Rafaella Mergener

8PUBLICATIONS
28CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Medical virology
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Publications (8)

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

|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

|Jul 27, 2024
invdup(8)(8q24.13q24.3)-A Complex Alteration and Its Clinical Consequences.

Rafaella Mergener, Marcela Rodrigues Nunes, Ana Kalise Böttcher

|Aug 26, 2023
16p11.2 Microduplication Syndrome with Increased Fluid in the Cisterna: Coincidence or Phenotype Extension?

Lívia Polisseni Cotta Nascimento, Rafaella Mergener, Marcela Rodrigues Nunes

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Frequent Collaborators

6 joint publications

Paulo Ricardo Gazzola Zen

6 joint publications

Ana Kalise Böttcher da Silveira

6 joint publications

Marcela Rodrigues Nunes

3 joint publications

Lívia Polisseni Cotta Nascimento