Author
University of IowaORCID 0000-0003-2239-8120Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
6 papers
Recent·Most cited
Aline Lourenço Petrin, Ligiane Alves Machado‐Paula, Julia Romanowska…·Lina M. Moreno Uribe
The paper identifies methylation quantitative loci (meQTLs) associated with nonsyndromic orofacial clefts, linking genetic variants to epigenetic changes that may explain missing heritability.
Christina Spencer, Ligiane Alves Machado‐Paula, Fang Qian…·Aline Lourenço Petrin
The paper analyzes the laterality, symmetry, and completeness of nonsyndromic orofacial clefts in a multiethnic cohort, finding sex, race, and ethnicity influence these traits but not completeness.
Aline Lourenço Petrin, Henry L. Keen, Lindsey Dunlay…·Lina M. Moreno Uribe
The paper identifies differentially methylated CpG sites in twins discordant for NSCL/P, linking them to retinoic acid signaling and chromatin regulation.
Aline Lourenço Petrin, Waheed A. Awotoye, Christina Spencer…·Lina M. Moreno‐Uribe
This study identifies genetic and epigenetic factors contributing to cleft laterality using monozygotic twins and replication cohorts, finding methylation differences in ARID5B, ZFP57, and HOOK2 associated with cleft side and severity.
Amanda Seaberg, Waheed A. Awotoye, Fang Qian…·Aline Lourenço Petrin
The paper investigates DNA methylation differences in IRF6 and TP63 regulatory regions in Van der Woude Syndrome patients and finds hypermethylation in IRF6 promoters correlates with more severe phenotypes.
Aline Lourenço Petrin, Ligiane Alves Machado‐Paula, Ashley Hinkle…·Lina M. Moreno Uribe
The paper identifies rare mutations in SIX1, PDGFRA, and KDR/VEGFR2 associated with OAVS phenotypes through whole genome sequencing and statistical analysis of a family.