Angelo Selicorni
ScholarGPS® ID: 92302943160757
Affiliation History
Field
Medicine
Discipline
Pediatrics
Top Specialties
Medical Genetics | Mutation | Human Genetics | Intellectual Disability | Chromosome | Disability | Birth Defect | Nutrition | Human Mutation | Molecular Genetics | DNA | Microcephaly | Prenatal Testing | Rare Disease | Adolescence
Metrics Summary
Publication Count
248
Predicted Citations
10,284
Predicted h-index
50
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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SMC1A epilepsy syndrome: clinical data from a large international cohort (journal article) American Journal of Medical Genetics Part A, volume 194, issue 7 (2024). |
No COVID‐19 pandemic impact on incidence and clinical presentation of celiac disease in Italian children (journal article) Acta Paediatrica (2024). |
Sindrome da microdelezione 22Q11.2 (journal article) Medico e Bambino, volume 43, issue 5, pages 321-323 (2024). |
Double somatic mosaicism in Cornelia de Lange syndrome (journal article) American Journal of Medical Genetics Part A, volume 194, issue 5 (2024). |
La sindrome di Stickler (journal article) Medico e Bambino, volume 43, issue 4, pages 251-253 (2024). |
La sindrome di Klinefelter (journal article) Medico e Bambino, volume 43, issue 3, pages 181-183 (2024). |
La sindrome di klinefelter (journal article) Medico e Bambino, volume 43, issue 3, pages 191-193 (2024). |
Application of the Face2Gene tool in an Italian dysmorphological pediatric clinic: Retrospective validation and future perspectives (journal article) American Journal of Medical Genetics Part A, volume 194, issue 3 (2024). |
La sindrome di Sotos (journal article) Medico e Bambino, volume 43, issue 2, pages 113-115 (2024). |
La sindrome di Noonan (journal article) Medico e Bambino, volume 42, issue 10, pages 657-659 (2023). |
How pain affect real life of children and adults with achondroplasia: A systematic review (journal article) European Journal of Medical Genetics, volume 66, issue 11, pages 104850- (2023). |
Spettro Oculo-Auricolo-Vertebrale (journal article) Medico e Bambino, volume 42, issue 8, pages 521-522 (2023). |
American Journal of Medical Genetics Part A, volume 191, issue 8, pages 2249-2251 (2023). |
Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum (journal article) Frontiers in Genetics, volume 14 (2023). |
Nasal polyposis in pediatric patients with Cornelia de Lange syndrome: endoscopic diagnosis, treatment and follow up in two case reports (journal article) Italian Journal of Pediatrics, volume 49, issue 1 (2023). |
Italian Journal of Pediatrics, volume 49, issue 1 (2023). |
American Journal of Medical Genetics Part A, volume 191, issue 3, pages 823-830 (2023). |
Sindrome dell’X Fragile (journal article) Medico e Bambino, volume 42, issue 2, pages 119-120 (2023). |
American Journal of Medical Genetics Part A, volume 191, issue 2, pages 424-436 (2023). |
Celiac disease prevalence and predisposing‐HLA in a cohort of 93 Williams‐Beuren syndrome patients (journal article) American Journal of Medical Genetics Part A, volume 191, issue 1, pages 84-89 (2023). |