Original Research
Published on 15 Jan 2024
Genome-wide association with footrot in hair and wool sheep
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1297444
- 4,981 views
- 3 citations
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14,353 articles
articles
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
Frontiers in Genetics
doi 10.3389/fgene.2023.1299599
- 4,366 views
- 7 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1286489
- 2,679 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1304661
- 5,028 views
- 11 citations
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
Frontiers in Genetics
doi 10.3389/fgene.2023.1278750
- 5,530 views
- 3 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1296383
- 3,457 views
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
Frontiers in Genetics
doi 10.3389/fgene.2023.1308116
- 3,941 views
- 1 citation
Original Research
Published on 12 Jan 2024
Genome-wide survey reveals the genetic background of Xinjiang Brown cattle in China
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1348329
- 4,141 views
- 6 citations
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
Frontiers in Genetics
doi 10.3389/fgene.2023.1259826
- 4,268 views
- 3 citations
Original Research
Published on 11 Jan 2024
Bibliometric and visual analysis of single-cell sequencing from 2010 to 2022
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1285599
- 5,058 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1292921
- 4,079 views
- 2 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1334646
- 4,214 views
- 2 citations
Original Research
Published on 11 Jan 2024
Genetics and clinical phenotypes in common variable immunodeficiency
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1272912
- 13,693 views
- 34 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1275633
- 3,352 views
Original Research
Published on 11 Jan 2024
Empirical validation of ProteinMPNN’s efficiency in enhancing protein fitness
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1347667
- 8,503 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1327258
- 3,604 views
- 6 citations
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
Frontiers in Genetics
doi 10.3389/fgene.2023.1329060
- 2,953 views
- 7 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1292073
- 10,230 views
- 3 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1286515
- 3,016 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
Frontiers in Genetics
doi 10.3389/fgene.2023.1321484
- 3,892 views
- 1 citation
Review
Published on 10 Jan 2024
The burden of cystic fibrosis in North Africa
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1295008
- 6,235 views
- 2 citations
Original Research
Published on 10 Jan 2024
QTL mapping: insights into genomic regions governing component traits of yield under combined heat and drought stress in wheat
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2023.1282240
- 5,125 views
- 15 citations
Original Research
Published on 09 Jan 2024
Applying negative sample denoising and multi-view feature for lncRNA-disease association prediction
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2023.1332273
- 2,151 views
- 3 citations
Original Research
Published on 09 Jan 2024
Molecular epidemiological investigation of G6PD deficiency in Yangjiang region, western Guangdong province
in Applied Genetic Epidemiology
Frontiers in Genetics
doi 10.3389/fgene.2023.1345537
- 3,836 views
- 5 citations