Endocrine Pathology

Papers
(The H4-Index of Endocrine Pathology is 16. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
Focal Tall Cell Change in Papillary Thyroid Carcinoma: Lessons Learned from Practices Adopting Rigid Criteria (Height to Width Ratio of 3)660
Evaluating CK20 and MCPyV Antibody Clones in Diagnosing Merkel Cell Carcinoma485
Deep Learning Enabled Scoring of Pancreatic Neuroendocrine Tumors Based on Cancer Infiltration Patterns311
Amphicrine Medullary Thyroid Carcinoma — a Case-Based Review Expanding on Its MUC Expression Profile221
The Presence of Typical “BRAFV600E-Like” Atypia in Papillary Thyroid Carcinoma is Highly Specific for the Presence of the BRAFV600E Mutation166
Recipient of the 2021 Endocrine Pathology Society Lifetime Achievement Award: Dr. Ronald A. DeLellis150
“Strumal Carcinoid”: A Well-Described but Unexplained Intratumoral Tumor40
In Memory of Kalman Kovacs and Eva Horvath37
External Validation of Three Available Grading Systems for Medullary Thyroid Carcinoma in a Single Institution Cohort35
The Spectrum of Familial Pituitary Neuroendocrine Tumors31
Next-Generation Immunohistochemistry in Thyroid Neoplasm: A Practical Review on the Applications in Diagnosis and Molecular Classification24
Primary Multiglandular Parathyroid Disease in the Setting of Pompe Disease21
Pathogenic ATM Variant-Harbouring Well-Differentiated Aggressive Type 1 Gastric Neuroendocrine Tumour with High-grade Features (G3 NET): a New Addition to the Clinical and Pathological Spectrum of Gas18
Insights into Biologic Evolution of Grade 3 Neuroendocrine Tumors Reflect Classification Challenges18
Pendred Syndrome with C Cell Hyperplasia17
Medullary Thyroid Carcinoma in the IARC/WHO Neuroendocrine Schema16
Intron 4–5 hTERT DNA Hypermethylation in Merkel Cell Carcinoma: Frequency, Association with Other Clinico-pathological Features and Prognostic Relevance16
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