Helena Fabbri-Scallet

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Top Venues

Sao Paulo medical journal = Revista paulista de medicina

Journal of clinical medicine

Life (Basel, Switzerland)

This page only lists publications with an associated author ORCID identifier.

Publications

Felipe Rodrigues de Oliveira, Taís Nitsch Mazzola, Maricilda Palandi de Mello, Ana Paula Francese-Santos, Sofia Helena V de Lemos-Marini, Andréa Trevas Maciel-Guerra, Olaf Hiort, Ralf Werner, Gil Guerra-Junior, Helena Fabbri-Scallet
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis. Life (Basel, Switzerland) 13 (5) (2023)
Verónica Calonga-Solís, Helena Fabbri-Scallet, Fabian Ott, Mostafa Al-Sharkawi, Axel Künstner, Lutz Wünsch, Olaf Hiort, Hauke Busch, Ralf Werner
MYRF: A New Regulator of Cardiac and Early Gonadal Development-Insights from Single Cell RNA Sequencing Analysis. Journal of clinical medicine 11 (16) (2022)
Luísa Riccetto, Társis Antonio Paiva Vieira, Nilma Lucia Viguetti-Campos, Taís Nitsch Mazzola, Mara Sanches Guaragna, Helena Fabbri-Scallet, Maricilda Palandi de Mello, Antonia Paula Marques-de-Faria, Andréa Trevas Maciel-Guerra, Gil Guerra Junior
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study. Sao Paulo medical journal = Revista paulista de medicina (2022)
Helena Fabbri-Scallet, Lizandra Maia de Sousa, Andréa Trevas Maciel-Guerra, Gil Guerra Junior, Maricilda Palandi de Mello
Mutation update for the NR5A1 gene involved in DSD and infertility. Human mutation 41 (1) (2019)
Helena Fabbri-Scallet, Maricilda Palandi de Mello, Gil Guerra-Júnior, Andréa Trevas Maciel-Guerra, Juliana Gabriel Ribeiro de Andrade, Camila Maia Costa de Queiroz, Isabella Lopes Monlleó, Dagmar Struve, Olaf Hiort, Ralf Werner
Functional characterization of five NR5A1 gene mutations found in patients with 46,XY disorders of sex development. Human mutation 39 (1) (2017)