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
- 2,758 views
- 1 citation
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846 articles
articles
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
- 5,363 views
- 13 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
- 2,639 views
- 3 citations
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
- 4,795 views
- 9 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
- 3,603 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
- 4,446 views
- 2 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
- 5,585 views
- 19 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
- 7,561 views
- 8 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
- 4,047 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
- 6,003 views
- 10 citations
Original Research
Published on 22 Nov 2022
Identification of subtypes of hepatocellular carcinoma and screening of prognostic molecular diagnostic markers based on cell adhesion molecule related genes
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1042540
- 4,508 views
- 4 citations
Editorial
Published on 18 Nov 2022
Editorial: Cancer systems biology
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1083902
- 3,293 views
Original Research
Published on 18 Nov 2022
Abnormal expression of TSG-6 disturbs extracellular matrix homeostasis in chondrocytes from endemic osteoarthritis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1064565
- 5,605 views
- 16 citations
Case Report
Published on 18 Nov 2022
Case report and a brief review: Analysis and challenges of prenatal imaging phenotypes and genotypes in Joubert syndrome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1038274
- 4,199 views
- 12 citations
Original Research
Published on 17 Nov 2022
Integration of small RNAs from plasma and cerebrospinal fluid for classification of multiple sclerosis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1042483
- 3,481 views
- 2 citations
Original Research
Published on 17 Nov 2022
Identification of four novel variants in the CDH23 gene from four affected families with hearing loss
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1027396
- 3,493 views
- 8 citations
Brief Research Report
Published on 14 Nov 2022
Establishment of transgenic pigs overexpressing human PKD2-D511V mutant
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1059682
- 2,646 views
Case Report
Published on 09 Nov 2022
Case Report: Novel pathogenic variant in NFIX in two sisters with Malan syndrome due to germline mosaicism
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1044660
- 2,692 views
- 3 citations
Original Research
Published on 09 Nov 2022
Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1035468
- 4,840 views
- 4 citations
Review
Published on 08 Nov 2022
Clinical detection, diagnosis and treatment of morphological abnormalities of sperm flagella: A review of literature
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1034951
- 10,074 views
- 33 citations
Original Research
Published on 07 Nov 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.953762
- 3,978 views
- 9 citations
Case Report
Published on 31 Oct 2022
Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1020525
- 3,305 views
- 1 citation
Editorial
Published on 28 Oct 2022
Editorial: Genetics and mechanism of ciliopathies
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1067168
- 2,535 views
Original Research
Published on 26 Oct 2022
Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.995488
- 5,792 views
- 14 citations