Graciela Moya

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L. Collins et al. · Nature Genetics · 2016 · 346 citations · Full text

Human Congenital Anomalies, Developmental Anomaly, Developmental Biology +8

Borate transporter <i>SLC4A11</i> mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

Julie Désir, Graciela Moya, Orit Reish et al. · Journal of Medical Genetics · 2007 · 163 citations · Full text

High frequency and founder effect of the CYP3A4*20 loss-of-function allele in the Spanish population classifies CYP3A4 as a polymorphic enzyme

María Apellániz-Ruiz, Lucía Inglada‐Pérez, M.E.G. Naranjo et al. · The Pharmacogenomics Journal · 2014 · 65 citations · Full text

Biology, Allelic Variant, Genetics +8

Genomic Ancestry,<i><scp>CYP</scp>2D6</i>,<i><scp>CYP</scp>2C9</i>, and<i><scp>CYP</scp>2C19</i>Among Latin Americans

Fernanda Rodrigues‐Soares, Eva Peñas‐Lledó, Eduardo Tarazona‐Santos et al. · Clinical Pharmacology & Therapeutics · 2019 · 52 citations · Full text

Interethnic Variability in <i>CYP2D6</i> , <i>CYP2C9</i> , and <i>CYP2C19</i> Genes and Predicted Drug Metabolism Phenotypes Among 6060 Ibero- and Native Americans: RIBEF-CEIBA Consortium Report on Population Pharmacogenomics

María-Eugenia G. Naranjo, Fernanda Rodrigues‐Soares, Eva Peñas‐Lledó et al. · OMICS A Journal of Integrative Biology · 2018 · 48 citations · Full text