The pathological and molecular genetic landscape of the hereditary renal cancer predisposition syndromes-Reference-Cited by-同舟云学术

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The pathological and molecular genetic landscape of the hereditary renal cancer predisposition syndromes

Published:2022-04-11 Issue:1 Volume:81 Page:15-31
ISSN:0309-0167
Container-title:Histopathology
language:en
Short-container-title:Histopathology

Author:

Al‐Obaidy Khaleel I¹^ORCID,Alruwaii Zainab I²,Williamson Sean R¹^ORCID,Cheng Liang³⁴^ORCID

Affiliation:

1. Department of Pathology, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic Cleveland OH USA

2. Department of Pathology, Dammam Regional Laboratory and Blood Bank Dammam Saudi Arabia

3. Department of Pathology Indiana University School of Medicine Indianapolis IN USA

4. Department of Urology Indiana University School of Medicine Indianapolis IN USA

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/his.14641

Reference136 articles.

1. Cancer statistics, 2022

2. Five decades of urologic pathology: the accelerating expansion of knowledge in renal cell neoplasia

3. A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas

4. Molecular and cytogenetic insights into the pathogenesis, classification, differential diagnosis, and prognosis of renal epithelial neoplasms

5. Uber eine sehr seltene Erkrankung der Netzhaut [about a very rare disease of the retina];Von‐Hippel E;Graefes Arch. Clin. Exp. Ophthalmol.,1904

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A 23-year bibliometric analysis of the development of global research on hereditary renal carcinoma;Frontiers in Oncology;2024-06-03

2. von Hippel–Lindau disease-related neoplasia with an emphasis on renal manifestations;Seminars in Diagnostic Pathology;2024-01

3. Wide morphological spectrums of renal neoplasms with TSC/mTOR, NF2, or monoallelic MUTYH germline mutation;Human Pathology Reports;2023-03

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