BRIEF RESEARCH REPORT
Published on 07 Aug 2023
Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?
doi 10.3389/fgene.2023.1031074
- 1,682 views
- 5 citations
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- The Nexus of Respiratory Control, Autonomic, and Hypothalamic Disorders: Overlapping Phenotypes in CCHS, ROHHAD, and Prader-Willi Syndromes
The Nexus of Respiratory Control, Autonomic, and Hypothalamic Disorders: Overlapping Phenotypes in CCHS, ROHHAD, and Prader-Willi Syndromes
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Articles
ORIGINAL RESEARCH
Published on 10 May 2023
Analysis and comparisons of gene expression changes in patient- derived neurons from ROHHAD, CCHS, and PWS
doi 10.3389/fped.2023.1090084
- 2,069 views
- 6 citations
CASE REPORT
Published on 22 Mar 2023
HIDEA syndrome: A new case report highlighting similarities with ROHHAD syndrome
doi 10.3389/fgene.2023.1137767
- 1,718 views
- 4 citations
CASE REPORT
Published on 15 Feb 2023
Case Report: A novel PHOX2B p.Ala248_Ala266dup variant causing congenital central hypoventilation syndrome
doi 10.3389/fped.2022.1070303
- 2,087 views
- 2 citations
ORIGINAL RESEARCH
Published on 31 Aug 2022
ROHHAD syndrome without rapid-onset obesity: A diagnosis challenge
doi 10.3389/fped.2022.910099
- 4,108 views
- 7 citations
Published in
Frontiers in Genetics
Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Pediatrics
- 2.1 impact factor
- 3.6 citescore