Original Research
Published on 15 Sep 2023
Pregnancy outcomes and genetic analysis for fetal ventriculomegaly
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1186660
- 2,982 views
- 1 citation
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797 articles
Original Research
Published on 15 Sep 2023
Association study of WNK1 genetic variants and essential hypertension risk in the Northern Han Chinese in Beijing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1234536
- 1,583 views
- 1 citation
Perspective
Published on 11 Sep 2023
Rare blood group registry in India-current challenges and future perspectives
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1264853
- 12,476 views
- 5 citations
Editorial
Published on 11 Sep 2023
Editorial: Statistical methods for genome-wide association studies (GWAS) and transcriptome-wide association studies (TWAS) and their applications
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1287673
- 3,013 views
Original Research
Published on 08 Sep 2023
Identification of potential key variants in mandibular premolar hypodontia through whole-exome sequencing
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1248326
- 2,406 views
- 1 citation
Editorial
Published on 08 Sep 2023
Editorial: Biomedical application of DNA modifications
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1286185
- 1,991 views
Review
Published on 08 Sep 2023
Characterization and therapeutic perspectives of differentiation-inducing therapy in malignant tumors
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1271381
- 4,169 views
- 4 citations
Original Research
Published on 07 Sep 2023
ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1234032
- 3,480 views
- 2 citations
Original Research
Published on 05 Sep 2023
eoPred: predicting the placental phenotype of early-onset preeclampsia using public DNA methylation data
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1248088
- 2,591 views
- 2 citations
Case Report
Published on 31 Aug 2023
Case report: identification of one frameshift variant and two in cis non-canonical splice variants of NEB gene in prenatal arthrogryposis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1220170
- 1,490 views
Original Research
Published on 31 Aug 2023
Transcriptome profiling of intact bowel wall reveals that PDE1A and SEMA3D are possible markers with roles in enteric smooth muscle apoptosis, proliferative disorders, and dysautonomia in Crohn’s disease
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1194882
- 3,072 views
Original Research
Published on 29 Aug 2023
Identification of human genetic variants modulating the course of COVID-19 infection with importance in other viral infections
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1240245
- 3,549 views
- 5 citations
Original Research
Published on 29 Aug 2023
Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1240067
- 3,442 views
- 6 citations
Original Research
Published on 25 Aug 2023
Functional analysis of a novel nonsense variant c.91A>T of the TRAPPC2 gene in a Chinese family with X-linked recessive autosomal spondyloepiphyseal dysplasia tarda
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1216592
- 1,956 views
Case Report
Published on 25 Aug 2023
Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1208673
- 2,571 views
- 3 citations
Case Report
Published on 17 Aug 2023
Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1213283
- 2,636 views
- 3 citations