Frontiers in Genetics | Human and Medical Genomics

Original Research

Published on 06 Jan 2023

Genome-wide imputed differential expression enrichment analysis identifies trait-relevant tissues

in Human and Medical Genomics

Ammarah Ghaffar
Dale R. Nyholt

Frontiers in Genetics

doi 10.3389/fgene.2022.1008511

2,575 views
2 citations

Editorial

Published on 06 Jan 2023

Editorial: Genomic alteration landscapes of aging, metabolic disorders, and cancer: Emerging overlaps and clinical importance

in Human and Medical Genomics

Jaspreet Kaur Dhanjal
Rajkumar Singh Kalra
Dhanendra Tomar
Amrendra K. Ajay

Frontiers in Genetics

doi 10.3389/fgene.2022.1102953

2,549 views

Original Research

Published on 06 Jan 2023

DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research

in Human and Medical Genomics

Yunlong Cui
Hongfeng Li
Pengfei Liu
Hailong Wang
Zhenzhen Zhang
Hongzhu Qu
Caijuan Tian
Xiangdong Fang

Frontiers in Genetics

doi 10.3389/fgene.2022.1118183

2,746 views
1 citation

Original Research

Published on 06 Jan 2023

Transcriptomic data analysis coupled with copy number aberrations reveals a blood-based 17-gene signature for diagnosis and prognosis of patients with colorectal cancer

in Human and Medical Genomics

Ibrahim H. Kaya
Olfat Al-Harazi
Dilek Colak

Frontiers in Genetics

doi 10.3389/fgene.2022.1031086

2,953 views
1 citation

Case Report

Published on 04 Jan 2023

Case report: A third variant in the 5′ UTR of TWIST1 creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome

in Human and Medical Genomics

Francisca Diaz-Gonzalez
Javier M. Sacedo-Gutiérrez
Stephen R. F. Twigg
Eduardo Calpena
Fernando E. Carceller-Benito
Manuel Parrón-Pajares
Fernando Santos-Simarro
Karen E. Heath

Frontiers in Genetics

doi 10.3389/fgene.2022.1089417

1,772 views
2 citations

Hypothesis and Theory

Published on 04 Jan 2023

Enrichment of titin-truncating variants in exon 327 in dilated cardiomyopathy and its relevance to reduced nonsense-mediated mRNA decay efficiency

in Human and Medical Genomics

Young-gon Kim
Changhee Ha
Sunghwan Shin
Jong-ho Park
Ja-Hyun Jang
Jong-Won Kim

Frontiers in Genetics

doi 10.3389/fgene.2022.1087359

2,807 views
4 citations

Original Research

Published on 04 Jan 2023

How many missed abortions are caused by embryonic chromosomal abnormalities and what are their risk factors?

in Human and Medical Genomics

Xin Li
Han Kang
Huifeng Yin
Tianjiao Liu
Qiannan Hou
Xiaolan Yu
Yuanlin Guo
Wei Shen
Huisheng Ge
Xiaoyan Zeng

Frontiers in Genetics

doi 10.3389/fgene.2022.1058261

5,155 views
1 citation

Original Research

Published on 04 Jan 2023

Genetic screening for hypertension and COVID-19 reveals functional variation of SPEG potentially associated with severe COVID-19 in women

in Human and Medical Genomics

Yu-Si Luo
Xiang-Chun Shen
Wei Li
Guo-Feng Wu
Xiao-Meng Yang
Ming-Yang Guo
Fang Chen
Hu-Yan Shen
Ping-Ping Zhang
Han Gao

Frontiers in Genetics

doi 10.3389/fgene.2022.1041470

2,388 views
2 citations

Brief Research Report

Published on 04 Jan 2023

siMS score- method for quantification of metabolic syndrome, confirms co-founding factors of metabolic syndrome

in Human and Medical Genomics

V. Dimitrijevic-Sreckovic
H. Petrovic
D. Dobrosavljevic
E. Colak
N. Ivanovic
D. Gostiljac
S. Ilic
D. Nikolic
J. Gacic
I. Soldatovic

Frontiers in Genetics

doi 10.3389/fgene.2022.1041383

3,574 views
5 citations

Review

Published on 04 Jan 2023

Single-cell omics: A new direction for functional genetic research in human diseases and animal models

in Human and Medical Genomics

Siyuan Kong
Rongrong Li
Yunhan Tian
Yaqiu Zhang
Yuhui Lu
Qiaoer Ou
Peiwen Gao
Kui Li
Yubo Zhang

Frontiers in Genetics

doi 10.3389/fgene.2022.1100016

8,453 views
20 citations

Perspective

Published on 15 Dec 2022

Precision medicine implementation challenges for APOL1 testing in chronic kidney disease in admixed populations

in Human and Medical Genomics

Giovanna Câmara Giudicelli
Celia Mariana Barbosa De Souza
Francisco Veríssimo Veronese
Lygia V. Pereira
Tábita Hünemeier
Fernanda Sales Luiz Vianna

Frontiers in Genetics

doi 10.3389/fgene.2022.1016341

3,056 views
3 citations

Case Report

Published on 09 Dec 2022

Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair

in Human and Medical Genomics

Qingming Wang
Shuangxi Cheng
Youqing Fu
Haiming Yuan

Frontiers in Genetics

doi 10.3389/fgene.2022.1040124

3,411 views
5 citations

Original Research

Published on 05 Dec 2022

Diagnostic signature, subtype classification, and immune infiltration of key m6A regulators in osteomyelitis patients

in Human and Medical Genomics

Xiangwen Shi
Haonan Ni
Yipeng Wu
Minzheng Guo
Bin Wang
Yue Zhang
Bihuan Zhang
Yongqing Xu

Frontiers in Genetics

doi 10.3389/fgene.2022.1044264

2,744 views
8 citations

Original Research

Published on 05 Dec 2022

Inflammation-related pathways involved in damaged articular cartilage of rats exposed to T-2 toxin based on RNA-sequencing analysis

in Human and Medical Genomics

Longyan Shi
Qiuliang Liu
Heying Yang
Qi Wang
Jiaxiang Wang
Yingzhong Fan

Frontiers in Genetics

doi 10.3389/fgene.2022.1079739

2,900 views
9 citations

Original Research

Published on 01 Dec 2022

Screening and functional analysis of the differential peptides from the placenta of patients with healthy pregnancy and preeclampsia using placental peptidome

in Human and Medical Genomics

Tingting Chen
Zhongxiao Zhang
Qin Lu
Jun Ma

Frontiers in Genetics

doi 10.3389/fgene.2022.1014836

2,145 views
2 citations

Editorial

Published on 01 Dec 2022

Editorial: Genome-wide association studies of COVID-19 among diverse human populations

in Human and Medical Genomics

Zhong-Shan Cheng

Frontiers in Genetics

doi 10.3389/fgene.2022.1088026

2,159 views
1 citation