Original Research

Published on 27 Sep 2024

A case of adrenomyeloneuropathy caused by a novel point mutation in the ABCD1 gene and functional verification

in Genetics of Common and Rare Diseases

Xiaoxue Shi
Xuelin Qi
Jinhua Zheng
Jianjun Ma
Dongsheng Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1421122

440 views

Original Research

Published on 27 Sep 2024

Genetic architecture of kernel-related traits in sweet and waxy maize revealed by genome-wide association analysis

in Genomics of Plants and the Phytoecosystem

Jingtao Qu
Diansi Yu
Wei Gu
Muhammad Hayder Bin Khalid
Huiyun Kuang
Dongdong Dang
Hui Wang
Boddupalli Prasanna
Xuecai Zhang
Ao Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1431043

573 views

Original Research

Published on 27 Sep 2024

Human complex mixture analysis by “FD Multi-SNP Mixture Kit”

in Statistical Genetics and Methodology

Anqi Chen
Lun Li
Junfei Zhou
Tiantian Li
Chunyan Yuan
Hai Peng
Chengtao Li
Suhua Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1432378

403 views

Editorial

Published on 27 Sep 2024

Editorial: The diversified role of mitochondria in cancer

in Cancer Genetics and Oncogenomics

Siyuan Song
Qingqing Xia
Yu’e Liu
Kuo Chen
Fengqian Chen
Jin Zhang
Yi Wang

Frontiers in Genetics

doi 10.3389/fgene.2024.1494075

517 views

Review

Published on 26 Sep 2024

Genetic etiology of autism spectrum disorder in the African population: a scoping review

in Genetics of Common and Rare Diseases

Olivier Hakizimana
Janvier Hitayezu
Jeanne P. Uyisenga
Hope Onohuean
Leonor Palmeira
Vincent Bours
Abdullateef Isiaka Alagbonsi
Annette Uwineza

Frontiers in Genetics

doi 10.3389/fgene.2024.1431093

1,102 views

Review

Published on 26 Sep 2024

Cell type specification and diversity in subpallial organoids

in Behavioral and Psychiatric Genetics

Narciso Pavon
Yubing Sun
ChangHui Pak

Frontiers in Genetics

doi 10.3389/fgene.2024.1440583

907 views

Case Report

Published on 26 Sep 2024

Case report: Two siblings with very late onset of holocarboxylase synthase deficiency and a mini-review

in Genetics of Common and Rare Diseases

Margaux Gaschignard
Louis Domenach
Delphine Lamireau
Claire Guibet
Sandrine Roche
Emmanuel Richard
Isabelle Redonnet-Vernhet
Samir Mesli
Louis Lebreton

Frontiers in Genetics

doi 10.3389/fgene.2024.1249480

504 views

Original Research

Published on 26 Sep 2024

Causal effects of specific gut microbiota on spinal stenosis diseases: a two-sample mendelian randomization study

in Statistical Genetics and Methodology

Kaihang Luo
Weizheng Zeng
Qiushuang Li
Yuliang Zhang
Shengkai Liu
Xizhe Liu
Shaoyu Liu

Frontiers in Genetics

doi 10.3389/fgene.2024.1400847

651 views

Brief Research Report

Published on 25 Sep 2024

Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males

in Genetics of Common and Rare Diseases

Yu-Ping Tseng
Ya-Sian Chang
Venugopala R. Mekala
Ting-Yuan Liu
Jan-Gowth Chang
Grace S. Shieh

Frontiers in Genetics

doi 10.3389/fgene.2024.1423714

526 views

Original Research

Published on 25 Sep 2024

ML-GAP: machine learning-enhanced genomic analysis pipeline using autoencoders and data augmentation

in RNA

Melih Agraz
Dincer Goksuluk
Peng Zhang
Bum-Rak Choi
Richard T. Clements
Gaurav Choudhary
George Em Karniadakis

