Michela Godi

466 total citations
18 papers, 323 citations indexed

About

Michela Godi is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Michela Godi has authored 18 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Endocrinology, Diabetes and Metabolism, 6 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Michela Godi's work include Growth Hormone and Insulin-like Growth Factors (10 papers), Genetic Syndromes and Imprinting (4 papers) and Cancer, Hypoxia, and Metabolism (3 papers). Michela Godi is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (10 papers), Genetic Syndromes and Imprinting (4 papers) and Cancer, Hypoxia, and Metabolism (3 papers). Michela Godi collaborates with scholars based in Italy, United States and Germany. Michela Godi's co-authors include Sandra D’Alfonso, Simona Mellone, Lucia Corrado, Letizia Mazzini, Gianni Bona, Mara Giordano, Paola Cerruti Mainardi, Yari Carlomagno, Chiara Castronovo and Alfredo Brusco and has published in prestigious journals such as Endocrine Reviews, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Michela Godi

18 papers receiving 318 citations

Peers

Countries citing papers authored by Michela Godi

Since Specialization

Citations

This map shows the geographic impact of Michela Godi'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 Michela Godi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michela Godi more than expected).

Fields of papers citing papers by Michela Godi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michela Godi. 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 Michela Godi. The network helps show where Michela Godi may publish in the future.

