A citation-based method for searching scientific literature

P M Barbaro, D S Ziegler, R R Reddel. Intern Med J 2016
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Telomeres shorten during ageing of human fibroblasts.
C B Harley, A B Futcher, C W Greider. Nature 1990
31



Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
Blanche P Alter, Gabriela M Baerlocher, Sharon A Savage, Stephen J Chanock, Babette B Weksler, Judith P Willner, June A Peters, Neelam Giri, Peter M Lansdorp. Blood 2007
234
31

Specific association of human telomerase activity with immortal cells and cancer.
N W Kim, M A Piatyszek, K R Prowse, C B Harley, M D West, P L Ho, G M Coviello, W E Wright, S L Weinrich, J W Shay. Science 1994
25

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
25

The genetics and clinical manifestations of telomere biology disorders.
Sharon A Savage, Alison A Bertuch. Genet Med 2010
133
25

Telomerase mutations in families with idiopathic pulmonary fibrosis.
Mary Y Armanios, Julian J-L Chen, Joy D Cogan, Jonathan K Alder, Roxann G Ingersoll, Cheryl Markin, William E Lawson, Mingyi Xie, Irma Vulto, John A Phillips,[...]. N Engl J Med 2007
791
25

Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.
Amanda J Walne, Tom Vulliamy, Michael Kirwan, Vincent Plagnol, Inderjeet Dokal. Am J Hum Genet 2013
131
25

Mammalian telomeres end in a large duplex loop.
J D Griffith, L Comeau, S Rosenfield, R M Stansel, A Bianchi, H Moss, T de Lange. Cell 1999
18

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
547
18


X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
628
18

How shelterin protects mammalian telomeres.
Wilhelm Palm, Titia de Lange. Annu Rev Genet 2008
18

Telomere measurement by quantitative PCR.
Richard M Cawthon. Nucleic Acids Res 2002
18

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
208
18

The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenita.
Shahinaz M Gadalla, Payal P Khincha, Hormuzd A Katki, Neelam Giri, Jason Y Y Wong, Stephen Spellman, Jack A Yanovski, Joan C Han, Immaculata De Vivo, Blanche P Alter,[...]. Mol Genet Genomic Med 2016
15
20

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
188
18

Telomere length is associated with disease severity and declines with age in dyskeratosis congenita.
Blanche P Alter, Philip S Rosenberg, Neelam Giri, Gabriela M Baerlocher, Peter M Lansdorp, Sharon A Savage. Haematologica 2012
115
18

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
235
18

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
78
18


Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
Tangui Le Guen, Laurent Jullien, Fabien Touzot, Michael Schertzer, Laetitia Gaillard, Mylène Perderiset, Wassila Carpentier, Patrick Nitschke, Capucine Picard, Gérard Couillault,[...]. Hum Mol Genet 2013
100
18

Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia.
Helen E Speedy, Ben Kinnersley, Daniel Chubb, Peter Broderick, Philip J Law, Kevin Litchfield, Sandrine Jayne, Martin J S Dyer, Claire Dearden, George A Follows,[...]. Blood 2016
47
18

Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
Caroline Kannengiesser, Raphael Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunes,[...]. Eur Respir J 2015
85
18

Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndrome.
Zhong Deng, Galina Glousker, Aliah Molczan, Alan J Fox, Noa Lamm, Jayaraju Dheekollu, Orr-El Weizman, Michael Schertzer, Zhuo Wang, Olga Vladimirova,[...]. Proc Natl Acad Sci U S A 2013
87
18

Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.
Galina Glousker, Fabien Touzot, Patrick Revy, Yehuda Tzfati, Sharon A Savage. Br J Haematol 2015
58
18

A DNA damage checkpoint response in telomere-initiated senescence.
Fabrizio d'Adda di Fagagna, Philip M Reaper, Lorena Clay-Farrace, Heike Fiegler, Philippa Carr, Thomas Von Zglinicki, Gabriele Saretzki, Nigel P Carter, Stephen P Jackson. Nature 2003
18




Blood cell telomere length is a dynamic feature.
Ulrika Svenson, Katarina Nordfjäll, Duncan Baird, Laureline Roger, Pia Osterman, Mai-Lis Hellenius, Göran Roos. PLoS One 2011
86
12

Telomeres shorten at equivalent rates in somatic tissues of adults.
Lily Daniali, Athanase Benetos, Ezra Susser, Jeremy D Kark, Carlos Labat, Masayuki Kimura, Kunji Desai, Mark Granick, Abraham Aviv. Nat Commun 2013
385
12

POT1 protects telomeres from a transient DNA damage response and determines how human chromosomes end.
Dirk Hockemeyer, Agnel J Sfeir, Jerry W Shay, Woodring E Wright, Titia de Lange. EMBO J 2005
215
12

Conservation of the human telomere sequence (TTAGGG)n among vertebrates.
J Meyne, R L Ratliff, R K Moyzis. Proc Natl Acad Sci U S A 1989
577
12

Telomere lengths are characteristic in each human individual.
Kaiyo Takubo, Naotaka Izumiyama-Shimomura, Naoko Honma, Motoji Sawabe, Tomio Arai, Motonobu Kato, Mitsuo Oshimura, Ken-Ichi Nakamura. Exp Gerontol 2002
209
12

Estimating telomere length from whole genome sequence data.
Zhihao Ding, Massimo Mangino, Abraham Aviv, Tim Spector, Richard Durbin. Nucleic Acids Res 2014
63
12

Human telomeres and telomere biology disorders.
Sharon A Savage. Prog Mol Biol Transl Sci 2014
40
12


A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes.
R K Moyzis, J M Buckingham, L S Cram, M Dani, L L Deaven, M D Jones, J Meyne, R L Ratliff, J R Wu. Proc Natl Acad Sci U S A 1988
12


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
12

Short telomere length, cancer survival, and cancer risk in 47102 individuals.
Maren Weischer, Børge G Nordestgaard, Richard M Cawthon, Jacob J Freiberg, Anne Tybjærg-Hansen, Stig E Bojesen. J Natl Cancer Inst 2013
150
12

The association of telomere length and cancer: a meta-analysis.
Ingrid M Wentzensen, Lisa Mirabello, Ruth M Pfeiffer, Sharon A Savage. Cancer Epidemiol Biomarkers Prev 2011
320
12

A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk.
Karen A Pooley, Stig E Bojesen, Maren Weischer, Sune F Nielsen, Deborah Thompson, Ali Amin Al Olama, Kyriaki Michailidou, Jonathan P Tyrer, Sara Benlloch, Judith Brown,[...]. Hum Mol Genet 2013
97
12

Telomere length in peripheral blood leukocytes and lung cancer risk: a large case-control study in Caucasians.
Beatriz Sanchez-Espiridion, Meng Chen, Joe Y Chang, Charles Lu, David W Chang, Jack A Roth, Xifeng Wu, Jian Gu. Cancer Res 2014
56
12

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
12

Shortened telomere length is associated with increased risk of cancer: a meta-analysis.
Hongxia Ma, Ziyuan Zhou, Sheng Wei, Zhensheng Liu, Karen A Pooley, Alison M Dunning, Ulrika Svenson, Göran Roos, H Dean Hosgood, Min Shen,[...]. PLoS One 2011
237
12

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
12

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.
Massimo Mangino, Shih-Jen Hwang, Timothy D Spector, Steven C Hunt, Masayuki Kimura, Annette L Fitzpatrick, Lene Christiansen, Inge Petersen, Clara C Elbers, Tamara Harris,[...]. Hum Mol Genet 2012
139
12


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.