Enrique Medina-Acosta

6PUBLICATIONS
16CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)Fish physiology and genetics
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Publications (6)

|May 08, 2024
Comprehensive genomic filtering algorithm to expose the cause of skewed X chromosome inactivation. The proof of concept in female haemophilia expression.

Betiana Michelle Ziegler, Miguel Martin Abelleyro, Vanina Daniela Marchione

|Nov 16, 2023
Identification of a novel epigenetic marker for typical and mosaic presentations of Fragile X syndrome.

Camilla Pereira da Silva, Diego Camuzi, Adriana Helena de Oliveira Reis

|Sep 24, 2021
MYH7 p.Glu903Gln Is a Pathogenic Variant Associated With Hypertrophic Cardiomyopathy.

Glauber M Dias, Arsonval Lamounier Júnior, Maila Seifert

|Jan 11, 2019
Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia.

Miguel Martín Abelleyro, Vanina Daniela Marchione, Micaela Palmitelli

|Aug 25, 2017
Population genetic structure of Guiana dolphin (Sotalia guianensis) from the southwestern Atlantic coast of Brazil.

Juliana Ywasaki Lima, Filipe Brum Machado, Ana Paula Cazerta Farro

|Apr 22, 2016
Trisomy 21 Alters DNA Methylation in Parent-of-Origin-Dependent and -Independent Manners.

Antônio Francisco Alves da Silva, Filipe Brum Machado, Érika Cristina Pavarino

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Frequent Collaborators

1 joint publications

Daniela Neme

1 joint publications

Glauber M Dias

1 joint publications

Maila Seifert

1 joint publications

Hector Barájas-Martinez