Atypical teratoid/rhabdoid tumour‐TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition-Reference-Cited by-同舟云学术

Atypical teratoid/rhabdoid tumour‐TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition

Published:2024-03-15 Issue:2 Volume:50 Page:
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology Appl Neurobio

Author:

Lee Julieann C.¹,Tran Quynh T.¹,McGee Rose B.²,Perrino Melissa R.²,Upadhyaya Santhosh A.³,Hanzlik Emily M.⁴,Pytel Nicholas⁴,Carroll Andrew J.⁵,Orisme Wilda¹,Eldomery Mohammad⁶,Wang Lu⁶,Blackburn Patrick R.⁶,Furtado Larissa V.⁶,Viaene Angela N.⁷,Luo Minjie⁷,Kalish Jennifer M.⁸⁹,Pinto Soniya N.¹⁰,Bag Asim K.¹⁰,Orr Brent A.¹^ORCID

Affiliation:

1. Department of Pathology, Neuropathology St. Jude Children's Research Hospital Memphis Tennessee USA

2. Department of Oncology, Division of Cancer Predisposition St. Jude Children's Research Hospital Memphis Tennessee USA

3. Department of Pediatrics and Communicable Diseases, C. S. Mott Children's Hospital University of Michigan Ann Arbor Michigan USA

4. Department of Pediatrics, Division of Neuro‐Oncology St. Jude Children's Research Hospital Memphis Tennessee USA

5. Department of Genetics University of Alabama Birmingham Alabama USA

6. Department of Pathology, Molecular Pathology St. Jude Children's Research Hospital Memphis Tennessee USA

7. Department of Pathology and Laboratory Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

8. Division of Human Genetics and Center for Childhood Cancer Research Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

9. Departments of Genetics and Pediatrics Perelman School of Medicine at the University of Pennsylvania Philadelphia Pennsylvania USA

10. Department of Diagnostic Imaging St. Jude Children's Research Hospital Memphis Tennessee USA

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12971

Reference16 articles.

1. Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22

2. Molecular and phenotypic characterization of ring chromosome 22

3. Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes