A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
572
33

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
486
33


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
160
26


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
811
26

The RNA component of human telomerase.
J Feng, W D Funk, S S Wang, S L Weinrich, A A Avilion, C P Chiu, R R Adams, E Chang, R C Allsopp, J Yu. Science 1995
20


InTERTpreting telomerase structure and function.
Haley D M Wyatt, Stephen C West, Tara L Beattie. Nucleic Acids Res 2010
101
20


The many facets of H/ACA ribonucleoproteins.
U Thomas Meier. Chromosoma 2005
206
20

Telomerase RNA deficiency in peripheral blood mononuclear cells in X-linked dyskeratosis congenita.
Judy M Y Wong, Mouhammed J Kyasa, Laura Hutchins, Kathleen Collins. Hum Genet 2004
46
20

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
274
20

Extension of life-span by introduction of telomerase into normal human cells.
A G Bodnar, M Ouellette, M Frolkis, S E Holt, C P Chiu, G B Morin, C B Harley, J W Shay, S Lichtsteiner, W E Wright. Science 1998
20

The POT1-TPP1 telomere complex is a telomerase processivity factor.
Feng Wang, Elaine R Podell, Arthur J Zaug, Yuting Yang, Paul Baciu, Thomas R Cech, Ming Lei. Nature 2007
469
20

Telomerase catalytic subunit homologs from fission yeast and human.
T M Nakamura, G B Morin, K B Chapman, S L Weinrich, W H Andrews, J Lingner, C B Harley, T R Cech. Science 1997
20

Short telomeres are a risk factor for idiopathic pulmonary fibrosis.
Jonathan K Alder, Julian J-L Chen, Lisa Lancaster, Sonye Danoff, Shu-chih Su, Joy D Cogan, Irma Vulto, Mingyi Xie, Xiaodong Qi, Rubin M Tuder,[...]. Proc Natl Acad Sci U S A 2008
469
20

Structure of active dimeric human telomerase.
Anselm Sauerwald, Sara Sandin, Gaël Cristofari, Sjors H W Scheres, Joachim Lingner, Daniela Rhodes. Nat Struct Mol Biol 2013
88
20

The accumulation and not the specific activity of telomerase ribonucleoprotein determines telomere maintenance deficiency in X-linked dyskeratosis congenita.
Xi-Lei Zeng, Naresh R Thumati, Helen B Fleisig, Kyle R Hukezalie, Sharon A Savage, Neelam Giri, Blanche P Alter, Judy M Y Wong. Hum Mol Genet 2012
21
20


Common variants near TERC are associated with mean telomere length.
Veryan Codd, Massimo Mangino, Pim van der Harst, Peter S Braund, Michael Kaiser, Alan J Beveridge, Suzanne Rafelt, Jasbir Moore, Chris Nelson, Nicole Soranzo,[...]. Nat Genet 2010
238
20

Identification of seven loci affecting mean telomere length and their association with disease.
Veryan Codd, Christopher P Nelson, Eva Albrecht, Massimo Mangino, Joris Deelen, Jessica L Buxton, Jouke Jan Hottenga, Krista Fischer, Tõnu Esko, Ida Surakka,[...]. Nat Genet 2013
583
20

How shelterin protects mammalian telomeres.
Wilhelm Palm, Titia de Lange. Annu Rev Genet 2008
13

Human box H/ACA pseudouridylation guide RNA machinery.
Arnold M Kiss, Beáta E Jády, Edouard Bertrand, Tamás Kiss. Mol Cell Biol 2004
136
13

Dyskeratosis congenita in all its forms.
I Dokal. Br J Haematol 2000
354
13

The human TruB family of pseudouridine synthase genes, including the Dyskeratosis Congenita 1 gene and the novel member TRUB1.
Cinzia Zucchini, Pierluigi Strippoli, Alessia Biolchi, Rossella Solmi, Luca Lenzi, Pietro D'Addabbo, Paolo Carinci, Luisa Valvassori. Int J Mol Med 2003
22
13


Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
292
13

Dyskeratosis congenita.
A Marrone, P J Mason. Cell Mol Life Sci 2003
52
13

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
683
13

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.
Blanche P Alter, Neelam Giri, Sharon A Savage, June A Peters, Jennifer T Loud, Lisa Leathwood, Ann G Carr, Mark H Greene, Philip S Rosenberg. Br J Haematol 2010
202
13

Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells.
Luis F Z Batista, Matthew F Pech, Franklin L Zhong, Ha Nam Nguyen, Kathleen T Xie, Arthur J Zaug, Sharon M Crary, Jinkuk Choi, Vittorio Sebastiano, Athena Cherry,[...]. Nature 2011
176
13

A novel DKC1 mutation, severe combined immunodeficiency (T+B-NK- SCID) and bone marrow transplantation in an infant with Hoyeraal-Hreidarsson syndrome.
Fausto Cossu, Tom J Vulliamy, Anna Marrone, Manuela Badiali, Antonio Cao, Inderjeet Dokal. Br J Haematol 2002
54
13

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
237
13

The biogenesis and regulation of telomerase holoenzymes.
Kathleen Collins. Nat Rev Mol Cell Biol 2006
209
13

Dyskeratosis congenita: telomerase, telomeres and anticipation.
Anna Marrone, Amanda Walne, Inderjeet Dokal. Curr Opin Genet Dev 2005
92
13

Syndromes of telomere shortening.
Mary Armanios. Annu Rev Genomics Hum Genet 2009
232
13

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
55
13


Noncoding RNAs of the H/ACA family.
M Terns, R Terns. Cold Spring Harb Symp Quant Biol 2006
38
13

An intronic mutation in DKC1 in an infant with Høyeraal-Hreidarsson syndrome.
Toni Pearson, Fiona Curtis, Ayman Al-Eyadhy, Salem Al-Tamemi, Bruce Mazer, Yigal Dror, Sharon Abish, Sherri Bale, John Compton, Reena Ray,[...]. Am J Med Genet A 2008
12
16

H/ACA guide RNAs, proteins and complexes.
Keqiong Ye. Curr Opin Struct Biol 2007
39
13

Protein composition of catalytically active human telomerase from immortal cells.
Scott B Cohen, Mark E Graham, George O Lovrecz, Nicolai Bache, Phillip J Robinson, Roger R Reddel. Science 2007
464
13

Subnuclear shuttling of human telomerase induced by transformation and DNA damage.
Judy M Y Wong, Leonard Kusdra, Kathleen Collins. Nat Cell Biol 2002
194
13


Telomere length in the newborn.
Koji Okuda, Arlene Bardeguez, Jeffrey P Gardner, Paulette Rodriguez, Vijaya Ganesh, Masayuki Kimura, Joan Skurnick, Girgis Awad, Abraham Aviv. Pediatr Res 2002
331
13

Real-time quantitative PCR of telomere length.
Marcel E Gil, Thérèsa L Coetzer. Mol Biotechnol 2004
102
13

Telomere length and risk of incident cancer and cancer mortality.
Peter Willeit, Johann Willeit, Agnes Mayr, Siegfried Weger, Friedrich Oberhollenzer, Anita Brandstätter, Florian Kronenberg, Stefan Kiechl. JAMA 2010
338
13

Structure of the Tribolium castaneum telomerase catalytic subunit TERT.
Andrew J Gillis, Anthony P Schuller, Emmanuel Skordalakes. Nature 2008
191
13


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.