Frontiers in Genetics

Brief Research Report

Published on 22 Nov 2022

Impact of polymorphisms in genes orchestrating innate immune responses on replication kinetics of Torque teno virus after kidney transplantation

Natalia Redondo
Isabel Rodríguez-Goncer
Patricia Parra
Eliseo Albert
Estela Giménez
Tamara Ruiz-Merlo
Francisco López-Medrano
Rafael San Juan
Esther González
Ángel Sevillano

Frontiers in Genetics

doi 10.3389/fgene.2022.1069890

2,527 views
1 citation

Original Research

Published on 22 Nov 2022

Causal effects of homocysteine levels on the components of sarcopenia: A two-sample mendelian randomization study

Hongwei Yu
Gan Luo
Tianwei Sun
Qiong Tang

Frontiers in Genetics

doi 10.3389/fgene.2022.1051047

6,003 views
10 citations

Original Research

Published on 22 Nov 2022

Identification of LTBP2 gene polymorphisms and their association with thoracolumbar vertebrae number, body size, and carcass traits in Dezhou donkeys

Ziwen Liu
Tianqi Wang
Xiaoyuan Shi
Xinrui Wang
Wei Ren
Bingjian Huang
Changfa Wang

Frontiers in Genetics

doi 10.3389/fgene.2022.969959

3,087 views
10 citations

Data Report

Published on 22 Nov 2022

Whole-exome sequencing of selected bread wheat recombinant inbred lines as a useful resource for allele mining and bulked segregant analysis

Salvatore Esposito
Nunzio D’Agostino
Francesca Taranto
Gabriella Sonnante
Francesco Sestili
Domenico Lafiandra
Pasquale De Vita

Frontiers in Genetics

doi 10.3389/fgene.2022.1058471

3,289 views
8 citations

Brief Research Report

Published on 22 Nov 2022

Mutational analysis of ribosomal proteins in a cohort of pediatric patients with T-cell acute lymphoblastic leukemia reveals Q123R, a novel mutation in RPL10

Lorenza Bacci
Valentina Indio
Guglielmo Rambaldelli
Cristina Bugarin
Franco Magliocchetti
Alberto Del Rio
Daniela Pollutri
Fraia Melchionda
Andrea Pession
Marina Lanciotti

Frontiers in Genetics

doi 10.3389/fgene.2022.1058468

3,692 views
6 citations

Original Research

Published on 22 Nov 2022

A novel heterozygous SIX1 missense mutation resulted in non-syndromic unilateral hearing loss

Ang Li
Siwen Liu
Peng Zhang
Xintong Hu
Guiying Li
Weiyue Gu
Yanfang Jiang

Frontiers in Genetics

doi 10.3389/fgene.2022.1047230

2,786 views
2 citations

Original Research

Published on 22 Nov 2022

Identification of subtypes of hepatocellular carcinoma and screening of prognostic molecular diagnostic markers based on cell adhesion molecule related genes

Ruge Sun
Yanchao Gao
Fengjun Shen

Frontiers in Genetics

doi 10.3389/fgene.2022.1042540

4,508 views
4 citations

Original Research

Published on 22 Nov 2022

Improving the prediction for the response to radiotherapy of clinical tumor samples by using combinatorial model of MicroRNA expression

Chao Tang
Jun Qi
Yan Wu
Ling Luo
Ying Wang
Yongzhong Wu
Xiaolong Shi

Frontiers in Genetics

doi 10.3389/fgene.2022.1069112

2,218 views
3 citations

Original Research

Published on 21 Nov 2022

A comprehensive prognostic and immune infiltration analysis of EXOC3L1 in pan-cancer

Zhan-Fei Zhang

Frontiers in Genetics

doi 10.3389/fgene.2022.1044100

8,648 views
10 citations

Original Research

Published on 21 Nov 2022

N6-methyladenosine-modified lncRNA and mRNA modification profiles in cerebral ischemia-reperfusion injury

