Mini Review
Published on 03 Sep 2024
Advances in stem cell therapy for diabetic foot
in Stem Cell Research
Frontiers in Genetics
doi 10.3389/fgene.2024.1427205
- 2,709 views
- 1 citation
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15,639 articles
Articles
Review
Published on 03 Sep 2024
A comprehensive review of artificial intelligence for pharmacology research
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1450529
- 3,077 views
- 1 citation
Original Research
Published on 02 Sep 2024
Lipids, lipid-lowering drugs and lateral epicondylitis of the humerus: a drug-targeted Mendelian randomization study
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2024.1437712
- 1,291 views
Original Research
Published on 02 Sep 2024
Evidence of survival bias in the association between APOE-Є4 and age at ischemic stroke onset
in Genetics of Aging
Frontiers in Genetics
doi 10.3389/fgene.2024.1392061
- 1,266 views
Original Research
Published on 02 Sep 2024
Elucidating the role of hepatic enzymes in spontaneous abortion: a Mendelian randomization approach
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2024.1336728
- 1,301 views
Case Report
Published on 02 Sep 2024
Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1382275
- 1,082 views
Review
Published on 30 Aug 2024
Nutrigenomic underpinnings of intestinal stem cells in inflammatory bowel disease and colorectal cancer development
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1349717
- 2,164 views
- 1 citation
Data Report
Published on 30 Aug 2024
Genome assembly, characterization, and mining of biosynthetic gene clusters (BGCs) from Chlorogloeopsis sp. ULAP02 isolated from Mt. Ulap, Itogon, Benguet, Philippines
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2024.1422274
- 1,102 views
Original Research
Published on 30 Aug 2024
Causal role of gut microbiota, serum metabolites, immunophenotypes in myocarditis: a mendelian randomization study
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2024.1382502
- 1,254 views
Correction
Published on 30 Aug 2024
Corrigendum: Evidence for a genetic contribution to the ossification of spinal ligaments in ossification of posterior longitudinal ligament and diffuse idiopathic skeletal hyperostosis: a narrative review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1477788
- 700 views
Mini Review
Published on 30 Aug 2024
Human sulfotransferase SULT2B1 physiological role and the impact of genetic polymorphism on enzyme activity and pathological conditions
in Pharmacogenetics and Pharmacogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1464243
- 1,373 views
Original Research
Published on 30 Aug 2024
Identification and expression analysis of bZIP transcription factors in Setaria italica in response to dehydration stress
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2024.1466486
- 767 views
- 1 citation
Data Report
Published on 30 Aug 2024
Genome of Methylomonas sp. AM2-LC, representing a methanotrophic bacterial species isolated from water column of a boreal, oxygen-stratified lake
in Evolutionary and Population Genetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1440435
- 1,063 views
Original Research
Published on 30 Aug 2024
Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing
in Behavioral and Psychiatric Genetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1352480
- 3,478 views
- 1 citation
Original Research
Published on 30 Aug 2024
Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1421943
- 1,368 views
Original Research
Published on 29 Aug 2024
Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature
in Molecular Cytogenetics
Frontiers in Genetics
doi 10.3389/fgene.2024.1448341
- 1,312 views