Claudia Carranza

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Denise Yan, Demet Tekin, Güney Bademci et al. · Human Genetics · 2016 · 139 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Down-regulation of EVI1 is associated with epigenetic alterations and good prognosis in patients with acute myeloid leukemia

Iria Vázquez, Miren Maicas, Javier Lizardi Cervera et al. · Haematologica · 2011 · 51 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Latin American Study of Hereditary Breast and Ovarian Cancer LACAM: A Genomic Epidemiology Approach

Javier Oliver, Rosalía Quezada Urban, Claudia Alejandra Franco Cortés et al. · Frontiers in Oncology · 2019 · 46 citations · Full text

Life Sciences, Genetics, Oncology +17

Dominant deafness–onychodystrophy syndrome caused by an <i><scp>ATP</scp>6V1B2</i> mutation

Ibis Menéndez, Claudia Carranza, Mariana Herrera‐Cruz et al. · Clinical Case Reports · 2017 · 30 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Frequency of the ETV6-RUNX1, BCR-ABL1, TCF3-PBX1, and MLL-AFF1 fusion genes in Guatemalan pediatric acute lymphoblastic leukemia patients and their ethnic associations

Claudia Carranza, Lilian Granados, Oneida Morales et al. · Cancer Genetics · 2013 · 25 citations

Life Sciences, Genetics, Oncology +14