Társis Paiva Vieira

21PUBLICATIONS
43CO-AUTHORS
Medical infection agents (incl. prions)Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (21)

|Sep 18, 2026
First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant.

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

|Jan 15, 2025
SMAD4 Pathogenic Variants in Seven New Brazilian Individuals With Myhre Syndrome Including a New Family.

Samira Spineli-Silva, Larissa Bretanha Pontes, Nicole de Leeuw

|Sep 27, 2024
Novel variants in the SOX11 gene: clinical description of seven new patients.

Beatriz Schincariol-Manhe, Érica Campagnolo, Samira Spineli-Silva

|Jun 26, 2024
Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries.

Patricia C Mazzonetto, Darine Villela, Ana C V Krepischi

|Apr 27, 2024
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.

Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno

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Frequent Collaborators

8 joint publications

Vera Lúcia Gil-da-Silva-Lopes

5 joint publications

Carlos Eduardo Steiner

4 joint publications

Mara Sanches Guaragna

3 joint publications

Vera Lúcia Gil-da-Silva-Lopes