Gunes Gundem

Memorial Sloan Kettering Cancer Center — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

53h-index33.3kcitations235works5.02yr avg
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Research Topics

Cancer Genomics and Diagnostics(84), Sarcoma Diagnosis and Treatment(30), Acute Myeloid Leukemia Research(24), Childhood Cancer Survivors' Quality of Life(19), CRISPR and Genetic Engineering(18)

Publications187 total

Enabling whole genome sequencing analysis from FFPE specimens in clinical oncology
Nature Communications·2025· 1 citedOpen Access
Low-Grade Fibro-Osseous Lesions With Isolated Chromosome 12 Chromothripsis: A Distinct Entity Or a Low-Grade Central Osteosarcoma With a Novel Driver?
Modern Pathology·2025
Integrating single-cell whole genome and transcriptome sequencing to track the clonal evolution of TP53-mutated myeloid neoplasms
Blood·2025
Feasibility and utility of unmatched whole-genome sequencing (uWGS)  for pediatric acute leukemias: An analysis of leukemia precision-based therapy (LEAP) study samples
Blood·2025Open Access
Author Correction: Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers
Nature Communications·2025Open Access
Author Correction: Clonal evolution during metastatic spread in high-risk neuroblastoma
Nature Genetics·2025Open Access
Clinical Significance of <i>TERT</i> Promoter Mutations in Neuroblastoma
JCO Precision Oncology·2025
Malignant <scp>CRTC1</scp>::<scp>TRIM11</scp> Cutaneous Tumor With Lethal Outcome: Histopathologic and Molecular Findings
Journal of Cutaneous Pathology·2025· 8 cited
Undifferentiated Pleomorphic Sarcoma in Children and Young Adults: A Comprehensive Clinicopathologic, Genomic, and Epigenetic Comparison With Adult Counterparts
Modern Pathology·2025· 1 cited
1090 Alterations in Epithelial-Mesenchymal Transition (EMT) and Histone Modification Genes Are Involved in the Pathogenesis of Gynecologic Carcinosarcoma (CS)
Laboratory Investigation·2025Open Access
Supernumerary ring chromosome 1 syndrome leads to fusion-driven B-cell acute lymphoblastic leukemia in monozygotic twins
Blood Advances·2025· 1 citedOpen Access
CD4+ T-Cell Lymphoma Harboring a Chimeric Antigen Receptor Integration in <i>TP53</i>
New England Journal of Medicine·2025· 49 citedOpen Access
Rhabdomyosarcoma With <scp><i>EWSR1::NF2</i></scp> Gene Fusion: A Case Report Potentially Expanding Its Genetic Spectrum
Genes Chromosomes and Cancer·2025· 1 citedOpen Access
Whole Genome Analysis Identifies Homologous Recombination Deficiency in Cancers with BRCA1/2 Wild-Type and BRCA1/2 Structural Variants
2024Open Access
Whole genome profiling of primary and metastatic adrenocortical carcinoma unravels significant molecular events
Pathology - Research and Practice·2024· 4 cited
Whole genome profiling of rare pediatric thoracic tumors elucidates a YAP1::LEUTX fusion in an unclassified biphasic embryonal neoplasm
Pathology - Research and Practice·2024· 4 cited
Genomic Characterization and Classification of BCL6 Rearranged Follicular Lymphomas
Blood·2024
Whole Genome Landscape Analysis of Homologous Recombination Deficiency in a Pan-Cancer Cohort
2024· 3 cited
Genomic evolution shapes prostate cancer disease type
Cell Genomics·2024· 13 citedOpen Access
Whole-Genome Sequencing Analysis of Male Breast Cancer Unveils Novel Structural Events and Potential Therapeutic Targets
Modern Pathology·2024· 14 citedOpen Access
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Frequent Co-authors

Elli Papaemmanuil(30), Peter J. Campbell(19), David C. Wedge(17), Peter Van Loo(16), Jon W. Teague(14), Michael R. Stratton(13), Keiran Raine(12), Adam P. Butler(12), Ludmil B. Alexandrov(11), Ultan McDermott(11), Max F. Levine(11), Daniel Brewer(10), Stuart McLaren(9), David Jones(9), Laura Mudie(9), Sarah O’Meara(9), Christopher S. Foster(9), Rosalind A. Eeles(9), Serena Nik‐Zainal(9), Juan S. Medina-Martínez(9)