Soara Menabò

402 total citations
19 papers, 248 citations indexed

About

Soara Menabò is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Soara Menabò has authored 19 papers receiving a total of 248 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Genetics. Recurrent topics in Soara Menabò's work include Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Soara Menabò is often cited by papers focused on Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Soara Menabò collaborates with scholars based in Italy, Germany and Sweden. Soara Menabò's co-authors include Lilia Baldazzi, Antonio Balsamo, Alessandro Cicognani, Alessandra Cassio, Annalisa Nicoletti, Federico Baronio, Felix G. Riepe, Milva Orquidea Bal, Flaminia Fanelli and Patrizia Agretti and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, International Journal of Molecular Sciences and Fertility and Sterility.

In The Last Decade

Soara Menabò

16 papers receiving 244 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Soara Menabò Italy 9 188 161 81 33 29 19 248
Athanasia Stoupa France 9 161 0.9× 197 1.2× 92 1.1× 6 0.2× 17 0.6× 23 261
Matthias Viemann Germany 7 217 1.2× 160 1.0× 80 1.0× 16 0.5× 13 0.4× 10 269
Jennifer Kyllo United States 9 170 0.9× 225 1.4× 69 0.9× 14 0.4× 59 2.0× 14 282
Rita Menassa France 8 181 1.0× 112 0.7× 71 0.9× 35 1.1× 31 1.1× 14 234
Diemud Simm Germany 9 269 1.4× 241 1.5× 71 0.9× 15 0.5× 95 3.3× 10 345
F Kurtz France 4 92 0.5× 71 0.4× 52 0.6× 22 0.7× 4 0.1× 6 155
Yanning Song China 8 124 0.7× 32 0.2× 62 0.8× 26 0.8× 6 0.2× 22 171
David H. Jelley United States 5 76 0.4× 107 0.7× 89 1.1× 19 0.6× 55 1.9× 9 181
Paul-Martin Holterhus Germany 5 99 0.5× 88 0.5× 50 0.6× 23 0.7× 1 0.0× 6 132
Marc Nicolino France 5 86 0.5× 73 0.5× 81 1.0× 30 0.9× 1 0.0× 6 177

Countries citing papers authored by Soara Menabò

Since Specialization
Citations

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

Fields of papers citing papers by Soara Menabò

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Soara Menabò

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

All Works

19 of 19 papers shown
1.
Corsi, Cristiana, Valeria Aiello, Amalia Conti, et al.. (2025). The need for clinical, genetic and radiological characterization of atypical polycystic kidney disease. Journal of Nephrology. 38(2). 621–631.
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Menabò, Soara, Lilia Baldazzi, Alexandra Kulle, et al.. (2020). Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations. European Journal of Human Genetics. 28(5). 692–692. 2 indexed citations
5.
Balsamo, Antonio, Federico Baronio, Rita Ortolano, et al.. (2020). Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant. Frontiers in Pediatrics. 8. 593315–593315. 10 indexed citations
6.
Fanelli, Flaminia, Silvia Trini Castelli, Marco Mezzullo, et al.. (2020). Steroid biomarkers for identifying non-classic adrenal hyperplasia due to 21-hydroxylase deficiency in a population of PCOS with suspicious levels of 17OH-progesterone. Journal of Endocrinological Investigation. 43(10). 1499–1509. 10 indexed citations
7.
Karlsson, Leif, Bengt Persson, Gil Guerra‐Júnior, et al.. (2019). Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia. Clinical Biochemistry. 73. 50–56. 2 indexed citations
8.
Baronio, Federico, Rita Ortolano, Soara Menabò, et al.. (2019). 46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features. International Journal of Molecular Sciences. 20(18). 4605–4605. 23 indexed citations
9.
Bonora, Elena, Annamaria Perri, Emanuela Scarano, et al.. (2018). <b><i>HDAC8</i></b> Loss of Function and <b><i>SHOX</i></b> Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype. Cytogenetic and Genome Research. 157(3). 135–140. 3 indexed citations
10.
Rocca, Maria Santa, Rita Ortolano, Soara Menabò, et al.. (2018). Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations. Fertility and Sterility. 109(6). 1105–1113. 15 indexed citations
11.
Scaramuzzo, Rosa Teresa, Soara Menabò, Lilia Baldazzi, et al.. (2017). Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia. Sexual Development. 11(2). 82–85. 5 indexed citations
12.
Gialluisi, Alessandro, Soara Menabò, Lilia Baldazzi, et al.. (2017). A genetic epidemiology study of congenital adrenal hyperplasia in Italy. Clinical Genetics. 93(2). 223–227. 7 indexed citations
13.
Menabò, Soara, Alessandra Gambineri, Antonio Balsamo, et al.. (2015). Improving the diagnosis of 11β-hydroxylase deficiency using home-made MLPA probes: identification of a novel chimeric CYP11B2/CYP11B1 gene in a Sicilian patient. Journal of Endocrinological Investigation. 39(3). 291–295. 8 indexed citations
14.
Menabò, Soara, Lilia Baldazzi, Alexandra Kulle, et al.. (2013). Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations. European Journal of Human Genetics. 22(5). 610–616. 37 indexed citations
15.
Menabò, Soara, Antonio Balsamo, Lilia Baldazzi, et al.. (2012). A sequence variation in 3'UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.. PubMed. 35(3). 298–305. 16 indexed citations
16.
Balsamo, Antonio, Lilia Baldazzi, Soara Menabò, & Alessandro Cicognani. (2010). Impact of Molecular Genetics on Congenital Adrenal Hyperplasia Management. Sexual Development. 4(4-5). 233–248. 38 indexed citations
17.
Nicoletti, Annalisa, Milva Orquidea Bal, Giuseppina De Marco, et al.. (2009). Thyrotropin-Stimulating Hormone Receptor Gene Analysis in Pediatric Patients with Non-Autoimmune Subclinical Hypothyroidism. The Journal of Clinical Endocrinology & Metabolism. 94(11). 4187–4194. 53 indexed citations
18.
Menabò, Soara, Antonio Balsamo, Annalisa Nicoletti, et al.. (2008). Three Novel <i>AMH</i>Gene Mutations in a Patient with Persistent Müllerian Duct Syndrome and Normal AMH Serum Dosage. Hormone Research in Paediatrics. 70(2). 124–128. 5 indexed citations
19.
Balsamo, Antonio, Alessandro Cicognani, Monia Gennari, et al.. (2007). Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1. European Journal of Endocrinology. 156(2). 249–256. 14 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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