Co-authorship network of co-authors of Michela Godi

This figure shows the co-authorship network connecting the top 25 collaborators of Michela Godi. A scholar is included among the top collaborators of Michela Godi 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 Michela Godi. Michela Godi 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	Topical nerve growth factor prevents neurodegenerative and vascular stages of diabetic retinopathy 2022 ·Frontiers in Pharmacology ·Gianpaolo Zerbini, Silvia Maestroni, Letizia Leocani, Andrea Mosca, Michela Godi, Renata Paleari, (unknown), (unknown), Paola Tirassa, Valerio Castoldi, Ilaria Viganò, Silvia Galbiati, (unknown), Alessandro Lambìase, Paolo Rama	11
2	Rare Variants in theTREX1Gene and Susceptibility to Autoimmune Diseases 2013 ·BioMed Research International ·Nadia Barizzone, Sara Monti, Simona Mellone, Michela Godi, Maurizio Marchini, R Scorza, Maria Giovanna Danieli, Sandra D’Alfonso	27
3	The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism. 2013 ·PubMed ·Stefania Moia, Michela Godi, (unknown), (unknown), Patrizia Agretti, Massimo Tonacchera, Rosario Berardi, Simonetta Bellone, Flavia Prodam, Mara Giordano, Gianni Bona	3
4	Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD) 2012 ·The Journal of Clinical Endocrinology & Metabolism ·Michela Godi, Simona Mellone, (unknown), (unknown), Claudio Bardelli, Mariacarolina Salerno, Flavia Prodam, Simonetta Bellone, Antonella Petri, Patricia Momigliano‐Richiardi, Gianni Bona, Mara Giordano	3
5	A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing 2011 ·European Journal of Endocrinology ·Daniela Vivenza, Michela Godi, Maria Felicia Faienza, Simona Mellone, Stefania Moia, Anna Rapa, Antonella Petri, Simonetta Bellone, (unknown), Luciano Cavallo, Mara Giordano, Gianni Bona	11
6	ATXN-2 CAG repeat expansions are interrupted in ALS patients 2011 ·Human Genetics ·Lucia Corrado, Letizia Mazzini, Gaia Donata Oggioni, (unknown), Michela Godi, Alfredo Brusco, Sandra D’Alfonso	47
7	A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient 2010 ·Neurobiology of Aging ·Lucia Corrado, Yari Carlomagno, (unknown), Simona Mellone, Michela Godi, Emanuela Cova, Cristina Cereda, Lucia Testa, Letizia Mazzini, Sandra D’Alfonso	46
8	Growth Hormone (GH)-Releasing Hormone Increases the Expression of the Dominant-Negative GH Isoform in Cases of Isolated GH Deficiency due to GH Splice-Site Mutations 2010 ·Endocrinology ·Vibor Petkovic, Michela Godi, (unknown), Andrée Eblé, Christa E. Flück, Iain C. A. F. Robinson, Primus E. Mullis	13
9	Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action 2010 ·Endocrine Reviews ·Vibor Petkovic, Michela Godi, Amit V. Pandey, (unknown), Charles Buchanan, Mehul Dattani, Andrée Eblé, Christa E. Flück, Primus E. Mullis	1
10	A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency 2009 ·Journal of Endocrinological Investigation ·Yari Carlomagno, Mariacarolina Salerno, Daniela Vivenza, Donatella Capalbo, Michela Godi, Simona Mellone, (unknown), G. Corneli, Patricia Momigliano‐Richiardi, Gianni Bona, Mara Giordano	12
11	A Recurrent Signal Peptide Mutation in the Growth Hormone Releasing Hormone Receptor with Defective Translocation to the Cell Surface and Isolated Growth Hormone Deficiency 2009 ·The Journal of Clinical Endocrinology & Metabolism ·Michela Godi, Simona Mellone, Antonella Petri, Teresa Arrigo, Claudio Bardelli, Lucia Corrado, Simonetta Bellone, Flavia Prodam, Patricia Momigliano‐Richiardi, Gianni Bona, Mara Giordano	17
12	Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action 2009 ·The Journal of Clinical Endocrinology & Metabolism ·Vibor Petkovic, Michela Godi, Amit V. Pandey, (unknown), Charles Buchanan, Mehul Dattani, Andrée Eblé, Christa E. Flück, Primus E. Mullis	17
13	A Functional Common Polymorphism in the Vitamin D-Responsive Element of theGH1Promoter Contributes to Isolated Growth Hormone Deficiency 2007 ·The Journal of Clinical Endocrinology & Metabolism ·Mara Giordano, Michela Godi, Simona Mellone, Antonella Petri, Daniela Vivenza, (unknown), Yari Carlomagno, Daniela Ferrante, Teresa Arrigo, G. Corneli, Simonetta Bellone, Francesca Giacopelli, Claudio Santoro, Gianni Bona, Patricia Momigliano‐Richiardi	14
14	The natural history of Cri du Chat Syndrome. A report from the Italian Register 2006 ·European Journal of Medical Genetics ·Paola Cerruti Mainardi, Guido Pastore, Chiara Castronovo, Michela Godi, Andrea Guala, Stefania Tamiazzo, (unknown), Mauro Pierluigi, F. Dagna Bricarelli	60
15	A Novel Deletion in theGH1Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency 2006 ·The Journal of Clinical Endocrinology & Metabolism ·Daniela Vivenza, Laura Guazzarotti, Michela Godi, Daniela Frasca, Berardo di Natale, Patricia Momigliano‐Richiardi, Gianni Bona, Mara Giordano	19
16	A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity 2006 ·Molecular and Cellular Endocrinology ·Mara Giordano, Michela Godi, Francesca Giacopelli, (unknown), Simona Mellone, (unknown), Antonella Petri, J. Bellone, Roberto Ravazzolo, Gianni Bona, Patricia Momigliano‐Richiardi	12
17	Genitourinary Anomalies in Mowat-Wilson Syndrome with Deletion/Mutation in the Zinc Finger Homeo Box 1B Gene (ZFHX1B) 2005 ·Hormone Research in Paediatrics ·Livia Garavelli, (unknown), R Virdis, (unknown), Guido Pastore, Michela Godi, (unknown), Anita Rauch, Christiane Zweier, Marcella Zollino, G Banchini, Nicola Longo, David Mowat, Giovanni Neri, Sergio Bernasconi	8
18	Mowat-Wilson syndrome and mutation of the Zinc Finger Homeo Box 1B gene: A new syndrome probably under-diagnosed 2005 ·Paola Cerruti Mainardi, Livia Garavelli, Guido Pastore, R Virdis, (unknown), Michela Godi, (unknown), Anita Rauch, Christiane Zweier, Chiara Castronovo, Marcella Zollino, G Banchini, Sergio Bernasconi, Giovanni Neri	2

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