ORIGINAL RESEARCH
Published on 19 Apr 2022
Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort
doi 10.3389/fgene.2022.818241
- 6,705 views
- 15 citations
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- Genetic and Environmental Factors in the Occurrence of Neonatal Disorders - Volume I
Genetic and Environmental Factors in the Occurrence of Neonatal Disorders - Volume I
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Articles
ORIGINAL RESEARCH
Published on 24 Mar 2022
SNP–SNP Interactions of Surfactant Protein Genes in Persistent Respiratory Morbidity Susceptibility in Previously Healthy Children
doi 10.3389/fgene.2022.815727
- 1,228 views
- 6 citations
CASE REPORT
Published on 14 Mar 2022
Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1
doi 10.3389/fgene.2022.843931
- 1,800 views
- 3 citations
ORIGINAL RESEARCH
Published on 10 Mar 2022
Novel Biallelic Variant in the BRAT1 Gene Caused Nonprogressive Cerebellar Ataxia Syndrome
doi 10.3389/fgene.2022.821587
- 2,627 views
- 5 citations
ORIGINAL RESEARCH
Published on 07 Mar 2022
LncRNA-RMST Functions as a Transcriptional Co-regulator of SOX2 to Regulate miR-1251 in the Progression of Hirschsprung's Disease
doi 10.3389/fped.2022.749107
- 1,708 views
- 10 citations
CASE REPORT
Published on 02 Feb 2022
Renal Involvement in IPEX Syndrome With a Novel Mutation of FOXP3: A Case Report
doi 10.3389/fgene.2021.752775
- 1,726 views
- 3 citations
ORIGINAL RESEARCH
Published on 18 Oct 2021
Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes?
doi 10.3389/fped.2021.727301
- 44,577 views
- 5 citations
ORIGINAL RESEARCH
Published on 04 Oct 2021
Single Nucleotide Polymorphisms Interactions of the Surfactant Protein Genes Associated With Respiratory Distress Syndrome Susceptibility in Preterm Infants
doi 10.3389/fped.2021.682160
- 2,034 views
- 9 citations
ORIGINAL RESEARCH
Published on 04 Aug 2021
High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing
doi 10.3389/fgene.2021.677748
- 1,961 views
- 5 citations
ORIGINAL RESEARCH
Published on 02 Jul 2021
Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information
doi 10.3389/fgene.2021.689071
- 3,134 views
- 29 citations
Published in
Frontiers in Genetics
- Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Pediatrics
- 2.1 impact factor
- 3.6 citescore
Impact
- 50kTopic views
- 39kArticle views
- 9,387Article downloads