A citation-based method for searching scientific literature

Bai-Wei Gu, Marisa Apicella, Jason Mills, Jian-Meng Fan, Dara A Reeves, Deborah French, Gregory M Podsakoff, Monica Bessler, Philip J Mason. PLoS One 2015
Times Cited: 19







List of co-cited articles
297 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
52

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
224
47

Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs.
Thomas Winkler, So Gun Hong, Jake E Decker, Mary J Morgan, Chuanfeng Wu, William M Hughes, Yanqin Yang, Danny Wangsa, Hesed M Padilla-Nash, Thomas Ried,[...]. J Clin Invest 2013
48
31

Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
31





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
631
21

Functional analysis of a chromosomal deletion associated with myelodysplastic syndromes using isogenic human induced pluripotent stem cells.
Andriana G Kotini, Chan-Jung Chang, Ibrahim Boussaad, Jeffrey J Delrow, Emily K Dolezal, Abhinav B Nagulapally, Fabiana Perna, Gregory A Fishbein, Virginia M Klimek, R David Hawkins,[...]. Nat Biotechnol 2015
97
21

Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice.
Jun He, Sandra Navarrete, Murek Jasinski, Tom Vulliamy, Inderjeet Dokal, Monica Bessler, Philip J Mason. Oncogene 2002
71
21

Induced pluripotent stem cell lines derived from human somatic cells.
Junying Yu, Maxim A Vodyanik, Kim Smuga-Otto, Jessica Antosiewicz-Bourget, Jennifer L Frane, Shulan Tian, Jeff Nie, Gudrun A Jonsdottir, Victor Ruotti, Ron Stewart,[...]. Science 2007
21

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
144
21

Enhancing a Wnt-Telomere Feedback Loop Restores Intestinal Stem Cell Function in a Human Organotypic Model of Dyskeratosis Congenita.
Dong-Hun Woo, Qijun Chen, Ting-Lin B Yang, M Rebecca Glineburg, Carla Hoge, Nicolae A Leu, F Brad Johnson, Christopher J Lengner. Cell Stem Cell 2016
33
21

Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.
Beverley H Anderson, Paul R Kasher, Josephine Mayer, Marcin Szynkiewicz, Emma M Jenkinson, Sanjeev S Bhaskar, Jill E Urquhart, Sarah B Daly, Jonathan E Dickerson, James O'Sullivan,[...]. Nat Genet 2012
162
21

H/ACA small RNA dysfunctions in disease reveal key roles for noncoding RNA modifications in hematopoietic stem cell differentiation.
Cristian Bellodi, Mary McMahon, Adrian Contreras, Dayle Juliano, Noam Kopmar, Tomoka Nakamura, David Maltby, Alma Burlingame, Sharon A Savage, Akiko Shimamura,[...]. Cell Rep 2013
73
21

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
322
21

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
21

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
21

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
345
15

Disease-specific induced pluripotent stem cells.
In-Hyun Park, Natasha Arora, Hongguang Huo, Nimet Maherali, Tim Ahfeldt, Akiko Shimamura, M William Lensch, Chad Cowan, Konrad Hochedlinger, George Q Daley. Cell 2008
15

Brief report: human pluripotent stem cell models of fanconi anemia deficiency reveal an important role for fanconi anemia proteins in cellular reprogramming and survival of hematopoietic progenitors.
Sun K Yung, Katarzyna Tilgner, Maria H Ledran, Saba Habibollah, Irina Neganova, Chatchawan Singhapol, Gabriele Saretzki, Miodrag Stojkovic, Lyle Armstrong, Stefan Przyborski,[...]. Stem Cells 2013
40
15


Wnt signaling controls the specification of definitive and primitive hematopoiesis from human pluripotent stem cells.
Christopher M Sturgeon, Andrea Ditadi, Geneve Awong, Marion Kennedy, Gordon Keller. Nat Biotechnol 2014
214
15

Congenital amegakaryocytic thrombocytopenia iPS cells exhibit defective MPL-mediated signaling.
Shinji Hirata, Naoya Takayama, Ryoko Jono-Ohnishi, Hiroshi Endo, Sou Nakamura, Takeaki Dohda, Masanori Nishi, Yuhei Hamazaki, Ei-ichi Ishii, Shin Kaneko,[...]. J Clin Invest 2013
40
15

Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells.
Angel Raya, Ignasi Rodríguez-Pizà, Guillermo Guenechea, Rita Vassena, Susana Navarro, María José Barrero, Antonella Consiglio, Maria Castellà, Paula Río, Eduard Sleep,[...]. Nature 2009
492
15

