A citation-based method for searching scientific literature

Anna Marrone, Amanda Walne, Hannah Tamary, Yuka Masunari, Michael Kirwan, Richard Beswick, Tom Vulliamy, Inderjeet Dokal. Blood 2007
Times Cited: 105







List of co-cited articles
1118 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
60

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
56

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
53

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
482
51

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
49

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
267
48

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
47


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
317
42


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
791
38

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
36

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
220
34

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
552
33

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
32

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
30

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
30


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
234
27

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
26

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

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
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
31


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
22

TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.
Hong-Yan Du, Elena Pumbo, Jennifer Ivanovich, Ping An, Richard T Maziarz, Ulrike M Reiss, Deborah Chirnomas, Akiko Shimamura, Adrianna Vlachos, Jeffrey M Lipton,[...]. Blood 2009
95
22


Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA.
Patrick F Fogarty, Hiroki Yamaguchi, Adrian Wiestner, Gabriela M Baerlocher, Elaine Sloand, Weihua S Zeng, Elizabeth J Read, Peter M Lansdorp, Neal S Young. Lancet 2003
188
20

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
302
19

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
19

Telomere shortening and tumor formation by mouse cells lacking telomerase RNA.
M A Blasco, H W Lee, M P Hande, E Samper, P M Lansdorp, R A DePinho, C W Greider. Cell 1997
17

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
157
17

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
17

Telomeres shorten during ageing of human fibroblasts.
C B Harley, A B Futcher, C W Greider. Nature 1990
16

Specific association of human telomerase activity with immortal cells and cancer.
N W Kim, M A Piatyszek, K R Prowse, C B Harley, M D West, P L Ho, G M Coviello, W E Wright, S L Weinrich, J W Shay. Science 1994
16

Complex inheritance pattern of dyskeratosis congenita in two families with 2 different mutations in the telomerase reverse transcriptase gene.
Hong-Yan Du, Elena Pumbo, Peter Manley, Joshua J Field, Susan J Bayliss, David B Wilson, Philip J Mason, Monica Bessler. Blood 2008
40
40

Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndrome.
Zhong Deng, Galina Glousker, Aliah Molczan, Alan J Fox, Noa Lamm, Jayaraju Dheekollu, Orr-El Weizman, Michael Schertzer, Zhuo Wang, Olga Vladimirova,[...]. Proc Natl Acad Sci U S A 2013
87
18

Congenital hypoplastic thrombocytopenia and cerebral malformations in two brothers.
H M Hoyeraal, J Lamvik, P J Moe. Acta Paediatr Scand 1970
90
16

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
123
15

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
83
18




A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure.
S Hreidarsson, K Kristjansson, G Johannesson, J H Johannsson. Acta Paediatr Scand 1988
82
17

Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia.
Michael Kirwan, Tom Vulliamy, Anna Marrone, Amanda J Walne, Richard Beswick, Peter Hillmen, Richard Kelly, Andrew Stewart, David Bowen, Stefan O Schonland,[...]. Hum Mutat 2009
80
17

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
454
13


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
122
13

The TEL patch of telomere protein TPP1 mediates telomerase recruitment and processivity.
Jayakrishnan Nandakumar, Caitlin F Bell, Ina Weidenfeld, Arthur J Zaug, Leslie A Leinwand, Thomas R Cech. Nature 2012
200
13

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
21


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.