Rolando Garcia, Ph.D. Titles and Appointments Assistant Professor School Medical School Department Pathology You have reached the Academic Profile. For more information on the doctor and patient care, please visit the clinical profile. Biography Education: Rutgers University 2011-2015 Biomedical Informatics PhD Fellowship: UT Southwestern 2016-2018 Clinical Genetics and Genomics UT Southwestern 2018-2019 Laboratory Genetics and Genomics Education Undergraduate School University of Texas at San Antonio (1990) Graduate School Rutgers University, the State University of New Jersey (2009) Graduate School Rutgers University, the State University of New Jersey (2015) Fellowship Pathology - Clinical Cytogenetics (2018), Cytogenetics Research Interest Clinical Genetics and Genomics Hematolymphoid Disorders Statistical Learning Publications Featured Publications Phenotypic and genotypic insights into concurrent tertiary trisomy for 9p and 18p. Wright CA, Scheuerle AE, Wilson K, García R, Koduru P, Mol Cytogenet 2025 Feb 18 1 1 Primary Pulmonary Hypoplasia With Congenital Alveolar Dysplasia Associated With TBX4 Gene Deletion: A Case With Autopsy and Molecular Findings. Ilori EO, Kahlow C, Garcia R, Ahmed S, Timmons C, Nesterenko TH, Pediatr Dev Pathol 2025 Feb 10935266251322326 MYC-r with a non-IG partner concurrently with a cryptic t(12;21) in B-lymphoblastic leukemia: A case and prognostic significance. Koduru P, Chen W, Fuda F, Pacheco M, Garcia R, Cancer Genet 2025 Feb 292-293 85-91 Clinicopathologic and Molecular Characterization of NUP98-Rearranged Acute Leukemias. Sajjan S, Oertling EE, Fuda F, Gagan J, Koduru P, Garcia R, Kwon A, Lin E, Cantu M, Wilson K, Weinberg OK, Chen M, Jaso JM, Slone TL, Truscott J, Thiebaud JA, Chung S, Madanat YF, Chen W, Int J Lab Hematol 2025 Jan Unveiling non-coding DMD variants: synergising RNA sequencing and DNA sequencing for enhanced molecular diagnosis. Pan Y, Nallamilli BRR, Liu R, Guruju N, Lesperance D, Ma Z, Mathur A, Banks K, Martin AS, García R, Guo F, Hegde M, J Med Genet 2024 Dec Recurrent cytogenetic abnormalities reveal alterations that promote progression and transformation in myelodysplastic syndrome. García R, Alkayyali T, Gomez LM, Wright C, Chen W, Oliver D, Koduru P, Cancer Genet 2024 Oct 288-289 92-105 Structural screening and molecular simulation identify potential ligands against the K700E hot spot variant and functional pockets of SF3B1 to modulate splicing in myelodysplastic syndrome. García R, Atis M, Cox A, Koduru P, Heliyon 2024 Jun 10 12 e32729 RNASeq Analysis for Accurate Identification of Fusion Partners in Tumor Specific Translocations Detected by Standard FISH Probes in Hematologic Malignancies. Koduru P, Chen W, Fuda F, Kaur G, Awan F, John S, Garcia R, Gagan J, Clin Pathol 2024 17 2632010X241230262 Automated prediction of acute promyelocytic leukemia from flow cytometry data using a graph neural network pipeline. Cox AM, Kim D, García R, Fuda FS, Weinberg OK, Chen W, Am J Clin Pathol 2023 Oct A t(11;14)(q13;q32)/CCND1::IGH carrying progenitor germinal B-cell with subsequent cytogenetic aberrations contributes to the development of classic Hodgkin lymphoma. García R, Timmons C, Luu H, Miller V, Fuda F, Chen W, Koduru P, Cancer Genet 2022 Oct 268-269 97-102 Results 1-10 of 36 1 2 3 4 Next Last
