers in Genetics

doi 10.3389/fgene.2024.1421943

3,013 views
1 citation

Original Research

Published on 29 Aug 2024

Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature

in Cytogenomics

Lei Liu
Tingying Lei
Fei Guo
Chunling Ma
Li Zhen
Lina Zhang
Dongzhi Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1448341

3,594 views
2 citations

16,551 articles

articles

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

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

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

Variation of tRNA modifications with and without intron dependency

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

Exploring the causal link among statin drugs and the osteoarthritis risk based on Mendelian randomization research

Construction of circRNA-mediated ceRNA network and immunoassay for investigating pathogenesis of COPD

A comprehensive review of artificial intelligence for pharmacology research

Advances in stem cell therapy for diabetic foot

Lipids, lipid-lowering drugs and lateral epicondylitis of the humerus: a drug-targeted Mendelian randomization study

Evidence of survival bias in the association between APOE-Є4 and age at ischemic stroke onset

Elucidating the role of hepatic enzymes in spontaneous abortion: a Mendelian randomization approach

Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3

Nutrigenomic underpinnings of intestinal stem cells in inflammatory bowel disease and colorectal cancer development

Genome assembly, characterization, and mining of biosynthetic gene clusters (BGCs) from Chlorogloeopsis sp. ULAP02 isolated from Mt. Ulap, Itogon, Benguet, Philippines

Corrigendum: Evidence for a genetic contribution to the ossification of spinal ligaments in ossification of posterior longitudinal ligament and diffuse idiopathic skeletal hyperostosis: a narrative review

Genome of Methylomonas sp. AM2-LC, representing a methanotrophic bacterial species isolated from water column of a boreal, oxygen-stratified lake

Human sulfotransferase SULT2B1 physiological role and the impact of genetic polymorphism on enzyme activity and pathological conditions

Identification and expression analysis of bZIP transcription factors in Setaria italica in response to dehydration stress

Causal role of gut microbiota, serum metabolites, immunophenotypes in myocarditis: a mendelian randomization study

Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing

Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis

Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature