Frontiers in Genetics

Methods

Published on 16 Jan 2024

Sister haplotypes and recombination disequilibrium: a new approach to identify associations of haplotypes with complex diseases

in Statistical Genetics and Methodology

Shun-Yao Liao
Yuan-De Tan

Frontiers in Genetics

doi 10.3389/fgene.2023.1295327

2,706 views

Case Report

Published on 16 Jan 2024

Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia

in Neurogenomics

Manal Alaamery
Salam Massadeh
Manar Aldarwish
Nour Albesher
Nora Aljawini
Othman Alahmed
Amna Kashgari
Christopher A. Walsh
Wafaa Eyaid

Frontiers in Genetics

doi 10.3389/fgene.2023.1294214

3,973 views
4 citations

Original Research

Published on 16 Jan 2024

An in silico approach to identify potential downstream targets of miR-153 involved in Alzheimer’s disease

in RNA

Sanila Amber
Saadia Zahid

Frontiers in Genetics

doi 10.3389/fgene.2024.1271404

3,601 views
2 citations

Original Research

Published on 15 Jan 2024

Methylenetetrahydrofolate reductase polymorphic variants C677T and A1298C in rectal cancer in Slavic population: significance for cancer risk and response to chemoradiotherapy

in Cancer Genetics and Oncogenomics

Aleksandra Stanojevic
Jelena Spasic
Mladen Marinkovic
Suzana Stojanovic-Rundic
Radmila Jankovic
Ana Djuric
Jerome Zoidakis
Remond J. A. Fijneman
Sergi Castellvi-Bel
Milena Cavic

Frontiers in Genetics

doi 10.3389/fgene.2023.1299599

4,387 views
7 citations

Original Research

Published on 15 Jan 2024

Genome-wide association with footrot in hair and wool sheep

in Livestock Genomics

Mehmet Ulas Cinar
Ryan D. Oliveira
Tracy S. Hadfield
Anne Lichtenwalner
Richard J. Brzozowski
C. Thomas Settlemire
Susan G. Schoenian
Charles Parker
Holly L. Neibergs
Noelle E. Cockett

Frontiers in Genetics

doi 10.3389/fgene.2023.1297444

5,004 views
3 citations

Case Report

Published on 15 Jan 2024

Case report: The evolving phenotype of ESCO2 spectrum disorder in a 15-year-old Malaysian child

in Genetics of Common and Rare Diseases

Sok-Kun Tae
Mazlan RA
Meow-Keong Thong

Frontiers in Genetics

doi 10.3389/fgene.2023.1286489

2,700 views
2 citations

Mini Review

Published on 12 Jan 2024

Machine learning and multi-omics data in chronic lymphocytic leukemia: the future of precision medicine?

in Cancer Genetics and Oncogenomics

Maria Tsagiopoulou
Ivo G. Gut

Frontiers in Genetics

doi 10.3389/fgene.2023.1304661

5,050 views
11 citations

Brief Research Report

Published on 12 Jan 2024

Mft1, identified from a genome-wide screen of the yeast haploid mutants, mediates cell cycle arrest to counteract quinoxaline-induced toxicity

in Predictive Toxicology and Exposomics

Abdallah Alhaj Sulaiman
Dana E. Al-Ansari
Reem Ali
Mustapha Aouida
Dindial Ramotar

Frontiers in Genetics

doi 10.3389/fgene.2023.1296383

3,474 views

Study Protocol

Published on 12 Jan 2024

Selective screening for inborn errors of metabolism using tandem mass spectrometry in West Kazakhstan children: study protocol

in Genetics of Common and Rare Diseases

Gulmira Zharmakhanova
Victoria Kononets
Saule Balmagambetova
Lyazzat Syrlybayeva
Eleonora Nurbaulina
Zhanna Zhussupova
Svetlana Sakhanova
Dinmukhamed Ayaganov
Svetlana Kim
Akmaral Zhumalina

Frontiers in Genetics

doi 10.3389/fgene.2023.1278750

5,561 views
3 citations

Original Research

Published on 12 Jan 2024

Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder

in Genetics of Common and Rare Diseases

Tayyaba Afsar
Hongxia Fu
Hammal Khan
Zain Ali
Zamrud Zehri
Gohar Zaman
Safdar Abbas
Arif Mahmood
Qamre Alam
Junjian Hu

