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International Journal of Surgery Case Reports|July 17, 2025
Post-radiation cranial fasciitis in a pediatric medulloblastoma survivor: A case report and systematic reviewMohsen Koosha, Roya Mostafavi, Azin Kheradmand, et al.AJP Reports|May 31, 2021
Kagami-Ogata Syndrome: Case Series and Review of LiteratureRishika P Sakaria, Roya Mostafavi, Stephen Miller, et al.Journal of Genetic Counseling|December 2, 2024
Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot studySusan Christian, Tara Dzwiniel, Amy Baker, et al.JCO Precision Oncology|October 20, 2022
Parental Preferences Surrounding Timing and Content of Consent Conversations for Clinical Germline Genetic Testing Following a Child's New Cancer DiagnosisBelinda N Mandrell, Liza Marie Johnson, Mary Caples, et al.Journal of Pediatric Hematology/Oncology Nursing|February 13, 2024
Genomes for Nurses: Understanding and Overcoming Barriers to Nurses Utilizing GenomicsStacy Hines-Dowell, Elizabeth McNamara, Roya Mostafavi, et al.JCO Oncology Practice|April 29, 2026
Parental Knowledge and Decisional Satisfaction Across Genomic Sequencing Consent Processes in Pediatric CancerMeaghann S Weaver, Liza-Marie Johnson, Katianne M Howard Sharp, et al.Cold Spring Harbor Molecular Case Studies|March 30, 2023
Progressive metastatic infantile fibrosarcoma with multiple acquired mutationsLarissa V Furtado, Marija Kacar, Roya Mostafavi, et al.Genes, Chromosomes & Cancer|August 7, 2023
Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndromePatrick R Blackburn, Rose B McGee, Roya Mostafavi, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 24, 2023
Pathogenic Variants in Adult-Onset Cancer Predisposition Genes in Pediatric Cancer: Prevalence and Impact on Tumor Molecular Features and Clinical ManagementRose B McGee, Ninad Oak, Lynn Harrison, et al.American Journal of Medical Genetics. Part A|February 27, 2020
Expanding the spectrum of CEP55-associated disease to viable phenotypesElizabeth S Barrie, Eline Overwater, Mieke M van Haelst, et al.Pageof 3