Ana Kalise Böttcher da Silveira

8PUBLICATIONS
24CO-AUTHORS
Cell and nuclear divisionMedical biochemistry - amino acids and metabolitesAutoimmunityEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (8)

|Aug 27, 2026
Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

|Apr 28, 2026
Oxidative Stress and Inflammation in Methylmalonic and Propionic Acidemias: A Review.

|Sep 26, 2025
Nitisinone treatment protect hereditary tyrosinemia type I patients against inflammation, DNA and protein oxidative damage by decreasing succinylacetone levels.

Roberta Barbizan Mascarello, Jéssica Lamberty Faverzani, Franciele Fátima Lopes

|Jan 22, 2025
First report of hypoplastic left heart syndrome in 3p- syndrome and review of candidate genes.

Ana Kalise Böttcher, Monique Banik Siqueira, Natasha Malgarezi

|Sep 12, 2024
What Can Really Be Considered a Syndrome? An Insight Based on 16p11.2 Microduplication.

Rafaella Mergener, Lívia Polisseni Cotta Nascimento, Ana Kalise Böttcher

|Sep 11, 2024
Turner syndrome and neuropsychological abnormalities: a review and case series.

Bruna Baierle Guaraná, Marcela Rodrigues Nunes, Victória Feitosa Muniz

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Frequent Collaborators

6 joint publications

Rafaella Mergener

6 joint publications

Marcela Rodrigues Nunes

6 joint publications

Paulo Ricardo Gazzola Zen

3 joint publications

Lívia Polisseni Cotta Nascimento