Frontiers in Genetics

Original Research

Published on 29 Nov 2024

Whole mitochondrial genome analyses of Han population from Shandong of China using massively parallel sequencing

in Evolutionary and Population Genetics

Jiashuo Zhang
XueBo Li
Anqi Chen
Mingxia Ding
Liangliang Li
Yinghua Qi
Chunli Ding
Dawei Cai
Suhua Zhang

Frontiers in Genetics

doi 10.3389/fgene.2024.1513412

898 views

Review

Published on 29 Nov 2024

PARP inhibitors in testicular germ cell tumors: what we know and what we are looking for

in Cancer Genetics and Oncogenomics

Sara Parola
Christoph Oing
Pasquale Rescigno
Salvatore Feliciano
Francesca Carlino
Luca Pompella
Antonella Lucia Marretta
Irene De Santo
Martina Viggiani
Margherita Muratore

Frontiers in Genetics

doi 10.3389/fgene.2024.1480417

757 views

Systematic Review

Published on 29 Nov 2024

Consumer-oriented (patient and family) outcomes from nursing in genomics: a scoping review of the literature (2012–2022)

in Human and Medical Genomics

Jordan N. Keels
Joanne Thomas
Kathleen A. Calzone
Laurie Badzek
Sarah Dewell
Vinaya Murthy
Rosie O’Shea
Emma T. Tonkin
Andrew A. Dwyer

Frontiers in Genetics

doi 10.3389/fgene.2024.1481948

1,217 views

Brief Research Report

Published on 29 Nov 2024

Genewise detection of variants in MEFV gene using nanopore sequencing

in Genetics of Common and Rare Diseases

Lilit Ghukasyan
Gisane Khachatryan
Tamara Sirunyan
Arpine Minasyan
Siras Hakobyan
Andranik Chavushyan
Varduhi Hayrapetyan
Hovsep Ghazaryan
Gevorg Martirosyan
Gohar Mkrtchyan

Frontiers in Genetics

doi 10.3389/fgene.2024.1493295

1,182 views

Original Research

Published on 29 Nov 2024

Gradient boosting reveals spatially diverse cholesterol gene signatures in colon cancer

in Cancer Genetics and Oncogenomics

Xiuxiu Yang
Debolina Chatterjee
Justin L. Couetil
Ziyu Liu
Valerie D. Ardon
Chao Chen
Jie Zhang
Kun Huang
Travis S. Johnson

Frontiers in Genetics

doi 10.3389/fgene.2024.1410353

841 views

Original Research

Published on 29 Nov 2024

Building a FAIR data ecosystem for incorporating single-cell transcriptomics data into agricultural genome to phenome research

in Livestock Genomics

Muskan Kapoor
Enrique Sapena Ventura
Amy Walsh
Alexey Sokolov
Nancy George
Sunita Kumari
Nicholas J. Provart
Benjamin Cole
Marc Libault
Timothy Tickle

Frontiers in Genetics

doi 10.3389/fgene.2024.1460351

893 views

Original Research

Published on 29 Nov 2024

Exome sequencing in 90 children with developmental delay: a single-center experience

in Epigenomics and Epigenetics

Oksana Boyarchuk
Liubov Volianska
Olena Smashna
Halyna Makukh

Frontiers in Genetics

doi 10.3389/fgene.2024.1505254

698 views

Original Research

Published on 29 Nov 2024

Correlating gene expression levels with transcription factor binding sites facilitates identification of key transcription factors from transcriptome data

in Computational Genomics

Tinghua Huang
Siqi Niu
Fanghong Zhang
Binyu Wang
Jianwu Wang
Guoping Liu
Min Yao

Frontiers in Genetics

doi 10.3389/fgene.2024.1511456

545 views
1 citation

Brief Research Report

Published on 29 Nov 2024

Case Report: Novel CNGA3 compound heterozygous variants cause achromatopsia in three patients from a family

in Genetics of Common and Rare Diseases

Xiaoqiang Zhou
Yasi Zhou
Shuijuan Wu
Xiaoling Guo
Liangfeng Yao
Xingkun Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1457569

