Frontiers in Genetics

Original Research

Published on 13 Dec 2024

Systemic inflammatory regulators and age-related macular degeneration: a bidirectional Mendelian randomization study

in Genetics of Common and Rare Diseases

Xi Liu
Yu Cao
Ying Wang
Lihua Kang
Guowei Zhang
Junfang Zhang
Bai Qin
Ling Yang
Jiawei Luo
Pengfei Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1391999

1,277 views
1 citation

Original Research

Published on 13 Dec 2024

Prenatal diagnosis of a silver-russell syndrome caused by 11p15 duplication and pedigree analysis

in Genetics of Common and Rare Diseases

Shurong Hong
Hua Wei
Xueyi Zhuang
Weirong Huang
Yu Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1465521

775 views

Brief Research Report

Published on 12 Dec 2024

Behind the scenes with genomics researchers

in ELSI in Science and Genetics

Renata Mont’Alverne
Lori Bradford
Cheryl Buckmaster
Graham Strickert
Jason MacLean
Diane Dupont

Frontiers in Genetics

doi 10.3389/fgene.2024.1467404

668 views

Systematic Review

Published on 12 Dec 2024

Mapping the current status and outlook of research on noonan syndrome over the last 26 years: a bibliometric and visual analysis

in Genetics of Common and Rare Diseases

Zhengjiu Cui
Yuanyuan Wang
Fei Luo
Juanjuan Diao
Bin Yuan

Frontiers in Genetics

doi 10.3389/fgene.2024.1488425

1,312 views
1 citation

Correction

Published on 12 Dec 2024

Corrigendum: 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.2024.1520519

981 views

Review

Published on 11 Dec 2024

Pathogenesis and management of TRPV3-related Olmsted syndrome

in Genetics of Common and Rare Diseases

Antong Lu
Kezhen Li
Cong Huang
Bo Yu
Weilong Zhong

Frontiers in Genetics

doi 10.3389/fgene.2024.1459109

1,031 views

Original Research

Published on 11 Dec 2024

Association between arthropathies and postpartum hemorrhage: a bidirectional Mendelian randomization study

in Statistical Genetics and Methodology

Zhao Wu
Chengyu Yuan
Xue Peng

Frontiers in Genetics

doi 10.3389/fgene.2024.1448754

980 views

Original Research

Published on 11 Dec 2024

Selection signature analysis reveals genes associated with tail phenotype in sheep

in Livestock Genomics

Yunxia Qi
Xiaolong He
Biao Wang
Chaoyun Yang
Lai Da
Bin Liu
Wenguang Zhang
Shaoyin Fu
Yongbin Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1509177

1,083 views

Original Research

Published on 11 Dec 2024

The frequent variant A57F in the GNE gene in patients from Russia has Finno-Ugric Mari origin

in Genetics of Common and Rare Diseases

Dmitrii Subbotin
Sofya Ionova
Andrey Marakhonov
Elena Saifullina
Artem Borovikov
Leila Akhmadeeva
Polina Chausova
Oksana Ryzhkova
Rena Zinchenko
Sergey Kutsev

Frontiers in Genetics

doi 10.3389/fgene.2024.1511304

692 views

Original Research

Published on 11 Dec 2024

Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome’s clinical and molecular spectrum through NALCN in-silico structural analysis

in Human and Medical Genomics

Davide Vecchio
Marina Macchiaiolo
Michaela V. Gonfiantini
Filippo M. Panfili
Francesco Petrizzelli
Niccolò Liorni
Fabiana Cortellessa
Lorenzo Sinibaldi
Ippolita Rana
Emanuele Agolini

Frontiers in Genetics

doi 10.3389/fgene.2024.1477940

1,199 views

Original Research

Published on 11 Dec 2024

The complete chloroplast genome of Illicium verum and comparative analysis with related species from Magnoliaceae and Illiciaceae

in Genomics of Plants and the Phytoecosystem

Yingying Cao
Yongxing Lai
Zhuxin Li
Shanshan Zhai
Yinghan Dai
Junyu Tao
Qing Wang
Ziheng Xu
Minjie Jiang
Li Yu

Frontiers in Genetics

doi 10.3389/fgene.2024.1452680

821 views
1 citation

Technology and Code

Published on 10 Dec 2024

MMPred: a tool to predict peptide mimicry events in MHC class II recognition

in Computational Genomics

Filippo Guerri
Valentin Junet
Judith Farrés
Xavier Daura

Frontiers in Genetics

doi 10.3389/fgene.2024.1500684

1,282 views

Original Research

Published on 10 Dec 2024

Comprehensive evaluation of AlphaMissense predictions by evidence quantification for variants of uncertain significance

in Human and Medical Genomics

Amina Kurtovic-Kozaric
Lejla Delalic
Belma Mutapcic
Lejla Comor
Eric Siciliano
Mark J. Kiel

Frontiers in Genetics

doi 10.3389/fgene.2024.1487608

1,576 views

Editorial

Published on 10 Dec 2024

Editorial: Multi-omic approaches decipher the pathogenesis of nervous system diseases and identify potential therapeutic drugs

in Neurogenomics

Robert Friedman
Yasin Mamatjan
Cuiping Pan
Patrícia Pelufo Silveira
Margarita Zachariou

Frontiers in Genetics

doi 10.3389/fgene.2024.1520148

766 views

Original Research

Published on 10 Dec 2024

Whole-exome sequencing identified a novel heterozygous variant in UBAP2L in a Chinese family with neurodevelopmental disorder characterized by impaired language, behavioral abnormalities, and dysmorphic facies

in Genetics of Common and Rare Diseases

Qi Yang
Qiang Zhang
Xunzhao Zhou
Juntan Feng
Shujie Zhang
Li Lin
Shang Yi
Zailong Qin
Jingsi Luo

Frontiers in Genetics

doi 10.3389/fgene.2024.1503048

1,195 views

Case Report

Published on 10 Dec 2024

Insights into diagnostic difficulties in spinal muscular atrophy: a Case Report series

in Genetics of Common and Rare Diseases

Kakha Bregvadze
Luka Abashishvili
Nana Nino Tatishvili
Teona Shatirishvili
Ana Bedoshvili
Gocha Chikvinidze
Arndt Rolfs
Volha Skrahina
Tinatin Tkemaladze

Frontiers in Genetics

doi 10.3389/fgene.2024.1502444

1,117 views