(Q44175459)

English

Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population

scientific article published on 11 July 2013

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scholarly article

1 reference

Europe PubMed Central

30 November 2017

Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population (English)

1 reference

Europe PubMed Central

30 November 2017

genome-wide association study

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susceptibility locus

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based on heuristic

inferred from title

papillary thyroid cancer

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based on heuristic

inferred from title

10

object named as

Li Jin

1 reference

Europe PubMed Central

30 November 2017

author name string

Yu-Long Wang

1

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Europe PubMed Central

30 November 2017

Shou-Hao Feng

2

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Europe PubMed Central

30 November 2017

Shi-Cheng Guo

3

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Europe PubMed Central

30 November 2017

Wen-Jun Wei

4

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Europe PubMed Central

30 November 2017

Duan-Shu Li

5

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Europe PubMed Central

30 November 2017

Yu Wang

6

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Europe PubMed Central

30 November 2017

Xiaofeng Wang

7

1 reference

Europe PubMed Central

30 November 2017

Zhuo-Ying Wang

8

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Europe PubMed Central

30 November 2017

Yan-Yun Ma

9

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Europe PubMed Central

30 November 2017

Qing-Hai Ji

11

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Europe PubMed Central

30 November 2017

Jiu-Cun Wang

12

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30 November 2017

language of work or name

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publication date

11 July 2013

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30 November 2017

Journal of Medical Genetics

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30 November 2017

50

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30 November 2017

10

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689-695

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30 November 2017

Cancer statistics, 2013

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https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Pathogenetic mechanisms in thyroid follicular-cell neoplasia

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Risk of thyroid cancer in first-degree relatives of patients with non-medullary thyroid cancer by histology type and age at diagnosis: a joint study from five Nordic countries.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The FOXE1 and NKX2-1 loci are associated with susceptibility to papillary thyroid carcinoma in the Japanese population.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Discovery of common variants associated with low TSH levels and thyroid cancer risk

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Rationales, design and recruitment of the Taizhou Longitudinal Study

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The ENCODE (ENCyclopedia Of DNA Elements) Project

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The UCSC Cancer Genomics Browser: update 2013.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

BEDTools: a flexible suite of utilities for comparing genomic features

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21).

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Extreme population differences across Neuregulin 1 gene, with implications for association studies.

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

The thyroid hormone receptor and the insulator protein CTCF: two different factors with overlapping functions

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

CTCF: master weaver of the genome

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

SNP-SNP interactions in breast cancer susceptibility

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

SNPassoc: an R package to perform whole genome association studies

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101687

21 January 2018

Identifiers

10.1136/JMEDGENET-2013-101687

1 reference

Europe PubMed Central

30 November 2017

1 reference

Europe PubMed Central

30 November 2017

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