Prioritization of predisposition genes for familial non-medullary thyroid cancer by whole-genome sequencing
Our results implicate the first germline variant in RET in a family with NMTC as well as the first germline variants in PTGIR, GALNT10, and UBN1 in TC.
Authors
- Asta Försti (ORCID: https://orcid.org/0000-0002-9857-4728)
- Diamanto Skopelitou
- Aayushi Srivastava (ORCID: https://orcid.org/0000-0002-2439-6797)
- Chiara Diquigiovanni (ORCID: https://orcid.org/0000-0003-3124-6946)
- Nagarajan Paramasivam (ORCID: https://orcid.org/0000-0002-7126-8472)
- Obul Reddy Bandapalli (ORCID: https://orcid.org/0000-0002-1132-1745)
- Kari Hemminki (ORCID: https://orcid.org/0000-0002-2769-3316)
- Abhishek Kumar (ORCID: https://orcid.org/0000-0003-4172-4059)
- Beiping Miao (ORCID: https://orcid.org/0000-0003-2307-3280)
- Elena Bonora
- Sara Giagiobbe
Institutions
- German Cancer Research Center (DE)
- Charles University (CZ)
- Heidelberg University (DE)
- University Hospital Heidelberg (DE)
- National Center for Tumor Diseases (DE)
- Hopp Children's Cancer Center Heidelberg (DE)
- Azienda USL di Bologna (IT)
- Heidelberg University (US)
- University of Bologna (IT)
Publication Details
- Journal
- European Journal of Endocrinology
- Published
- 2025-03-27
- DOI
- https://doi.org/10.1093/ejendo/lvaf045
- Citations
- 2
- Primary Topic
- Thyroid Cancer Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 2.59
Funders
- Deutsches Krebsforschungszentrum
- European Commission