Concepedia

Author

Anna Maria Barbieri

University of MilanORCID

Also Known As

A M Barbieri, A. BARBIERI, A. M. Barbieri, A.M. Barbieri, Anna Maria Barbieri, Anna Maria Barbieri, Barbieri, Anna Maria

58

Publications

1.4K

Citations

19

H-Index

58

Concepts

All Affiliations

University of MilanFondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoIstituti di Ricovero e Cura a Carattere ScientificoHumanitas UniversityOspedale Maggiore
AM

About

Anna Maria Barbieri is an author at University of Milan specializing in medicine, genetics, and natural sciences.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

11

11

574

2

Natural Sciences

4

4

275

3

Cell Biology

3

3

167

4

Biochemistry

2

2

29

5

Biology

1

1

227

Anna Maria Barbieri

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27

Publications

1.4K

Citations

19

H-Index

YearCitations

Eukaryotic initiation factor 6 is rate-limiting in translation, growth and transformation

Valentina Gandin, Annarita Miluzio, Anna Maria Barbieri,

Nature

2008

227

A homeobox gene, <i>vax2</i> , controls the patterning of the eye dorsoventral axis

Anna Maria Barbieri, Giuseppe Lupo, Alessandro Bulfone,

Proceedings of the National Academy of Sciences

1999

151

Pseudohypoparathyroidism and<i>GNAS</i>Epigenetic Defects: Clinical Evaluation of Albright Hereditary Osteodystrophy and Molecular Analysis in 40 Patients

Giovanna Mantovani, Luisa De Sanctis, Anna Maria Barbieri,

The Journal of Clinical Endocrinology & Metabolism

2010

146

<i>Vax2</i>inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma

Anna Maria Barbieri, Vania Broccoli, Paola Bovolenta,

Development

2002

131

The limited role of midnight salivary cortisol levels in the diagnosis of subclinical hypercortisolism in patients with adrenal incidentaloma

Benedetta Masserini, Valentina Morelli, S. Bergamaschi,

European Journal of Endocrinology

2008

105

Pseudohypoparathyroidism Type Ia and Pseudo-Pseudohypoparathyroidism: The Growing Spectrum of<i>GNAS</i>Inactivating Mutations

Francesca Marta Elli, Luisa deSanctis, Barbara Ceoloni,

Human Mutation

2012

75

Quantitative Analysis of Methylation Defects and Correlation With Clinical Characteristics in Patients With Pseudohypoparathyroidism Type I and GNAS Epigenetic Alterations

Francesca Marta Elli, Luisa De Sanctis, Valentina Bollati,

The Journal of Clinical Endocrinology & Metabolism

2014

59

Adrenalectomy Improves Blood Pressure and Metabolic Control in Patients With Possible Autonomous Cortisol Secretion: Results of a RCT

Valentina Morelli, Sofía Frigerio, Carmen Aresta,

Frontiers in Endocrinology

2022

47

Dopamine D2 receptor gene polymorphisms and response to cabergoline therapy in patients with prolactin-secreting pituitary adenomas

Marcello Filopanti, Anna Maria Barbieri, Anita R. Angioni,

The Pharmacogenomics Journal

2008

41

Two novel nonsense mutations in GALNT3 gene are responsible for familial tumoral calcinosis

Anna Maria Barbieri, Marcello Filopanti, Guido Bua,

Journal of Human Genetics

2007

38

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