Original Research
Published on 03 Sep 2021
Intratumor Epigenetic Heterogeneity—A Panel Gene Methylation Study in Thyroid Cancer
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.714071
- 3,288 views
- 8 citations
Type at least 3 characters
773 articles
Articles
Original Research
Published on 03 Sep 2021
A Functional Variant of CXCL16 Is Associated With Predisposition to Sepsis and MODS in Trauma Patients: Genetic Association Studies
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.720313
- 2,656 views
- 4 citations
Review
Published on 01 Sep 2021
DNA Double-Strand Break Repair: All Roads Lead to HeterochROMAtin Marks
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.730696
- 7,610 views
- 19 citations
Original Research
Published on 31 Aug 2021
PLCE1 Polymorphisms Are Associated With Gastric Cancer Risk: The Changes in Protein Spatial Structure May Play a Potential Role
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.714915
- 2,776 views
- 6 citations
Original Research
Published on 30 Aug 2021
No Casual Relationship Between T2DM and the Risk of Infectious Diseases: A Two-Sample Mendelian Randomization Study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.720874
- 5,894 views
- 7 citations
Original Research
Published on 26 Aug 2021
Chromoanagenesis Event Underlies a de novo Pericentric and Multiple Paracentric Inversions in a Single Chromosome Causing Coffin–Siris Syndrome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.708348
- 4,239 views
- 7 citations
Original Research
Published on 26 Aug 2021
Exome Sequencing Reveals a Putative Role for HLA-C*03:02 in Control of HIV-1 in African Pediatric Populations
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.720213
- 4,015 views
- 5 citations
Original Research
Published on 19 Aug 2021
Clinical Utility of Rapid Exome Sequencing Combined With Mitochondrial DNA Sequencing in Critically Ill Pediatric Patients With Suspected Genetic Disorders
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.725259
- 5,766 views
- 13 citations
Original Research
Published on 19 Aug 2021
Identification of a Novel Glycolysis-Related LncRNA Signature for Predicting Overall Survival in Patients With Bladder Cancer
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.720421
- 3,351 views
- 14 citations
Original Research
Published on 17 Aug 2021
Protective Effect of TNFRSF11A rs7239667 G > C Gene Polymorphism on Coronary Outcome of Kawasaki Disease in Southern Chinese Population
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.691282
- 2,421 views
Case Report
Published on 10 Aug 2021
Case Report: A Novel Mutation in NFKB1 Associated With Pyoderma Gangrenosum
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.673453
- 3,604 views
- 11 citations
Mini Review
Published on 06 Aug 2021
The Path to Conserved Extended Haplotypes: Megabase-Length Haplotypes at High Population Frequency
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.716603
- 2,931 views
- 5 citations
Case Report
Published on 05 Aug 2021
Case Report: Whole Exome Sequencing Revealed Two Novel Mutations of PIEZO1 Implicated in Nonimmune Hydrops Fetalis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.684555
- 3,502 views
- 7 citations
Original Research
Published on 05 Aug 2021
Splicing Outcomes of 5′ Splice Site GT>GC Variants That Generate Wild-Type Transcripts Differ Significantly Between Full-Length and Minigene Splicing Assays
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.701652
- 6,849 views
- 12 citations
Mini Review
Published on 02 Aug 2021
Homologous Recombination Subpathways: A Tangle to Resolve
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.723847
- 13,854 views
- 32 citations
Original Research
Published on 30 Jul 2021
Deep Phenotyping and Genetic Characterization of a Cohort of 70 Individuals With 5p Minus Syndrome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2021.645595
- 8,514 views
- 9 citations