Mara Sanches Guaragna

11PUBLICATIONS
38CO-AUTHORS
Genetic immunologyComputational neuroscience (incl. mathematical neuroscience and theoretical neuroscience)Adolescent healthDevelopmental genetics (incl. sex determination)Medical biochemistry - nucleic acids
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Publications (11)

|Jul 29, 2026
Whole-genome sequencing in Brazilian patients with neurofibromatosis type 1, including novel variants, incidental findings, and dual diagnoses.

|Jan 30, 2025
Past and future in vitro and in vivo approaches toward circulating factors and biomarkers in idiopathic nephrotic syndrome.

Mara S Guaragna, Fernanda M S Casimiro, Patrícia Varela

|Apr 27, 2024
Syndromic Retinitis Pigmentosa: A 15-Patient Study.

Ianne Pessoa Holanda, Priscila Hae Hyun Rim, Rare Genomes Project Consortium

|Jan 20, 2024
X-linked congenital adrenal hypoplasia: Report of long clinical follow-up and description of a new complex variant in the NR0B1 gene.

Adriana Mangue Esquiaveto-Aun, Maricilda Palandi de Mello, Mara Sanches Guaragna

|Nov 30, 2022
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.

Luísa Riccetto, Tarsis Paiva Vieira, Nilma Lucia Viguetti-Campos

|Nov 23, 2022
SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.

Flávia Marcorin de Oliveira, Beatriz Amstalden Barros, Ana Paula Dos Santos

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Frequent Collaborators

5 joint publications

Maricilda Palandi de Mello

4 joint publications

Gil Guerra-Júnior

4 joint publications

Andréa Trevas Maciel-Guerra

4 joint publications

Tarsis Paiva Vieira