Stefania Moia

407 total citations
14 papers, 297 citations indexed

About

Stefania Moia is a scholar working on Endocrinology, Diabetes and Metabolism, Endocrine and Autonomic Systems and Physiology. According to data from OpenAlex, Stefania Moia has authored 14 papers receiving a total of 297 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Endocrinology, Diabetes and Metabolism, 4 papers in Endocrine and Autonomic Systems and 4 papers in Physiology. Recurrent topics in Stefania Moia's work include Growth Hormone and Insulin-like Growth Factors (6 papers), Regulation of Appetite and Obesity (4 papers) and Thyroid Disorders and Treatments (3 papers). Stefania Moia is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (6 papers), Regulation of Appetite and Obesity (4 papers) and Thyroid Disorders and Treatments (3 papers). Stefania Moia collaborates with scholars based in Italy. Stefania Moia's co-authors include Gianni Bona, Simonetta Bellone, Flavia Prodam, Anna Rapa, Alice Monzani, Gillian E. Walker, Roberta Ricotti, Antonella Petri, Francesca Teofoli and Alessandra Cassio and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Stefania Moia

14 papers receiving 282 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefania Moia Italy	8	158	78	48	47	45	14	297
Barbara Krzyżanowska‐Świniarska Poland	11	92 0.6×	34 0.4×	80 1.7×	61 1.3×	29 0.6×	36	324
Joanna Smyczyńska Poland	12	244 1.5×	51 0.7×	33 0.7×	19 0.4×	21 0.5×	55	350
Süheyla Görar Türkiye	11	110 0.7×	34 0.4×	38 0.8×	41 0.9×	14 0.3×	26	327
Yuka Miyatani Japan	11	108 0.7×	22 0.3×	56 1.2×	80 1.7×	32 0.7×	13	387
Mira S. Zantout Lebanon	12	268 1.7×	56 0.7×	166 3.5×	56 1.2×	19 0.4×	21	539
Başak Karbek Türkiye	13	262 1.7×	34 0.4×	48 1.0×	41 0.9×	43 1.0×	22	438
Anissa Djemli Canada	11	141 0.9×	60 0.8×	27 0.6×	41 0.9×	28 0.6×	16	356
Eva Venegas Spain	10	190 1.2×	73 0.9×	48 1.0×	57 1.2×	42 0.9×	20	296
Sandra Williams United States	4	162 1.0×	35 0.4×	56 1.2×	43 0.9×	26 0.6×	6	352
Maciej Hilczer Poland	13	238 1.5×	60 0.8×	46 1.0×	14 0.3×	23 0.5×	59	403

Countries citing papers authored by Stefania Moia

Since Specialization

Citations

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

Fields of papers citing papers by Stefania Moia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Moia

This figure shows the co-authorship network connecting the top 25 collaborators of Stefania Moia. A scholar is included among the top collaborators of Stefania Moia 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 Stefania Moia. Stefania Moia is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Moia, Stefania, Daniele Tessaris, Silvia Einaudi, et al.. (2017). Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 43(1). 94–94. 7 indexed citations

Monzani, Alice, Michela Perrone, Flavia Prodam, et al.. (2017). Unacylated ghrelin and obestatin: promising biomarkers of protein energy wasting in children with chronic kidney disease. Pediatric Nephrology. 33(4). 661–672. 16 indexed citations

Grossini, Elena, Giulia Raina, Serena Farruggio, et al.. (2016). Intracoronary Des-Acyl Ghrelin Acutely Increases Cardiac Perfusion Through a Nitric Oxide-Related Mechanism in Female Anesthetized Pigs. Endocrinology. 157(6). 2403–2415. 14 indexed citations

Prodam, Flavia, Letizia Trovato, Roberta Ricotti, et al.. (2015). Adiponectin oligomers are similarly distributed in adequate-for-gestational-age obese children irrespective of feeding in their first year. Pediatric Research. 77(6). 808–813. 6 indexed citations

Walker, Gillian E., Roberta Ricotti, Stefania Moia, et al.. (2014). Pediatric Obesity and Vitamin D Deficiency: A Proteomic Approach Identifies Multimeric Adiponectin as a Key Link between These Conditions. PLoS ONE. 9(1). e83685–e83685. 50 indexed citations

Prodam, Flavia, Francesco Cadario, Simonetta Bellone, et al.. (2014). Obestatin Levels Are Associated With C-Peptide and Antiinsulin Antibodies at the Onset, Whereas Unacylated and Acylated Ghrelin Levels Are Not Predictive of Long-Term Metabolic Control in Children With Type 1 Diabetes. The Journal of Clinical Endocrinology & Metabolism. 99(4). E599–E607. 17 indexed citations

Varrasi, Claudia, et al.. (2014). Interictal ghrelin levels in adult patients with epilepsy. Seizure. 23(10). 852–855. 4 indexed citations

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

Monzani, Alice, Flavia Prodam, Anna Rapa, et al.. (2012). ENDOCRINE DISORDERS IN CHILDHOOD AND ADOLESCENCE: Natural history of subclinical hypothyroidism in children and adolescents and potential effects of replacement therapy: a review. European Journal of Endocrinology. 168(1). R1–R11. 73 indexed citations

10.

Trovato, Letizia, Flavia Prodam, Giulia Genoni, et al.. (2012). Involvement of genes related to inflammation and cell cycle in Idiopathic Short Stature. Pituitary. 16(1). 83–90. 6 indexed citations

11.

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

12.

Trovato, Letizia, Flavia Prodam, Giulia Genoni, et al.. (2011). Isolated GHD: investigation and implication of JAK/STAT related genes before and after rhGH treatment. Pituitary. 15(4). 482–489. 6 indexed citations

13.

Prodam, Flavia, Letizia Trovato, Antonella Petri, et al.. (2011). Unacylated, acylated ghrelin and obestatin levels are differently inhibited by oral glucose load in pediatric obesity: Association with insulin sensitivity and metabolic alterations. e-SPEN the European e-Journal of Clinical Nutrition and Metabolism. 6(3). e109–e115. 11 indexed citations

14.

Rapa, Anna, Alice Monzani, Stefania Moia, et al.. (2009). Subclinical Hypothyroidism in Children and Adolescents: A Wide Range of Clinical, Biochemical, and Genetic Factors Involved. The Journal of Clinical Endocrinology & Metabolism. 94(7). 2414–2420. 73 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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