A citation-based method for searching scientific literature

Deanna E MacNeil, Patrick Lambert-Lanteigne, Chantal Autexier. Nucleic Acids Res 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity



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
55

Inhibition of telomerase RNA decay rescues telomerase deficiency caused by dyskerin or PARN defects.
Siddharth Shukla, Jens C Schmidt, Katherine C Goldfarb, Thomas R Cech, Roy Parker. Nat Struct Mol Biol 2016
61
55

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
547
55

Disruption of Telomerase RNA Maturation Kinetics Precipitates Disease.
Caitlin M Roake, Lu Chen, Ananya L Chakravarthy, James E Ferrell, Grazia D Raffa, Steven E Artandi. Mol Cell 2019
20
55


Cryo-EM structure of substrate-bound human telomerase holoenzyme.
Thi Hoang Duong Nguyen, Jane Tam, Robert A Wu, Basil J Greber, Daniel Toso, Eva Nogales, Kathleen Collins. Nature 2018
87
44

Human Telomerase RNA Processing and Quality Control.
Chi-Kang Tseng, Hui-Fang Wang, Allison M Burns, Morgan R Schroeder, Martina Gaspari, Peter Baumann. Cell Rep 2015
76
44

Posttranscriptional modulation of TERC by PAPD5 inhibition rescues hematopoietic development in dyskeratosis congenita.
Wilson Chun Fok, Siddharth Shukla, Alexandre Teixeira Vessoni, Kirsten Ann Brenner, Roy Parker, Christopher M Sturgeon, Luis Francisco Zirnberger Batista. Blood 2019
17
44

A Polyadenylation-Dependent 3' End Maturation Pathway Is Required for the Synthesis of the Human Telomerase RNA.
Duy Nguyen, Valérie Grenier St-Sauveur, Danny Bergeron, Fabien Dupuis-Sandoval, Michelle S Scott, François Bachand. Cell Rep 2015
68
44

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
338
44

An Activity Switch in Human Telomerase Based on RNA Conformation and Shaped by TCAB1.
Lu Chen, Caitlin M Roake, Adam Freund, Pedro J Batista, Siqi Tian, Yi A Yin, Chandresh R Gajera, Shengda Lin, Byron Lee, Matthew F Pech,[...]. Cell 2018
23
44

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
163
44

Poly(A)-specific ribonuclease (PARN) mediates 3'-end maturation of the telomerase RNA component.
Diane H Moon, Matthew Segal, Baris Boyraz, Eva Guinan, Inga Hofmann, Patrick Cahan, Albert K Tai, Suneet Agarwal. Nat Genet 2015
99
44

ZCCHC8, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.
Dustin L Gable, Valeriya Gaysinskaya, Christine C Atik, C Conover Talbot, Byunghak Kang, Susan E Stanley, Elizabeth W Pugh, Nuria Amat-Codina, Kara M Schenk, Murat O Arcasoy,[...]. Genes Dev 2019
28
44

Telomerase Regulation from Beginning to the End.
Deanna Elise MacNeil, Hélène Jeanne Bensoussan, Chantal Autexier. Genes (Basel) 2016
46
44

Regulation of human telomerase in homeostasis and disease.
Caitlin M Roake, Steven E Artandi. Nat Rev Mol Cell Biol 2020
43
44


Transcriptome-wide mapping reveals widespread dynamic-regulated pseudouridylation of ncRNA and mRNA.
Schraga Schwartz, Douglas A Bernstein, Maxwell R Mumbach, Marko Jovanovic, Rebecca H Herbst, Brian X León-Ricardo, Jesse M Engreitz, Mitchell Guttman, Rahul Satija, Eric S Lander,[...]. Cell 2014
433
33


Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients.
Suneet Agarwal, Yuin-Han Loh, Erin M McLoughlin, Junjiu Huang, In-Hyun Park, Justine D Miller, Hongguang Huo, Maja Okuka, Rosana Maria Dos Reis, Sabine Loewer,[...]. Nature 2010
223
33