Frontiers in Genetics

doi 10.3389/fgene.2024.1442759

591 views

Original Research

Published on 25 Sep 2024

Personality and COMT gene: molecular-genetic and epigenetic associations with NEO-PI-R personality domains and facets in monozygotic twins

in Epigenomics and Epigenetics

Dušanka Mitrović
Snežana Smederevac
Lissette Delgado-Cruzata
Selka Sadiković
Dejan Pajić
Mechthild Prinz
Zoran Budimlija
Milan Oljača
Jelena Kušić-Tišma
Nataša Vučinić

Frontiers in Genetics

doi 10.3389/fgene.2024.1455872

821 views

Original Research

Published on 25 Sep 2024

Integrating transcriptomics, eQTL, and Mendelian randomization to dissect monocyte roles in severe COVID-19 and gout flare

in Genetics of Common and Rare Diseases

Jiajia Li
Guixian Yang
Junnan Liu
Guofeng Li
Huiling Zhou
Yuan He
Xinru Fei
Dongkai Zhao

Frontiers in Genetics

doi 10.3389/fgene.2024.1385316

1,090 views

Original Research

Published on 25 Sep 2024

Quantifying uncertainty of molecular mismatch introduced by mislabeled ancestry using haplotype-based HLA genotype imputation

in Immunogenetics

Benedict M. Matern
Eric Spierings
Selle Bandstra
Abeer Madbouly
Stefan Schaub
Eric T. Weimer
Matthias Niemann

Frontiers in Genetics

doi 10.3389/fgene.2024.1444554

812 views

Editorial

Published on 25 Sep 2024

Editorial: Application of novel statistical and machine-learning methods to high-dimensional clinical cancer and (multi-) omics data volume II

in Statistical Genetics and Methodology

Chao Xu
Shaolong Cao
Md Ashad Alam

Frontiers in Genetics

doi 10.3389/fgene.2024.1487893

283 views

Original Research

Published on 24 Sep 2024

TimeNorm: a novel normalization method for time course microbiome data

in Statistical Genetics and Methodology

Qianwen Luo
Meng Lu
Hamza Butt
Nicholas Lytal
Ruofei Du
Hongmei Jiang
Lingling An

Frontiers in Genetics

doi 10.3389/fgene.2024.1417533

526 views

Original Research

Published on 24 Sep 2024

Optimizing purebred selection to improve crossbred performance

in Livestock Genomics

Somayeh Barani
Sayed Reza Miraie Ashtiani
Ardeshir Nejati Javaremi
Majid Khansefid
Hadi Esfandyari

Frontiers in Genetics

doi 10.3389/fgene.2024.1384973

517 views

Navigation group

Articles

A case of adrenomyeloneuropathy caused by a novel point mutation in the ABCD1 gene and functional verification

Genetic architecture of kernel-related traits in sweet and waxy maize revealed by genome-wide association analysis

Human complex mixture analysis by “FD Multi-SNP Mixture Kit”

Editorial: The diversified role of mitochondria in cancer

Genetic etiology of autism spectrum disorder in the African population: a scoping review

Cell type specification and diversity in subpallial organoids

Case report: Two siblings with very late onset of holocarboxylase synthase deficiency and a mini-review

Causal effects of specific gut microbiota on spinal stenosis diseases: a two-sample mendelian randomization study

Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males

ML-GAP: machine learning-enhanced genomic analysis pipeline using autoencoders and data augmentation

Personality and COMT gene: molecular-genetic and epigenetic associations with NEO-PI-R personality domains and facets in monozygotic twins

Integrating transcriptomics, eQTL, and Mendelian randomization to dissect monocyte roles in severe COVID-19 and gout flare

Quantifying uncertainty of molecular mismatch introduced by mislabeled ancestry using haplotype-based HLA genotype imputation

Editorial: Application of novel statistical and machine-learning methods to high-dimensional clinical cancer and (multi-) omics data volume II

TimeNorm: a novel normalization method for time course microbiome data

Optimizing purebred selection to improve crossbred performance