Frontiers in Genetics | Human and Medical Genomics

Review

Published on 24 Nov 2022

Genes in pediatric pulmonary arterial hypertension and the most promising BMPR2 gene therapy

in Human and Medical Genomics

Lingling Dai
Lizhong Du

Frontiers in Genetics

doi 10.3389/fgene.2022.961848

5,687 views
6 citations

Original Research

Published on 22 Nov 2022

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

in Human and Medical Genomics

Hongwei Yu
Gan Luo
Tianwei Sun
Qiong Tang

Frontiers in Genetics

doi 10.3389/fgene.2022.1051047

5,142 views
6 citations

Original Research

Published on 22 Nov 2022

Identifying key m6A-methylated lncRNAs and genes associated with neural tube defects via integrative MeRIP and RNA sequencing analyses

in Human and Medical Genomics

Jing Yang
Jing Xu
Luting Zhang
Yingting Li
Min Chen

Frontiers in Genetics

doi 10.3389/fgene.2022.974357

3,125 views
5 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

in Human and Medical Genomics

Ruge Sun
Yanchao Gao
Fengjun Shen

Frontiers in Genetics

doi 10.3389/fgene.2022.1042540

3,335 views
4 citations

Editorial

Published on 18 Nov 2022

Editorial: Cancer systems biology

in Human and Medical Genomics

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

Frontiers in Genetics

doi 10.3389/fgene.2022.1083902

2,583 views

Original Research

Published on 18 Nov 2022

Abnormal expression of TSG-6 disturbs extracellular matrix homeostasis in chondrocytes from endemic osteoarthritis

in Human and Medical Genomics

Yujie Ning
Pan Zhang
Feiyu Zhang
Sijie Chen
Yanli Liu
Feihong Chen
Yifan Wu
Shujin Li
Chaowei Wang
Yi Gong

Frontiers in Genetics

doi 10.3389/fgene.2022.1064565

3,644 views
9 citations

Case Report

Published on 18 Nov 2022

Case report and a brief review: Analysis and challenges of prenatal imaging phenotypes and genotypes in Joubert syndrome

in Human and Medical Genomics

Ling-Xi Huang
Xian-Gui Lu
Jiao-Xiang Liu
Ling Xu
Ning Shang
Li Guo
Yan-Chun OuYang

Frontiers in Genetics

doi 10.3389/fgene.2022.1038274

3,193 views
10 citations

Original Research

Published on 17 Nov 2022

Integration of small RNAs from plasma and cerebrospinal fluid for classification of multiple sclerosis

in Human and Medical Genomics

Maria Needhamsen
Payam Emami Khoonsari
Galina Yurevna Zheleznyakova
Eliane Piket
Michael Hagemann-Jensen
Yanan Han
Jannik Gierlich
Diana Ekman
Maja Jagodic

Frontiers in Genetics

doi 10.3389/fgene.2022.1042483

2,687 views

Original Research

Published on 17 Nov 2022

Identification of four novel variants in the CDH23 gene from four affected families with hearing loss

in Human and Medical Genomics

Baoling Kang
Xinshu Lu
Jianjun Xiong
Yuan Li
Jinwen Zhu
Tao Cai

Frontiers in Genetics

doi 10.3389/fgene.2022.1027396

2,429 views
4 citations

Brief Research Report

Published on 14 Nov 2022

Establishment of transgenic pigs overexpressing human PKD2-D511V mutant

in Human and Medical Genomics

Yuan Zhang
Saifei Xu
Qiao Jin
Jianing Luo
Ce Gao
Sakthidasan Jayaprakash
Huanan Wang
Lenan Zhuang
Jin He

Frontiers in Genetics

doi 10.3389/fgene.2022.1059682

2,055 views

Case Report

Published on 09 Nov 2022

Case Report: Novel pathogenic variant in NFIX in two sisters with Malan syndrome due to germline mosaicism

in Human and Medical Genomics

Elizabeth Langley
Laura S. Farach
Kate Mowrey

Frontiers in Genetics

doi 10.3389/fgene.2022.1044660

2,084 views

Original Research

Published on 09 Nov 2022

Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations

in Human and Medical Genomics

Jianzheng Fang
Xiaoyi Wang
Xueping Sun
Yugui Cui
Feiyang Diao
Xiaoyu Yang

Frontiers in Genetics

doi 10.3389/fgene.2022.1035468

3,424 views
3 citations

Review

Published on 08 Nov 2022

Clinical detection, diagnosis and treatment of morphological abnormalities of sperm flagella: A review of literature

in Human and Medical Genomics

Jiaxiong Wang
Weizhuo Wang
Liyan Shen
Aiyan Zheng
Qingxia Meng
Hong Li
Shenmin Yang

Frontiers in Genetics

doi 10.3389/fgene.2022.1034951

7,242 views
29 citations

Original Research

Published on 07 Nov 2022

Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder

in Human and Medical Genomics

Leonardo Caporali
Claudio Fiorini
Flavia Palombo
Martina Romagnoli
Flavia Baccari
Corrado Zenesini
Paola Visconti
Annio Posar
Maria Cristina Scaduto
Danara Ormanbekova

Frontiers in Genetics

doi 10.3389/fgene.2022.953762

3,085 views
8 citations

Case Report

Published on 31 Oct 2022

Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing

in Human and Medical Genomics

Jialing Yu
Na Chen
Min Chen
Min Shen
Yeqing Qian
Minyue Dong

Frontiers in Genetics

doi 10.3389/fgene.2022.1020525

2,168 views
1 citation

Editorial

Published on 28 Oct 2022

Editorial: Genetics and mechanism of ciliopathies

in Human and Medical Genomics

Steven Lim Cho Pei
Brian Hon Yin Chung

Frontiers in Genetics

doi 10.3389/fgene.2022.1067168

2,020 views