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

No abstract is available for this paper.

• Publication year

  1998

• Venue

  American Journal of Human Genetics

• Publication date

  1998-12-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1086/302164PMID 9837827PMCID PMC1377646
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Solitary, multiple, and familial oxyphil tumours of the thyroid gland

  1998cited by this paper
• Familial papillary carcinoma of the thyroid.

  1997cited by this paper
• Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.

  1997cited by this paper
• Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

  1997cited by this paper
• Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid.

  1997cited by this paper
• Physical and genetic mapping of novel microsatellite polymorphisms on human chromosome 19.

  1996cited by this paper
• RET mutations in human disease.

  1996cited by this paper
• Parametric and nonparametric linkage analysis: a unified multipoint approach.

  1996influential reference
• An integrated metric physical map of human chromosome 19

  1995influential reference
• Familial Nonmedullary Thyroid Cancer: An Emerging Entity That Warrants Aggressive Treatment

  1995cited by this paper
• Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands.

  1994cited by this paper
• Expression of adhesion molecule ICAM-1 (CD54) in thyroid papillary adenocarcinoma

  1994cited by this paper
• Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm

  1994cited by this paper
• Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidism

  1994cited by this paper
• Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

  1993cited by this paper
• Familial Papillary Carcinoma of the Thyroid

  1992influential reference
• Overexpression of the c-MET/HGF receptor gene in human thyroid carcinomas.

  1992cited by this paper
• High frequency of activation of tyrosine kinase oncogenes in human papillary thyroid carcinoma.

  1989cited by this paper
• Computer-simulation methods in human linkage analysis.

  1989influential reference
• Familial occurrence of differentiated, nonmedullary thyroid carcinoma

  1988cited by this paper
• An autosomal dominant form of adolescent multinodular goiter.

  1986influential reference
• Familial papillary carcinoma of the thyroid.

  1986cited by this paper
• Easy calculations of lod scores and genetic risks on small computers.

  1984influential reference
• Congenital goiter and the development of metastatic follicular carcinoma with evidence for a leak of nonhormonal iodide: clinical, pathological, kinetic, and biochemical studies and a review of the literature.

  1981influential reference
• Familial occurrence of papillary thyroid carcinoma

  1980influential reference

• Familial Thyroid Cancers Syndromes.

  2025cites this paper
• Chromosomal localization of mutated genes in non-syndromic familial thyroid cancer

  2024cites this paper
• Identification of P21 (CDKN1A) Activated Kinase 4 as a Susceptibility Gene for Familial Non-Medullary Thyroid Carcinoma

  2024cites this paper
• Familial nonmedullary thyroid cancer: a case series in Iranian patients with a meta-review of case series.

  2023cites this paper
• Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome Sequencing

  2023cites this paper
• Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes

  2022cites this paper
• Susceptibility Genes and Chromosomal Regions Associated With Non-Syndromic Familial Non-Medullary Thyroid Carcinoma: Some Pathogenetic and Diagnostic Keys

  2022influential citation
• Prognostic Relevance of ZNF844 and Chr 19p13.2 KRAB-Zinc Finger Proteins in Clear Cell Renal Carcinoma

  2022cites this paper
• Genetic susceptibility to hereditary non-medullary thyroid cancer

  2022cites this paper
• Familial Nonmedullary Thyroid Cancer

  2021cites this paper
• Identification of NID1 as a novel candidate susceptibility gene for familial non-medullary thyroid carcinoma using whole-exome sequencing

  2021cites this paper
• Inherited Follicular Epithelial-Derived Thyroid Carcinomas: From Molecular Biology to Histological Correlates

  2021cites this paper
• A pathogenic variant in CHEK2 shows a founder effect in Portuguese Roma patients with thyroid cancer

  2021cites this paper
• Inherited Thyroid Tumors With Oncocytic Change

  2021cites this paper
• Genetics of Familial Non-Medullary Thyroid Carcinoma (FNMTC)

  2021influential citation
• Unexpected Widespread Bone Metastases from a BRAF K601N Mutated Follicular Thyroid Carcinoma within a Previously Resected Multinodular Goiter

  2021cites this paper
• Il carcinoma familiare non midollare della tiroide non sindromico

  2021cites this paper
• Papillary Thyroid Cancer Affecting Multiple Family Members: A Case Report and Literature Review of Familial Nonmedullary Thyroid Cancer

  2021cites this paper
• Pathogenic Mitochondrial DNA Mutation Load Inversely Correlates with Malignant Features in Familial Oncocytic Parathyroid Tumors Associated with Hyperparathyroidism-Jaw Tumor Syndrome

  2021cites this paper
• Familial non-medullary thyroid cancer: a critical review

  2020cites this paper
• Családi halmozódást mutató papillaris pajzsmirigy-carcinoma

  2020cites this paper
• Myosins and Disease.