Proteostatic control of telomerase function through TRiC-mediated folding of TCAB1.
Adam Freund, Franklin L Zhong, Andrew S Venteicher, Zhaojing Meng, Timothy D Veenstra, Judith Frydman, Steven E Artandi. Cell 2014
72
33

Cell cycle-regulated trafficking of human telomerase to telomeres.
Rebecca L Tomlinson, Tania D Ziegler, Teerawit Supakorndej, Rebecca M Terns, Michael P Terns. Mol Biol Cell 2006
195
33

Stepwise RNP assembly at the site of H/ACA RNA transcription in human cells.
Xavier Darzacq, Nupur Kittur, Sujayita Roy, Yaron Shav-Tal, Robert H Singer, U Thomas Meier. J Cell Biol 2006
121
33



CRM1 controls the composition of nucleoplasmic pre-snoRNA complexes to licence them for nucleolar transport.
Bérengère Pradet-Balade, Cyrille Girard, Séverine Boulon, Conception Paul, Karim Azzag, Rémy Bordonné, Edouard Bertrand, Céline Verheggen. EMBO J 2011
29
33

The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN.
Chi-Kang Tseng, Hui-Fang Wang, Morgan R Schroeder, Peter Baumann. Nat Commun 2018
14
33

TPP1 OB-fold domain controls telomere maintenance by recruiting telomerase to chromosome ends.
Franklin L Zhong, Luis F Z Batista, Adam Freund, Matthew F Pech, Andrew S Venteicher, Steven E Artandi. Cell 2012
184
33

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
33

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
33

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
292
33

Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita.
Hemanth Tummala, Amanda Walne, Laura Collopy, Shirleny Cardoso, Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed,[...]. J Clin Invest 2015
102
33

How shelterin protects mammalian telomeres.
Wilhelm Palm, Titia de Lange. Annu Rev Genet 2008
33

Posttranscriptional manipulation of TERC reverses molecular hallmarks of telomere disease.
Baris Boyraz, Diane H Moon, Matthew Segal, Maud Z Muosieyiri, Asli Aykanat, Albert K Tai, Patrick Cahan, Suneet Agarwal. J Clin Invest 2016
33
33

Absence of cancer-associated changes in human fibroblasts immortalized with telomerase.
C P Morales, S E Holt, M Ouellette, K J Kaur, Y Yan, K S Wilson, M A White, W E Wright, J W Shay. Nat Genet 1999
616
33

Structure and function of telomerase RNA.
Carla A Theimer, Juli Feigon. Curr Opin Struct Biol 2006
142
33


The regulation and functions of the nuclear RNA exosome complex.
Cornelia Kilchert, Sina Wittmann, Lidia Vasiljeva. Nat Rev Mol Cell Biol 2016
163
33

Effects of dyskeratosis congenita mutations in dyskerin, NHP2 and NOP10 on assembly of H/ACA pre-RNPs.
Christian Trahan, Caroline Martel, François Dragon. Hum Mol Genet 2010
37
33

Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells.
Neha Nagpal, Jianing Wang, Jing Zeng, Emily Lo, Diane H Moon, Kevin Luk, Roman O Braun, Lauri M Burroughs, Sioban B Keel, Christopher Reilly,[...]. Cell Stem Cell 2020
15
33

Non-coding RNAs: lessons from the small nuclear and small nucleolar RNAs.
A Gregory Matera, Rebecca M Terns, Michael P Terns. Nat Rev Mol Cell Biol 2007
477
33




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
33

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
33

Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Susan E Stanley, Dustin L Gable, Christa L Wagner, Thomas M Carlile, Vidya Sagar Hanumanthu, Joshua D Podlevsky, Sara E Khalil, Amy E DeZern, Maria F Rojas-Duran, Carolyn D Applegate,[...]. Sci Transl Med 2016
96
33

Differences in disease severity but similar telomere lengths in genetic subgroups of patients with telomerase and shelterin mutations.
Tom J Vulliamy, Michael J Kirwan, Richard Beswick, Upal Hossain, Charlotte Baqai, Anna Ratcliffe, Judith Marsh, Amanda Walne, Inderjeet Dokal. PLoS One 2011
60
33

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
203
33


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.