A citation-based method for searching scientific literature

Isabelle Schmutz, Arjen R Mensenkamp, Kaori K Takai, Maaike Haadsma, Liesbeth Spruijt, Richarda M de Voer, Seunga Sara Choo, Franziska K Lorbeer, Emma J van Grinsven, Dirk Hockemeyer, Marjolijn Cj Jongmans, Titia de Lange. Elife 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
Jianxin Shi, Xiaohong R Yang, Bari Ballew, Melissa Rotunno, Donato Calista, Maria Concetta Fargnoli, Paola Ghiorzo, Brigitte Bressac-de Paillerets, Eduardo Nagore, Marie Francoise Avril,[...]. Nat Genet 2014
188
100

Genetic and molecular identification of three human TPP1 functions in telomerase action: recruitment, activation, and homeostasis set point regulation.
Alec N Sexton, Samuel G Regalado, Christine S Lai, Gregory J Cost, Colleen M O'Neil, Fyodor D Urnov, Philip D Gregory, Rudolf Jaenisch, Kathleen Collins, Dirk Hockemeyer. Genes Dev 2014
75
100

TPP1 is a homologue of ciliate TEBP-beta and interacts with POT1 to recruit telomerase.
Huawei Xin, Dan Liu, Ma Wan, Amin Safari, Hyeung Kim, Wen Sun, Matthew S O'Connor, Zhou Songyang. Nature 2007
355
100

Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice.
S E Artandi, S Chang, S L Lee, S Alson, G J Gottlieb, L Chin, R A DePinho. Nature 2000
834
100

The POT1-TPP1 telomere complex is a telomerase processivity factor.
Feng Wang, Elaine R Podell, Arthur J Zaug, Yuting Yang, Paul Baciu, Thomas R Cech, Ming Lei. Nature 2007
456
100

The TEL patch of telomere protein TPP1 mediates telomerase recruitment and processivity.
Jayakrishnan Nandakumar, Caitlin F Bell, Ina Weidenfeld, Arthur J Zaug, Leslie A Leinwand, Thomas R Cech. Nature 2012
200
100

A DNA damage checkpoint response in telomere-initiated senescence.
Fabrizio d'Adda di Fagagna, Philip M Reaper, Lorena Clay-Farrace, Heike Fiegler, Philippa Carr, Thomas Von Zglinicki, Gabriele Saretzki, Nigel P Carter, Stephen P Jackson. Nature 2003
100


POT1-interacting protein PIP1: a telomere length regulator that recruits POT1 to the TIN2/TRF1 complex.
Jeffrey Zheng-Sheng Ye, Dirk Hockemeyer, Andrew N Krutchinsky, Diego Loayza, Sarah M Hooper, Brian T Chait, Titia de Lange. Genes Dev 2004
314
100

TPP1 OB-fold domain controls telomere maintenance by recruiting telomerase to chromosome ends.
Franklin L Zhong, Luis F Z Batista, Adam Freund, Matthew F Pech, Andrew S Venteicher, Steven E Artandi. Cell 2012
184
100


Telomerase activity in human germline and embryonic tissues and cells.
W E Wright, M A Piatyszek, W E Rainey, W Byrd, J W Shay. Dev Genet 1996
951
100

A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres.
Huiling He, Wei Li, Daniel F Comiskey, Sandya Liyanarachchi, Taina T Nieminen, Yanqiang Wang, Katherine E DeLap, Pamela Brock, Albert de la Chapelle. Thyroid 2020
11
100

Specific association of human telomerase activity with immortal cells and cancer.
N W Kim, M A Piatyszek, K R Prowse, C B Harley, M D West, P L Ho, G M Coviello, W E Wright, S L Weinrich, J W Shay. Science 1994
100

Telomeres shorten during ageing of human fibroblasts.
C B Harley, A B Futcher, C W Greider. Nature 1990
100

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.
Yiran Guo, Melissa Kartawinata, Jiankang Li, Hilda A Pickett, Juliana Teo, Tatjana Kilo, Pasquale M Barbaro, Brendan Keating, Yulan Chen, Lifeng Tian,[...]. Blood 2014
62
50

A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16) (q22).
K Taysi, M Fishman, G S Sekhon. Birth Defects Orig Artic Ser 1978
11
50

Structural and functional consequences of a disease mutation in the telomere protein TPP1.
Kamlesh Bisht, Eric M Smith, Valerie M Tesmer, Jayakrishnan Nandakumar. Proc Natl Acad Sci U S A 2016
24
50

Telomere shortening triggers senescence of human cells through a pathway involving ATM, p53, and p21(CIP1), but not p16(INK4a).
Utz Herbig, Wendy A Jobling, Benjamin P C Chen, David J Chen, John M Sedivy. Mol Cell 2004
819
50

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
50

CTCF deletion syndrome: clinical features and epigenetic delineation.
Ikumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, Hidetaka Watanabe, Ken Higashimoto, Junko Tomikawa, Daisuke Ieda, Kei Ohashi, Yutaka Negishi, Ayako Hattori,[...]. J Med Genet 2017
11
50

Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics.
Linn Fagerberg, Björn M Hallström, Per Oksvold, Caroline Kampf, Dijana Djureinovic, Jacob Odeberg, Masato Habuka, Simin Tahmasebpoor, Angelika Danielsson, Karolina Edlund,[...]. Mol Cell Proteomics 2014
450
50

Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1.
Hande Kocak, Bari J Ballew, Kamlesh Bisht, Rebecca Eggebeen, Belynda D Hicks, Shalabh Suman, Adri O'Neil, Neelam Giri, Ivan Maillard, Blanche P Alter,[...]. Genes Dev 2014
70
50

Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma.
Kim Wong, Carla Daniela Robles-Espinoza, David Rodriguez, Saskia S Rudat, Susana Puig, Miriam Potrony, Chi C Wong, James Hewinson, Paula Aguilera, Joan Anton Puig-Butille,[...]. JAMA Dermatol 2019
15
50

Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
Lauren G Aoude, Antonia L Pritchard, Carla Daniela Robles-Espinoza, Karin Wadt, Mark Harland, Jiyeon Choi, Michael Gartside, Víctor Quesada, Peter Johansson, Jane M Palmer,[...]. J Natl Cancer Inst 2014
95
50

A mutation in the POT1 gene is responsible for cardiac angiosarcoma in TP53-negative Li-Fraumeni-like families.
Oriol Calvete, Paula Martinez, Pablo Garcia-Pavia, Carlos Benitez-Buelga, Beatriz Paumard-Hernández, Victoria Fernandez, Fernando Dominguez, Clara Salas, Nuria Romero-Laorden, Jesus Garcia-Donas,[...]. Nat Commun 2015
78
50

A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure.
S Hreidarsson, K Kristjansson, G Johannesson, J H Johannsson. Acta Paediatr Scand 1988
82
50

Interstitial 16q deletion with typical dysmorphic syndrome.
J P Fryns, W Proesmans, G Van Hoey, H Van den Berghe. Ann Genet 1981
30
50

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
50

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

Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics.
Linn Fagerberg, Björn M Hallström, Per Oksvold, Caroline Kampf, Dijana Djureinovic, Jacob Odeberg, Masato Habuka, Simin Tahmasebpoor, Angelika Danielsson, Karolina Edlund,[...]. Mol Cell Proteomics 2014
50


One protein to rule them all: The role of CCCTC-binding factor in shaping human genome in health and disease.
Michal Lazniewski, Wayne K Dawson, Anna Maria Rusek, Dariusz Plewczynski. Semin Cell Dev Biol 2019
7
50



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
50

Specificity requirements for human telomere protein interaction with telomerase holoenzyme.
Alec N Sexton, Daniel T Youmans, Kathleen Collins. J Biol Chem 2012
74
50

A dynamic molecular link between the telomere length regulator TRF1 and the chromosome end protector TRF2.
Benjamin R Houghtaling, Leanora Cuttonaro, William Chang, Susan Smith. Curr Biol 2004
204
50

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.
Blanche P Alter, Neelam Giri, Sharon A Savage, June A Peters, Jennifer T Loud, Lisa Leathwood, Ann G Carr, Mark H Greene, Philip S Rosenberg. Br J Haematol 2010
194
50

A syndrome of primary combined immunodeficiency with microcephaly, cerebellar hypoplasia, growth failure and progressive pancytopenia.
F Berthet, R Caduff, U B Schaad, H Roten, P Tuchschmid, E Boltshauser, R A Seger. Eur J Pediatr 1994
31
50

Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.
Galina Glousker, Fabien Touzot, Patrick Revy, Yehuda Tzfati, Sharon A Savage. Br J Haematol 2015
58
50

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase.
Erin M Parry, Jonathan K Alder, Xiaodong Qi, Julian J-L Chen, Mary Armanios. Blood 2011
98
50

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
50

Pulmonary fibrosis linked to variants in the ACD gene, encoding the telomere protein TPP1.
Thijs W Hoffman, Joanne J van der Vis, Jasper J van der Smagt, Maarten P G Massink, Jan C Grutters, Coline H M van Moorsel. Eur Respir J 2019
4
50

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
Blanche P Alter, Gabriela M Baerlocher, Sharon A Savage, Stephen J Chanock, Babette B Weksler, Judith P Willner, June A Peters, Neelam Giri, Peter M Lansdorp. Blood 2007
234
50


Prognostic significance of pulmonary function tests in dyskeratosis congenita, a telomere biology disorder.
Neelam Giri, Sandhiya Ravichandran, Youjin Wang, Shahinaz M Gadalla, Blanche P Alter, Joseph Fontana, Sharon A Savage. ERJ Open Res 2019
5
50

NIH Image to ImageJ: 25 years of image analysis.
Caroline A Schneider, Wayne S Rasband, Kevin W Eliceiri. Nat Methods 2012
50

Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia.
Helen E Speedy, Ben Kinnersley, Daniel Chubb, Peter Broderick, Philip J Law, Kevin Litchfield, Sandrine Jayne, Martin J S Dyer, Claire Dearden, George A Follows,[...]. Blood 2016
47
50

Monosomy 16q: a distinct syndrome. Apropos of a de novo del(16) (q2100q2300).
H Rivera, E Vargas-Moyeda, M Möller, A Torres-Lamas, J M Cantú. Clin Genet 1985
24
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.