A citation-based method for searching scientific literature

Gabrielle Henslee, Christopher L Williams, Pengfei Liu, Alison A Bertuch. Cold Spring Harb Mol Case Stud 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Development of a New Monochrome Multiplex qPCR Method for Relative Telomere Length Measurement in Cancer.
Paige N Dahlgren, Kanokwan Bishop, Shatovisha Dey, Brittney-Shea Herbert, Hiromi Tanaka. Neoplasia 2018
10
100

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
Richard J Allen, Joanne Porte, Rebecca Braybrooke, Carlos Flores, Tasha E Fingerlin, Justin M Oldham, Beatriz Guillen-Guio, Shwu-Fan Ma, Tsukasa Okamoto, Alison E John,[...]. Lancet Respir Med 2017
107
100


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



Targeting telomerase-expressing cancer cells.
Michel M Ouellette, Woodring E Wright, Jerry W Shay. J Cell Mol Med 2011
50
100



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
100

Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials.
Paul W Noble, Carlo Albera, Williamson Z Bradford, Ulrich Costabel, Roland M du Bois, Elizabeth A Fagan, Robert S Fishman, Ian Glaspole, Marilyn K Glassberg, Lisa Lancaster,[...]. Eur Respir J 2016
195
100

Interaction profiling identifies the human nuclear exosome targeting complex.
Michal Lubas, Marianne S Christensen, Maiken S Kristiansen, Michal Domanski, Lasse G Falkenby, Søren Lykke-Andersen, Jens S Andersen, Andrzej Dziembowski, Torben Heick Jensen. Mol Cell 2011
249
100

Short telomere length and its correlation with gene mutations in myelodysplastic syndrome.
Sang Mee Hwang, Seon Young Kim, Jung Ah Kim, Hee-Sue Park, Si Nae Park, Kyongok Im, Kwantae Kim, Sung-Min Kim, Dong Soon Lee. J Hematol Oncol 2016
16
100

Obesity, cigarette smoking, and telomere length in women.
A M Valdes, T Andrew, J P Gardner, M Kimura, E Oelsner, L F Cherkas, A Aviv, T D Spector. Lancet 2005
928
100

Association of immune abnormalities with telomere shortening in autosomal-dominant dyskeratosis congenita.
Matt Knudson, Shashikant Kulkarni, Zuhair K Ballas, Monica Bessler, Frederick Goldman. Blood 2005
55
100

Danazol Treatment for Telomere Diseases.
Danielle M Townsley, Bogdan Dumitriu, Delong Liu, Angélique Biancotto, Barbara Weinstein, Christina Chen, Nathan Hardy, Andrew D Mihalek, Shilpa Lingala, Yun Ju Kim,[...]. N Engl J Med 2016
164
100

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
100

Telomere shortening in familial and sporadic pulmonary fibrosis.
Jennifer T Cronkhite, Chao Xing, Ganesh Raghu, Kelly M Chin, Fernando Torres, Randall L Rosenblatt, Christine Kim Garcia. Am J Respir Crit Care Med 2008
314
100

Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts.
Anne Polvi, Tarja Linnankivi, Tero Kivelä, Riitta Herva, James P Keating, Outi Mäkitie, Davide Pareyson, Leena Vainionpää, Jenni Lahtinen, Iiris Hovatta,[...]. Am J Hum Genet 2012
102
100

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
100

Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells.
Neha Nagpal, Jianing Wang, Jing Zeng, Emily Lo, Diane H Moon, Kevin Luk, Roman O Braun, Lauri M Burroughs, Sioban B Keel, Christopher Reilly,[...]. Cell Stem Cell 2020
15
100

Measurement of telomere length by the Southern blot analysis of terminal restriction fragment lengths.
Masayuki Kimura, Rivka C Stone, Steven C Hunt, Joan Skurnick, Xiaobin Lu, Xiaojian Cao, Calvin B Harley, Abraham Aviv. Nat Protoc 2010
259
100

A Natural Product Telomerase Activator Lengthens Telomeres in Humans: A Randomized, Double Blind, and Placebo Controlled Study.
Laura Salvador, Gunasekaran Singaravelu, Calvin B Harley, Peter Flom, Anitha Suram, Joseph M Raffaele. Rejuvenation Res 2016
34
100

Mammalian telomeres end in a large duplex loop.
J D Griffith, L Comeau, S Rosenfield, R M Stansel, A Bianchi, H Moss, T de Lange. Cell 1999
100

