A citation-based method for searching scientific literature

Noa Lamm, Elly Ordan, Rotem Shponkin, Carmelit Richler, Memet Aker, Yehuda Tzfati. PLoS One 2009
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


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
631
45


Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.
Hiroki Yamaguchi, Rodrigo T Calado, Hinh Ly, Sachiko Kajigaya, Gabriela M Baerlocher, Stephen J Chanock, Peter M Lansdorp, Neal S Young. N Engl J Med 2005
483
37

The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita.
T Vulliamy, A Marrone, F Goldman, A Dearlove, M Bessler, P J Mason, I Dokal. Nature 2001
681
37

Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10.
Amanda J Walne, Tom Vulliamy, Anna Marrone, Richard Beswick, Michael Kirwan, Yuka Masunari, Fat-Hia Al-Qurashi, Mahmoud Aljurf, Inderjeet Dokal. Hum Mol Genet 2007
204
37

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
205
37


TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.
Sharon A Savage, Neelam Giri, Gabriela M Baerlocher, Nick Orr, Peter M Lansdorp, Blanche P Alter. Am J Hum Genet 2008
269
37

Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.
Mary Armanios, Jiunn-Liang Chen, Yen-Pei Christy Chang, Robert A Brodsky, Anita Hawkins, Constance A Griffin, James R Eshleman, Alan R Cohen, Aravinda Chakravarti, Ada Hamosh,[...]. Proc Natl Acad Sci U S A 2005
295
37

Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation.
Tom J Vulliamy, Anna Marrone, Stuart W Knight, Amanda Walne, Philip J Mason, Inderjeet Dokal. Blood 2006
223
37

RTEL1 dismantles T loops and counteracts telomeric G4-DNA to maintain telomere integrity.
Jean-Baptiste Vannier, Visnja Pavicic-Kaltenbrunner, Mark I R Petalcorin, Hao Ding, Simon J Boulton. Cell 2012
292
37

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
105
33

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
33

Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal-Hreidarsson syndrome.
Fabien Touzot, Isabelle Callebaut, Jean Soulier, Laetitia Gaillard, Chantal Azerrad, Anne Durandy, Alain Fischer, Jean-Pierre de Villartay, Patrick Revy. Proc Natl Acad Sci U S A 2010
54
33

Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.
Amanda J Walne, Tom Vulliamy, Michael Kirwan, Vincent Plagnol, Inderjeet Dokal. Am J Hum Genet 2013
132
33

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia.
Rodrigo T Calado, Joshua A Regal, Mark Hills, William T Yewdell, Leandro F Dalmazzo, Marco A Zago, Peter M Lansdorp, Donna Hogge, Stephen J Chanock, Elihu H Estey,[...]. Proc Natl Acad Sci U S A 2009
126
29

Dyskeratosis congenita in all its forms.
I Dokal. Br J Haematol 2000
352
29


DNA damage foci at dysfunctional telomeres.
Hiroyuki Takai, Agata Smogorzewska, Titia de Lange. Curr Biol 2003
968
29

Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
Tom Vulliamy, Anna Marrone, Richard Szydlo, Amanda Walne, Philip J Mason, Inderjeet Dokal. Nat Genet 2004
321
29

How shelterin protects mammalian telomeres.
Wilhelm Palm, Titia de Lange. Annu Rev Genet 2008
29

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
29

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

Telomerase activity in human germline and embryonic tissues and cells.
W E Wright, M A Piatyszek, W E Rainey, W Byrd, J W Shay. Dev Genet 1996
951
25

A human telomerase holoenzyme protein required for Cajal body localization and telomere synthesis.
Andrew S Venteicher, Eladio B Abreu, Zhaojing Meng, Kelly E McCann, Rebecca M Terns, Timothy D Veenstra, Michael P Terns, Steven E Artandi. Science 2009
340
25

Association between aplastic anaemia and mutations in telomerase RNA.
Tom Vulliamy, Anna Marrone, Inderjeet Dokal, Philip J Mason. Lancet 2002
211
25


Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1.
S W Knight, N S Heiss, T J Vulliamy, C M Aalfs, C McMahon, P Richmond, A Jones, R C Hennekam, A Poustka, P J Mason,[...]. Br J Haematol 1999
150
25

Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification.
Davide Ruggero, Silvia Grisendi, Francesco Piazza, Eduardo Rego, Francesca Mari, Pulivarthi H Rao, Carlos Cordon-Cardo, Pier Paolo Pandolfi. Science 2003
303
25

A spectrum of severe familial liver disorders associate with telomerase mutations.
Rodrigo T Calado, Joshua A Regal, David E Kleiner, David S Schrump, Nathan R Peterson, Veronica Pons, Stephen J Chanock, Peter M Lansdorp, Neal S Young. PLoS One 2009
123
25

Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita.
Franklin Zhong, Sharon A Savage, Marina Shkreli, Neelam Giri, Lea Jessop, Timothy Myers, Renee Chen, Blanche P Alter, Steven E Artandi. Genes Dev 2011
164
25


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
142
25

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.
Beverley H Anderson, Paul R Kasher, Josephine Mayer, Marcin Szynkiewicz, Emma M Jenkinson, Sanjeev S Bhaskar, Jill E Urquhart, Sarah B Daly, Jonathan E Dickerson, James O'Sullivan,[...]. Nat Genet 2012
160
25

Functional characterization of natural telomerase mutations found in patients with hematologic disorders.
Zhong-Tao Xin, Adam D Beauchamp, Rodrigo T Calado, Jennifer W Bradford, Joshua A Regal, Aarthi Shenoy, Yuying Liang, Peter M Lansdorp, Neal S Young, Hinh Ly. Blood 2007
72
20

Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome.
Hiroki Yamaguchi, Gabriela M Baerlocher, Peter M Lansdorp, Stephen J Chanock, Olga Nunez, Elaine Sloand, Neal S Young. Blood 2003
215
20


The effect of TERC haploinsufficiency on the inheritance of telomere length.
Fred Goldman, Rachida Bouarich, Shashikant Kulkarni, Sara Freeman, Hong-Yan Du, Lea Harrington, Philip J Mason, Arturo Londoño-Vallejo, Monica Bessler. Proc Natl Acad Sci U S A 2005
77
20

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
20

A conserved WD40 protein binds the Cajal body localization signal of scaRNP particles.
Kazimierz T Tycowski, Mei-Di Shu, Abiodun Kukoyi, Joan A Steitz. Mol Cell 2009
143
20

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
795
20

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
236
20

Mouse dyskerin mutations affect accumulation of telomerase RNA and small nucleolar RNA, telomerase activity, and ribosomal RNA processing.
Yuko Mochizuki, Jun He, Shashikant Kulkarni, Monica Bessler, Philip J Mason. Proc Natl Acad Sci U S A 2004
134
20

Adult-onset pulmonary fibrosis caused by mutations in telomerase.
Kalliopi D Tsakiri, Jennifer T Cronkhite, Phillip J Kuan, Chao Xing, Ganesh Raghu, Jonathan C Weissler, Randall L Rosenblatt, Jerry W Shay, Christine Kim Garcia. Proc Natl Acad Sci U S A 2007
556
20

Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood.
G S Sasa, A Ribes-Zamora, N D Nelson, A A Bertuch. Clin Genet 2012
50
20

TIN2 protein dyskeratosis congenita missense mutants are defective in association with telomerase.
Dong Yang, Quanyuan He, Hyeung Kim, Wenbin Ma, Zhou Songyang. J Biol Chem 2011
45
20

Impaired control of IRES-mediated translation in X-linked dyskeratosis congenita.
Andrew Yoon, Guang Peng, Yves Brandenburger, Ornella Zollo, Wei Xu, Eduardo Rego, Davide Ruggero. Science 2006
294
20

Dyskeratosis congenita as a disorder of telomere maintenance.
Nya D Nelson, Alison A Bertuch. Mutat Res 2012
87
20

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
556
20

CTC1 Mutations in a patient with dyskeratosis congenita.
Rachel B Keller, Katelyn E Gagne, G Naheed Usmani, George K Asdourian, David A Williams, Inga Hofmann, Suneet Agarwal. Pediatr Blood Cancer 2012
84
20


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.