Luz C. Ramirez-Valencia
Medellin, ANT, Colombia
Last Updated: 09/26/2026
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Found 11 publications
Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanation.
Journal: medRxiv : the preprint server for health sciences
Published: February 06, 2026
Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanation.
Journal: medRxiv : the preprint server for health sciences
Published: February 06, 2026
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 18, 2023
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes.
Journal: Genetic epidemiology
Published: October 06, 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.
Journal: Frontiers in cell and developmental biology
Published: October 26, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Journal: American journal of human genetics
Published: March 30, 2020
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.
Journal: Human genetics
Published: September 26, 2019
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
Journal: American journal of human genetics
Published: January 02, 2018
Dental Decay Phenotype in Nonsyndromic Orofacial Clefting.
Journal: Journal of dental research
Published: May 24, 2017
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
Journal: Human molecular genetics
Published: January 17, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Journal: American journal of human genetics
Published: December 02, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026