A citation-based method for searching scientific literature

Yingqi Shao, Sizhou Feng, Jinbo Huang, Jiali Huo, Yahong You, Yizhou Zheng. BMC Med Genet 2018
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
100

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
100

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
100

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
100

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
100

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
100

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
100

Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome.
Anna Marrone, Amanda Walne, Hannah Tamary, Yuka Masunari, Michael Kirwan, Richard Beswick, Tom Vulliamy, Inderjeet Dokal. Blood 2007
105
100

Neuropsychiatric conditions among patients with dyskeratosis congenita: a link with telomere biology?
Sandra Rackley, Maryland Pao, Guillermo F Seratti, Neelam Giri, J J Rasimas, Blanche P Alter, Sharon A Savage. Psychosomatics 2012
17
66

Dyskeratosis congenita induced cirrhosis for liver transplantation-perioperative management.
Anshuman Singh, V K Pandey, Manish Tandon, C K Pandey. Indian J Anaesth 2015
3
66


Dyskeratosis congenita.
V Gupta, B D Bhatia. Indian Pediatr 2008
5
66

Cytogenetic abnormalities in dyskeratosis congenita--report of five cases.
A Aguilar-Martinez, M J Lautre-Ecenarro, F Urbina-González, M C Cristóbal-Gil, P Guerra-Rodriguez, A García-Pérez. Clin Exp Dermatol 1988
18
66

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
66


Dyskeratosis congenita: unusual presenting features within a kindred.
G L Forni, C Melevendi, S Jappelli, A Rasore-Quartino. Pediatr Hematol Oncol 1993
19
66

Dyskeratosis congenita with esophageal and anal stricture.
Ercan Arca, Ahmet Tüzün, H Bülent Tastan, Ahmet Akar, Osman Köse. Int J Dermatol 2003
5
66

Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature review.
Neelam Giri, Rees Lee, Albert Faro, Charles B Huddleston, Frances V White, Blanche P Alter, Sharon A Savage. BMC Blood Disord 2011
39
66

Late manifestation of dyskeratosis congenita presenting as chronic dermal ulcer in a 37-year-old man.
C Reimann, B Kloeckener-Gruissem, C M Niemeyer, W Vanscheidt. J Eur Acad Dermatol Venereol 2008
9
66

Late death after unrelated-BMT for dyskeratosis congenita following conditioning with alemtuzumab, fludarabine and melphalan.
K Amarasinghe, C Dalley, I Dokal, A Laurie, V Gupta, J Marsh. Bone Marrow Transplant 2007
26
66

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
66

Dyskeratosis congenita: clinical report and review of the literature.
I Baran, R Nalcaci, M Kocak. Int J Dent Hyg 2010
15
66

Beyond the triad: Inheritance, mucocutaneous phenotype, and mortality in a cohort of patients with dyskeratosis congenita.
Suzanne C Ward, Sharon A Savage, Neelam Giri, Blanche P Alter, Philip S Rosenberg, Dominique C Pichard, Edward W Cowen. J Am Acad Dermatol 2018
10
66

Dyskeratosis congenita.
M J Cheesbrough. Br J Dermatol 1978
5
66

Dyskeratosis congenita.
Alexander Röth, Gabriela M Baerlocher. Br J Haematol 2008
4
66

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
66

Fatal interstitial pulmonary disease in a patient with dyskeratosis congenita after allogeneic bone marrow transplantation.
M Yabe, H Yabe, K Hattori, T Morimoto, T Hinohara, I Takakura, T Shimizu, K Shimamura, X Tang, S Kato. Bone Marrow Transplant 1997
60
66


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
66

Telomere length is associated with disease severity and declines with age in dyskeratosis congenita.
Blanche P Alter, Philip S Rosenberg, Neelam Giri, Gabriela M Baerlocher, Peter M Lansdorp, Sharon A Savage. Haematologica 2012
115
66

Nonmyeloablative allogeneic hematopoietic stem cell transplantation for treatment of Dyskeratosis congenita.
T Güngör, S Corbacioglu, R Storb, R A Seger. Bone Marrow Transplant 2003
32
66

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
158
66


Reduced intensity conditioning is effective for hematopoietic SCT in dyskeratosis congenita-related BM failure.
M Ayas, A Nassar, A A Hamidieh, M Kharfan-Dabaja, T B Othman, A Elhaddad, A Seraihy, F Hussain, K Alimoghaddam, S Ladeb,[...]. Bone Marrow Transplant 2013
38
66

Successful umbilical cord blood transplantation in a child with dyskeratosis congenita after a fludarabine-based reduced-intensity conditioning regimen.
Bruno Nobili, Gabriele Rossi, Piero De Stefano, Marco Zecca, Giovanna Giorgiani, Silverio Perrotta, Anna Canazzio, Franco Locatelli. Br J Haematol 2002
33
66


A case of dyskeratosis congenita with primary amenorrhea and adenocarcinoma of stomach.
Nandini Chakrabarti, Nilendu Sarma, Chandan Chattopadhyay, Atanu Roy Chowdhuri, Chanchal Das, Salil K Pal. Indian J Dermatol 2011
4
66

Unusual complications after bone marrow transplantation for dyskeratosis congenita.
V Rocha, A Devergie, G Socié, P Ribaud, H Espérou, N Parquet, E Gluckman. Br J Haematol 1998
86
66

Dyskeratosis congenita associated with three malignancies.
C Baykal, A Kavak, P Gülcan, N Büyükbabani. J Eur Acad Dermatol Venereol 2003
22
66

T cell immunodeficiency in dyskeratosis congenita.
B W Lee, H K Yap, T C Quah, A Chong, C C Seah. Arch Dis Child 1992
22
66

Dyskeratosis congenita and the DNA damage response.
Michael Kirwan, Richard Beswick, Amanda J Walne, Upal Hossain, Colin Casimir, Tom Vulliamy, Inderjeet Dokal. Br J Haematol 2011
23
66

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
66

Response to androgen therapy in patients with dyskeratosis congenita.
Payal P Khincha, Ingrid M Wentzensen, Neelam Giri, Blanche P Alter, Sharon A Savage. Br J Haematol 2014
55
66

Advances in the understanding of dyskeratosis congenita.
Amanda J Walne, Inderjeet Dokal. Br J Haematol 2009
111
66

[Dyskeratosis congenita: short telomeres are not the rule].
Fabien Touzot, Tangui Le Guen, Jean-Pierre de Villartay, Patrick Revy. Med Sci (Paris) 2012
7
66

Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.
Hemanth Tummala, Laura C Collopy, Amanda J Walne, Alicia Ellison, Shirleny Cardoso, Tekin Aksu, Nese Yarali, Deniz Aslan, Rüştü Fikret Akata, Juliana Teo,[...]. Blood 2018
8
66


Liver failure due to hepatic angiosarcoma in an adolescent with dyskeratosis congenita.
Timothy S Olson, Elaine S Chan, Michele E Paessler, Kathleen E Sullivan, Christopher N Frantz, Piere Russo, Monica Bessler. J Pediatr Hematol Oncol 2014
8
66

Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
Charles A Johnson, Mark Hatfield, Jose S Pulido. Ophthalmic Genet 2009
15
66

Dyskeratosis Congenita Without Oral Involvement: A Rare Hereditary Disease.
Fariba Iraji, Kioumars Jamshidi, Mohsen Pourazizi, Bahareh Abtahi-Naeini. Oman Med J 2015
6
66


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.