A citation-based method for searching scientific literature

Valerie M Tesmer, Eric M Smith, Oana Danciu, Shilpa Padmanaban, Jayakrishnan Nandakumar. Proc Natl Acad Sci U S A 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
28

Essential role of mouse telomerase in highly proliferative organs.
H W Lee, M A Blasco, G J Gottlieb, J W Horner, C W Greider, R A DePinho. Nature 1998
993
28

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
290
28


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
141
28

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
28

Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Jonathan K Alder, Susan E Stanley, Christa L Wagner, Makenzie Hamilton, Vidya Sagar Hanumanthu, Mary Armanios. Chest 2015
88
28

Stn1-Ten1 is an Rpa2-Rpa3-like complex at telomeres.
Jia Sun, Eun Young Yu, Yuting Yang, Laura A Confer, Steven H Sun, Ke Wan, Neal F Lue, Ming Lei. Genes Dev 2009
105
28

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
28

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
28

CDK phosphorylation of TRF2 controls t-loop dynamics during the cell cycle.
Grzegorz Sarek, Panagiotis Kotsantis, Phil Ruis, David Van Ly, Pol Margalef, Valerie Borel, Xiao-Feng Zheng, Helen R Flynn, Ambrosius P Snijders, Dipanjan Chowdhury,[...]. Nature 2019
27
28

N-terminal residues of human dyskerin are required for interactions with telomerase RNA that prevent RNA degradation.
Deanna E MacNeil, Patrick Lambert-Lanteigne, Chantal Autexier. Nucleic Acids Res 2019
9
28

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
28

Mice with Pulmonary Fibrosis Driven by Telomere Dysfunction.
Juan M Povedano, Paula Martinez, Juana M Flores, Francisca Mulero, Maria A Blasco. Cell Rep 2015
115
28

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
28


Crystal structure of a Cbf5-Nop10-Gar1 complex and implications in RNA-guided pseudouridylation and dyskeratosis congenita.
Rumana Rashid, Bo Liang, Daniel L Baker, Osama A Youssef, Yang He, Kathleen Phipps, Rebecca M Terns, Michael P Terns, Hong Li. Mol Cell 2006
126
28

Recognition and elongation of telomeres by telomerase.
E H Blackburn, C W Greider, E Henderson, M S Lee, J Shampay, D Shippen-Lentz. Genome 1989
129
28

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
79
28


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
28

TRF2 recruits RTEL1 to telomeres in S phase to promote t-loop unwinding.
Grzegorz Sarek, Jean-Baptiste Vannier, Stephanie Panier, John H J Petrini, Simon J Boulton. Mol Cell 2015
89
28

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
28

Telomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybrids.
Shira Sagie, Shir Toubiana, Stella R Hartono, Hagar Katzir, Aya Tzur-Gilat, Shany Havazelet, Claire Francastel, Guillaume Velasco, Frédéric Chédin, Sara Selig. Nat Commun 2017
52
28

A triple helix within a pseudoknot is a conserved and essential element of telomerase RNA.
Kinneret Shefer, Yogev Brown, Valentin Gorkovoy, Tamar Nussbaum, Nikolai B Ulyanov, Yehuda Tzfati. Mol Cell Biol 2007
65
28

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
28


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
28


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
28

Pulmonary fibrosis associated with TINF2 gene mutation: is somatic reversion required?
Caroline Kannengiesser, Raphael Borie, Patrick Revy. Eur Respir J 2014
12
28

A POT1 mutation implicates defective telomere end fill-in and telomere truncations in Coats plus.
Hiroyuki Takai, Emma Jenkinson, Shaheen Kabir, Riyana Babul-Hirji, Nasrin Najm-Tehrani, David A Chitayat, Yanick J Crow, Titia de Lange. Genes Dev 2016
45
28

RTEL1: functions of a disease-associated helicase.
Jean-Baptiste Vannier, Grzegorz Sarek, Simon J Boulton. Trends Cell Biol 2014
68
28

Longevity, stress response, and cancer in aging telomerase-deficient mice.
K L Rudolph, S Chang, H W Lee, M Blasco, G J Gottlieb, C Greider, R A DePinho. Cell 1999
981
28


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
28

RTEL1 is a replisome-associated helicase that promotes telomere and genome-wide replication.
Jean-Baptiste Vannier, Sumit Sandhu, Mark I R Petalcorin, Xiaoli Wu, Zinnatun Nabi, Hao Ding, Simon J Boulton. Science 2013
121
28

Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure.
Tom J Vulliamy, Amanda Walne, Aroon Baskaradas, Philip J Mason, Anna Marrone, Inderjeet Dokal. Blood Cells Mol Dis 2005
140
28

Human CST Facilitates Genome-wide RAD51 Recruitment to GC-Rich Repetitive Sequences in Response to Replication Stress.
Megan Chastain, Qing Zhou, Olga Shiva, Maria Fadri-Moskwik, Leanne Whitmore, Pingping Jia, Xueyu Dai, Chenhui Huang, Ping Ye, Weihang Chai. Cell Rep 2016
29
28

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
28

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
28


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
28



Investigation of chromosome X inactivation and clinical phenotypes in female carriers of DKC1 mutations.
Jialin Xu, Payal P Khincha, Neelam Giri, Blanche P Alter, Sharon A Savage, Judy M Y Wong. Am J Hematol 2016
15
28

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
28

N-terminal domains of the human telomerase catalytic subunit required for enzyme activity in vivo.
B N Armbruster, S S Banik, C Guo, A C Smith, C M Counter. Mol Cell Biol 2001
138
28

Many disease-associated variants of hTERT retain high telomerase enzymatic activity.
Arthur J Zaug, Sharon M Crary, Matthew Jesse Fioravanti, Kristina Campbell, Thomas R Cech. Nucleic Acids Res 2013
47
28

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
28


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.