Francesca Teofoli

1.0k total citations
23 papers, 329 citations indexed

About

Francesca Teofoli is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Francesca Teofoli has authored 23 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Endocrinology, Diabetes and Metabolism, 12 papers in Molecular Biology and 8 papers in Clinical Biochemistry. Recurrent topics in Francesca Teofoli's work include Metabolism and Genetic Disorders (8 papers), Thyroid Disorders and Treatments (7 papers) and Sexual Differentiation and Disorders (5 papers). Francesca Teofoli is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Thyroid Disorders and Treatments (7 papers) and Sexual Differentiation and Disorders (5 papers). Francesca Teofoli collaborates with scholars based in Italy, Germany and United States. Francesca Teofoli's co-authors include Marta Camilot, Luciano Tatò, Paolo Cavarzere, Gianni Bona, Anna Rapa, Andrea Corrias, Rossella Gaudino, Franco Antoniazzi, Alberto Gandini and Giorgio Radetti and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Fertility and Sterility and Clinical Endocrinology.

In The Last Decade

Francesca Teofoli

23 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francesca Teofoli Italy 10 181 150 54 45 39 23 329
Rulai Yang China 12 55 0.3× 128 0.9× 141 2.6× 99 2.2× 13 0.3× 31 336
Mahoko Furujo Japan 10 71 0.4× 99 0.7× 59 1.1× 48 1.1× 11 0.3× 27 319
Daniela Lapa Italy 8 233 1.3× 42 0.3× 21 0.4× 30 0.7× 14 0.4× 10 352
Arianna Passoni Italy 6 315 1.7× 112 0.7× 27 0.5× 138 3.1× 93 2.4× 7 387
Yoshihide Ohyama Japan 9 348 1.9× 159 1.1× 8 0.1× 74 1.6× 33 0.8× 12 396
Brenda M. Wiedijk Netherlands 9 496 2.7× 149 1.0× 32 0.6× 196 4.4× 123 3.2× 11 559
Chantal Zevenbergen Netherlands 7 154 0.9× 56 0.4× 12 0.2× 28 0.6× 16 0.4× 10 275
I. Pela Italy 10 26 0.1× 124 0.8× 48 0.9× 35 0.8× 11 0.3× 26 285
Tennille S. Leak United States 10 68 0.4× 102 0.7× 15 0.3× 11 0.2× 16 0.4× 12 324
Yuichi Mushimoto Japan 12 126 0.7× 262 1.7× 222 4.1× 45 1.0× 4 0.1× 30 425

Countries citing papers authored by Francesca Teofoli

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Teofoli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Teofoli

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

All Works

20 of 20 papers shown
1.
Maines, Evelina, Roberto Franceschi, Francesca Rivieri, et al.. (2024). Biochemical Pattern of Methylmalonyl-CoA Epimerase Deficiency Identified in Newborn Screening: A Case Report. International Journal of Neonatal Screening. 10(3). 53–53. 1 indexed citations
2.
Cavarzere, Paolo, Marta Camilot, Silvana Lauriola, et al.. (2022). Twenty Years of Neonatal Screening for Congenital Adrenal Hyperplasia in North-Eastern Italy: Role of Liquid Chromatography-Tandem Mass Spectrometry as a Second-Tier Test. Hormone Research in Paediatrics. 95(3). 255–263. 5 indexed citations
3.
Maguolo, Alice, Erika Rigotti, Andrea Pasini, et al.. (2021). Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy. Frontiers in Pediatrics. 9. 661416–661416. 17 indexed citations
4.
Salviati, Leonardo, Andrea Bordugo, Marta Camilot, et al.. (2020). Multiple acyl-COA dehydrogenase deficiency in elderly carriers. Journal of Neurology. 267(5). 1414–1419. 22 indexed citations
5.
Cavarzere, Paolo, Silvana Lauriola, Francesca Teofoli, et al.. (2018). Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 10–10. 4 indexed citations
6.
Maines, Evelina, Angelo Pietrobelli, Natascia Campostrini, et al.. (2017). High-protein goat’s milk diet identified through newborn screening: clinical warning of a potentially dangerous dietetic practice. Public Health Nutrition. 20(15). 2806–2809. 5 indexed citations
7.
Corradi, Massimiliano, Alberto Gandini, Francesca Teofoli, et al.. (2016). Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns.. PubMed. 68(3). 157–61. 2 indexed citations
8.
Maines, Evelina, Natascia Campostrini, Andrea Pasini, et al.. (2016). Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient. JIMD Reports. 35. 29–31. 4 indexed citations
9.
Cavarzere, Paolo, Marta Camilot, Silvana Lauriola, et al.. (2016). Congenital hypothyroidism with delayed TSH elevation in low-birth-weight infants: incidence, diagnosis and management. European Journal of Endocrinology. 175(5). 395–402. 32 indexed citations
10.
Camilot, Marta, Eleonora Ferrarini, Francesca Teofoli, et al.. (2014). Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism. BMC Endocrine Disorders. 14(1). 69–69. 9 indexed citations
11.
12.
Cavarzere, Paolo, Rossella Gaudino, Roberto Franceschi, et al.. (2010). Possible andrologic markers in elevated neonatal 17-hydroxyprogesterone. Fertility and Sterility. 94(6). 2350–2352. 1 indexed citations
13.
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
14.
Teofoli, Francesca, et al.. (2008). Anthropometric traits and aging: A cross-sectional survey in diabetic elderly women. Archives of Gerontology and Geriatrics. 48(2). 197–200. 6 indexed citations
15.
Camilot, Marta, et al.. (2008). A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis. Journal of Endocrinological Investigation. 31(1). 1–7. 6 indexed citations
16.
Marco, Giuseppina De, Patrizia Agretti, Marta Camilot, et al.. (2008). Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia. Clinical Endocrinology. 70(2). 335–338. 20 indexed citations
17.
Gaudino, Rossella, Paolo Cavarzere, Marta Camilot, et al.. (2008). Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy. Fertility and Sterility. 90(6). 2217–2221. 19 indexed citations
18.
19.
Cavarzere, Paolo, Marta Camilot, Francesca Teofoli, & Luciano Tatò. (2005). Neonatal Screening for Congenital Adrenal Hyperplasia in North-Eastern Italy: A Report Three Years into the Program. Hormone Research in Paediatrics. 63(4). 180–186. 16 indexed citations
20.
Camilot, Marta, Francesca Teofoli, Alberto Gandini, et al.. (2005). Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. Clinical Endocrinology. 63(2). 146–151. 52 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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