BRIEF RESEARCH REPORT
Published on 09 Jan 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
doi 10.3389/fgene.2022.1018062
- 1,824 views
- 1 citation
- Frontiers in Pediatrics
- Genetics of Common and Rare Diseases
- Research Topics
- Next-Generation Sequencing: An Ongoing Revolution in Pediatrics
Next-Generation Sequencing: An Ongoing Revolution in Pediatrics
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CASE REPORT
Published on 06 Oct 2022
Case report: Robust response of metastatic clear cell sarcoma treated with cabozantinib and immunotherapy
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- 2 citations
ORIGINAL RESEARCH
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Vici syndrome in Israel: Clinical and molecular insights
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BRIEF RESEARCH REPORT
Published on 14 Sep 2022
Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genes
doi 10.3389/fgene.2022.945296
- 1,428 views
- 7 citations
ORIGINAL RESEARCH
Published on 08 Sep 2022
Differences in severity of cardiovascular anomalies in children with Noonan syndrome based on the causative gene
doi 10.3389/fped.2022.946071
- 1,009 views
- 3 citations
CORRECTION
Published on 10 Aug 2022
Corrigendum: Transcriptional and epigenetic response to sedentary behavior and physical activity in children and adolescents: A systematic review
doi 10.3389/fped.2022.993123
- 909 views
ORIGINAL RESEARCH
Published on 04 Aug 2022
Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary Tract
doi 10.3389/fped.2022.898773
- 2,750 views
- 3 citations
ORIGINAL RESEARCH
Published on 27 Jul 2022
Novel NHEJ1 pathogenic variant linked to severe combined immunodeficiency, microcephaly, and abnormal T and B cell receptor repertoires
doi 10.3389/fped.2022.883173
- 1,810 views
- 3 citations
BRIEF RESEARCH REPORT
Published on 22 Jul 2022
Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center
doi 10.3389/fgene.2022.887698
- 998 views
- 2 citations
SYSTEMATIC REVIEW
Published on 24 Jun 2022
Transcriptional and Epigenetic Response to Sedentary Behavior and Physical Activity in Children and Adolescents: A Systematic Review
doi 10.3389/fped.2022.917152
- 4,154 views
- 10 citations
ORIGINAL RESEARCH
Published on 13 Jun 2022
A Collaborative Psychiatric-Genetics Inpatient Care Delivery Model Improves Access to Clinical Genetic Evaluation, Testing, and Diagnosis for Patients With Neurodevelopmental Disorders
doi 10.3389/fgene.2022.901458
- 1,684 views
- 2 citations
ORIGINAL RESEARCH
Published on 17 May 2022
A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay
doi 10.3389/fped.2022.859034
- 1,800 views
- 3 citations
Published in
Frontiers in Pediatrics
- Genetics of Common and Rare Diseases
- Children and Health
Participating Journals
Frontiers in Genetics
- 2.8 impact factor
- 5.5 citescore
Frontiers in Public Health
- 3.0 impact factor
- 4.8 citescore
Impact
- 34kTopic views
- 24kArticle views
- 9,289Article downloads