Frontiers in Genetics

Original Research

Published on 19 Jan 2023

ABI3BP is a prognosis biomarker related with clinicopathological features and immunity infiltration of lung tumor

Yan Feng
Xiaolei Han
Zhe Zhang
Han Qiao
Huaping Tang

Frontiers in Genetics

doi 10.3389/fgene.2022.1085785

4,192 views
12 citations

Original Research

Published on 19 Jan 2023

Investigating nicotine pathway-related long non-coding RNAs in tobacco

Xiaodong Xie
Jingjing Jin
Chen Wang
Peng Lu
Zefeng Li
Jiemeng Tao
Peijian Cao
Yalong Xu

Frontiers in Genetics

doi 10.3389/fgene.2022.1102183

3,330 views
7 citations

Brief Research Report

Published on 19 Jan 2023

Draft genome assembly for the colombian freshwater bocachico fish, Prochilodus magdalenae

Jonny Andrés Yepes-Blandón
Chao Bian
María José Benítez-Galeano
Jorge Luis Aristizabal-Regino
Ana Lucía Estrada-Posada
Daiana Mir
Gersson Vásquez-Machado
Víctor Julio Atencio-García
Qiong Shi
Nélida Rodríguez-Osorio

Frontiers in Genetics

doi 10.3389/fgene.2022.989788

5,422 views
7 citations

Original Research

Published on 18 Jan 2023

RNA modification writers pattern in relation to tumor microenvironment and prognosis in prostate cancer

Xu Cheng
Xuanzi Yi

Frontiers in Genetics

doi 10.3389/fgene.2022.1065424

2,423 views
1 citation

Review

Published on 17 Jan 2023

Biochemical exploration of β-lactamase inhibitors

Varshaa Arer
Debasish Kar

Frontiers in Genetics

doi 10.3389/fgene.2022.1060736

15,381 views
33 citations

Original Research

Published on 17 Jan 2023

Preclinical species gene expression database: Development and meta-analysis

Caitlin Krause
Kinga Suwada
Eric A. G. Blomme
Kenneth Kowalkowski
Michael J. Liguori
Prathap Kumar Mahalingaiah
Scott Mittelstadt
Richard Peterson
Lauren Rendino
Andy Vo

Frontiers in Genetics

doi 10.3389/fgene.2022.1078050

12,093 views
13 citations

Case Report

Published on 17 Jan 2023

Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia

Misbahuddin M. Rafeeq
Hussam Aly Sayed Murad
Najumuddin
Samee Ullah
Zaheer Ahmed
Qamre Alam
Muhammad Bilal
Alaa Hamed Habib
Ziaullah M. Sain
Muhammad Jawad Khan

Frontiers in Genetics

doi 10.3389/fgene.2022.1117500

3,475 views
3 citations

Original Research

Published on 17 Jan 2023

Genome-wide association mapping of bread wheat genotypes using yield and grain morphology-related traits under different environments

Hafiz Ghulam Muhu-Din Ahmed
Yawen Zeng
Muhammad Ahsan Khan
Muhammad Abdul Rehman Rashid
Muhammad Ameen
Ahmed Akrem
Amjad Saeed

Frontiers in Genetics

doi 10.3389/fgene.2022.1008024

4,526 views
10 citations

Brief Research Report

Published on 17 Jan 2023

Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2

Yu Toyoda
Sung Kweon Cho
Velibor Tasic
Kateřina Pavelcová
Jana Bohatá
Hiroshi Suzuki
Victor A. David
Jaeho Yoon
Anna Pallaiova
Jana Šaligová

Frontiers in Genetics

doi 10.3389/fgene.2022.1048330

6,375 views
8 citations

Methods

Published on 17 Jan 2023

A shortest path-based approach for copy number variation detection from next-generation sequencing data

Guojun Liu
Hongzhi Yang
Xiguo Yuan

Frontiers in Genetics

doi 10.3389/fgene.2022.1084974

2,696 views
6 citations

Review

Published on 16 Jan 2023

LncRNAs could play a vital role in osteosarcoma treatment: Inhibiting osteosarcoma progression and improving chemotherapy resistance

Shi Xiaotong
Li Xiao
Liao Shiyu
Bi Zhiguo
Feng Chunyang
Liu Jianguo

Frontiers in Genetics

doi 10.3389/fgene.2022.1022155

2,759 views
2 citations

Original Research

Published on 16 Jan 2023

Addressing disparities in pharmacogenomics through rural and underserved workforce education

Jacob T. Brown
Erin McGonagle
Randall Seifert
Marilyn Speedie
Pamala A. Jacobson

Frontiers in Genetics

doi 10.3389/fgene.2022.1082985

3,078 views
9 citations

Original Research

Published on 16 Jan 2023

Candidate targets of copy number deletion events across 17 cancer types

Qingyao Huang
Michael Baudis

Frontiers in Genetics

doi 10.3389/fgene.2022.1017657

2,949 views

Correction

Published on 16 Jan 2023

Corrigendum: Transmembrane and coiled-coil domains 3 is a diagnostic biomarker for predicting immune checkpoint blockade efficacy in hepatocellular carcinoma

Xinyao Hu
Hua Zhu
Shi Feng
Chaoqun Wang
Yingze Ye
Xiaoxing Xiong

Frontiers in Genetics

doi 10.3389/fgene.2022.1117731

1,672 views
1 citation

Original Research

Published on 16 Jan 2023

Integrative analysis of WDR12 as a potential prognostic and immunological biomarker in multiple human tumors

