Helena Fabbri‐Scallet

411 citations

22 papers · 222 indexed · h-index 9

Co-authors: 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
Topics: Sexual Differentiation and Disorders (18 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers)Urological Disorders and Treatments (7 papers)
Cited by: Urology Reproductive Medicine Genetics
Journals: International Journal of Molecular Sciences Human Mutation Journal of Clinical Medicine
Partner nations: Brazil Germany Australia

In The Last Decade

Helena Fabbri‐Scallet

18 papers receiving 216 citations

Peers

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

#	Work	Indexed citations
1	Replication of Missense OTOG Gene Variants in a Brazilian Patient with Menière’s Disease 2025 ·Genes ·(unknown),(unknown),Helena Fabbri‐Scallet,(unknown),(unknown),(unknown),Fernando Freitas Ganança,Juan Carlos Amor‐Dorado,Andrés Soto-Varela,José A. López‐Escámez,Edi Lúcia Sartorato	0
2	DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis 2023 ·Life ·(unknown),Taís Nitsch Mazzola,Maricilda Palandi de Mello,(unknown),Sofia Helena Valente de Lemos‐Marini,Andréa Trevas Maciel‐Guerra,Olaf Hiort,Ralf Werner,Gil Guerra‐Júnior,Helena Fabbri‐Scallet	12
3	DHX37 and the Implications in Disorders of Sex Development: An Update Review 2023 ·Hormone Research in Paediatrics ·(unknown),(unknown),Andréa Trevas Maciel‐Guerra,(unknown),Maricilda Palandi de Mello,Gil Guerra‐Júnior,Helena Fabbri‐Scallet	3
4	Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil 2023 ·Fetal Diagnosis and Therapy ·(unknown),(unknown),(unknown),Taís Nitsch Mazzola,Helena Fabbri‐Scallet,(unknown),Társis Paiva Vieira,Maricilda Palandi de Mello,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior	0
5	Sex dimorphism of weight and length at birth: evidence based on disorders of sex development 2022 ·Annals of Human Biology ·(unknown),(unknown),(unknown),Juliana Gabriel Ribeiro de Andrade,Sofia Helena Valente de Lemos‐Marini,Maricilda Palandi de Mello,Antonia Paula Marques‐de‐Faria,Taís Nitsch Mazzola,(unknown),Helena Fabbri‐Scallet,Társis Paiva Vieira,(unknown),André Moreno Morcillo,Olaf Hiort,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior	0
6	Can Non-Coding NR5A1 Gene Variants Explain Phenotypes of Disorders of Sex Development? 2022 ·Sexual Development ·Helena Fabbri‐Scallet,Ralf Werner,(unknown),Juliana Gabriel Ribeiro de Andrade,Andréa Trevas Maciel‐Guerra,Nadine Hornig,Olaf Hiort,Gil Guerra‐Júnior,Maricilda Palandi de Mello	7
7	Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review 2022 ·Sexual Development ·(unknown),(unknown),Helena Fabbri‐Scallet,Maricilda Palandi de Mello,Gil Guerra‐Júnior,Andréa Trevas Maciel‐Guerra	3
8	Trends in Time Regarding Sex Assignment of Patients with Disorders of Sex Development: Experience of an Interdisciplinary Service 2022 ·Sexual Development ·(unknown),(unknown),(unknown),Juliana Gabriel Ribeiro de Andrade,(unknown),(unknown),(unknown),(unknown),Társis Paiva Vieira,Taís Nitsch Mazzola,(unknown),Helena Fabbri‐Scallet,Maricilda Palandi de Mello,Antonia Paula Marques‐de‐Faria,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior	1
9	MYRF: A New Regulator of Cardiac and Early Gonadal Development—Insights from Single Cell RNA Sequencing Analysis 2022 ·Journal of Clinical Medicine ·(unknown),Helena Fabbri‐Scallet,(unknown),(unknown),Axel Künstner,Lutz Wünsch,Olaf Hiort,Hauke Busch,Ralf Werner	5
10	So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity 2022 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·(unknown),(unknown),Fernanda Caroline Soardi,(unknown),Taís Nitsch Mazzola,Helena Fabbri‐Scallet,Maricilda Palandi de Mello,(unknown),(unknown),Isabella Lopes Monlleó	1
