Gabriela Stangoni

591 total citations
24 papers, 257 citations indexed

About

Gabriela Stangoni is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Gabriela Stangoni has authored 24 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Gabriela Stangoni's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Gabriela Stangoni is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Gabriela Stangoni collaborates with scholars based in Italy, United States and Netherlands. Gabriela Stangoni's co-authors include Paolo Prontera, Daniela Rogaia, Emilio Donti, Amedea Mencarelli, Giuseppe Merla, Alberto Verrotti, Rita Romani, Bruno Dallapiccola, Lucia Micale and Anna Capalbo and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, International Journal of Molecular Sciences and Bone.

In The Last Decade

Gabriela Stangoni

23 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
Gabriela Stangoni Italy 9 166 122 35 32 23 24 257
Sandesh C. Sreenath Nagamani United States 6 218 1.3× 194 1.6× 70 2.0× 46 1.4× 12 0.5× 8 349
Jamal Ghoumid France 11 160 1.0× 209 1.7× 21 0.6× 62 1.9× 9 0.4× 34 352
Ruolan Guo China 11 120 0.7× 158 1.3× 62 1.8× 31 1.0× 6 0.3× 41 332
Konstantina Kosma Greece 10 137 0.8× 130 1.1× 37 1.1× 21 0.7× 12 0.5× 30 288
Frances Elmslie United Kingdom 10 99 0.6× 117 1.0× 43 1.2× 22 0.7× 50 2.2× 16 291
Kent E. Kruckeberg United States 8 132 0.8× 180 1.5× 12 0.3× 31 1.0× 13 0.6× 9 350
C. Verellen‐Dumoulin Belgium 9 170 1.0× 166 1.4× 26 0.7× 39 1.2× 6 0.3× 17 289
Fılız Hazan Türkiye 10 119 0.7× 183 1.5× 27 0.8× 34 1.1× 23 1.0× 54 309
Lars Geffers Germany 8 57 0.3× 188 1.5× 22 0.6× 14 0.4× 46 2.0× 12 280
Andrew Lane United States 10 203 1.2× 257 2.1× 51 1.5× 51 1.6× 81 3.5× 22 428

Countries citing papers authored by Gabriela Stangoni

Since Specialization
Citations

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

Fields of papers citing papers by Gabriela Stangoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabriela Stangoni

This figure shows the co-authorship network connecting the top 25 collaborators of Gabriela Stangoni. A scholar is included among the top collaborators of Gabriela Stangoni 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 Gabriela Stangoni. Gabriela Stangoni 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.
Bedetti, Chiara, Amedea Mencarelli, Daniela Rogaia, et al.. (2020). A patient with novel MBOAT7 variant: The cerebellar atrophy is progressive and displays a peculiar neurometabolic profile. American Journal of Medical Genetics Part A. 182(10). 2377–2383. 9 indexed citations
2.
Prontera, Paolo, et al.. (2020). Porencephaly in an Italian neonate with foetal alcohol spectrum disorder. Medicine. 99(31). e21384–e21384. 1 indexed citations
3.
Fattorusso, Antonella, Giovanni Battista Dell’Isola, Paolo Prontera, et al.. (2020). Intestinal lymphangiectasia in a 3-month-old girl. Medicine. 99(27). e20995–e20995. 1 indexed citations
4.
Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2019). Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene. European Journal of Human Genetics. 27(8). 1260–1266. 1 indexed citations
5.
Prontera, Paolo, Amedea Mencarelli, Marta Cofini, et al.. (2018). Report of a Novel SHOX Missense Variant in a Boy With Short Stature and His Mother With Leri–Weill Dyschondrosteosis. Frontiers in Endocrinology. 9. 163–163. 3 indexed citations
6.
Palagano, Eleonora, Paolo Prontera, Renato Borgatti, et al.. (2018). Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1. Bone. 114. 125–136. 16 indexed citations
7.
Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2017). Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature. International Journal of Molecular Sciences. 18(9). 1998–1998. 8 indexed citations
8.
Prontera, Paolo, et al.. (2017). Epileptogenic Brain Malformations and Mutations in Tubulin Genes: A Case Report and Review of the Literature. International Journal of Molecular Sciences. 18(11). 2273–2273. 7 indexed citations
9.
Sparaneo, Angelo, Laura Penta, Amedea Mencarelli, et al.. (2017). Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism. The Journal of Clinical Endocrinology & Metabolism. 102(11). 3961–3969. 20 indexed citations
10.
Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2016). A novel MED12 mutation: Evidence for a fourth phenotype. American Journal of Medical Genetics Part A. 170(9). 2377–2382. 23 indexed citations
11.
12.
Prontera, Paolo, Lucia Micale, Alberto Verrotti, et al.. (2015). A New HomozygousIGF1RVariant Defines a Clinically Recognizable Incomplete Dominant form of SHORT Syndrome. Human Mutation. 36(11). 1043–1047. 34 indexed citations
13.
Giglio, Sabrina, Maurizio Cecconi, Alberto Verrotti, et al.. (2015). MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATION.. PubMed. 26(3). 327–32. 4 indexed citations
14.
Prontera, Paolo, et al.. (2014). Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephaly. American Journal of Medical Genetics Part A. 164(12). 3137–3141. 27 indexed citations
15.
Prontera, Paolo, Sabrina Siliquini, Gabriela Stangoni, et al.. (2011). Acrofrontofacionasal dysostosis 1 in two sisters of Indian origin. American Journal of Medical Genetics Part A. 155(12). 3125–3127. 6 indexed citations
16.
Prontera, Paolo, Laura Bernardini, Gabriela Stangoni, et al.. (2011). Deletion 2p15–16.1 syndrome: Case report and review. American Journal of Medical Genetics Part A. 155(10). 2473–2478. 26 indexed citations
17.
Prontera, Paolo, et al.. (2011). Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. American Journal of Medical Genetics Part A. 155(4). 928–930. 20 indexed citations
18.
Prontera, Paolo, et al.. (2009). Encephalocraniocutaneous lipomatosis (ECCL) in a patient with history of familial multiple lipomatosis (FML). American Journal of Medical Genetics Part A. 149A(3). 543–545. 7 indexed citations
19.
Prontera, Paolo, Laura Bernardini, Gabriela Stangoni, et al.. (2009). 2q31.2q32.3 deletion syndrome: Report of an adult patient. American Journal of Medical Genetics Part A. 149A(4). 706–712. 24 indexed citations
20.
Bellomo, Gianni, et al.. (1995). Twenty four-hour ambulatory blood pressure monitoring in women with pre-eclampsia.. PubMed. 9(8). 617–21. 6 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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