Aldo Giannotti - Concepedia

Author

Aldo Giannotti

Bambino Gesù Children's Hospital

Also Known As

A D Giannotti, A GIANNOTTI, A Giannotti, A. GIANNOTTI, A. Giannotti, Aldo Giannotti, April Giannotti

167

Publications

Citations

H-Index

132

Concepts

All Affiliations

Bambino Gesù Children's Hospital University of Rome Tor Vergata Istituti di Ricovero e Cura a Carattere Scientifico Sapienza University of Rome Casa Sollievo della Sofferenza

About

Aldo Giannotti is an author at Bambino Gesù Children's Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	39	2.1K
2	Health Sciences	4	4	114
3	Arts	1	1	67
4	Education	1	1	17
5	Natural Sciences	1	1	11

Aldo Giannotti

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly Luisa Nanni, Jeffrey E. Ming, Maureen Bocian, Human Molecular Genetics	1999	359
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal Bruno Marino, Maria Cristina Digilio, Alessandra Toscano, The Journal of Pediatrics Expanded Cardiac SpectrumHeart FailurePediatric Heart DiseasePediatricsCongenital Heart Defect	1999	254
Complete Transposition of the Great Arteries M. Cristina Digilio, Brett Casey, Alessandra Toscano, Circulation	2001	157
Anatomic patterns of conotruncal defects associated with deletion 22q11 Bruno Marino, M. Cristina Digilio, Alessandra Toscano, Genetics in Medicine Developmental AnomalyGross AnatomyDeletion 22Q11Surgical PathologyCongenital Disorders	2001	151
Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study Margherita Bonamico, P. Mariani, Helene Maria Danesi, Journal of Pediatric Gastroenterology and Nutrition	2001	143
Apparent preferential loss of heterozygosity atTSC2 overTSC1 chromosomal region in tuberous sclerosis hamartomas Caterina Carbonara, Lucia Longa, Enrico Grosso, Genes Chromosomes and Cancer	1996	133
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome Francesca Amati, Emanuela Conti, Antonio Novelli, European Journal of Human Genetics Cardiovascular DiseasePhysiologyDigeorge/velo-cardio-facial SyndromeCardiac PathologyNeurology	1999	133
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies MC Digilio, Adriano Angioni, Marco De Santis, Clinical Genetics	2003	126
22q11 deletions in isolated and syndromic patients with tetralogy of Fallot Francesca Amati, Aldo Mari, MariaCristina Digilio, Human Genetics Down SyndromeClinical DisordersNeurological DisorderClinical NeurologySyndromic Patients	1995	124
Coeliac disease in Williams syndrome: Table 1 Aldo Giannotti Journal of Medical Genetics	2001	112

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