11	Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study 2022 ·Sao Paulo Medical Journal ·(unknown),Társis Paiva Vieira,(unknown),Taís Nitsch Mazzola,(unknown),Helena Fabbri‐Scallet,Maricilda Palandi de Mello,Antonia Paula Marques‐de‐Faria,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior	0
12	A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication 2022 ·International Journal of Molecular Sciences ·(unknown),(unknown),(unknown),Juliana Gabriel Ribeiro de Andrade,(unknown),Helena Fabbri‐Scallet,Vera Lúcia Gil‐da‐Silva‐Lopes,Gil Guerra‐Júnior,Axel Künstner,Hauke Busch,Olaf Hiort,Maricilda Palandi de Mello,Ralf Werner,Andréa Trevas Maciel‐Guerra	4
13	Mutation update for theNR5A1gene involved in DSD and infertility 2019 ·Human Mutation ·Helena Fabbri‐Scallet,(unknown),Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior,Maricilda Palandi de Mello	55
14	Clinical Findings and Follow-Up of 46,XY and 45,X/46,XY Testicular Dysgenesis 2019 ·Sexual Development ·Juliana Gabriel Ribeiro de Andrade,Helena Fabbri‐Scallet,Ana Paula Santos,Martine Cools,Ralf Werner,Olaf Hiort,Maricilda Palandi de Mello,Gil Guerra‐Júnior,Andréa Trevas Maciel‐Guerra	17
15	Why pediatricians need to know the disorders of sex development: experience of 709 cases in a specialized service 2019 ·Jornal de Pediatria ·(unknown),(unknown),(unknown),Juliana Gabriel Ribeiro de Andrade,Guilherme Guaragna‐Filho,(unknown),(unknown),(unknown),Helena Fabbri‐Scallet,Taís Nitsch Mazzola,(unknown),Társis Paiva Vieira,Sofia Helena Valente de Lemos‐Marini,Antonia Paula Marques‐de‐Faria,(unknown),Maricilda Palandi de Mello,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior	5
16	A Search for Disorders of Sex Development among Infertile Men 2018 ·Sexual Development ·(unknown),(unknown),(unknown),Helena Fabbri‐Scallet,Taís Nitsch Mazzola,(unknown),(unknown),Gil Guerra‐Júnior,Maricilda Palandi de Mello,Andréa Trevas Maciel‐Guerra	4
17	<b><i>NR5A1</i></b> Loss-of-Function Mutations Lead to 46,XY Partial Gonadal Dysgenesis Phenotype: Report of Three Novel Mutations 2016 ·Sexual Development ·Helena Fabbri‐Scallet,Juliana Gabriel Ribeiro de Andrade,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior,Maricilda Palandi de Mello	19
18	The novel p.Cys65Tyr mutation in NR5A1gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency 2014 ·BMC Medical Genetics ·Helena Fabbri‐Scallet,Juliana Gabriel Ribeiro de Andrade,Fernanda Caroline Soardi,(unknown),(unknown),Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior,Maricilda Palandi de Mello	28
19	Multifunctional role of steroidogenic factor 1 and disorders of sex development 2011 ·Arquivos Brasileiros de Endocrinologia & Metabologia ·Maricilda Palandi de Mello,(unknown),Helena Fabbri‐Scallet,Andréa Trevas Maciel‐Guerra,Gil Guerra‐Júnior	15
20	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 2010 ·Arquivos Brasileiros de Endocrinologia & Metabologia ·Helena Fabbri‐Scallet,Maricilda Palandi de Mello,Fernanda Caroline Soardi,(unknown),(unknown),(unknown),Arnaldo Moura Neto,Heraldo Mendes Garmes,Maria Tereza Matias Baptista,Patrícia Matos,Sofia Helena Valente de Lemos‐Marini,Lilia Freire Rodrigues D’Souza-Li,Gil Guerra‐Júnior	12

About Helena Fabbri‐Scallet

Helena Fabbri‐Scallet is a scholar working on Urology, Reproductive Medicine and Genetics, having authored 22 papers that have together received 222 indexed citations. Recurring topics across this 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). The work is most often cited by research in Urology (61 citations), Reproductive Medicine (56 citations) and Genetics (168 citations). Helena Fabbri‐Scallet has collaborated with scholars based in Brazil, Germany and Australia. Frequent 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. Their work appears in journals such as International Journal of Molecular Sciences, Human Mutation and Journal of Clinical Medicine.

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