Frontiers in Genetics

Review

Published on 02 Oct 2024

Prenatal finding of isolated ventricular septal defect: genetic association, outcomes and counseling

Xin Chen
Qian Zhang
Man Lu
Qiuxia Feng
Litao Qin
Shixiu Liao

Frontiers in Genetics

doi 10.3389/fgene.2024.1447216

5,390 views
2 citations

Original Research

Published on 01 Oct 2024

Integrated PacBio SMRT and Illumina sequencing uncovers transcriptional and physiological responses to drought stress in whole-plant Nitraria tangutorum

Meiying Wei
Bo Wang
Chaoqun Li
Xiaolan Li
Cai He
Yi Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1474259

2,256 views
2 citations

Original Research

Published on 01 Oct 2024

MicroRNA binding site variants–new potential markers of primary osteoporosis in men and women

Bulat Yalaev
Roman Deev
Anton Tyurin
Ramil Salakhov
Kirill Smirnov
Anna Eremkina
Natalia Mokrysheva
Ildar Minniakhmetov
Rita Khusainova

Frontiers in Genetics

doi 10.3389/fgene.2024.1470310

2,261 views
2 citations

Original Research

Published on 01 Oct 2024

Transparent sparse graph pathway network for analyzing the internal relationship of lung cancer

Zhibin Jin
Yuhu Shi
Lili Zhou

Frontiers in Genetics

doi 10.3389/fgene.2024.1437174

1,501 views
1 citation

Original Research

Published on 01 Oct 2024

A statistical model to identify hereditary and epigenetic fusion genes associated with dilated cardiomyopathy

Ling Fei
Jun Zhang
Degen Zhuo

Frontiers in Genetics

doi 10.3389/fgene.2024.1438887

1,914 views

Editorial

Published on 30 Sep 2024

Editorial: Emerging talents in human and medical genomics

Vanessa Meyer
Stephen J. Bush
Angela Botes
Mandeep Kaur

Frontiers in Genetics

doi 10.3389/fgene.2024.1497486

1,144 views

Original Research

Published on 27 Sep 2024

Allogeneic mesenchymal stromal cell therapy in kidney transplantation: should repeated human leukocyte antigen mismatches be avoided?

Suzanne Bezstarosti
Pauline Erpicum
Gianni Maggipinto
Geertje J. Dreyer
Marlies E. J. Reinders
Soufian Meziyerh
Dave L. Roelen
Johan W. De Fijter
Jesper Kers
Laurent Weekers

Frontiers in Genetics

doi 10.3389/fgene.2024.1436194

2,415 views
2 citations

Editorial

Published on 27 Sep 2024

Editorial: Personalized therapies for monogenic diabetes

Maurizio Delvecchio
Ming Liu
Novella Rapini
Fabrizio Barbetti

Frontiers in Genetics

doi 10.3389/fgene.2024.1496367

2,115 views
1 citation

Brief Research Report

Published on 27 Sep 2024

Multi-omic analysis of longitudinal acute myeloid leukemia patient samples reveals potential prognostic markers linked to disease progression

Nisar Ahmed
Irene Cavattoni
William Villiers
Chiara Cugno
Sara Deola
Borbala Mifsud

Frontiers in Genetics

doi 10.3389/fgene.2024.1442539

3,383 views
4 citations

Original Research

Published on 27 Sep 2024

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

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

1,856 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

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

2,682 views
4 citations

Brief Research Report

Published on 27 Sep 2024

Inorganic pyrophosphate plasma levels in patients with GGCX-associated PXE-like phenotypes

Qiaoli Li
Catherine Troutman
Mary Peckiconis
Tamara Wurst
Sharon F. Terry

Frontiers in Genetics

doi 10.3389/fgene.2024.1429320

1,790 views
2 citations

Original Research

Published on 27 Sep 2024

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

Xiaoxue Shi
Xuelin Qi
Jinhua Zheng
Jianjun Ma
Dongsheng Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1421122

1,886 views

Editorial

Published on 27 Sep 2024

Editorial: The diversified role of mitochondria in cancer

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

Frontiers in Genetics

doi 10.3389/fgene.2024.1494075

2,391 views
1 citation

Review

Published on 26 Sep 2024

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

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

7,800 views
1 citation

Review

Published on 26 Sep 2024

Cell type specification and diversity in subpallial organoids

Narciso Pavon
Yubing Sun
ChangHui Pak

Frontiers in Genetics

doi 10.3389/fgene.2024.1440583

4,528 views
3 citations

Original Research

Published on 26 Sep 2024

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

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

Frontiers in Genetics

doi 10.3389/fgene.2024.1400847

2,350 views
1 citation

Case Report

Published on 26 Sep 2024

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

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

1,659 views

Original Research

Published on 25 Sep 2024

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

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

3,971 views
8 citations

Brief Research Report

Published on 25 Sep 2024

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

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

2,429 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

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

3,837 views
1 citation

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

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

6,547 views
3 citations

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

Chao Xu
Shaolong Cao
Md Ashad Alam

Frontiers in Genetics

doi 10.3389/fgene.2024.1487893

1,224 views

Original Research

Published on 25 Sep 2024

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

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

2,736 views
10 citations

1,121 Publications

volumes

Prenatal finding of isolated ventricular septal defect: genetic association, outcomes and counseling

Integrated PacBio SMRT and Illumina sequencing uncovers transcriptional and physiological responses to drought stress in whole-plant Nitraria tangutorum

MicroRNA binding site variants–new potential markers of primary osteoporosis in men and women

Transparent sparse graph pathway network for analyzing the internal relationship of lung cancer

A statistical model to identify hereditary and epigenetic fusion genes associated with dilated cardiomyopathy

Editorial: Emerging talents in human and medical genomics

Allogeneic mesenchymal stromal cell therapy in kidney transplantation: should repeated human leukocyte antigen mismatches be avoided?

Editorial: Personalized therapies for monogenic diabetes

Multi-omic analysis of longitudinal acute myeloid leukemia patient samples reveals potential prognostic markers linked to disease progression

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

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

Inorganic pyrophosphate plasma levels in patients with GGCX-associated PXE-like phenotypes

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

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

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

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

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

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

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

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

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

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