Helena Fabbri‐Scallet

411 total citations
22 papers, 222 citations indexed

About

Helena Fabbri‐Scallet is a scholar working on Molecular Biology, Genetics and Urology. According to data from OpenAlex, Helena Fabbri‐Scallet has authored 22 papers receiving a total of 222 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 17 papers in Genetics and 7 papers in Urology. Recurrent topics in Helena Fabbri‐Scallet's work include Sexual Differentiation and Disorders (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers) and Urological Disorders and Treatments (7 papers). Helena Fabbri‐Scallet is often cited by papers focused on Sexual Differentiation and Disorders (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers) and Urological Disorders and Treatments (7 papers). Helena Fabbri‐Scallet collaborates with scholars based in Brazil, Germany and Australia. Helena Fabbri‐Scallet's co-authors include Gil Guerra‐Júnior, Maricilda Palandi de Mello, Andréa Trevas Maciel‐Guerra, Juliana Gabriel Ribeiro de Andrade, Olaf Hiort, Ralf Werner, Fernanda Caroline Soardi, Antonia Paula Marques‐de‐Faria, Martine Cools and Sofia Helena Valente de Lemos‐Marini and has published in prestigious journals such as International Journal of Molecular Sciences, Human Mutation and Journal of Clinical Medicine.

In The Last Decade

Helena Fabbri‐Scallet

18 papers receiving 216 citations

Peers

Helena Fabbri‐Scallet

GENET

UROLO

EDM

Vasiliki Karageorgou Germany

Zita Halász Hungary

GS Conway United Kingdom

Denise R. Archambeault United States

Juliana Gabriel Ribeiro de Andrade Brazil

A. Nyström Sweden

M. Doco‐Fenzy France

Christiane Pleuger Germany

Gianluca Spena Italy

Doris Fadoju United States

Vasiliki Karageorgou Germany

Helena Fabbri‐Scallet

141 ×0.8

112 ×0.7

GENET

47 ×0.8

UROLO

41 ×0.7

9 ×0.3

EDM

Citations per year, relative to Helena Fabbri‐Scallet Helena Fabbri‐Scallet (= 1×) peers Vasiliki Karageorgou

Countries citing papers authored by Helena Fabbri‐Scallet

Since Specialization

Citations

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

Fields of papers citing papers by Helena Fabbri‐Scallet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helena Fabbri‐Scallet. 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 Helena Fabbri‐Scallet. The network helps show where Helena Fabbri‐Scallet may publish in the future.

Co-authorship network of co-authors of Helena Fabbri‐Scallet

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

All Works

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20 of 20 papers shown

Fabbri‐Scallet, Helena, Fernando Freitas Ganança, Juan Carlos Amor‐Dorado, et al.. (2025). Replication of Missense OTOG Gene Variants in a Brazilian Patient with Menière’s Disease. Genes. 16(6). 654–654.

Mazzola, Taís Nitsch, Maricilda Palandi de Mello, Sofia Helena Valente de Lemos‐Marini, et al.. (2023). DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis. Life. 13(5). 1093–1093. 12 indexed citations

Maciel‐Guerra, Andréa Trevas, et al.. (2023). DHX37 and the Implications in Disorders of Sex Development: An Update Review. Hormone Research in Paediatrics. 97(5). 433–444. 3 indexed citations

Mazzola, Taís Nitsch, Helena Fabbri‐Scallet, Társis Paiva Vieira, et al.. (2023). Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil. Fetal Diagnosis and Therapy. 51(1). 49–54.

Andrade, Juliana Gabriel Ribeiro de, Sofia Helena Valente de Lemos‐Marini, Maricilda Palandi de Mello, et al.. (2022). Sex dimorphism of weight and length at birth: evidence based on disorders of sex development. Annals of Human Biology. 49(7-8). 274–279.

Fabbri‐Scallet, Helena, Ralf Werner, Juliana Gabriel Ribeiro de Andrade, et al.. (2022). Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development?. Sexual Development. 16(4). 252–260. 7 indexed citations

Fabbri‐Scallet, Helena, et al.. (2022). Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review. Sexual Development. 16(4). 242–251. 3 indexed citations

Andrade, Juliana Gabriel Ribeiro de, Társis Paiva Vieira, Taís Nitsch Mazzola, et al.. (2022). Trends in Time Regarding Sex Assignment of Patients with Disorders of Sex Development: Experience of an Interdisciplinary Service. Sexual Development. 16(4). 236–241. 1 indexed citations

Fabbri‐Scallet, Helena, Axel Künstner, Lutz Wünsch, et al.. (2022). MYRF: A New Regulator of Cardiac and Early Gonadal Development—Insights from Single Cell RNA Sequencing Analysis. Journal of Clinical Medicine. 11(16). 4858–4858. 5 indexed citations

10.

Soardi, Fernanda Caroline, et al.. (2022). So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity. The Italian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 89–89. 1 indexed citations

11.

Vieira, Társis Paiva, Taís Nitsch Mazzola, Helena Fabbri‐Scallet, et al.. (2022). Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study. Sao Paulo Medical Journal. 141(4). e2022281–e2022281.

12.

Andrade, Juliana Gabriel Ribeiro de, Helena Fabbri‐Scallet, Vera Lúcia Gil‐da‐Silva‐Lopes, et al.. (2022). A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication. International Journal of Molecular Sciences. 24(1). 494–494. 4 indexed citations

13.

Fabbri‐Scallet, Helena, et al.. (2019). Mutation update for theNR5A1gene involved in DSD and infertility. Human Mutation. 41(1). 58–68. 55 indexed citations

14.

Andrade, Juliana Gabriel Ribeiro de, Helena Fabbri‐Scallet, Ana Paula Santos, et al.. (2019). Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis. Sexual Development. 13(4). 171–177. 17 indexed citations

15.

Andrade, Juliana Gabriel Ribeiro de, Guilherme Guaragna‐Filho, Helena Fabbri‐Scallet, et al.. (2019). Why pediatricians need to know the disorders of sex development: experience of 709 cases in a specialized service. Jornal de Pediatria. 96(5). 607–613. 5 indexed citations

16.

Fabbri‐Scallet, Helena, et al.. (2018). A Search for Disorders of Sex Development among Infertile Men. Sexual Development. 12(6). 275–280. 4 indexed citations

17.

Fabbri‐Scallet, Helena, Juliana Gabriel Ribeiro de Andrade, Andréa Trevas Maciel‐Guerra, Gil Guerra‐Júnior, & Maricilda Palandi de Mello. (2016). <b><i>NR5A1</i></b> Loss-of-Function Mutations Lead to 46,XY Partial Gonadal Dysgenesis Phenotype: Report of Three Novel Mutations. Sexual Development. 10(4). 191–199. 19 indexed citations

18.

Fabbri‐Scallet, Helena, Juliana Gabriel Ribeiro de Andrade, Fernanda Caroline Soardi, et al.. (2014). The novel p.Cys65Tyr mutation in NR5A1gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency. BMC Medical Genetics. 15(1). 7–7. 28 indexed citations

19.

Mello, Maricilda Palandi de, et al.. (2011). Multifunctional role of steroidogenic factor 1 and disorders of sex development. Arquivos Brasileiros de Endocrinologia & Metabologia. 55(8). 607–612. 15 indexed citations

20.

Fabbri‐Scallet, Helena, Maricilda Palandi de Mello, Fernanda Caroline Soardi, et al.. (2010). Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1. Arquivos Brasileiros de Endocrinologia & Metabologia. 54(8). 754–760. 12 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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