Original Research
Published on 06 Sep 2022
Potential gene identification and pathway crosstalk analysis of age-related macular degeneration
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.992328
- 2,210 views
- 2 citations
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772 articles
Articles
Original Research
Published on 05 Sep 2022
The role of ACE1 I/D and ACE2 polymorphism in the outcome of Iranian COVID-19 patients: A case-control study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.955965
- 4,837 views
- 10 citations
Review
Published on 05 Sep 2022
Non-canonical DNA structures: Diversity and disease association
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.959258
- 15,392 views
- 37 citations
Original Research
Published on 02 Sep 2022
Family-based exome sequencing identifies candidate genes related to keratoconus in Chinese families
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.988620
- 1,864 views
- 4 citations
Original Research
Published on 02 Sep 2022
Interpreting the spectrum of gamma-secretase complex missense variation in the context of hidradenitis suppurativa—An in-silico study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.962449
- 2,805 views
- 12 citations
Original Research
Published on 02 Sep 2022
Association of genetic variants in ULK4 with the age of first onset of type B aortic dissection
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.956866
- 3,346 views
- 1 citation
Original Research
Published on 02 Sep 2022
Identifying celiac disease-related chemicals by transcriptome-wide association study and chemical-gene interaction analyses
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.990483
- 2,680 views
- 2 citations
Review
Published on 01 Sep 2022
Population-based screening of newborns: Findings from the newborn screening expansion study (part two)
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.867354
- 2,793 views
- 5 citations
Original Research
Published on 30 Aug 2022
Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.900574
- 4,230 views
- 17 citations
Review
Published on 30 Aug 2022
Non-canonical DNA/RNA structures associated with the pathogenesis of Fragile X-associated tremor/ataxia syndrome and Fragile X syndrome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.866021
- 2,921 views
- 2 citations
Original Research
Published on 29 Aug 2022
Implementation of a biochemical, clinical, and genetic screening programme for familial hypercholesterolemia in 26 centres in Spain: The ARIAN study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.971651
- 3,318 views
- 2 citations
Original Research
Published on 25 Aug 2022
Decoding regulatory associations of G-quadruplex with epigenetic and transcriptomic functional components
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.957023
- 2,837 views
- 5 citations
Editorial
Published on 25 Aug 2022
Editorial: Progress in understanding the immunogenetic basis of disease susceptibility and outcomes
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1007825
- 912 views
Correction
Published on 24 Aug 2022
Corrigendum: A potential indicator ARRDC2 has feasibility to evaluate prognosis and immune microenvironment in ovarian cancer
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.978493
- 964 views
Original Research
Published on 23 Aug 2022
DDX59-AS1 is a prognostic biomarker and correlated with immune infiltrates in OSCC
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.892727
- 2,843 views
- 4 citations
Editorial
Published on 23 Aug 2022
Editorial: Reproductive genomics
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1002458
- 2,724 views
- 1 citation