Elisa Vaiani

477 total citations
22 papers, 328 citations indexed

About

Elisa Vaiani is a scholar working on Endocrinology, Diabetes and Metabolism, Surgery and Molecular Biology. According to data from OpenAlex, Elisa Vaiani has authored 22 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Endocrinology, Diabetes and Metabolism, 6 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in Elisa Vaiani's work include Sexual Differentiation and Disorders (5 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Hormonal and reproductive studies (3 papers). Elisa Vaiani is often cited by papers focused on Sexual Differentiation and Disorders (5 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Hormonal and reproductive studies (3 papers). Elisa Vaiani collaborates with scholars based in Argentina, United States and Switzerland. Elisa Vaiani's co-authors include Alicia Belgorosky, Marco A. Rivarola, Roxana Marino, Gabriela Guercio, Nora Saraco, Carolina Pepe, Pablo Ramírez, Eduardo Chaler, S Iorcansky and Lilien Chertkoff and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Clinical Endocrinology and European Journal of Endocrinology.

In The Last Decade

Elisa Vaiani

22 papers receiving 324 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisa Vaiani Argentina 9 151 125 115 55 49 22 328
Semih Bolu Türkiye 7 67 0.4× 68 0.5× 62 0.5× 24 0.4× 20 0.4× 37 192
Heves Kırmızıbekmez Türkiye 9 48 0.3× 68 0.5× 42 0.4× 25 0.5× 23 0.5× 38 263
Sanjay Saran India 10 49 0.3× 134 1.1× 52 0.5× 44 0.8× 9 0.2× 27 249
Molka Chaieb Tunisia 9 106 0.7× 94 0.8× 88 0.8× 45 0.8× 8 0.2× 17 338
Pauline Smit Netherlands 8 62 0.4× 161 1.3× 52 0.5× 29 0.5× 9 0.2× 10 324
Georgia Kassi Greece 11 130 0.9× 248 2.0× 46 0.4× 165 3.0× 16 0.3× 27 436
Sebahat Yılmaz Ağladıoğlu Türkiye 12 111 0.7× 193 1.5× 124 1.1× 96 1.7× 13 0.3× 31 355
Bonita Franklin United States 9 130 0.9× 225 1.8× 39 0.3× 141 2.6× 10 0.2× 19 330
Fatma Dursun Türkiye 9 60 0.4× 68 0.5× 63 0.5× 25 0.5× 35 0.7× 37 218
Mercedes Maceiras Argentina 12 157 1.0× 253 2.0× 231 2.0× 55 1.0× 80 1.6× 24 469

Countries citing papers authored by Elisa Vaiani

Since Specialization
Citations

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

Fields of papers citing papers by Elisa Vaiani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Vaiani