Refaat A. Eid
Muhammad Alaa Eldeen
Mohamed A. Soltan
Mubarak Al-Shraim
Majed Aldehri
Leena S. Alqahtani
Ghadi Alsharif
Sarah Albogami
Ibrahim Jafri
Eman Fayad

Frontiers in Genetics

doi 10.3389/fgene.2022.1008502

4,426 views
9 citations

Original Research

Published on 16 Jan 2023

The role of smoking and alcohol in mediating the effect of gastroesophageal reflux disease on lung cancer: A Mendelian randomization study

Jing Yang
Duorui Nie
Yujing Chen
Zixing Liu
Mengzhao Li
Chun Gong
Qiong Liu

Frontiers in Genetics

doi 10.3389/fgene.2022.1054132

9,036 views
7 citations

Original Research

Published on 16 Jan 2023

A systems level approach to study metabolic networks in prokaryotes with the aromatic amino acid biosynthesis pathway

Priya V. K
Somdatta Sinha

Frontiers in Genetics

doi 10.3389/fgene.2022.1084727

3,275 views

Original Research

Published on 13 Jan 2023

Biological gene extraction path based on knowledge graph and natural language processing

Canlin Zhang
Xiaopei Cao

Frontiers in Genetics

doi 10.3389/fgene.2022.1086379

2,643 views
1 citation

Original Research

Published on 13 Jan 2023

Distinct traces of mixed ancestry in western commercial pig genomes following gene flow from Chinese indigenous breeds

Yebo Peng
Martijn FL Derks
Martien AM Groenen
Yiqiang Zhao
Mirte Bosse

Frontiers in Genetics

doi 10.3389/fgene.2022.1070783

3,819 views
7 citations

Original Research

Published on 13 Jan 2023

Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China

Yongyi Zou
Chuanxin Feng
Jiawei Qin
Xinrong Wang
Tingting Huang
Yan Yang
Kang Xie
Huizhen Yuan
Shuhui Huang
Bicheng Yang

Frontiers in Genetics

doi 10.3389/fgene.2022.1073851

7,074 views
12 citations

Original Research

Published on 13 Jan 2023

Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved

Brian E. Gawronski
Emily J. Cicali
Caitrin W. McDonough
Linda B. Cottler
Julio D. Duarte

Frontiers in Genetics

doi 10.3389/fgene.2022.1085994

5,587 views
16 citations

Original Research

Published on 13 Jan 2023

Prenatal diagnosis of recurrent moderate skeletal dysplasias in lamin B receptors

Xueping Shen
Zhi Li
Xuekui Pan
Juan Yao
Guosong Shen
Su Zhang
Minyue Dong
Lihong Fan

Frontiers in Genetics

doi 10.3389/fgene.2022.1020475

2,636 views
4 citations

Case Report

Published on 13 Jan 2023

Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review

Shaohua Bi
Liying Dai
Liangliang Jiang
Lili Wang
Mia Teng
Guanghui Liu
Ru-Jeng Teng

Frontiers in Genetics

doi 10.3389/fgene.2022.970204

5,227 views
6 citations

Original Research

Published on 13 Jan 2023

Interferon gamma-related gene signature based on anti-tumor immunity predicts glioma patient prognosis

Zhe Zhang
Xiaoli Shen
Zilong Tan
Yuran Mei
Tianzhu Lu
Yulong Ji
Sida Cheng
Yu Xu
Zekun Wang
Xinxian Liu

Frontiers in Genetics

doi 10.3389/fgene.2022.1053263

8,241 views
15 citations

3,801 Publications

volumes

ABI3BP is a prognosis biomarker related with clinicopathological features and immunity infiltration of lung tumor

Investigating nicotine pathway-related long non-coding RNAs in tobacco

Draft genome assembly for the colombian freshwater bocachico fish, Prochilodus magdalenae

RNA modification writers pattern in relation to tumor microenvironment and prognosis in prostate cancer

Biochemical exploration of β-lactamase inhibitors

Preclinical species gene expression database: Development and meta-analysis

Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia

Genome-wide association mapping of bread wheat genotypes using yield and grain morphology-related traits under different environments

Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2

A shortest path-based approach for copy number variation detection from next-generation sequencing data

LncRNAs could play a vital role in osteosarcoma treatment: Inhibiting osteosarcoma progression and improving chemotherapy resistance

Addressing disparities in pharmacogenomics through rural and underserved workforce education

Candidate targets of copy number deletion events across 17 cancer types

Corrigendum: Transmembrane and coiled-coil domains 3 is a diagnostic biomarker for predicting immune checkpoint blockade efficacy in hepatocellular carcinoma

Integrative analysis of WDR12 as a potential prognostic and immunological biomarker in multiple human tumors

The role of smoking and alcohol in mediating the effect of gastroesophageal reflux disease on lung cancer: A Mendelian randomization study

A systems level approach to study metabolic networks in prokaryotes with the aromatic amino acid biosynthesis pathway

Biological gene extraction path based on knowledge graph and natural language processing

Distinct traces of mixed ancestry in western commercial pig genomes following gene flow from Chinese indigenous breeds

Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China

Exploring perceptions, knowledge, and attitudes regarding pharmacogenetic testing in the medically underserved

Prenatal diagnosis of recurrent moderate skeletal dysplasias in lamin B receptors

Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review

Interferon gamma-related gene signature based on anti-tumor immunity predicts glioma patient prognosis