Editorial
Published on 10 Jul 2023
Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1249585
- 2,163 views
- 2 citations
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772 articles
Articles
Correction
Published on 10 Jul 2023
Corrigendum: 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.2023.1198975
- 1,314 views
Case Report
Published on 06 Jul 2023
Homozygous deep intronic variant in SNX14 cause autosomal recessive Spinocerebellar ataxia 20: a case report
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1197681
- 2,860 views
- 1 citation
Case Report
Published on 05 Jul 2023
Case report: A novel SON mutation in a Colombian patient with ZTTK syndrome
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1183362
- 3,675 views
- 1 citation
Original Research
Published on 05 Jul 2023
Integrative profiling of extrachromosomal circular DNA in placenta and maternal plasma provides insights into the biology of fetal growth restriction and reveals potential biomarkers
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1128082
- 4,758 views
- 1 citation
Original Research
Published on 04 Jul 2023
Gene set variation analysis-based aging and senescence score as a prognostic indicator and therapeutic guide in lung adenocarcinoma
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1176292
- 2,468 views
- 2 citations
Original Research
Published on 29 Jun 2023
Chromatin structure and context-dependent sequence features control prime editing efficiency
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1222112
- 4,480 views
- 4 citations
Original Research
Published on 29 Jun 2023
COVID-19 severity: does the genetic landscape of rare variants matter?
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1152768
- 4,465 views
- 7 citations
Original Research
Published on 28 Jun 2023
Genetic insight into the putative causal proteins and druggable targets of osteoporosis: a large-scale proteome-wide mendelian randomization study
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1161817
- 7,154 views
- 3 citations
Editorial
Published on 26 Jun 2023
Editorial: Enhanced biological mechanism study, drug discovery and individualized medicine with single-cell multiomics data and integrative analysis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1236126
- 1,134 views
Original Research
Published on 22 Jun 2023
Double whammy: the genetic variants in CECR2 and high Hcy on the development of neural tube defects
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1189847
- 2,183 views
Original Research
Published on 16 Jun 2023
Integrative analysis of DNA methylomes reveals novel cell-free biomarkers in lung adenocarcinoma
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1175784
- 3,101 views
Case Report
Published on 16 Jun 2023
Case report: Application of targeted NGS for the detection of non-canonical driver variants in MPN
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1198834
- 3,190 views
- 1 citation
Original Research
Published on 15 Jun 2023
Advanced maternal age: copy number variations and pregnancy outcomes
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1206855
- 3,620 views
- 3 citations
Original Research
Published on 14 Jun 2023
Altered DNA methylome profiles of blood leukocytes in Chinese patients with mild cognitive impairment and Alzheimer’s disease
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1175864
- 2,868 views
- 3 citations
Original Research
Published on 13 Jun 2023
Identification of a novel candidate HSD3B2 gene variant for familial hypospadias by whole-exome sequencing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1106933
- 1,629 views