Pluripotent stem cell models of Shwachman-Diamond syndrome reveal a common mechanism for pancreatic and hematopoietic dysfunction.
Asmin Tulpule, James M Kelley, M William Lensch, Jade McPherson, In Hyun Park, Odelya Hartung, Tomoka Nakamura, Thorsten M Schlaeger, Akiko Shimamura, George Q Daley. Cell Stem Cell 2013
55
15

Overcoming reprogramming resistance of Fanconi anemia cells.
Lars U W Müller, Michael D Milsom, Chad E Harris, Rutesh Vyas, Kristina M Brumme, Kalindi Parmar, Lisa A Moreau, Axel Schambach, In-Hyun Park, Wendy B London,[...]. Blood 2012
106
15

Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients.
Loïc Garçon, Jingping Ge, Shwetha H Manjunath, Jason A Mills, Marisa Apicella, Shefali Parikh, Lisa M Sullivan, Gregory M Podsakoff, Paul Gadue, Deborah L French,[...]. Blood 2013
62
15

Embryonic stem cell lines derived from human blastocysts.
J A Thomson, J Itskovitz-Eldor, S S Shapiro, M A Waknitz, J J Swiergiel, V S Marshall, J M Jones. Science 1998
15

Telomere diseases.
Rodrigo T Calado, Neal S Young. N Engl J Med 2009
511
15


T lymphocyte potential marks the emergence of definitive hematopoietic progenitors in human pluripotent stem cell differentiation cultures.
Marion Kennedy, Geneve Awong, Christopher M Sturgeon, Andrea Ditadi, Ross LaMotte-Mohs, Juan Carlos Zúñiga-Pflücker, Gordon Keller. Cell Rep 2012
239
15

Generation of engraftable hematopoietic stem cells from induced pluripotent stem cells by way of teratoma formation.
Nao Suzuki, Satoshi Yamazaki, Tomoyuki Yamaguchi, Motohito Okabe, Hideki Masaki, Satoshi Takaki, Makoto Otsu, Hiromitsu Nakauchi. Mol Ther 2013
142
15

Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity.
F Ann Ran, Patrick D Hsu, Chie-Yu Lin, Jonathan S Gootenberg, Silvana Konermann, Alexandro E Trevino, David A Scott, Azusa Inoue, Shogo Matoba, Yi Zhang,[...]. Cell 2013
15

Dyskeratosis congenita: two examples of this multisystem disorder.
R Womer, J E Clark, P Wood, H Sabio, T E Kelly. Pediatrics 1983
52
15

Dyskeratosis congenita in all its forms.
I Dokal. Br J Haematol 2000
353
15

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
562
15

Molecular insights into the heterogeneity of telomere reprogramming in induced pluripotent stem cells.
Fang Wang, Yu Yin, Xiaoying Ye, Kai Liu, Haiying Zhu, Lingling Wang, Maria Chiourea, Maja Okuka, Guangzhen Ji, Jiameng Dan,[...]. Cell Res 2012
59
15

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
269
15

Multiplex genome engineering using CRISPR/Cas systems.
Le Cong, F Ann Ran, David Cox, Shuailiang Lin, Robert Barretto, Naomi Habib, Patrick D Hsu, Xuebing Wu, Wenyan Jiang, Luciano A Marraffini,[...]. Science 2013
15

Telomeres acquire embryonic stem cell characteristics in induced pluripotent stem cells.
Rosa M Marion, Katerina Strati, Han Li, Agueda Tejera, Stefan Schoeftner, Sagrario Ortega, Manuel Serrano, Maria A Blasco. Cell Stem Cell 2009
335
15

Three novel truncating TINF2 mutations causing severe dyskeratosis congenita in early childhood.
G S Sasa, A Ribes-Zamora, N D Nelson, A A Bertuch. Clin Genet 2012
50
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
85
15


Dyskeratosis congenita caused by a novel TERT point mutation in siblings with pancytopenia and exudative retinopathy.
Akshay Sharma, Kasiani Myers, Zhan Ye, John D'Orazio. Pediatr Blood Cancer 2014
13
23

Bilateral retinal vasculopathy associated with autosomal dominant dyskeratosis congenita.
Sara Vaz-Pereira, Patricio A Pacheco, Shreyans Gandhi, Austin G Kulasekararaj, Judith C Marsh, Bishwanath Pal, Ghulam J Mufti. Eur J Ophthalmol 2013
13
23

Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
Charles A Johnson, Mark Hatfield, Jose S Pulido. Ophthalmic Genet 2009
15
20


Retinal vasculopathy in autosomal dominant dyskeratosis congenita due to TINF2 mutation.
Mary Gleeson, Aengus O'Marcaigh, Melanie Cotter, Donal Brosnahan, Tom Vulliamy, Owen P Smith. Br J Haematol 2012
9
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.