Le Shao
Bowei Chen
Qibiao Wu
Yaqian Xu
Jian Yi
Zhihua Guo
Baiyan Liu

Frontiers in Genetics

doi 10.3389/fgene.2022.973979

5,198 views
13 citations

Original Research

Published on 21 Nov 2022

Single-step genomic BLUP with many metafounders

Andrei A. Kudinov
Minna Koivula
Gert P. Aamand
Ismo Strandén
Esa A. Mäntysaari

Frontiers in Genetics

doi 10.3389/fgene.2022.1012205

4,006 views
13 citations

Review

Published on 21 Nov 2022

LncRNAs-associated to genomic instability: A barrier to cancer therapy effectiveness

Marco A Andonegui-Elguera
Rodrigo E. Cáceres-Gutiérrez
Diego Oliva-Rico
José Díaz-Chávez
Luis A. Herrera

Frontiers in Genetics

doi 10.3389/fgene.2022.984329

5,038 views
2 citations

Original Research

Published on 21 Nov 2022

Construction of a mitochondrial dysfunction related signature of diagnosed model to obstructive sleep apnea

Qian Liu
Tao Hao
Lei Li
Daqi Huang
Ze Lin
Yipeng Fang
Dong Wang
Xin Zhang

Frontiers in Genetics

doi 10.3389/fgene.2022.1056691

7,389 views
8 citations

Original Research

Published on 21 Nov 2022

Circulating tumour cell combined with DNA methylation for early detection of hepatocellular carcinoma

Wenjin Liang
Zhigao Xu
Fangyu Kong
Xiao Huang
Yuxin Xiao
Wei Zhou
Shaojun Ye
Qifa Ye

Frontiers in Genetics

doi 10.3389/fgene.2022.1065693

4,376 views
14 citations

Methods

Published on 21 Nov 2022

A depth-first search algorithm for oligonucleotide design in gene assembly

Hanjie Liang
Zengrui Chen
Gang Fang

Frontiers in Genetics

doi 10.3389/fgene.2022.1023092

3,406 views
5 citations

Original Research

Published on 21 Nov 2022

Distinct clinical pattern of colorectal cancer patients with POLE mutations: A retrospective study on real-world data

Miao Jiang
Yongliang Jia
Jinming Han
Jianxiang Shi
Chang Su
Rui Zhang
Menglu Xing
Shuiling Jin
Hong Zong

Frontiers in Genetics

doi 10.3389/fgene.2022.963964

6,441 views
9 citations

Review

Published on 21 Nov 2022

Heterochromatin in the fungal plant pathogen, Zymoseptoria tritici: Control of transposable elements, genome plasticity and virulence

Callum J. Fraser
Simon K. Whitehall

Frontiers in Genetics

doi 10.3389/fgene.2022.1058741

3,593 views
2 citations

Original Research

Published on 21 Nov 2022

Candidate pigmentation genes related to feather color variation in an indigenous chicken breed revealed by whole genome data

Huie Wang
Junhui Wen
Haiying Li
Tao Zhu
Xiurong Zhao
Jinxin Zhang
Xinye Zhang
Chi Tang
Lujiang Qu
M. Gemingguli

Frontiers in Genetics

doi 10.3389/fgene.2022.985228

6,444 views
14 citations

Original Research

Published on 21 Nov 2022

Genomic profiling and network-level understanding uncover the potential genes and the pathways in hepatocellular carcinoma

Sherif A. El-Kafrawy
Mai M. El-Daly
Leena H. Bajrai
Thamir A. Alandijany
Arwa A. Faizo
Mohammad Mobashir
Sunbul S. Ahmed
Sarfraz Ahmed
Shoaib Alam
Raja Jeet

Frontiers in Genetics

doi 10.3389/fgene.2022.880440

7,152 views
14 citations

Mini Review

Published on 21 Nov 2022

Keeping the balance: Trade-offs between human brain evolution, autism, and schizophrenia

Eryk Duński
Aleksandra Pękowska

Frontiers in Genetics

doi 10.3389/fgene.2022.1009390

6,562 views

Original Research

Published on 21 Nov 2022

Identification of a novel AIFM1 variant from a Chinese family with auditory neuropathy

