Review
Published on 04 Jan 2023
Single-cell omics: A new direction for functional genetic research in human diseases and animal models
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1100016
- 6,800 views
- 16 citations
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772 articles
Articles
Perspective
Published on 15 Dec 2022
Precision medicine implementation challenges for APOL1 testing in chronic kidney disease in admixed populations
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1016341
- 2,709 views
- 2 citations
Case Report
Published on 09 Dec 2022
Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1040124
- 2,881 views
- 4 citations
Original Research
Published on 05 Dec 2022
Diagnostic signature, subtype classification, and immune infiltration of key m6A regulators in osteomyelitis patients
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1044264
- 2,368 views
- 6 citations
Original Research
Published on 05 Dec 2022
Inflammation-related pathways involved in damaged articular cartilage of rats exposed to T-2 toxin based on RNA-sequencing analysis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1079739
- 2,457 views
- 8 citations
Original Research
Published on 01 Dec 2022
Screening and functional analysis of the differential peptides from the placenta of patients with healthy pregnancy and preeclampsia using placental peptidome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1014836
- 1,949 views
- 1 citation
Editorial
Published on 01 Dec 2022
Editorial: Genome-wide association studies of COVID-19 among diverse human populations
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1088026
- 1,975 views
- 1 citation
Original Research
Published on 30 Nov 2022
Targeted screening of genetic associations with COVID-19 susceptibility and severity
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1073880
- 3,623 views
- 9 citations
Original Research
Published on 29 Nov 2022
The role of angiotensin I converting enzyme insertion/deletion polymorphism in the severity and outcomes of COVID-19 patients
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1035796
- 1,589 views
- 1 citation
Original Research
Published on 28 Nov 2022
Identification and characterization of novel elastin gene mutations in eleven families with supravalvular aortic stenosis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1059640
- 2,689 views
- 4 citations
Case Report
Published on 25 Nov 2022
Case report: Identification of a frameshift mutation in GC enrichment and the GCC repeat region of the androgen insensitivity receptor (AR) gene in a patient with complete androgen insensitivity syndrome by whole-exome sequencing (WES) combined with specific PCR and deep sequencing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1038997
- 2,526 views
- 2 citations
Original Research
Published on 24 Nov 2022
Epigenomic signatures associated with spontaneous and replication stress-induced DNA double strand breaks
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.907547
- 3,216 views
- 2 citations
Review
Published on 24 Nov 2022
Genes in pediatric pulmonary arterial hypertension and the most promising BMPR2 gene therapy
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.961848
- 3,978 views
- 3 citations
Original Research
Published on 24 Nov 2022
Analyzing the Korean reference genome with meta-imputation increased the imputation accuracy and spectrum of rare variants in the Korean population
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1008646
- 3,304 views
- 5 citations
Original Research
Published on 22 Nov 2022
Causal effects of homocysteine levels on the components of sarcopenia: A two-sample mendelian randomization study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1051047
- 4,419 views
- 2 citations
Original Research
Published on 22 Nov 2022
Identifying key m6A-methylated lncRNAs and genes associated with neural tube defects via integrative MeRIP and RNA sequencing analyses
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.974357
- 2,494 views
- 5 citations