Whole Exome-Wide Association Identifies Rare Variants in GALNT9 Associated with Middle Eastern Papillary Thyroid Carcinoma Risk
Simple Summary This study targeted the identification of rare variants in Middle Eastern
papillary thyroid carcinoma (PTC) through an exome-wide association study. It was found …
papillary thyroid carcinoma (PTC) through an exome-wide association study. It was found …
[HTML][HTML] rs965513 polymorphism as a common risk marker is associated with papillary thyroid cancer
F Wang, D Yan, X Ji, J Han, M Chen, H Qiao, S Zhang - Oncotarget, 2016 - ncbi.nlm.nih.gov
Papillary thyroid cancer (PTC) is the most common type of thyroid cancer. With the rapid
development of genome-wide association studies (GWAS), many genome variants …
development of genome-wide association studies (GWAS), many genome variants …
Variants in LRRC34 reveal distinct mechanisms for predisposition to papillary thyroid carcinoma
DF Comiskey Jr, H He, S Liyanarachchi… - Journal of Medical …, 2020 - jmg.bmj.com
Background Papillary thyroid carcinoma (PTC) demonstrates high heritability and a low
somatic mutation burden relative to other cancers. Therefore, the genetic risk predisposing …
somatic mutation burden relative to other cancers. Therefore, the genetic risk predisposing …
Papillary thyroid carcinoma: association between germline DNA variant markers and clinical parameters
J Jendrzejewski, S Liyanarachchi, R Nagy, L Senter… - Thyroid, 2016 - liebertpub.com
Background: Papillary thyroid cancer (PTC) is reported to be highly heritable in
epidemiological studies. Genome-wide association studies (GWAS) have uncovered several …
epidemiological studies. Genome-wide association studies (GWAS) have uncovered several …
Association of polygenic score with tumor molecular subtypes in papillary thyroid carcinoma
Context Genome-wide association studies have identified germline variants associated with
elevated PTC risk. It is also known that somatic driver mutations contribute to PTC …
elevated PTC risk. It is also known that somatic driver mutations contribute to PTC …
Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer
Thyroid cancer is the most common cancer in Korea. Several susceptibility loci of
differentiated thyroid cancer (DTC) were identified by previous genome-wide association …
differentiated thyroid cancer (DTC) were identified by previous genome-wide association …
Novel somatic alterations underlie Chinese papillary thyroid carcinoma
C Yang, W Xu, J Gong, Z Liu, D Cui - Cancer Biomarkers, 2020 - content.iospress.com
To characterize the somatic alterations of papillary thyroid carcinomas (PTC) in Chinese
patients, we performed the next-generation-sequencing (NGS) study of the tumor-normal …
patients, we performed the next-generation-sequencing (NGS) study of the tumor-normal …
Fine mapping of 14q13 reveals novel variants associated with different histological subtypes of papillary thyroid carcinoma
J Jendrzejewski, S Liyanarachchi… - … journal of cancer, 2019 - Wiley Online Library
The first two genome wide association studies (GWAS) of papillary thyroid carcinoma (PTC)
detected five variants associated with PTC. Two of them (rs944289 and rs116909374) are …
detected five variants associated with PTC. Two of them (rs944289 and rs116909374) are …
Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese …
Background Five single nucleotide polymorphisms (SNPs) were previously reported to be
associated with thyroid cancer in European populations in two genome-wide association …
associated with thyroid cancer in European populations in two genome-wide association …
Cumulative risk impact of five genetic variants associated with papillary thyroid carcinoma
S Liyanarachchi, A Wojcicka, W Li, M Czetwertynska… - Thyroid, 2013 - liebertpub.com
Background: Two recent genome-wide association studies (GWASs) identified five single
nucleotide polymorphisms (SNPs; rs965513, rs944289, rs966423, rs2439302, and …
nucleotide polymorphisms (SNPs; rs965513, rs944289, rs966423, rs2439302, and …