Eyleen Corrales
San Jose, SJ, Costa Rica
Last Updated: 09/26/2026
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Found 8 publications
Analysis of muscle and blood RNA samples from patients with myotonic dystrophy type 1 reveals the presence of new mis-splicing biomarkers of disease severity.
Journal: Journal of medical genetics
Published: May 14, 2025
Individual-specific levels of CTG•CAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1.
Journal: Human molecular genetics
Published: April 08, 2022
Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent.
Journal: Human molecular genetics
Published: June 11, 2021
Aerial strategies advance volcanic gas measurements at inaccessible, strongly degassing volcanoes.
Journal: Science advances
Published: April 06, 2020
Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset.
Journal: Human molecular genetics
Published: December 09, 2019
Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1.
Journal: PloS one
Published: November 23, 2018
Candidate gene study reveals DRD1 and DRD2 as putative interacting risk factors for youth depression.
Journal: Psychiatry research
Published: March 23, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026