Frontiers in Genetics

doi 10.3389/fgene.2023.1308116

3,956 views
1 citation

Original Research

Published on 12 Jan 2024

Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing

in Genetics of Common and Rare Diseases

Ismail Gouiza
Meriem Hechmi
Abir Zioudi
Hamza Dallali
Nadia Kheriji
Majida Charif
Morgane Le Mao
Said Galai
Lilia Kraoua
Ilhem Ben Youssef-Turki

Frontiers in Genetics

doi 10.3389/fgene.2023.1259826

4,294 views
3 citations

Original Research

Published on 12 Jan 2024

Genome-wide survey reveals the genetic background of Xinjiang Brown cattle in China

in Livestock Genomics

Xiao Wang
Zhen Ma
Liang Gao
Lixin Yuan
Zhibing Ye
Fanrong Cui
Xiaoping Guo
Wujun Liu
Xiangmin Yan

Frontiers in Genetics

doi 10.3389/fgene.2023.1348329

4,170 views
6 citations

Original Research

Published on 11 Jan 2024

Bibliometric and visual analysis of single-cell sequencing from 2010 to 2022

in Computational Genomics

Ling Chen
Yantong Wan
Tingting Yang
Qi Zhang
Yuting Zeng
Shuqi Zheng
Zhishan Ling
Yupeng Xiao
Qingyi Wan
Ruili Liu

Frontiers in Genetics

doi 10.3389/fgene.2023.1285599

5,081 views
8 citations

Original Research

Published on 11 Jan 2024

Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case–control study based on the China Neonatal Genomes Project

in Human and Medical Genomics

Xiao Wang
Tiantian Xiao
Jin Wang
Bingbing Wu
Huijun Wang
Yulan Lu
Yaqiong Wang
Bin Chen
Liyuan Hu
Yun Cao

Frontiers in Genetics

doi 10.3389/fgene.2023.1292921

4,097 views
3 citations

Original Research

Published on 11 Jan 2024

Diversity of antibiotic resistance gene variants at subsequent stages of the wastewater treatment process revealed by a metagenomic analysis of PCR amplicons

in Evolutionary and Genomic Microbiology

Adrian Gorecki
Piotr Ostapczuk
Lukasz Dziewit

Frontiers in Genetics

doi 10.3389/fgene.2023.1334646

4,241 views
2 citations

Original Research

Published on 11 Jan 2024

Novel cis compound heterozygous variants in MYO6 causes early onset of non-syndromic hearing loss in a Chinese family

in Genetics of Common and Rare Diseases

Haiting Ji
Lichun Zhang
Hafiz Muhammad Jafar Hussain
Ayesha Aftab
Huiqian Yu
Min Xiao

Frontiers in Genetics

doi 10.3389/fgene.2023.1275633

3,372 views

Original Research

Published on 11 Jan 2024

Genetics and clinical phenotypes in common variable immunodeficiency

in Genetics of Common and Rare Diseases

Charlotte Cunningham-Rundles
Jean-Laurent Casanova
Bertrand Boisson

Frontiers in Genetics

doi 10.3389/fgene.2023.1272912

14,410 views
34 citations

Original Research

Published on 11 Jan 2024

Empirical validation of ProteinMPNN’s efficiency in enhancing protein fitness

in Computational Genomics

Tianshu Wang
Xiaocheng Jin
Xiaoli Lu
Xiaoping Min
Shengxiang Ge
Shaowei Li

Frontiers in Genetics

doi 10.3389/fgene.2023.1347667

8,533 views
6 citations

Original Research

Published on 11 Jan 2024

Hereditary deafness carrier screening in 9,993 Chinese individuals

in Genetics of Common and Rare Diseases

Yanqiu Liu
Lei Wang
Lanlai Yuan
Yaqing Li
Zhengshi Chen
Bicheng Yang
Daqing Wang
Yu Sun