  2020cites this paper
• Variants in LRRC34 reveal distinct mechanisms for predisposition to papillary thyroid carcinoma

  2020cites this paper
• Characterizing the function of EPB41L4A in the predisposition to papillary thyroid carcinoma

  2020cites this paper
• Nonsyndromic Familial Thyroid Cancer

  2020cites this paper
• Familial Nonmedullary Thyroid Cancer

  2020cites this paper
• The American Association of Endocrine Surgeons Guidelines for the Definitive Surgical Management of Thyroid Disease in Adults.

  2020cites this paper
• mtDNA mutations in cancer

  2020cites this paper
• Genetic Mutations and Variants in the Susceptibility of Familial Non-Medullary Thyroid Cancer

  2020cites this paper
• Familial non-medullary thyroid carcinoma: clinico-pathological features, current knowledge and novelty regarding genetic risk factors.

  2020cites this paper
• A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres

  2020cites this paper
• Oncocytic thyroid neoplasms: from histology to molecular biology

  2019cites this paper
• Familial Non-Medullary Thyroid Cancer

  2018cites this paper
• An InDel in Phospholipase-CB-1 is linked with euthyroid multinodular goiter 1 2 *

  2018cites this paper
• An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter

  2018cites this paper
• Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer

  2018influential citation
• Biología molecular del carcinoma de tiroides de estirpe folicular (II). Aplicaciones clínicas

  2018cites this paper
• C14orf93 (RTFC) is identified as a novel susceptibility gene for familial nonmedullary thyroid cancer.

  2017cites this paper
• Inherited variants in genes somatically mutated in thyroid cancer

  2017cites this paper
• Etiopathogenesis of oncocytomas.

  2017cites this paper
• Clinical Presentation and Diagnosis of Hürthle Cell Thyroid Cancer

  2017cites this paper
• Etude des facteurs de risque génétiques et des interactions gène-environnement dans les cancers différenciés de la thyroïde

  2017cites this paper
• Familial thyroid carcinoma: the road less traveled in thyroid pathology – an update

  2017cites this paper
• Familial non-medullary thyroid cancer: unraveling the genetic maze.

  2016cites this paper
• Thyroid Hürthle cell tumors: research of potential markers of malignancy

  2016cites this paper
• Diagnosis and Management of Hereditary Thyroid Cancer.

  2016cites this paper
• The Role of Genetics in the Development of Familial Nonmedullary Thyroid Cancer

  2016cites this paper
• Familial non-medullary thyroid cancer: an update on the genetic and pathologic features

  2016cites this paper
• FOXE1 Polymorphism Interacts with Dietary Iodine Intake in Differentiated Thyroid Cancer Risk in the Cuban Population

  2016cites this paper
• Clinicopathological features and prognosis of familial papillary thyroid carcinoma – a large‐scale, matched, case–control study

  2016cites this paper
• The impact of family history on non-medullary thyroid cancer.

  2016cites this paper
• The HABP2 G534E variant is an unlikely cause of familial non-medullary thyroid cancer.

  2016cites this paper
• Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer

  2015cites this paper
• Emergency JJ Stent for Septic Shock under Remifentanil Sedation - An Option when Interventional Radiology is not available

  2015cites this paper
• An Overview of Thyroid Cancer Genetics and Inheritance

  2015cites this paper
• A germline mutation in SRRM2, a splicing factor gene, is implicated in papillary thyroid carcinoma predisposition

  2015cites this paper
• Single nucleotide polymorphisms of the Fas gene are associated with papillary thyroid cancer.

  2015cites this paper
• Genetic Predisposition for Nonmedullary Thyroid Cancer

  2015cites this paper
• [Thyroid pathology. Case n(o) 2: Follicular oncocytic adenoma].

  2015cites this paper
• Hereditary thyroid cancer syndromes and genetic testing

  2015cites this paper
• Familial vs sporadic papillary thyroid carcinoma: a matched-case comparative study showing similar clinical/prognostic behaviour.

