A citation-based method for searching scientific literature

Warrick Chilton, Brendan O'Brien, Fadi Charchar. Int J Mol Sci 2017
Times Cited: 11







List of co-cited articles
33 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Telomere length measurement by fluorescence in situ hybridization and flow cytometry: tips and pitfalls.
Gabriela M Baerlocher, Jennifer Mak, Teri Tien, Peter M Lansdorp. Cytometry 2002
102
9

Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data.
Jianxin Shi, Ju-Hyun Park, Jubao Duan, Sonja T Berndt, Winton Moy, Kai Yu, Lei Song, William Wheeler, Xing Hua, Debra Silverman,[...]. PLoS Genet 2016
39
9

Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148.
Jun Fang, Jinping Jia, Matthew Makowski, Mai Xu, Zhaoming Wang, Tongwu Zhang, Jason W Hoskins, Jiyeon Choi, Younghun Han, Mingfeng Zhang,[...]. Nat Commun 2017
17
9

Mediterranean diet and telomere length in high cardiovascular risk subjects from the PREDIMED-NAVARRA study.
Sonia García-Calzón, Miguel A Martínez-González, Cristina Razquin, Fernando Arós, José Lapetra, J Alfredo Martínez, Guillermo Zalba, Amelia Marti. Clin Nutr 2016
37
9

Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.
Bari J Ballew, Meredith Yeager, Kevin Jacobs, Neelam Giri, Joseph Boland, Laurie Burdett, Blanche P Alter, Sharon A Savage. Hum Genet 2013
134
9


Telomere length in white blood cell DNA and lung cancer: a pooled analysis of three prospective cohorts.
Wei Jie Seow, Richard M Cawthon, Mark P Purdue, Wei Hu, Yu-Tang Gao, Wen-Yi Huang, Stephanie J Weinstein, Bu-Tian Ji, Jarmo Virtamo, H Dean Hosgood,[...]. Cancer Res 2014
79
9

X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.
S W Knight, N S Heiss, T J Vulliamy, S Greschner, G Stavrides, G S Pai, G Lestringant, N Varma, P J Mason, I Dokal,[...]. Am J Hum Genet 1999
138
9

Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Bridget D Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, Carlos E Girod,[...]. Nat Genet 2015
225
9


Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.
Alberto Diaz de Leon, Jennifer T Cronkhite, Anna-Luise A Katzenstein, J David Godwin, Ganesh Raghu, Craig S Glazer, Randall L Rosenblatt, Carlos E Girod, Edward R Garrity, Chao Xing,[...]. PLoS One 2010
190
9

Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome.
R Yaghmai, A Kimyai-Asadi, K Rostamiani, N S Heiss, A Poustka, W Eyaid, J Bodurtha, H C Nousari, A Hamosh, A Metzenberg. J Pediatr 2000
43
9

Telomere Length and the Cancer-Atherosclerosis Trade-Off.
Rivka C Stone, Kent Horvath, Jeremy D Kark, Ezra Susser, Sarah A Tishkoff, Abraham Aviv. PLoS Genet 2016
49
9

Telomere dysfunction: a potential cancer predisposition factor.
Xifeng Wu, Christopher I Amos, Yong Zhu, Hua Zhao, Barton H Grossman, Jerry W Shay, Sherry Luo, Waun Ki Hong, Margaret R Spitz. J Natl Cancer Inst 2003
332
9

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
195
9

Association between exposure to second-hand smoke and telomere length: cross-sectional study of 1303 non-smokers.
Liya Lu, Cathy Johnman, Liane McGlynn, Daniel F Mackay, Paul G Shiels, Jill P Pell. Int J Epidemiol 2017
9
11



Short Telomere Length and Ischemic Heart Disease: Observational and Genetic Studies in 290 022 Individuals.
Alexander Scheller Madrid, Line Rode, Børge G Nordestgaard, Stig E Bojesen. Clin Chem 2016
61
9

Stress and telomere biology: a lifespan perspective.
Idan Shalev, Sonja Entringer, Pathik D Wadhwa, Owen M Wolkowitz, Eli Puterman, Jue Lin, Elissa S Epel. Psychoneuroendocrinology 2013
192
9

The association between leukocyte telomere length and cigarette smoking, dietary and physical variables, and risk of prostate cancer.
Lisa Mirabello, Wen-Yi Huang, Jason Y Y Wong, Nilanjan Chatterjee, Douglas Reding, E David Crawford, Immaculata De Vivo, Richard B Hayes, Sharon A Savage. Aging Cell 2009
146
9

Shorter telomere length in Europeans than in Africans due to polygenetic adaptation.
Matthew E B Hansen, Steven C Hunt, Rivka C Stone, Kent Horvath, Utz Herbig, Alessia Ranciaro, Jibril Hirbo, William Beggs, Alexander P Reiner, James G Wilson,[...]. Hum Mol Genet 2016
56
9

Short telomere length and breast cancer risk: a study in sister sets.
Jing Shen, Mary Beth Terry, Irina Gurvich, Yuyan Liao, Ruby T Senie, Regina M Santella. Cancer Res 2007
110
9

The association between telomere length and cancer risk in population studies.
Xun Zhu, Wei Han, Wenjie Xue, Yuxia Zou, Cuiwei Xie, Jiangbo Du, Guangfu Jin. Sci Rep 2016
73
9

TERT promoter mutations in familial and sporadic melanoma.
Susanne Horn, Adina Figl, P Sivaramakrishna Rachakonda, Christine Fischer, Antje Sucker, Andreas Gast, Stephanie Kadel, Iris Moll, Eduardo Nagore, Kari Hemminki,[...]. Science 2013
9

