Original Research
Accepted on 16 May 2024
The performance evaluation of NIPT for fetal chromosome microdeletion/microduplication detection: a retrospective analysis of 68,588 Chinese cases
Frontiers in Genetics
doi 10.3389/fgene.2024.1390539
Volumes
14,835 Publications
Volume 15 - 2024
Original Research
Accepted on 16 May 2024
Comparison of the classifiers based on mRNA, microRNA and lncRNA expression and DNA methylation profiles for the tumor origin detection
Frontiers in Genetics
doi 10.3389/fgene.2024.1383852
Editorial
Accepted on 16 May 2024
Editorial: Full Landscape of Human Genomic Diversity and Its Impact on Precision Medicine
Frontiers in Genetics
doi 10.3389/fgene.2024.1432509
Editorial
Accepted on 16 May 2024
Editorial : Seaweed Phylogenetics, Evolution, and Biogeography
Frontiers in Genetics
doi 10.3389/fgene.2024.1429024
Original Research
Accepted on 16 May 2024
Association between genetically proxied glucosamine and risk of cancer and non-neoplastic disease: A Mendelian randomization study
Frontiers in Genetics
doi 10.3389/fgene.2024.1293668
Original Research
Accepted on 16 May 2024
Revealing the Genetic Complexity of Hypothyroidism: Integrating Complementary Association Methods
Frontiers in Genetics
doi 10.3389/fgene.2024.1409226
Original Research
Published on 16 May 2024
Community-based breeding programs can realize sustainable genetic gain and economic benefits in tropical dairy cattle systems
Frontiers in Genetics
doi 10.3389/fgene.2024.1106709
- 177 views
Methods
Published on 16 May 2024
Longitudinal method comparison: modeling polygenic risk for post-traumatic stress disorder over time in individuals of African and European ancestry
Frontiers in Genetics
doi 10.3389/fgene.2024.1203577
- 115 views
Mini Review
Published on 16 May 2024
Histone methylation: at the crossroad between circadian rhythms in transcription and metabolism
Frontiers in Genetics
doi 10.3389/fgene.2024.1343030
- 191 views
Original Research
Published on 16 May 2024
The NM_033380.2 transcript of the COL4A5 gene contains a variable splice site c.4822–10T>C, which has been identified as a causative factor for Alport syndrome
Frontiers in Genetics
doi 10.3389/fgene.2024.1330525
- 104 views
Original Research
Published on 16 May 2024
A panel based on three-miRNAs as diagnostic biomarker for prostate cancer
Frontiers in Genetics
doi 10.3389/fgene.2024.1371441
- 122 views
Data Report
Published on 16 May 2024
Assessing the impact of sequencing platforms and analytical pipelines on whole-exome sequencing
Frontiers in Genetics
doi 10.3389/fgene.2024.1334075
- 137 views
Original Research
Published on 16 May 2024
A novel homozygous RSPH4A variant in a family with primary ciliary dyskinesia and literature review
Frontiers in Genetics
doi 10.3389/fgene.2024.1364476
- 119 views
Original Research
Published on 16 May 2024
Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities: case report and literature review
Frontiers in Genetics
doi 10.3389/fgene.2024.1351710
- 163 views
Original Research
Accepted on 15 May 2024
The causal effect of Alzheimer's disease and family history of Alzheimer's disease on non-ischemic cardiomyopathy and left ventricular structure and function: A Mendelian randomization study
Frontiers in Genetics
doi 10.3389/fgene.2024.1379865
Original Research
Accepted on 15 May 2024
Karyotype depends on sperm head morphology in some amniote groups
Frontiers in Genetics
doi 10.3389/fgene.2024.1396530