I. Zamproni

1.5k total citations · 1 hit paper
18 papers, 1.1k citations indexed

About

I. Zamproni is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Emergency Medicine. According to data from OpenAlex, I. Zamproni has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Endocrinology, Diabetes and Metabolism, 6 papers in Molecular Biology and 6 papers in Emergency Medicine. Recurrent topics in I. Zamproni's work include HIV-related health complications and treatments (6 papers), Thyroid Disorders and Treatments (5 papers) and Neonatal Health and Biochemistry (3 papers). I. Zamproni is often cited by papers focused on HIV-related health complications and treatments (6 papers), Thyroid Disorders and Treatments (5 papers) and Neonatal Health and Biochemistry (3 papers). I. Zamproni collaborates with scholars based in Italy, United States and Switzerland. I. Zamproni's co-authors include Stefano Mora, Giovanna Weber, Laura Fugazzola, Stefania Di Candia, Maria Cristina Vigone, Luca Persani, Maria Carla Proverbio, G Chiumello, Paola Sogno Valin and A. Gessi and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Bone and Mineral Research.

In The Last Decade

I. Zamproni

18 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy

2013 387 citations Paola Sogno Valin, Maria Carla Proverbio et al. Hormone Research in Paediatrics profile →

Peers

Countries citing papers authored by I. Zamproni

Since Specialization

Citations

This map shows the geographic impact of I. Zamproni's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by I. Zamproni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I. Zamproni more than expected).

Fields of papers citing papers by I. Zamproni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I. Zamproni. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by I. Zamproni. The network helps show where I. Zamproni may publish in the future.

