Graziella Pinto - Concepedia

Author

Graziella Pinto

Hôpital Necker-Enfants Malades ORCID

Also Known As

G Pinto, G. N. Pinto, G. Neves Pinto, G. Pinto, Genevive Baujat, Graziella Pinto, J. Cavaillé

127

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Assistance Publique – Hôpitaux de Paris Inserm Université Paris Cité Sorbonne Université

About

Graziella Pinto is an author at Hôpital Necker-Enfants Malades specializing in medicine, anesthesiology, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	517
2	Endocrinology	2	2	102
3	Health Sciences	1	1	72
4	Public Health	1	1	79
5	Molecular Genetics	1	1	16

Graziella Pinto

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations Irène Netchine, Sylvie Rossignol, Marie‐Noëlle Dufourg, The Journal of Clinical Endocrinology & Metabolism	2007	312
Long‐term efficacy of the interleukin‐1 receptor antagonist anakinra in ten patients with neonatal‐onset multisystem inflammatory disease/chronic infantile neurologic, cutaneous, articular syndrome Bénédicte Neven, Isabelle Marvillet, C. Terrada, Arthritis & Rheumatism	2009	252
Childhood Craniopharyngioma: Hypothalamus-Sparing Surgery Decreases the Risk of Obesity Églantine Elowe-Gruau, Jacques Beltrand, Raja Brauner, The Journal of Clinical Endocrinology & Metabolism	2013	206
Mutations in the Iodotyrosine Deiodinase Gene and Hypothyroidism J.C. Moreno, Hans van Toor, Graziella Pinto, New England Journal of Medicine	2008	194
Recurrent <i>PRKAR1A</i> Mutation in Acrodysostosis with Hormone Resistance Agnès Linglart, Alain Couvineau, Colette Auzan, New England Journal of Medicine	2011	172
CHARGE Syndrome Includes Hypogonadotropic Hypogonadism and Abnormal Olfactory Bulb Development Graziella Pinto, Véronique Abadie, Robin Mesnage, The Journal of Clinical Endocrinology & Metabolism	2005	150
Androgen Insensitivity Syndrome: Somatic Mosaicism of the Androgen Receptor in Seven Families and Consequences for Sex Assignment and Genetic Counseling Birgit Köhler, Serge Lumbroso, Juliane Léger, The Journal of Clinical Endocrinology & Metabolism	2005	115
Update on Lysinuric Protein Intolerance, a Multi-faceted Disease Retrospective cohort analysis from birth to adulthood Wladimir Mauhin, Florence Habarou, Stéphanie Gobin, Orphanet Journal of Rare Diseases	2017	111
Pituitary Stalk Interruption Syndrome: A Clinical-Biological-Genetic Assessment of Its Pathogenesis<sup>1</sup> Graziella Pinto, Irène Netchine, Marie‐Laure Sobrier, The Journal of Clinical Endocrinology & Metabolism	1997	108
Long-Term Outcome of Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Anne Bachelot, Geneviève Plu‐Bureau, E Thibaud, Hormone Research in Paediatrics	2006	105

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