A citation-based method for searching scientific literature

Valeriya Gaysinskaya, Susan E Stanley, Soheir Adam, Mary Armanios. Chest 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


The telomerase database.
Joshua D Podlevsky, Christopher J Bley, Rebecca V Omana, Xiaodong Qi, Julian J-L Chen. Nucleic Acids Res 2008
137
50

Understanding the contribution of synonymous mutations to human disease.
Zuben E Sauna, Chava Kimchi-Sarfaty. Nat Rev Genet 2011
521
50

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
50

Short Telomere Syndromes in Clinical Practice: Bridging Bench and Bedside.
Abhishek A Mangaonkar, Mrinal M Patnaik. Mayo Clin Proc 2018
32
50

From organ to cell: Multi-level telomere length assessment in patients with idiopathic pulmonary fibrosis.
Aernoud A van Batenburg, Karin M Kazemier, Matthijs F M van Oosterhout, Joanne J van der Vis, Hendrik W van Es, Jan C Grutters, Roel Goldschmeding, Coline H M van Moorsel. PLoS One 2020
6
50

The effect of TERC haploinsufficiency on the inheritance of telomere length.
Fred Goldman, Rachida Bouarich, Shashikant Kulkarni, Sara Freeman, Hong-Yan Du, Lea Harrington, Philip J Mason, Arturo Londoño-Vallejo, Monica Bessler. Proc Natl Acad Sci U S A 2005
77
50

Molecular mechanisms of disease-causing missense mutations.
Shannon Stefl, Hafumi Nishi, Marharyta Petukh, Anna R Panchenko, Emil Alexov. J Mol Biol 2013
126
50

The genetics of dyskeratosis congenita.
Philip J Mason, Monica Bessler. Cancer Genet 2011
86
50

Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease.
Jonathan A Kropski, Jason M Pritchett, Donald F Zoz, Peter F Crossno, Cheryl Markin, Errine T Garnett, Amber L Degryse, Daphne B Mitchell, Vasiliy V Polosukhin, Otis B Rickman,[...]. Am J Respir Crit Care Med 2015
87
50

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
50

Pulmonary Fibrosis and a TERT Founder Mutation With a Latency Period of 300 Years.
Joanne J van der Vis, Jasper J van der Smagt, Frederic A M Hennekam, Jan C Grutters, Coline H M van Moorsel. Chest 2020
4
50

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
50

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
50


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
50



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



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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50

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
50


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
50

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
50

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
50


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.