Társis Paiva Vieira

19PUBLICATIONS
40CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Optical technologyAnalytical spectrometry
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Publications (19)

|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

|Apr 27, 2024
Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis.

Ruy Pires de Oliveira-Sobrinho, Simone Appenzeller, Ianne Pessoa Holanda

|Feb 24, 2024
Variants in <i>KMT2A</i> in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome.

Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli

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Frequent Collaborators

7 joint publications

Vera Lúcia Gil-da-Silva-Lopes

3 joint publications

Vera Lúcia Gil-da-Silva-Lopes

3 joint publications

Milena Atique-Tacla

3 joint publications

Andréa Trevas Maciel-Guerra