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The American Journal of Surgical Pathology|September 7, 2022
Morphologic and Molecular Heterogeneity of Cervical Neuroendocrine Neoplasia: A Report of 14 CasesZehra Ordulu, Mari Mino-Kenudson, Robert H Young, et al.
The American Journal of Surgical Pathology|June 23, 2020
Inflammatory Myofibroblastic Tumor of the Uterus: An Immunohistochemical Study of 23 CasesJennifer A Bennett, Sabrina Croce, Anna Pesci, et al.
The American Journal of Surgical Pathology|November 5, 2021
Solitary Fibrous Tumors of the Female Genital Tract: A Study of 27 Cases Emphasizing Nonvulvar Locations, Variant Histology, and Prognostic FactorsKyle M Devins, Robert H Young, Sabrina Croce, et al.
Genes, Chromosomes & Cancer|December 7, 2013
Continuous tissue microarray based identification of cancers with homogeneous target expression for successful targeted therapy in clinical routine practiceEike Burandt, Melanie Schreiber, Alexander Stein, et al.
Cancers|December 24, 2021
Transcriptome Analysis in Vulvar Squamous Cell CancerKatharina Prieske, Malik Alawi, Anna Jaeger, et al.
Virchows Archiv : an International Journal of Pathology|December 8, 2019
High homogeneity of mismatch repair deficiency in advanced prostate cancerChristoph Fraune, Ronald Simon, Doris Höflmayer, et al.
Translational Andrology and Urology|April 14, 2021
Mismatch repair deficiency occurs very rarely in seminomasDavid Dum, Stefan Steurer, Ronald Simon, et al.
Urologic Oncology|February 19, 2020
MMR deficiency in urothelial carcinoma of the bladder presents with temporal and spatial homogeneity throughout the tumor massChristoph Fraune, Ronald Simon, Claudia Hube-Magg, et al.
Breast Cancer (Tokyo, Japan)|May 28, 2014
Cyclin D1 gene amplification is highly homogeneous in breast cancerEike Burandt, Martin Grünert, Annette Lebeau, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 21, 2021
Embryonal rhabdomyosarcoma of the uterine corpus: a clinicopathological and molecular analysis of 21 cases highlighting a frequent association with DICER1 mutationsJennifer A Bennett, Zehra Ordulu, Robert H Young, et al.
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