Huiling He, Wei Li, Daniel F Comiskey, Sandya Liyanarachchi, Taina T Nieminen, Yanqiang Wang, Katherine E DeLap, Pamela Brock, Albert de la Chapelle. Thyroid 2020
Times Cited: 15
Times Cited: 15
Times Cited
Times Co-cited
Similarity
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
Jianxin Shi, Xiaohong R Yang, Bari Ballew, Melissa Rotunno, Donato Calista, Maria Concetta Fargnoli, Paola Ghiorzo, Brigitte Bressac-de Paillerets, Eduardo Nagore, Marie Francoise Avril,[...]. Nat Genet 2014
Jianxin Shi, Xiaohong R Yang, Bari Ballew, Melissa Rotunno, Donato Calista, Maria Concetta Fargnoli, Paola Ghiorzo, Brigitte Bressac-de Paillerets, Eduardo Nagore, Marie Francoise Avril,[...]. Nat Genet 2014
33
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
Lauren G Aoude, Antonia L Pritchard, Carla Daniela Robles-Espinoza, Karin Wadt, Mark Harland, Jiyeon Choi, Michael Gartside, Víctor Quesada, Peter Johansson, Jane M Palmer,[...]. J Natl Cancer Inst 2014
Lauren G Aoude, Antonia L Pritchard, Carla Daniela Robles-Espinoza, Karin Wadt, Mark Harland, Jiyeon Choi, Michael Gartside, Víctor Quesada, Peter Johansson, Jane M Palmer,[...]. J Natl Cancer Inst 2014
33
A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer.
Aayushi Srivastava, Beiping Miao, Diamanto Skopelitou, Varun Kumar, Abhishek Kumar, Nagarajan Paramasivam, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli. Cancers (Basel) 2020
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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Identification of Rare Variants Predisposing to Thyroid Cancer.
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Yanqiang Wang, Sandya Liyanarachchi, Katherine E Miller, Taina T Nieminen, Daniel F Comiskey, Wei Li, Pamela Brock, David E Symer, Keiko Akagi, Katherine E DeLap,[...]. Thyroid 2019
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A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.
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Tremika Le-Shan Wilson, Namita Hattangady, Antonio Marcondes Lerario, Carmen Williams, Erika Koeppe, Shane Quinonez, Jenae Osborne, Kelly B Cha, Tobias Else. Fam Cancer 2017
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Genetic variation in POT1 and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study.
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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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A genome-wide association study yields five novel thyroid cancer risk loci.
Julius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, Lilja Stefansdottir, Jon G Jonasson, Sigurjon A Gudjonsson, Daniel F Gudbjartsson, Gisli Masson, Hrefna Johannsdottir, Gisli H Halldorsson,[...]. Nat Commun 2017
Julius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, Lilja Stefansdottir, Jon G Jonasson, Sigurjon A Gudjonsson, Daniel F Gudbjartsson, Gisli Masson, Hrefna Johannsdottir, Gisli H Halldorsson,[...]. Nat Commun 2017
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Identification, genetic testing, and management of hereditary melanoma.
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POT1 loss-of-function variants predispose to familial melanoma.
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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Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non-CDKN2A/CDK4 melanoma families.
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POT1 as a terminal transducer of TRF1 telomere length control.
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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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30
Assessing thyroid cancer risk using polygenic risk scores.
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Sandya Liyanarachchi, Julius Gudmundsson, Egil Ferkingstad, Huiling He, Jon G Jonasson, Vinicius Tragante, Folkert W Asselbergs, Li Xu, Lambertus A Kiemeney, Romana T Netea-Maier,[...]. Proc Natl Acad Sci U S A 2020
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NOP53 as A Candidate Modifier Locus for Familial Non-Medullary Thyroid Cancer.
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Discovery of common variants associated with low TSH levels and thyroid cancer risk.
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20
Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma.
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20
A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma.
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20
A germline mutation in SRRM2, a splicing factor gene, is implicated in papillary thyroid carcinoma predisposition.
Jerneja Tomsic, Huiling He, Keiko Akagi, Sandya Liyanarachchi, Qun Pan, Blake Bertani, Rebecca Nagy, David E Symer, Benjamin J Blencowe, Albert de la Chapelle. Sci Rep 2015
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Lack of mutations of the telomerase RNA component in familial papillary thyroid cancer with short telomeres.
Silvia Cantara, Serena Capuano, Marco Capezzone, Michele Benigni, Milena Pisu, Stefania Marchisotta, Furio Pacini. Thyroid 2012
Silvia Cantara, Serena Capuano, Marco Capezzone, Michele Benigni, Milena Pisu, Stefania Marchisotta, Furio Pacini. Thyroid 2012
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Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21.
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SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility.
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The enigma of excessively long telomeres in cancer: lessons learned from rare human POT1 variants.
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Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma.
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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.