Caroline B. Teixeira
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 7 publications
ACMG secondary findings in the Brazilian rare genomes project: insights from 5402 genome sequencing.
ACMG secondary findings in the Brazilian rare genomes project: insights from 5402 genome sequencing.
Journal: Journal of human genetics
Published: January 28, 2025
Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies.
Journal: Pediatric research
Published: September 11, 2023
A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation.
Journal: Pediatric blood & cancer
Published: February 05, 2023
LHX6 promoter hypermethylation in oncological pediatric patients conceived by IVF.
Journal: Journal of developmental origins of health and disease
Published: September 26, 2022
Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes.
Journal: Frontiers in genetics
Published: April 15, 2022
Expanding the role of SETD5 haploinsufficiency in neurodevelopment and neuroblastoma.
Journal: Pediatric blood & cancer
Published: October 21, 2019
Showing 1-7 of 7
Last Updated: 09/26/2026