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Vaiani. A scholar is included among the top collaborators of Elisa Vaiani 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 Elisa Vaiani. Elisa Vaiani 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.
Jørgensen, Flemming Steen, Roxana Marino, Natalia Pérez Garrido, et al.. (2025). A Novel POR G88S Mutation Causes Severe PORD and Establishes a Critical Pharmacogenomic Risk Profile. The Journal of Clinical Endocrinology & Metabolism. 1 indexed citations
2.
Vaiani, Elisa, et al.. (2023). Treatment with TRIAC in pediatric patients with MCT8. Archivos Argentinos de Pediatria. 121(6). e202202968–e202202968. 1 indexed citations
3.
Vaiani, Elisa, et al.. (2021). Paediatric Langerhans Cell Histiocytosis Disease: Long-Term Sequelae in the Hypothalamic Endocrine System. Hormone Research in Paediatrics. 94(1-2). 9–17. 8 indexed citations
4.
Marino, Roxana, Natalia Pérez Garrido, Pablo Ramírez, et al.. (2021). Ehlers–Danlos Syndrome: Molecular and Clinical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 106(7). e2789–e2802. 12 indexed citations
5.
Vaiani, Elisa, et al.. (2020). SAT-093 Two Cases of Autosomal Dominant Familial Central Diabetes Insipidus: A Novel Variant in Neurophysin II Region of AVP Gene. Journal of the Endocrine Society. 4(Supplement_1). 1 indexed citations
6.
Vaiani, Elisa, Pablo Ramírez, Mariana Costanzo, et al.. (2019). The Low-Dose ACTH Test: Usefulness of Combined Analysis of Serum and Salivary Maximum Cortisol Response in Pediatrics. The Journal of Clinical Endocrinology & Metabolism. 104(10). 4323–4330. 6 indexed citations
7.
Vaiani, Elisa, et al.. (2019). Use of Desmopressin for Bilateral Inferior Petrosal Sinus Sampling (BIPSS) in Pediatric Patients with Cushing Disease (CD). 92. 1 indexed citations
8.
Vaiani, Elisa, et al.. (2018). Presentación atípica de un prolactinoma gigante en un adolescente de 15 años. Archivos Argentinos de Pediatria. 116(2). e325–e330. 1 indexed citations
9.
10.
Vaiani, Elisa, et al.. (2014). Central Adrenal Insufficiency Could Not Be Confirmed by Measurement of Basal Serum DHEAS Levels in Pubertal Children. Hormone Research in Paediatrics. 82(5). 332–337. 7 indexed citations
11.
Baquedano, María Sonia, Gabriela Guercio, Roxana Marino, et al.. (2013). [Novel heterozygous mutation in the steroidogenic acute regulatory protein gene in a 46,XY patient with congenital lipoid adrenal hyperplasia].. PubMed. 73(4). 297–302. 1 indexed citations
12.
Baquedano, María Sonia, Gabriela Guercio, Roxana Marino, et al.. (2012). Unique Dominant Negative Mutation in the N-Terminal Mitochondrial Targeting Sequence of StAR, Causing a Variant Form of Congenital Lipoid Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 98(1). E153–E161. 17 indexed citations
13.
Gil, Silvia, Elisa Vaiani, Gabriela Guercio, et al.. (2012). Effectiveness of rhGH treatment on final height of renal-transplant recipients in childhood. Pediatric Nephrology. 27(6). 1005–1009. 16 indexed citations
14.
Vaiani, Elisa, et al.. (2010). Thyroid axis dysfunction in patients with Prader‐Willi syndrome during the first 2 years of life. Clinical Endocrinology. 73(4). 546–550. 41 indexed citations
15.
Ciaccio, Marta, Silvia Gil, Gabriela Guercio, et al.. (2010). Effectiveness of rhGH Treatment on Adult Height in GH-Deficient Childhood Survivors of Medulloblastoma. Hormone Research in Paediatrics. 73(4). 281–286. 9 indexed citations
16.
Chantada, Guillermo, Myriam Guitter, Adriana Fandiño, et al.. (2008). Treatment results in patients with retinoblastoma and invasion to the cut end of the optic nerve. Pediatric Blood & Cancer. 52(2). 218–222. 35 indexed citations
17.
Pepe, Carolina, Nora Saraco, María Sonia Baquedano, et al.. (2007). The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues. Clinical Endocrinology. 67(5). 698–705. 26 indexed citations
18.
Vaiani, Elisa, Roxana Marino, Pablo Ramírez, et al.. (2006). Unexpected Peripheral Markers of Thyroid Function in a Patient with a Novel Mutation of the MCT8 Thyroid Hormone Transporter Gene. Hormone Research in Paediatrics. 67(1). 1–6. 65 indexed citations
19.
Belgorosky, Alicia, Carolina Pepe, Roxana Marino, et al.. (2003). Hypothalamic-Pituitary-Ovarian Axis during Infancy, Early and Late Prepuberty in an Aromatase-Deficient Girl Who Is a Compound Heterocygote for Two New Point Mutations of the CYP19 Gene. The Journal of Clinical Endocrinology & Metabolism. 88(11). 5127–5131. 69 indexed citations
20.
Vaiani, Elisa, Mirta Ciocca, Miriam Cuarterolo, et al.. (2002). Hypothalamic-Pituitary-Testicular Function in Prepubertal Children with Chronic Liver Disease. Journal of Pediatric Endocrinology and Metabolism. 15(3). 289–95. 1 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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