  2014cites this paper
• Controversies in familial thyroid cancer 2014.

  2014cites this paper
• Common genetic variant on 14q13.3 contributes to thyroid cancer susceptibility: evidence based on 12 studies

  2014cites this paper
• Ailesel tiroid kanseri hakkinda tartişmali konular 2014

  2014cites this paper
• Common genetic variants on FOXE1 contributes to thyroid cancer susceptibility: evidence based on 16 studies

  2014cites this paper
• Controversies in familial thyroid cancer 2014

  2014cites this paper
• Familial nonmedullary thyroid cancer: screening, clinical, molecular and genetic findings.

  2014cites this paper
• Molecular approaches to thyroid cancer diagnosis.

  2014cites this paper
• Variants in the ATM‐CHEK2‐BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma

  2014cites this paper
• The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma

  2014cites this paper
• Oncocytic Lesions of the Neuroendocrine System

  2014cites this paper
• SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility.

  2013cites this paper
• 当センターで治療経験した家族性非髄様甲状腺癌（familial nonmedullary thyroid cancer：FNMTC）症例の検討

  2013cites this paper
• Genome-wide association study on differentiated thyroid cancer.

  2013cites this paper
• Cumulative Risk Impact of Five Genetic Variants Associated with Papillary Thyroid Carcinoma

  2013cites this paper
• CQ25. Does Prognosis of Oxyphilic (Hurthle Cell) Follicular Carcinoma Differ from That of Conventional Follicular Carcinoma

  2013cites this paper
• Unraveling the Genetic Predisposition to Differentiated Thyroid Carcinoma

  2013cites this paper
• Familial Nonmedullary Thyroid Carcinoma

  2013cites this paper
• Association Study of Chemokine (C–C motif) Ligand 5 Gene Polymorphism and Papillary Thyroid Cancer

  2013cites this paper
• Unraveling the genetic predisposition to differentiated thyroid carcinoma.

  2013cites this paper
• MATCHED-CASE COMPARATIVE STUDY SHOWING SIMILAR 2

  2013cites this paper
• Association study of integrins beta 1 and beta 2 gene polymorphism and papillary thyroid cancer.

  2013cites this paper
• Ultra-Rare Mutation in Long-Range Enhancer Predisposes to Thyroid Carcinoma with High Penetrance

  2013cites this paper
• Approach to and treatment of differentiated thyroid carcinoma.

  2012cites this paper
• Family history of malignant and benign thyroid diseases and risk of thyroid cancer: a population-based case–control study in New Caledonia

  2012cites this paper
• A genetic association analysis of polymorphisms, rs2282695 and rs12373539, in the FOSB gene and papillary thyroid cancer

  2012cites this paper
• The role of GRIM-19 and STAT3 interaction in renal tumorigenesis

  2012cites this paper
• Telomere abnormalities and chromosome fragility in patients affected by familial papillary thyroid cancer.

  2012cites this paper
• Associations between promoter polymorphism -106A/G of interleukin-11 receptor alpha and papillary thyroid cancer in Korean population.

  2012cites this paper
• Analysis of loss of heterozygsity effect on thyroid tumor with oxyphilia cell locus in familial non medullary thyroid carcinoma in Iranian families

  2012cites this paper
• 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

  2012cites this paper
• Radioactive iodine-refractory differentiated thyroid cancer: unmet needs and future directions

  2012cites this paper
• Allelic loss of susceptibility loci and the occurrence of BRAF and RAS mutations in patients with familial non‐medullary thyroid cancer

  2012cites this paper
• The biology and the genetics of Hurthle cell tumors of the thyroid.

  2012cites this paper
• Association between a promoter polymorphism (rs2192752, –1028A/C) of interleukin 1 receptor, type I (IL1R1) and location of papillary thyroid carcinoma in a Korean population

  2012cites this paper
• FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility

  2012cites this paper
• Discipline : Santé Publique ʹ Epidémiologie

  2012cites this paper
• Lack of Mutations of the Telomerase RNA Component in Familial Papillary Thyroid Cancer with Short Telomeres

  2012cites this paper
• Rôle des facteurs de risque familiaux, individuels et environnementaux dans les cancers de la thyroïde : analyse d'études cas-témoins

  2012cites this paper
• Genomic profiling of mitochondrion-rich breast carcinoma: chromosomal changes may be relevant for mitochondria accumulation and tumour biology

  2012cites this paper