498 views

Original Research

Published on 29 Nov 2024

Detection of gene variants associated with recessive limb–girdle muscular weakness and Pompe disease in a global cohort of patients through the application of next-generation sequencing analysis

in Genetics of Common and Rare Diseases

Jorge Alfredo Bevilacqua
Abdullah Mohammed Al-Salti
Abubaker Al Madani
Armando Alves da Fonseca
Hacer Durmus
Josiah Chai
Ali Alshehri
Márcia Gonçalves Ribeiro
Paulo Sgobbi
Sergey S. Nikitin

Frontiers in Genetics

doi 10.3389/fgene.2024.1477291

1,054 views

Case Report

Published on 28 Nov 2024

Novel pathogenic ATM mutation with ataxia-telangiectasia in a Chinese family

in Genetics of Common and Rare Diseases

Qiaomin Zhou
Minling Chen
Enfu Tao

Frontiers in Genetics

doi 10.3389/fgene.2024.1491649

558 views

Case Report

Published on 28 Nov 2024

Case Report: Concurrent de novo pathogenic variants in the LMNA gene as a cause of sporadic partial lipodystrophy

in Genetics of Common and Rare Diseases

José L. Santos
José Patricio Miranda
Carlos F. Lagos
Víctor A. Cortés

Frontiers in Genetics

doi 10.3389/fgene.2024.1468878

880 views

Review

Published on 28 Nov 2024

Application of next-generation sequencing in the detection of transgenic crop

in Genomic Assay Technology

Shitian He
Yueyuan Fan
Shaomin Tao
Yanxia Zhang
Chuanlin Yin
Xiaoping Yu

Frontiers in Genetics

doi 10.3389/fgene.2024.1461115

869 views

Original Research

Published on 27 Nov 2024

Exploring the therapeutic potency of cryptotanshinone in cervical cancer: a multi-omics and network pharmacology approach

in Cancer Genetics and Oncogenomics

Zenghong Lu
Gangfeng Zhu
Xiaofei Feng
Yi Xiang
Cixiang Chen
Huiting Yuan
Zhixing Chen

Frontiers in Genetics

doi 10.3389/fgene.2024.1435132

976 views

Original Research

Published on 27 Nov 2024

Global deletion of the immune cell transcription factor, T-bet, alters gut microbiota and insulin sensitivity in mice

in Immunogenetics

E. Stolarczyk
C. T. Vong
N. Garrido-Mesa
E. Marks
D. Abdel-Aziz
Q. Ju
I. Jackson
N. Powell
G. M. Lord
J. K. Howard

Frontiers in Genetics

doi 10.3389/fgene.2024.1502832

948 views

Editorial

Published on 27 Nov 2024

Editorial: Multi-omics strategy toward identifying and managing hereditary and metabolic liver diseases

in Statistical Genetics and Methodology

Mingjie Wang
Sujun Zheng
Xinhua Li

Frontiers in Genetics

doi 10.3389/fgene.2024.1520721

524 views

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Articles

Whole mitochondrial genome analyses of Han population from Shandong of China using massively parallel sequencing

PARP inhibitors in testicular germ cell tumors: what we know and what we are looking for

Consumer-oriented (patient and family) outcomes from nursing in genomics: a scoping review of the literature (2012–2022)

Genewise detection of variants in MEFV gene using nanopore sequencing

Gradient boosting reveals spatially diverse cholesterol gene signatures in colon cancer

Building a FAIR data ecosystem for incorporating single-cell transcriptomics data into agricultural genome to phenome research

Exome sequencing in 90 children with developmental delay: a single-center experience

Correlating gene expression levels with transcription factor binding sites facilitates identification of key transcription factors from transcriptome data

Case Report: Novel CNGA3 compound heterozygous variants cause achromatopsia in three patients from a family

Detection of gene variants associated with recessive limb–girdle muscular weakness and Pompe disease in a global cohort of patients through the application of next-generation sequencing analysis

Novel pathogenic ATM mutation with ataxia-telangiectasia in a Chinese family

Case Report: Concurrent de novo pathogenic variants in the LMNA gene as a cause of sporadic partial lipodystrophy

Application of next-generation sequencing in the detection of transgenic crop

Exploring the therapeutic potency of cryptotanshinone in cervical cancer: a multi-omics and network pharmacology approach

Global deletion of the immune cell transcription factor, T-bet, alters gut microbiota and insulin sensitivity in mice

Editorial: Multi-omics strategy toward identifying and managing hereditary and metabolic liver diseases