Co-authorship network of co-authors of I. Zamproni

This figure shows the co-authorship network connecting the top 25 collaborators of I. Zamproni. A scholar is included among the top collaborators of I. Zamproni based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with I. Zamproni. I. Zamproni is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	The Clinical and Molecular Characterization of Patients With Dyshormonogenic Congenital Hypothyroidism Reveals Specific Diagnostic Clues for DUOX2 Defects 2014 ·The Journal of Clinical Endocrinology & Metabolism ·Marina Muzza, (unknown), Maria Cristina Vigone, I. Zamproni, Valentina Cirello, (unknown), (unknown), Nadia Schoenmakers, Luciano Beccaria, Francesco Gallo, (unknown), P. Beck‐Peccoz, Luca Persani, Giovanna Weber, Laura Fugazzola	55
2	Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy breakdown → 2013 ·Hormone Research in Paediatrics ·Paola Sogno Valin, Maria Carla Proverbio, Cecilia Diceglie, A. Gessi, Stefania Di Candia, Benedetta Mariani, I. Zamproni, Eleonora Mangano, Rosanna Asselta, Cristina Battaglia, Manuela Caruso‐Nicoletti, Stefano Mora, Alessandro Salvatoni	387
3	Whole Genome SNP Genotyping and Exome Sequencing Reveal Novel Genetic Variants and Putative Causative Genes in Congenital Hyperinsulinism 2013 ·PLoS ONE ·Maria Carla Proverbio, Eleonora Mangano, A. Gessi, Roberta Bordoni, Roberta Spinelli, Rosanna Asselta, Paola Sogno Valin, Stefania Di Candia, I. Zamproni, Cecilia Diceglie, Stefano Mora, Manuela Caruso‐Nicoletti, Alessandro Salvatoni, Gianluca De Bellis, Cristina Battaglia	37
4	Congenital Hypothyroidism With Eutopic Thyroid Gland: Analysis of Clinical and Biochemical Features at Diagnosis and After Re-Evaluation 2013 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Maria Cristina Vigone, Francesca Cortinovis, I. Zamproni, Laura Fugazzola, Luca Persani, Carlo Corbetta, G Chiumello, Giovanna Weber	99
5	Genetic defects of hydrogen peroxide generation in the thyroid gland. 2013 ·PubMed ·Giovanna Weber, (unknown), I. Zamproni, Laura Fugazzola	27
6	Tenofovir Disoproxil Fumarate and Bone Mineral Density: A 60-Month Longitudinal Study in a Cohort of H V -Infected Youths 2010 ·Antiviral Therapy ·M Viganò, Gianvincenzo Zuccotti, (unknown), (unknown), I. Zamproni, Chiara Cerini, Valentina Fabiano, Vania Giacomet, Stefano Mora	35
7	Pseudohypoparathyroidism, an often delayed diagnosis: a case series 2009 ·Cases Journal ·(unknown), Stefano Mora, I. Zamproni, G Chiumello, Giovanna Weber	11
8	Differential effect of age, gender and puberty on bone formation rate assessed by measurement of bone-specific alkaline phosphatase in healthy Italian children and adolescents 2009 ·Journal of Bone and Mineral Metabolism ·Stefano Mora, (unknown), (unknown), (unknown), I. Zamproni, Vania Giacomet, M Viganò	15
9	Biallelic Inactivation of the Dual Oxidase Maturation Factor 2 (DUOXA2) Gene as a Novel Cause of Congenital Hypothyroidism 2007 ·The Journal of Clinical Endocrinology & Metabolism ·I. Zamproni, Helmut Grasberger, Francesca Cortinovis, Maria Cristina Vigone, G Chiumello, Stefano Mora, Kazumichi Onigata, Laura Fugazzola, Samuel Refetoff, Luca Persani, Giovanna Weber	119
10	Identification of two Novel Frameshift Mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy 2007 ·Experimental and Molecular Pathology ·(unknown), Maria Carla Proverbio, (unknown), F. Gervasi, Ermanna Rovida, (unknown), (unknown), Paola Sogno Valin, Luca Albarello, I. Zamproni, (unknown), Claudio Doglioni, Stefano Mora, G Chiumello, Ida Biunno	5
11	Alterations in circulating osteoimmune factors may be responsible for high bone resorption rate in HIV-infected children and adolescents 2007 ·AIDS ·Stefano Mora, I. Zamproni, (unknown), Vania Giacomet, (unknown), Gianvincenzo Zuccotti, M Viganò	26
12	Normalization of Fat Accrual in Lipoatrophic, HIV-Infected Children Switched from Stavudine to Tenofovir and from Protease Inhibitor to Efavirenz 2007 ·Antiviral Therapy ·M Viganò, Paolo Brambilla, (unknown), Vania Giacomet, (unknown), I. Zamproni, Gianvincenzo Zuccotti, Stefano Mora	29
13	Analysis of Bone Mineral Content in Horizontally HIV-Infected Children Naïve to Antiretroviral Treatment 2005 ·Calcified Tissue International ·Stefano Mora, I. Zamproni, Vania Giacomet, (unknown), (unknown), M Viganò	7
14	Persistent mild hypothyroidism associated with novel sequence variants of theDUOX2 gene in two siblings 2005 ·Human Mutation ·Maria Cristina Vigone, Laura Fugazzola, I. Zamproni, Arianna Passoni, Stefania Di Candia, G Chiumello, Luca Persani, Giovanna Weber	95
15	Analysis of Bone Mineral Content in Horizontally HIV-Infected Children Naïve to Antiretroviral Treatment 2004 ·Calcified Tissue International ·Stefano Mora, I. Zamproni, Vania Giacomet, (unknown), (unknown), M Viganò	31
16	Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancy 2004 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·(unknown), Maria Carla Proverbio, Giulia Malferrari, (unknown), P. Boettcher, Roberto Dominici, Eugenia Monferini, (unknown), Monica Cattaneo, Davide Antonello, (unknown), I. Zamproni, Matteo Viscardi, G Chiumello, Ida Biunno	4
17	Longitudinal Changes of Bone Mineral Density and Metabolism in Antiretroviral-Treated Human Immunodeficiency Virus-Infected Children 2004 ·The Journal of Clinical Endocrinology & Metabolism ·Stefano Mora, I. Zamproni, Sabrina Beccio, Roberta Bianchi, Vania Giacomet, M Viganò	74
18	Autosomal Dominant Hypocalcemia in Monozygotic Twins Caused by a De Novo Germline Mutation Near the Amino-Terminus of the Human Calcium Receptor 2004 ·Journal of Bone and Mineral Research ·Jianxin Hu, Stefano Mora, Giovanna Weber, I. Zamproni, Maria Carla Proverbio, Allen M. Spiegel	19

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