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
100

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
100

Results and follow-up of a phase III randomized study of recombinant human-granulocyte stimulating factor as support for immunosuppressive therapy in patients with severe aplastic anaemia.
Eliane Gluckman, Riitta Rokicka-Milewska, Ian Hann, Emmanouel Nikiforakis, Filipos Tavakoli, Sophie Cohen-Scali, Andrea Bacigalupo. Br J Haematol 2002
71
100

Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature.
Luba Nalysnyk, Javier Cid-Ruzafa, Philip Rotella, Dirk Esser. Eur Respir Rev 2012
259
100

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
100

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
100

Telomere length: a review of methods for measurement.
Alison J Montpetit, Areej A Alhareeri, Marty Montpetit, Angela R Starkweather, Lynne W Elmore, Kristin Filler, Lathika Mohanraj, Candace W Burton, Victoria S Menzies, Debra E Lyon,[...]. Nurs Res 2014
131
100

Correlation of Leukocyte Telomere Length Measurement Methods in Patients with Dyskeratosis Congenita and in Their Unaffected Relatives.
Payal P Khincha, Casey L Dagnall, Belynda Hicks, Kristine Jones, Abraham Aviv, Masayuki Kimura, Hormuzd Katki, Geraldine Aubert, Neelam Giri, Blanche P Alter,[...]. Int J Mol Sci 2017
20
100

Loss of telomeric DNA during aging of normal and trisomy 21 human lymphocytes.
H Vaziri, F Schächter, I Uchida, L Wei, X Zhu, R Effros, D Cohen, C B Harley. Am J Hum Genet 1993
631
100

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
100

Common troublesome symptoms and their impact on quality of life in patients with myelodysplastic syndromes (MDS): results of a large internet-based survey.
David P Steensma, Kathleen V Heptinstall, Victor M Johnson, Paul J Novotny, Jeff A Sloan, John K Camoriano, Joyce Niblack, John M Bennett, Ruben A Mesa. Leuk Res 2008
66
100


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
100

Eltrombopag restores trilineage hematopoiesis in refractory severe aplastic anemia that can be sustained on discontinuation of drug.
Ronan Desmond, Danielle M Townsley, Bogdan Dumitriu, Matthew J Olnes, Phillip Scheinberg, Margaret Bevans, Ankur R Parikh, Kinneret Broder, Katherine R Calvo, Colin O Wu,[...]. Blood 2014
209
100

Therapeutic effect of androgen therapy in a mouse model of aplastic anemia produced by short telomeres.
Christian Bär, Nicolas Huber, Fabian Beier, Maria A Blasco. Haematologica 2015
44
100

Determinants of telomere length across human tissues.
Kathryn Demanelis, Farzana Jasmine, Lin S Chen, Meytal Chernoff, Lin Tong, Dayana Delgado, Chenan Zhang, Justin Shinkle, Mekala Sabarinathan, Hannah Lin,[...]. Science 2020
44
100


The Spectrum of Hepatic Involvement in Patients With Telomere Disease.
Devika Kapuria, Gil Ben-Yakov, Rebecca Ortolano, Min Ho Cho, Or Kalchiem-Dekel, Varun Takyar, Shilpa Lingala, Naveen Gara, Michele Tana, Yun Ju Kim,[...]. Hepatology 2019
13
100

Telomere length and genetic variant associations with interstitial lung disease progression and survival.
Chad A Newton, Justin M Oldham, Brett Ley, Vikram Anand, Ayodeji Adegunsoye, Gabrielle Liu, Kiran Batra, Jose Torrealba, Julia Kozlitina, Craig Glazer,[...]. Eur Respir J 2019
47
100

A method for measuring the distribution of the shortest telomeres in cells and tissues.
Tsung-Po Lai, Ning Zhang, Jungsik Noh, Ilgen Mender, Enzo Tedone, Ejun Huang, Woodring E Wright, Gaudenz Danuser, Jerry W Shay. Nat Commun 2017
45
100

Short Telomere Length Predicts Non-Relapse Mortality after Stem Cell Transplantation for Myelodysplastic Syndrome.
Mikko Myllymäki, Robert Allyn Redd, Christopher R Reilly, Wael Saber, Stephen Spellman, Christopher James Gibson, Zhen-Huan Hu, Tao Wang, Esther H Orr, Jaclyn Garza Grenier,[...]. Blood 2020
5
100

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
100

Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2018
93
100

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
18
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


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.