Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort-Reference-Cited by-同舟云学术

Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort

Published:2021-12-06 Issue: Volume: Page:
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Winzeler Bettina¹²³^ORCID,Tufton Nicola⁴⁵^ORCID,Lim Eugenie⁴⁵,Challis Ben G.⁶^ORCID,Park Soo‐Mi⁷,Izatt Louise⁸^ORCID,Carroll Paul V.⁹,Velusamy Anand⁹,Hulse Tony¹⁰,Whitelaw Benjamin C.¹¹,Martin Ezequiel³¹²,Rodger Fay³,Maranian Melanie³,Clark Graeme R.³,Akker Scott⁴⁵^ORCID,Maher Eamonn R.³,Casey Ruth T.³⁶^ORCID

Affiliation:

1. Department of Endocrinology, Diabetology and Metabolism University Hospital Basel Basel Switzerland

2. Department of Clinical Research University of Basel Basel Switzerland

3. Department of Medical Genetics, and Cancer Research, UK Cambridge Centre, University of Cambridge Cambridge Biomedical Campus Cambridge UK

4. Department of Endocrinology St. Bartholomew's Hospital, Barts Health NHS Trust London UK

5. Department of Endocrinology, William Harvey Research Institute Queen Mary University of London London

6. Department of Endocrinology, Cambridge University Hospital NHS Foundation Trust Cambridge UK

7. Department of Clinical Genetics, Cambridge University Hospital NHS Foundation Trust Cambridge UK

8. Department of Clinical Genetics Guy's and St. Thomas' NHS Foundation Trust London UK

9. Department of Endocrinology Guy's and St. Thomas' NHS Foundation Trust London UK

10. Department of Paediatric Endocrinology Evelina London Children's Hospital, Guy's and St. Thomas' NHS Foundation Trust London UK

11. Department of Endocrinology King's College Hospital NHS Foundation Trust London UK

12. Oncology Department, Cancer Molecular Diagnostics Laboratory University of Cambridge Cambridge UK

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14639

Reference43 articles.

1. Occurrence of pheochromocytoma in Rochester, Minnesota, 1950 through 1979;Beard CM;Mayo Clin Proc,1983

2. Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours

3. Year of Diagnosis, Features at Presentation, and Risk of Recurrence in Patients with Pheochromocytoma or Secreting Paraganglioma

4. Pheochromocytoma and functional paraganglioma syndrome: No longer the 10% tumor

5. Paraganglioma and phaeochromocytoma: from genetics to personalized medicine

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1. International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescents;Nature Reviews Endocrinology;2024-08-15

2. Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma;Gene;2023-07

3. Somatic EPAS1 Variants in Pheochromocytoma and Paraganglioma in Patients With Sickle Cell Disease;The Journal of Clinical Endocrinology & Metabolism;2023-06-07

4. Editorial for Clinical Endocrinology special issue on “Genetics in Endocrinology”;Clinical Endocrinology;2022-09-05