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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Michela Godi Italy 12 109 108 98 80 70 18 323
Malini Sathanoori United States 10 132 1.2× 153 1.4× 45 0.5× 31 0.4× 120 1.7× 21 462
Daniel Chesik Netherlands 15 60 0.6× 132 1.2× 129 1.3× 30 0.4× 14 0.2× 20 439
Louise Gregory United Kingdom 14 171 1.6× 224 2.1× 258 2.6× 31 0.4× 58 0.8× 25 520
Audrey Briand‐Suleau France 11 122 1.1× 168 1.6× 32 0.3× 151 1.9× 35 0.5× 16 437
Sietske H. Kevelam Netherlands 10 83 0.8× 283 2.6× 31 0.3× 100 1.3× 15 0.2× 11 473
Adam Mp 6 113 1.0× 180 1.7× 16 0.2× 30 0.4× 27 0.4× 286 388
Corinne Morel Switzerland 10 152 1.4× 179 1.7× 126 1.3× 57 0.7× 41 0.6× 16 506
Ardinger Hh United States 6 124 1.1× 192 1.8× 16 0.2× 30 0.4× 27 0.4× 287 402
Bean Ljh 6 113 1.0× 180 1.7× 16 0.2× 29 0.4× 26 0.4× 285 386
Esther Kinning United Kingdom 13 256 2.3× 321 3.0× 68 0.7× 34 0.4× 56 0.8× 28 556

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

18 of 18 papers shown
1.
Zerbini, Gianpaolo, Silvia Maestroni, Letizia Leocani, et al.. (2022). Topical nerve growth factor prevents neurodegenerative and vascular stages of diabetic retinopathy. Frontiers in Pharmacology. 13. 1015522–1015522. 11 indexed citations
2.
Barizzone, Nadia, Sara Monti, Simona Mellone, et al.. (2013). Rare Variants in theTREX1Gene and Susceptibility to Autoimmune Diseases. BioMed Research International. 2013. 1–6. 27 indexed citations
3.
Moia, Stefania, Michela Godi, Patrizia Agretti, et al.. (2013). The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism.. PubMed. 36(9). 716–21. 3 indexed citations
4.
Godi, Michela, Simona Mellone, Claudio Bardelli, et al.. (2012). Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD). The Journal of Clinical Endocrinology & Metabolism. 97(9). E1791–E1797. 3 indexed citations
5.
Vivenza, Daniela, Michela Godi, Maria Felicia Faienza, et al.. (2011). A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing. European Journal of Endocrinology. 164(5). 705–713. 11 indexed citations
6.
Corrado, Lucia, Letizia Mazzini, Gaia Donata Oggioni, et al.. (2011). ATXN-2 CAG repeat expansions are interrupted in ALS patients. Human Genetics. 130(4). 575–580. 47 indexed citations
7.
Corrado, Lucia, Yari Carlomagno, Simona Mellone, et al.. (2010). A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient. Neurobiology of Aging. 32(3). 552.e1–552.e6. 46 indexed citations
8.
Petkovic, Vibor, Michela Godi, Andrée Eblé, et al.. (2010). 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. Endocrinology. 151(6). 2650–2658. 13 indexed citations
9.
Petkovic, Vibor, Michela Godi, Amit V. Pandey, et al.. (2010). Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action. Endocrine Reviews. 31(1). 135–135. 1 indexed citations
10.
Carlomagno, Yari, Mariacarolina Salerno, Daniela Vivenza, et al.. (2009). A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency. Journal of Endocrinological Investigation. 32(8). 653–658. 12 indexed citations
11.
Godi, Michela, Simona Mellone, Antonella Petri, et al.. (2009). A Recurrent Signal Peptide Mutation in the Growth Hormone Releasing Hormone Receptor with Defective Translocation to the Cell Surface and Isolated Growth Hormone Deficiency. The Journal of Clinical Endocrinology & Metabolism. 94(10). 3939–3947. 17 indexed citations
12.
Petkovic, Vibor, Michela Godi, Amit V. Pandey, et al.. (2009). Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action. The Journal of Clinical Endocrinology & Metabolism. 95(2). 731–739. 17 indexed citations
13.
Giordano, Mara, Michela Godi, Simona Mellone, et al.. (2007). A Functional Common Polymorphism in the Vitamin D-Responsive Element of theGH1Promoter Contributes to Isolated Growth Hormone Deficiency. The Journal of Clinical Endocrinology & Metabolism. 93(3). 1005–1012. 14 indexed citations
14.
Mainardi, Paola Cerruti, Guido Pastore, Chiara Castronovo, et al.. (2006). The natural history of Cri du Chat Syndrome. A report from the Italian Register. European Journal of Medical Genetics. 49(5). 363–383. 60 indexed citations
15.
Vivenza, Daniela, Laura Guazzarotti, Michela Godi, et al.. (2006). A Novel Deletion in theGH1Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency. The Journal of Clinical Endocrinology & Metabolism. 91(3). 980–986. 19 indexed citations
16.
Giordano, Mara, Michela Godi, Francesca Giacopelli, et al.. (2006). A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity. Molecular and Cellular Endocrinology. 249(1-2). 51–57. 12 indexed citations
17.
Garavelli, Livia, R Virdis, Guido Pastore, et al.. (2005). Genitourinary Anomalies in Mowat-Wilson Syndrome with Deletion/Mutation in the Zinc Finger Homeo Box 1B Gene (ZFHX1B). Hormone Research in Paediatrics. 63(4). 187–192. 8 indexed citations
18.
Mainardi, Paola Cerruti, Livia Garavelli, Guido Pastore, et al.. (2005). Mowat-Wilson syndrome and mutation of the Zinc Finger Homeo Box 1B gene: A new syndrome probably under-diagnosed. 31(2). 116–125. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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