Frontiers in Genetics

doi 10.3389/fgene.2023.1327258

3,641 views
6 citations

Case Report

Published on 11 Jan 2024

Case Report: From epilepsy and uterus didelphys to Turner syndrome-associated dysgerminoma

in Genetics of Common and Rare Diseases

Jinghua Li
Haipeng Zhu
Xuelian Ma
Jia Li
Jing Xue
Limin Feng

Frontiers in Genetics

doi 10.3389/fgene.2023.1286515

3,031 views
1 citation

Original Research

Published on 11 Jan 2024

Genetically predicted circulating levels of cytokines and the risk of oral cavity and pharyngeal cancer: a bidirectional mendelian-randomization study

in Statistical Genetics and Methodology

Kehan Wu
Qianhui Sun
Dongxu Liu
Jiayi Lu
Deyu Wen
Xiyan Zang
Li Gao

Frontiers in Genetics

doi 10.3389/fgene.2023.1321484

3,915 views
1 citation

Original Research

Published on 11 Jan 2024

Assembly and analysis of the complete mitochondrial genome of the Chinese wild dwarf almond (Prunus tenella)

in Genomics of Plants and the Phytoecosystem

Xingyue Liu
Dongdong Zhang
Zhenfan Yu
Bin Zeng

Frontiers in Genetics

doi 10.3389/fgene.2023.1329060

2,972 views
8 citations

Original Research

Published on 11 Jan 2024

Identification of gene mutations associated with type 1 diabetes by next-generation sequencing in affected Palestinian families

in Genetics of Common and Rare Diseases

Abrar Bawatneh
Alaa Darwish
Hasan Eideh
Hisham M. Darwish

Frontiers in Genetics

doi 10.3389/fgene.2023.1292073

10,270 views
3 citations

Review

Published on 10 Jan 2024

The burden of cystic fibrosis in North Africa

in Genetics of Common and Rare Diseases

Nada El Makhzen
Houria Daimi
Laila Bouguenouch
Hugues Abriel

Frontiers in Genetics

doi 10.3389/fgene.2023.1295008

6,275 views
3 citations

16,588 articles

articles

Sister haplotypes and recombination disequilibrium: a new approach to identify associations of haplotypes with complex diseases

Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia

An in silico approach to identify potential downstream targets of miR-153 involved in Alzheimer’s disease

Methylenetetrahydrofolate reductase polymorphic variants C677T and A1298C in rectal cancer in Slavic population: significance for cancer risk and response to chemoradiotherapy

Genome-wide association with footrot in hair and wool sheep

Case report: The evolving phenotype of ESCO2 spectrum disorder in a 15-year-old Malaysian child

Machine learning and multi-omics data in chronic lymphocytic leukemia: the future of precision medicine?

Mft1, identified from a genome-wide screen of the yeast haploid mutants, mediates cell cycle arrest to counteract quinoxaline-induced toxicity

Selective screening for inborn errors of metabolism using tandem mass spectrometry in West Kazakhstan children: study protocol

Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder

Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing

Genome-wide survey reveals the genetic background of Xinjiang Brown cattle in China

Bibliometric and visual analysis of single-cell sequencing from 2010 to 2022

Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case–control study based on the China Neonatal Genomes Project

Diversity of antibiotic resistance gene variants at subsequent stages of the wastewater treatment process revealed by a metagenomic analysis of PCR amplicons

Novel cis compound heterozygous variants in MYO6 causes early onset of non-syndromic hearing loss in a Chinese family

Genetics and clinical phenotypes in common variable immunodeficiency

Empirical validation of ProteinMPNN’s efficiency in enhancing protein fitness

Hereditary deafness carrier screening in 9,993 Chinese individuals

Case Report: From epilepsy and uterus didelphys to Turner syndrome-associated dysgerminoma

Genetically predicted circulating levels of cytokines and the risk of oral cavity and pharyngeal cancer: a bidirectional mendelian-randomization study

Assembly and analysis of the complete mitochondrial genome of the Chinese wild dwarf almond (Prunus tenella)

Identification of gene mutations associated with type 1 diabetes by next-generation sequencing in affected Palestinian families

The burden of cystic fibrosis in North Africa