A citation-based method for searching scientific literature

Erin M Parry, Jonathan K Alder, Xiaodong Qi, Julian J-L Chen, Mary Armanios. Blood 2011
Times Cited: 98







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



Times Cited
  Times     Co-cited
Similarity


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
58

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
40

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
39

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
547
34

Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.
Alberto Diaz de Leon, Jennifer T Cronkhite, Anna-Luise A Katzenstein, J David Godwin, Ganesh Raghu, Craig S Glazer, Randall L Rosenblatt, Carlos E Girod, Edward R Garrity, Chao Xing,[...]. PLoS One 2010
206
32

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
31

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
31

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
28

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
27


Lung transplantation in telomerase mutation carriers with pulmonary fibrosis.
Leann L Silhan, Pali D Shah, Daniel C Chambers, Laurie D Snyder, Gerdt C Riise, Christa L Wagner, Eva Hellström-Lindberg, Jonathan B Orens, Juliette F Mewton, Sonye K Danoff,[...]. Eur Respir J 2014
101
27

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
26


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
25

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
24

The gastrointestinal manifestations of telomere-mediated disease.
Naudia L Jonassaint, Nini Guo, Joseph A Califano, Elizabeth A Montgomery, Mary Armanios. Aging Cell 2013
55
43

Telomerase mutations in smokers with severe emphysema.
Susan E Stanley, Julian J L Chen, Joshua D Podlevsky, Jonathan K Alder, Nadia N Hansel, Rasika A Mathias, Xiaodong Qi, Nicholas M Rafaels, Robert A Wise, Edwin K Silverman,[...]. J Clin Invest 2015
97
23

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
23

Syndromes of telomere shortening.
Mary Armanios. Annu Rev Genomics Hum Genet 2009
228
22

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
22

Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.
Jonathan K Alder, Joy D Cogan, Andrew F Brown, Collin J Anderson, William E Lawson, Peter M Lansdorp, John A Phillips, James E Loyd, Julian J-L Chen, Mary Armanios. PLoS Genet 2011
70
31

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
25

Telomeres shorten during ageing of human fibroblasts.
C B Harley, A B Futcher, C W Greider. Nature 1990
21

Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene.
Jonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, Christa L Wagner, Lawrence M Lieblich, Robert Auerbach, Arleen D Auerbach, Sarah J Wheelan, Mary Armanios. Hum Mutat 2013
57
36

Short telomeres, even in the presence of telomerase, limit tissue renewal capacity.
Ling-Yang Hao, Mary Armanios, Margaret A Strong, Baktiar Karim, David M Feldser, David Huso, Carol W Greider. Cell 2005
200
20

Short telomeres are sufficient to cause the degenerative defects associated with aging.
Mary Armanios, Jonathan K Alder, Erin M Parry, Baktiar Karim, Margaret A Strong, Carol W Greider. Am J Hum Genet 2009
150
20

Telomere length is a determinant of emphysema susceptibility.
Jonathan K Alder, Nini Guo, Frant Kembou, Erin M Parry, Collin J Anderson, Amany I Gorgy, Michael F Walsh, Thomas Sussan, Shyam Biswal, Wayne Mitzner,[...]. Am J Respir Crit Care Med 2011
156
20

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
19

An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management.
Ganesh Raghu, Harold R Collard, Jim J Egan, Fernando J Martinez, Juergen Behr, Kevin K Brown, Thomas V Colby, Jean-François Cordier, Kevin R Flaherty, Joseph A Lasky,[...]. Am J Respir Crit Care Med 2011
19

Rare variants in RTEL1 are associated with familial interstitial pneumonia.
Joy D Cogan, Jonathan A Kropski, Min Zhao, Daphne B Mitchell, Lynette Rives, Cheryl Markin, Errine T Garnett, Keri H Montgomery, Wendi R Mason, David F McKean,[...]. Am J Respir Crit Care Med 2015
105
19

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
18


Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita.
A C Dietz, P J Orchard, K S Baker, R H Giller, S A Savage, B P Alter, J Tolar. Bone Marrow Transplant 2011
94
19

Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Susan E Stanley, Dustin L Gable, Christa L Wagner, Thomas M Carlile, Vidya Sagar Hanumanthu, Joshua D Podlevsky, Sara E Khalil, Amy E DeZern, Maria F Rojas-Duran, Carolyn D Applegate,[...]. Sci Transl Med 2016
96
18

Flow cytometry and FISH to measure the average length of telomeres (flow FISH).
Gabriela M Baerlocher, Irma Vulto, Gary de Jong, Peter M Lansdorp. Nat Protoc 2006
278
17

Hepatopulmonary syndrome is a frequent cause of dyspnea in the short telomere disorders.
Amany I Gorgy, Naudia L Jonassaint, Susan E Stanley, Ayman Koteish, Amy E DeZern, Jolan E Walter, Sabrina C Sopha, James P Hamilton, Julie Hoover-Fong, Allen R Chen,[...]. Chest 2015
47
36


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
16

Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
Caroline Kannengiesser, Raphael Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunes,[...]. Eur Respir J 2015
85
18

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
15

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
15


Diagnostic utility of telomere length testing in a hospital-based setting.
Jonathan K Alder, Vidya Sagar Hanumanthu, Margaret A Strong, Amy E DeZern, Susan E Stanley, Clifford M Takemoto, Ludmila Danilova, Carolyn D Applegate, Stephen G Bolton, David W Mohr,[...]. Proc Natl Acad Sci U S A 2018
71
21

Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita.
Erin M Parry, Jonathan K Alder, Stella S Lee, John A Phillips, James E Loyd, Priya Duggal, Mary Armanios. J Med Genet 2011
38
36

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
14

Telomere diseases.
Rodrigo T Calado, Neal S Young. N Engl J Med 2009
503
14

A common MUC5B promoter polymorphism and pulmonary fibrosis.
Max A Seibold, Anastasia L Wise, Marcy C Speer, Mark P Steele, Kevin K Brown, James E Loyd, Tasha E Fingerlin, Weiming Zhang, Gunnar Gudmundsson, Steve D Groshong,[...]. N Engl J Med 2011
587
14

Subclinical lung disease, macrocytosis, and premature graying in kindreds with telomerase (TERT) mutations.
Alberto Diaz de Leon, Jennifer T Cronkhite, Cuneyt Yilmaz, Cecelia Brewington, Richard Wang, Chao Xing, Connie C W Hsia, Christine Kim Garcia. Chest 2011
59
23

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.
Tasha E Fingerlin, Elissa Murphy, Weiming Zhang, Anna L Peljto, Kevin K Brown, Mark P Steele, James E Loyd, Gregory P Cosgrove, David Lynch, Steve Groshong,[...]. Nat Genet 2013
403
14

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
16


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.