Review
Published on 30 Sep 2022
Genetic heterogeneity in corpus callosum agenesis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.958570
- 21,339 views
- 32 citations
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847 articles
articles
Original Research
Published on 30 Sep 2022
Identification of CD161 expression as a novel prognostic biomarker in breast cancer correlated with immune infiltration
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.996345
- 3,912 views
- 4 citations
Original Research
Published on 30 Sep 2022
A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1017302
- 3,937 views
- 8 citations
Original Research
Published on 30 Sep 2022
CFAP300 mutation causing primary ciliary dyskinesia in Finland
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.985227
- 4,750 views
- 13 citations
Review
Published on 29 Sep 2022
Pharmacogenomics of drug transporters for antiretroviral long-acting pre-exposure prophylaxis for HIV
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.940661
- 5,547 views
- 7 citations
Original Research
Published on 29 Sep 2022
Comprehensive analysis of m7G modification patterns based on potential m7G regulators and tumor microenvironment infiltration characterization in lung adenocarcinoma
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.996950
- 3,463 views
- 3 citations
Original Research
Published on 29 Sep 2022
Study on complications of osteoporosis based on network pharmacology
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.941098
- 4,388 views
- 3 citations
Original Research
Published on 28 Sep 2022
Polymorphisms of pharmacogenetic candidate genes affect etomidate anesthesia susceptibility
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.999132
- 3,343 views
- 5 citations
Case Report
Published on 27 Sep 2022
Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1001105
- 6,466 views
- 24 citations
Original Research
Published on 27 Sep 2022
FISH analysis of numerical chromosomal abnormalities in the sperm of robertsonian translocation der(13; 14)(q10;q10) carriers
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1010568
- 3,801 views
- 3 citations
Original Research
Published on 26 Sep 2022
Leader gene identification for digestive system cancers based on human subcellular location and cancer-related characteristics in protein–protein interaction networks
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.919210
- 2,359 views
- 2 citations
Case Report
Published on 23 Sep 2022
Birth of a boy after intracytoplasmic sperm injection using ejaculated spermatozoa from a nonmosaic klinefelter syndrome man with normal sperm motility: A case report
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.989701
- 3,616 views
- 6 citations
Original Research
Published on 19 Sep 2022
Systemic lupus erythematosus variants modulate the function of an enhancer upstream of TNFAIP3
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1011965
- 4,650 views
- 12 citations
Original Research
Published on 19 Sep 2022
Causal effect of serum 25-hydroxyvitamin D levels on low back pain: A two-sample mendelian randomization study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1001265
- 7,522 views
- 19 citations
Original Research
Published on 15 Sep 2022
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.951829
- 3,480 views
- 2 citations
Editorial
Published on 15 Sep 2022
Editorial: Time, genetics, and complex disease
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1016049
- 3,228 views
Original Research
Published on 15 Sep 2022
Economic evaluation of using polygenic risk score to guide risk screening and interventions for the prevention of type 2 diabetes in individuals with high overall baseline risk
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.880799
- 5,232 views
- 13 citations
Editorial
Published on 15 Sep 2022
Editorial: Cholesterol and cancer drug resistance: Molecular, signaling, and therapeutic aspects
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.994181
- 2,137 views
- 2 citations
Original Research
Published on 13 Sep 2022
Microtubule modification defects underlie cilium degeneration in cell models of retinitis pigmentosa associated with pre-mRNA splicing factor mutations
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1009430
- 5,808 views
- 10 citations
Original Research
Published on 13 Sep 2022
Synergistic effects of rare variants of ARHGAP31 and FBLN1 in vitro in terminal transverse limb defects
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.946854
- 3,871 views
- 4 citations
Original Research
Published on 12 Sep 2022
Comprehensive analysis of the expression of N6-methyladenosine RNA methylation regulators in pulmonary artery hypertension
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.974740
- 7,713 views
- 15 citations
Brief Research Report
Published on 09 Sep 2022
A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.988202
- 3,373 views
- 4 citations
Mini Review
Published on 09 Sep 2022
Molecular mechanism of ferroptosis and its role in the occurrence and treatment of diabetes
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1018829
- 7,916 views
- 17 citations
Case Report
Published on 09 Sep 2022
A novel mutation in SPINK5 gene underlies a case of atypical Netherton syndrome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.943264
- 5,340 views
- 2 citations