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Paper Details

Assessing thyroid cancer risk using polygenic risk scores.
Proc Natl Acad Sci U S A
32
2020
10-SNP PRS, 592,475 common variants, PRS, PTC, SNPs, germline variants, papillary thyroid cancer, patients, single-nucleotide polymorphisms, thyroid cancer
Author NameAffiliation
Sandya LiyanarachchiComprehensive Cancer Center, The Ohio State University
Sandya LiyanarachchiComprehensive Cancer Center, The Ohio State University
Egil FerkingstaddeCODE genetics/Amgen Inc.
Huiling HeComprehensive Cancer Center, The Ohio State University
Huiling HeComprehensive Cancer Center, The Ohio State University
Lambertus A KiemeneyRadboud Institute for Health Sciences, Radboud University Medical Centre
Gudmar ThorleifssondeCODE genetics/Amgen Inc.
Gudmar ThorleifssondeCODE genetics/Amgen Inc.
Matthew D RingelThe Ohio State University
Kari StefanssondeCODE genetics/Amgen Inc.
Kari StefanssonUniversity of Iceland
Kari StefanssondeCODE genetics/Amgen Inc.
Kari StefanssonUniversity of Iceland
Albert de la ChapelleComprehensive Cancer Center, The Ohio State University
Albert de la ChapelleComprehensive Cancer Center, The Ohio State University
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