(Q38261984)

1 September 2017

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title

Genetic predisposition for nonmedullary thyroid cancer (English)

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1 September 2017

Rebecca Nagy

1

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PubMed ID

25338077

1 September 2017

Matthew D Ringel

series ordinal

2

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1 September 2017

22 October 2014

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1 September 2017

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1 September 2017

6

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1 September 2017

1

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1 September 2017

13-20

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https://scigraph.springernature.com/pub.10.1007/s12672-014-0205-y

1 September 2017

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cites work

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21 January 2018

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21 January 2018

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Papillary thyroid carcinoma in Iceland. A study of the occurrence in families and the coexistence of other primary tumours

21 January 2018

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Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria

21 January 2018

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Cowden syndrome: a critical review of the clinical literature

21 January 2018

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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 January 2018

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Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations

21 January 2018

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FAP associated cribriform morular variant of PTC: striking female prevalence and indolent course.

21 January 2018

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Cribriform-morular variant of papillary thyroid carcinoma: an indication to screen for occult FAP.

21 January 2018

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Familial adenomatous polyposis-associated, cribriform morular variant of papillary thyroid carcinoma harboring a K-RAS mutation: case presentation and review of molecular mechanisms

21 January 2018

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Carney complex: the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis

21 January 2018

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A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

21 January 2018

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Spectrum and risk of neoplasia in Werner syndrome: a systematic review

21 January 2018

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Familial thyroid cancer: a review

21 January 2018

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Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer

21 January 2018

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Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series

21 January 2018

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Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer

21 January 2018

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A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

21 January 2018

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Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21

21 January 2018

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Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: a SNP array-based linkage analysis of 38 families

21 January 2018

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

21 January 2018

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SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility

21 January 2018

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Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway

21 January 2018

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Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance

21 January 2018

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Common SNP in pre-miR-146a decreases mature miR expression and predisposes to papillary thyroid carcinoma

21 January 2018

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Polymorphic mature microRNAs from passenger strand of pre-miR-146a contribute to thyroid cancer

21 January 2018

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Common obesity-related genetic variants and papillary thyroid cancer risk

21 January 2018

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Investigation of insulin resistance gene polymorphisms in patients with differentiated thyroid cancer.

21 January 2018

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Common variants of the thyroglobulin gene are associated with differentiated thyroid cancer risk

21 January 2018

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Polymorphisms of DNA damage response genes in radiation-related and sporadic papillary thyroid carcinoma.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Association of BRCA1 functional single nucleotide polymorphisms with risk of differentiated thyroid carcinoma

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

XRCC1 polymorphisms and differentiated thyroid carcinoma risk: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Significance of MDM2 and P14 ARF polymorphisms in susceptibility to differentiated thyroid carcinoma

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma

21 January 2018

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Common genetic variants related to genomic integrity and risk of papillary thyroid cancer

21 January 2018

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Role of genetic variants of autophagy genes in susceptibility for non-medullary thyroid cancer and patients outcome

21 January 2018

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Common genetic variants in metabolism and detoxification pathways and the risk of papillary thyroid cancer

21 January 2018

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Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer

21 January 2018

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Association between single-nucleotide polymorphisms of BRAF and papillary thyroid carcinoma in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Genome-wide association study on differentiated thyroid cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Common genetic variants on FOXE1 contributes to thyroid cancer susceptibility: evidence based on 16 studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Cumulative risk impact of five genetic variants associated with papillary thyroid carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Significant SNPs have limited prediction ability for thyroid cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Localization of the gene for Cowden disease to chromosome 10q22–23

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12672-014-0205-Y

Association studies of OGG1, XRCC1, XRCC2 and XRCC3 polymorphisms with differentiated thyroid cancer

21 January 2018

1 reference

12 December 2020

The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches

1 reference

12 December 2020

Associations between rs965513/rs944289 and papillary thyroid carcinoma risk: a meta-analysis

1 reference

12 December 2020

Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome

1 reference

12 December 2020

Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population

1 reference

12 December 2020

Modification of cancer risks in offspring by sibling and parental cancers from 2,112,616 nuclear families.

1 reference

12 December 2020

Familial nonmedullary thyroid carcinoma

1 reference

12 December 2020

Mapping a New Familial Thyroid Epithelial Neoplasia Susceptibility Locus to Chromosome 8p23.1-p22 by High-Density Single-Nucleotide Polymorphism Genome-Wide Linkage Analysis

1 reference

12 December 2020

In patients with thyroid cancer of follicular cell origin, a family history of nonmedullary thyroid cancer in one first-degree relative is associated with more aggressive disease

1 reference

12 December 2020

Familial occurrence of nonmedullary thyroid cancer: a population-based study of 5673 first-degree relatives of thyroid cancer patients from Norway.

1 reference

12 December 2020

Biological behavior and prognosis of familial papillary thyroid carcinoma

1 reference

12 December 2020

Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands

1 reference

12 December 2020

Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk.

1 reference

12 December 2020

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

1 reference

12 December 2020

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

1 reference

12 December 2020

Germline mutations of the APC gene in patients with familial adenomatous polyposis-associated thyroid carcinoma: results from a European cooperative study

1 reference

12 December 2020

10.1007/S12672-014-0205-Y

Identifiers

DOI

1 reference

PubMed ID

25338077

Dimensions Publication ID

1 September 2017

0 references

1 reference

PubMed ID

25338077