A citation-based method for searching scientific literature

Alison A Bertuch. RNA Biol 2016
Times Cited: 82







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



Times Cited
  Times     Co-cited
Similarity



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
8

Skewed X-inactivation in carriers of X-linked dyskeratosis congenita.
T J Vulliamy, S W Knight, I Dokal, P J Mason. Blood 1997
50
8

Diamond Blackfan anemia: a model for the translational approach to understanding human disease.
Adrianna Vlachos, Lionel Blanc, Jeffrey M Lipton. Expert Rev Hematol 2014
43
9

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
Adrianna Vlachos, Sarah Ball, Niklas Dahl, Blanche P Alter, Sujit Sheth, Ugo Ramenghi, Joerg Meerpohl, Stefan Karlsson, Johnson M Liu, Thierry Leblanc,[...]. Br J Haematol 2008
252
4

Triple-helix structure in telomerase RNA contributes to catalysis.
Feng Qiao, Thomas R Cech. Nat Struct Mol Biol 2008
90
4

Clonal hematopoiesis in patients with dyskeratosis congenita.
Nieves Perdigones, Juan C Perin, Irene Schiano, Peter Nicholas, Jaclyn A Biegel, Philip J Mason, Daria V Babushok, Monica Bessler. Am J Hematol 2016
24
16

Structure and function of the telomeric CST complex.
Cory Rice, Emmanuel Skordalakes. Comput Struct Biotechnol J 2016
52
7

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
464
4

Dyskeratosis congenita.
Tom Vulliamy, Inderjeet Dokal. Semin Hematol 2006
75
5

Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry.
Kasiani C Myers, Audrey Anna Bolyard, Barbara Otto, Trisha E Wong, Amanda T Jones, Richard E Harris, Stella M Davies, David C Dale, Akiko Shimamura. J Pediatr 2014
71
5

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.
Marcin W Wlodarski, Shinsuke Hirabayashi, Victor Pastor, Jan Starý, Henrik Hasle, Riccardo Masetti, Michael Dworzak, Markus Schmugge, Marry van den Heuvel-Eibrink, Marek Ussowicz,[...]. Blood 2016
167
4

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.
Daniel A Arber, Attilio Orazi, Robert Hasserjian, Jürgen Thiele, Michael J Borowitz, Michelle M Le Beau, Clara D Bloomfield, Mario Cazzola, James W Vardiman. Blood 2016
4

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
4

Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation.
Lisa Mirabello, Payal P Khincha, Steven R Ellis, Neelam Giri, Seth Brodie, Settara C Chandrasekharappa, Frank X Donovan, Weiyin Zhou, Belynda D Hicks, Joseph F Boland,[...]. J Med Genet 2017
55
7


RNaseH1 regulates TERRA-telomeric DNA hybrids and telomere maintenance in ALT tumour cells.
Rajika Arora, Yongwoo Lee, Harry Wischnewski, Catherine M Brun, Tobias Schwarz, Claus M Azzalin. Nat Commun 2014
201
4


Telomeres and aging.
Geraldine Aubert, Peter M Lansdorp. Physiol Rev 2008
636
4

Cell biology of disease: Telomeropathies: an emerging spectrum disorder.
Brody Holohan, Woodring E Wright, Jerry W Shay. J Cell Biol 2014
107
4

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
4

Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono,[...]. Blood 2017
60
6

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.
Polina Stepensky, Montserrat Chacón-Flores, Katherine H Kim, Omar Abuzaitoun, Arnulfo Bautista-Santos, Natalia Simanovsky, Dritan Siliqi, Davide Altamura, Alfonso Méndez-Godoy, Abril Gijsbers,[...]. J Med Genet 2017
54
7

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
569
4

Phenotypes in mTERT⁺/⁻ and mTERT⁻/⁻ mice are due to short telomeres, not telomere-independent functions of telomerase reverse transcriptase.
Margaret A Strong, Sofia L Vidal-Cardenas, Baktiar Karim, Huimin Yu, Nini Guo, Carol W Greider. Mol Cell Biol 2011
85
4

p53 Mediates Failure of Human Definitive Hematopoiesis in Dyskeratosis Congenita.
Wilson Chun Fok, Evandro Luis de Oliveira Niero, Carissa Dege, Kirsten Ann Brenner, Christopher Michael Sturgeon, Luis Francisco Zirnberger Batista. Stem Cell Reports 2017
17
23


Telomeres in cancer: tumour suppression and genome instability.
John Maciejowski, Titia de Lange. Nat Rev Mol Cell Biol 2017
272
4

Telomere restoration and extension of proliferative lifespan in dyskeratosis congenita fibroblasts.
Erik R Westin, Elizabeth Chavez, Kimberly M Lee, Francoise A Gourronc, Soraya Riley, Peter M Lansdorp, Frederick D Goldman, Aloysius J Klingelhutz. Aging Cell 2007
44
9

Triallelic and epigenetic-like inheritance in human disorders of telomerase.
Laura C Collopy, Amanda J Walne, Shirleny Cardoso, Josu de la Fuente, Mahfuzah Mohamed, Helga Toriello, Hannah Tamary, Adam J Y V Ling, Timothy Lloyd, Rebecca Kassam,[...]. Blood 2015
28
14

Telomere diseases.
Rodrigo T Calado, Neal S Young. N Engl J Med 2009
511
4

Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.
Payal P Khincha, Alison A Bertuch, Suneet Agarwal, Danielle M Townsley, Neal S Young, Siobán Keel, Akiko Shimamura, Farid Boulad, Tregony Simoneau, Henri Justino,[...]. Eur Respir J 2017
21
19

Poly(A)-specific ribonuclease (PARN): an allosterically regulated, processive and mRNA cap-interacting deadenylase.
Anders Virtanen, Niklas Henriksson, Per Nilsson, Mikael Nissbeck. Crit Rev Biochem Mol Biol 2013
46
8

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
124
4


Current Insights to Regulation and Role of Telomerase in Human Diseases.
Mert Burak Ozturk, Yinghui Li, Vinay Tergaonkar. Antioxidants (Basel) 2017
34
11

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
396
4

Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation.
R Coleman Lindsley, Wael Saber, Brenton G Mar, Robert Redd, Tao Wang, Michael D Haagenson, Peter V Grauman, Zhen-Huan Hu, Stephen R Spellman, Stephanie J Lee,[...]. N Engl J Med 2017
324
4

Outcome of haematopoietic stem cell transplantation in dyskeratosis congenita.
Francesca Fioredda, Simona Iacobelli, Elisabeth T Korthof, Cora Knol, Anja van Biezen, Dorine Bresters, Paul Veys, Ayami Yoshimi, Franca Fagioli, Brune Mats,[...]. Br J Haematol 2018
26
15

Telomere length in inherited bone marrow failure syndromes.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2015
39
10




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
17
23

Replicating through telomeres: a means to an end.
Paula Martínez, Maria A Blasco. Trends Biochem Sci 2015
80
5

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
6


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
24
16

Telomeres and telomerase: three decades of progress.
Jerry W Shay, Woodring E Wright. Nat Rev Genet 2019
190
4



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.