The association of telomere length and genetic variation in telomere biology genes.
Lisa Mirabello, Kai Yu, Peter Kraft, Immaculata De Vivo, David J Hunter, Jennifer Prescott, Jason Y Y Wong, Nilanjan Chatterjee, Richard B Hayes, Sharon A Savage. Hum Mutat 2010
76
9

Extensive Proliferation of Human Cancer Cells with Ever-Shorter Telomeres.
Rebecca A Dagg, Hilda A Pickett, Axel A Neumann, Christine E Napier, Jeremy D Henson, Erdahl T Teber, Jonathan W Arthur, C Patrick Reynolds, Jayne Murray, Michelle Haber,[...]. Cell Rep 2017
32
9

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.
Amos J Simon, Atar Lev, Yong Zhang, Batia Weiss, Anna Rylova, Eran Eyal, Nitzan Kol, Ortal Barel, Keren Cesarkas, Michalle Soudack,[...]. J Exp Med 2016
52
9

Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2018
76
9

Telomeres in molecular epidemiology studies.
Clara Bodelon, Sharon A Savage, Shahinaz M Gadalla. Prog Mol Biol Transl Sci 2014
15
9

Fine mapping of the dyskeratosis congenita locus in Xq28.
S W Knight, T Vulliamy, G L Forni, D Oscier, P J Mason, I Dokal. J Med Genet 1996
22
9

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Stig E Bojesen, Karen A Pooley, Sharon E Johnatty, Jonathan Beesley, Kyriaki Michailidou, Jonathan P Tyrer, Stacey L Edwards, Hilda A Pickett, Howard C Shen, Chanel E Smart,[...]. Nat Genet 2013
368
9

Telomere dysfunction accurately predicts clinical outcome in chronic lymphocytic leukaemia, even in patients with early stage disease.
Thet Thet Lin, Kevin Norris, Nicole H Heppel, Guy Pratt, James M Allan, David J Allsup, James Bailey, Lynn Cawkwell, Robert Hills, Julia W Grimstead,[...]. Br J Haematol 2014
62
9

A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.
Bari J Ballew, Vijai Joseph, Saurav De, Grzegorz Sarek, Jean-Baptiste Vannier, Travis Stracker, Kasmintan A Schrader, Trudy N Small, Richard O'Reilly, Chris Manschreck,[...]. PLoS Genet 2013
77
9

Short telomeres limit tumor progression in vivo by inducing senescence.
David M Feldser, Carol W Greider. Cancer Cell 2007
202
9

Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita.
Tom Vulliamy, Richard Beswick, Michael Kirwan, Anna Marrone, Martin Digweed, Amanda Walne, Inderjeet Dokal. Proc Natl Acad Sci U S A 2008
193
9

Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome.
Anna Marrone, Amanda Walne, Hannah Tamary, Yuka Masunari, Michael Kirwan, Richard Beswick, Tom Vulliamy, Inderjeet Dokal. Blood 2007
101
9

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.
Yiran Guo, Melissa Kartawinata, Jiankang Li, Hilda A Pickett, Juliana Teo, Tatjana Kilo, Pasquale M Barbaro, Brendan Keating, Yulan Chen, Lifeng Tian,[...]. Blood 2014
60
9

A role for the Rb family of proteins in controlling telomere length.
Marta García-Cao, Susana Gonzalo, Douglas Dean, María A Blasco. Nat Genet 2002
74
9


Telomere length and the risk of lung cancer.
Jin Sung Jang, Yi Young Choi, Won Kee Lee, Jin Eun Choi, Sung Ick Cha, Yeon Jae Kim, Chang Ho Kim, Sin Kam, Tae Hoon Jung, Jae Yong Park. Cancer Sci 2008
130
9

Highly recurrent TERT promoter mutations in human melanoma.
Franklin W Huang, Eran Hodis, Mary Jue Xu, Gregory V Kryukov, Lynda Chin, Levi A Garraway. Science 2013
9

Prenatal Air Pollution and Newborns' Predisposition to Accelerated Biological Aging.
Dries S Martens, Bianca Cox, Bram G Janssen, Diana B P Clemente, Antonio Gasparrini, Charlotte Vanpoucke, Wouter Lefebvre, Harry A Roels, Michelle Plusquin, Tim S Nawrot. JAMA Pediatr 2017
84
9

Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN).
Santhosh Dhanraj, Sethu Madhava Rao Gunja, Adam P Deveau, Mikael Nissbeck, Boonchai Boonyawat, Andrew J Coombs, Alessandra Renieri, Mafalda Mucciolo, Annabella Marozza, Sabrina Buoni,[...]. J Med Genet 2015
51
9

Telomere and telomerase stability in human diseases and cancer.
Ilaria Chiodi, Chiara Mondello. Front Biosci (Landmark Ed) 2016
9
11

Telomere length and depression: prospective cohort study and Mendelian randomisation study in 67 306 individuals.
Marie Kim Wium-Andersen, David Dynnes Ørsted, Line Rode, Stig Egil Bojesen, Børge Grønne Nordestgaard. Br J Psychiatry 2017
15
9

Perceived stress and telomere length: A systematic review, meta-analysis, and methodologic considerations for advancing the field.
Maya B Mathur, Elissa Epel, Shelley Kind, Manisha Desai, Christine G Parks, Dale P Sandler, Nayer Khazeni. Brain Behav Immun 2016
111
9

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
89
9

Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.
Amanda J Walne, Tom Vulliamy, Michael Kirwan, Vincent Plagnol, Inderjeet Dokal. Am J Hum Genet 2013
125
9

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
75
9


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.