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Times Cited: 11
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Times Co-cited
Similarity
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.
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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
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Identification of Rare Variants Predisposing to Thyroid Cancer.
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POT1 loss-of-function variants predispose to familial melanoma.
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Carla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, Lauren G Aoude, Víctor Quesada, Zhihao Ding, Karen A Pooley, Antonia L Pritchard, Jessamy C Tiffen, Mia Petljak,[...]. Nat Genet 2014
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Diego Loayza, Titia De Lange. Nature 2003
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A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer.
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Aayushi Srivastava, Beiping Miao, Diamanto Skopelitou, Varun Kumar, Abhishek Kumar, Nagarajan Paramasivam, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli. Cancers (Basel) 2020
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Genetic variation in POT1 and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study.
Melissa A Richard, Philip J Lupo, Lindsay M Morton, Yutaka A Yasui, Yadav A Sapkota, Michael A Arnold, Geraldine Aubert, Joseph P Neglia, Lucie M Turcotte, Wendy M Leisenring,[...]. PLoS One 2020
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Short telomeres, telomerase reverse transcriptase gene amplification, and increased telomerase activity in the blood of familial papillary thyroid cancer patients.
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Assessing thyroid cancer risk using polygenic risk scores.
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A genome-wide association study yields five novel thyroid cancer risk loci.
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The TEL patch of telomere protein TPP1 mediates telomerase recruitment and processivity.
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The enigma of excessively long telomeres in cancer: lessons learned from rare human POT1 variants.
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TPP1 OB-fold domain controls telomere maintenance by recruiting telomerase to chromosome ends.
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Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma.
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Structural and functional analysis of the human POT1-TPP1 telomeric complex.
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Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non-CDKN2A/CDK4 melanoma families.
Thomas P Potjer, Sander Bollen, Anneliese J E M Grimbergen, Remco van Doorn, Nelleke A Gruis, Christi J van Asperen, Frederik J Hes, Nienke van der Stoep. Int J Cancer 2019
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A mutation in the POT1 gene is responsible for cardiac angiosarcoma in TP53-negative Li-Fraumeni-like families.
Oriol Calvete, Paula Martinez, Pablo Garcia-Pavia, Carlos Benitez-Buelga, Beatriz Paumard-Hernández, Victoria Fernandez, Fernando Dominguez, Clara Salas, Nuria Romero-Laorden, Jesus Garcia-Donas,[...]. Nat Commun 2015
Oriol Calvete, Paula Martinez, Pablo Garcia-Pavia, Carlos Benitez-Buelga, Beatriz Paumard-Hernández, Victoria Fernandez, Fernando Dominguez, Clara Salas, Nuria Romero-Laorden, Jesus Garcia-Donas,[...]. Nat Commun 2015
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Insights into Genetic Susceptibility to Melanoma by Gene Panel Testing: Potential Pathogenic Variants in ACD, ATM, BAP1, and POT1.
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Lorenza Pastorino, Virginia Andreotti, Bruna Dalmasso, Irene Vanni, Giulia Ciccarese, Mario Mandalà, Giuseppe Spadola, Maria Antonietta Pizzichetta, Giovanni Ponti, Maria Grazia Tibiletti,[...]. Cancers (Basel) 2020
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Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
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TPP1 Blocks an ATR-Mediated Resection Mechanism at Telomeres.
Tatsuya Kibe, Michal Zimmermann, Titia de Lange. Mol Cell 2016
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Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity.
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Leukocyte Telomere Length and Risk of Papillary Thyroid Carcinoma.
Ji Li, Changming An, Haitao Zheng, Tianshui Lei, Nasha Zhang, Yan Zheng, Ming Yang. J Clin Endocrinol Metab 2019
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The genetics of hereditary nonmedullary thyroid carcinoma.
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On the prevalence of familial nonmedullary thyroid cancer in multiply affected kindreds.
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Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer.
Sudheer Kumar Gara, Li Jia, Maria J Merino, Sunita K Agarwal, Lisa Zhang, Maggie Cam, Dhaval Patel, Electron Kebebew. N Engl J Med 2015
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2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer.
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Current Knowledge of Germline Genetic Risk Factors for the Development of Non-Medullary Thyroid Cancer.
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Endocrine tumours: familial nonmedullary thyroid carcinoma is a more aggressive disease: a systematic review and meta-analysis.
Xiaofei Wang, Wenli Cheng, Jingdong Li, Anping Su, Tao Wei, Feng Liu, Jingqiang Zhu. Eur J Endocrinol 2015
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Prevalence, clinicopathologic features, and somatic genetic mutation profile in familial versus sporadic nonmedullary thyroid cancer.
Willieford Moses, Julie Weng, Electron Kebebew. Thyroid 2011
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Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series.
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A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.
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MYH9 binds to lncRNA gene PTCSC2 and regulates FOXE1 in the 9q22 thyroid cancer risk locus.
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Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
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NOP53 as A Candidate Modifier Locus for Familial Non-Medullary Thyroid Cancer.
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Telomere length is shorter in affected members of families with familial nonmedullary thyroid cancer.
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DICER1 mutations in familial pleuropulmonary blastoma.
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A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24.
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Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer.
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18
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.