Rongrong Wang
Xiaohui Bai
Huiming Yang
Jingyu Ma
Shudong Yu
Zhiming Lu

Frontiers in Genetics

doi 10.3389/fgene.2022.1064823

2,970 views
4 citations

Editorial

Published on 18 Nov 2022

Editorial: Cancer systems biology

Jesús Espinal-Enríquez
Claudia Rangel-Escareño
Frank Emmert-Streib

Frontiers in Genetics

doi 10.3389/fgene.2022.1083902

3,293 views

Case Report

Published on 18 Nov 2022

Case Report: Precision genetic diagnosis in a case of Dyggve-Melchior-Clausen syndrome reveals paternal isodisomy and heterodisomy of chromosome 18 with imprinting clinical implications

María-Pilar López-Garrido
María-Carmen Carrascosa-Romero
Minerva Montero-Hernández
Caridad-María Serrano-Martínez
Francisco Sánchez-Sánchez

Frontiers in Genetics

doi 10.3389/fgene.2022.1005573

3,532 views
5 citations

Original Research

Published on 18 Nov 2022

Identification of susceptibility modules and hub genes of osteoarthritis by WGCNA analysis

Yanchao Wang
Wenjun Zhou
Yan Chen
Dong He
Zhen Qin
Zhao Wang
Song Liu
Lei Zhou
Jianwen Su
Chi Zhang

Frontiers in Genetics

doi 10.3389/fgene.2022.1036156

8,629 views
8 citations

3,801 Publications

volumes

Impact of polymorphisms in genes orchestrating innate immune responses on replication kinetics of Torque teno virus after kidney transplantation

Causal effects of homocysteine levels on the components of sarcopenia: A two-sample mendelian randomization study

Identification of LTBP2 gene polymorphisms and their association with thoracolumbar vertebrae number, body size, and carcass traits in Dezhou donkeys

Whole-exome sequencing of selected bread wheat recombinant inbred lines as a useful resource for allele mining and bulked segregant analysis

Mutational analysis of ribosomal proteins in a cohort of pediatric patients with T-cell acute lymphoblastic leukemia reveals Q123R, a novel mutation in RPL10

A novel heterozygous SIX1 missense mutation resulted in non-syndromic unilateral hearing loss

Identification of subtypes of hepatocellular carcinoma and screening of prognostic molecular diagnostic markers based on cell adhesion molecule related genes

Improving the prediction for the response to radiotherapy of clinical tumor samples by using combinatorial model of MicroRNA expression

A comprehensive prognostic and immune infiltration analysis of EXOC3L1 in pan-cancer

N6-methyladenosine-modified lncRNA and mRNA modification profiles in cerebral ischemia-reperfusion injury

Single-step genomic BLUP with many metafounders

LncRNAs-associated to genomic instability: A barrier to cancer therapy effectiveness

Construction of a mitochondrial dysfunction related signature of diagnosed model to obstructive sleep apnea

Circulating tumour cell combined with DNA methylation for early detection of hepatocellular carcinoma

A depth-first search algorithm for oligonucleotide design in gene assembly

Distinct clinical pattern of colorectal cancer patients with POLE mutations: A retrospective study on real-world data

Heterochromatin in the fungal plant pathogen, Zymoseptoria tritici: Control of transposable elements, genome plasticity and virulence

Candidate pigmentation genes related to feather color variation in an indigenous chicken breed revealed by whole genome data

Genomic profiling and network-level understanding uncover the potential genes and the pathways in hepatocellular carcinoma

Keeping the balance: Trade-offs between human brain evolution, autism, and schizophrenia

Identification of a novel AIFM1 variant from a Chinese family with auditory neuropathy

Editorial: Cancer systems biology

Case Report: Precision genetic diagnosis in a case of Dyggve-Melchior-Clausen syndrome reveals paternal isodisomy and heterodisomy of chromosome 18 with imprinting clinical implications

Identification of susceptibility modules and hub genes of osteoarthritis by WGCNA analysis