A citation-based method for searching scientific literature

Evert-Jan Uringa, Kathleen Lisaingo, Hilda A Pickett, Julie Brind'Amour, Jan-Hendrik Rohde, Alex Zelensky, Jeroen Essers, Peter M Lansdorp. Mol Biol Cell 2012
Times Cited: 74







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



Times Cited
  Times     Co-cited
Similarity


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
67

Regulation of murine telomere length by Rtel: an essential gene encoding a helicase-like protein.
Hao Ding, Mike Schertzer, Xiaoli Wu, Marina Gertsenstein, Sara Selig, Makoto Kammori, Reza Pourvali, Steven Poon, Irma Vulto, Elizabeth Chavez,[...]. Cell 2004
234
47

RTEL1 maintains genomic stability by suppressing homologous recombination.
Louise J Barber, Jillian L Youds, Jordan D Ward, Michael J McIlwraith, Nigel J O'Neil, Mark I R Petalcorin, Julie S Martin, Spencer J Collis, Sharon B Cantor, Melissa Auclair,[...]. Cell 2008
251
43

Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication.
Agnel Sfeir, Settapong T Kosiyatrakul, Dirk Hockemeyer, Sheila L MacRae, Jan Karlseder, Carl L Schildkraut, Titia de Lange. Cell 2009
636
41

RTEL1 is a replisome-associated helicase that promotes telomere and genome-wide replication.
Jean-Baptiste Vannier, Sumit Sandhu, Mark I R Petalcorin, Xiaoli Wu, Zinnatun Nabi, Hao Ding, Simon J Boulton. Science 2013
121
40

Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
Tangui Le Guen, Laurent Jullien, Fabien Touzot, Michael Schertzer, Laetitia Gaillard, Mylène Perderiset, Wassila Carpentier, Patrick Nitschke, Capucine Picard, Gérard Couillault,[...]. Hum Mol Genet 2013
100
32

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
28

RTEL-1 enforces meiotic crossover interference and homeostasis.
Jillian L Youds, David G Mets, Michael J McIlwraith, Julie S Martin, Jordan D Ward, Nigel J ONeil, Ann M Rose, Stephen C West, Barbara J Meyer, Simon J Boulton. Science 2010
118
27

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
27

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
27

Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndrome.
Zhong Deng, Galina Glousker, Aliah Molczan, Alan J Fox, Noa Lamm, Jayaraju Dheekollu, Orr-El Weizman, Michael Schertzer, Zhuo Wang, Olga Vladimirova,[...]. Proc Natl Acad Sci U S A 2013
87
27

RTEL1: an essential helicase for telomere maintenance and the regulation of homologous recombination.
Evert-Jan Uringa, Jillian L Youds, Kathleen Lisaingo, Peter M Lansdorp, Simon J Boulton. Nucleic Acids Res 2011
68
26

A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.
Bari J Ballew, Vijai Joseph, Saurav De, Grzegorz Sarek, Jean-Baptiste Vannier, Travis Stracker, Kasmintan A Schrader, Trudy N Small, Richard O'Reilly, Chris Manschreck,[...]. PLoS Genet 2013
79
24

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
Margaret Wrensch, Robert B Jenkins, Jeffrey S Chang, Ru-Fang Yeh, Yuanyuan Xiao, Paul A Decker, Karla V Ballman, Mitchel Berger, Jan C Buckner, Susan Chang,[...]. Nat Genet 2009
359
22

Genome-wide association study identifies five susceptibility loci for glioma.
Sanjay Shete, Fay J Hosking, Lindsay B Robertson, Sara E Dobbins, Marc Sanson, Beatrice Malmer, Matthias Simon, Yannick Marie, Blandine Boisselier, Jean-Yves Delattre,[...]. Nat Genet 2009
585
22

TRF2 recruits RTEL1 to telomeres in S phase to promote t-loop unwinding.
Grzegorz Sarek, Jean-Baptiste Vannier, Stephanie Panier, John H J Petrini, Simon J Boulton. Mol Cell 2015
89
21


RTEL1: functions of a disease-associated helicase.
Jean-Baptiste Vannier, Grzegorz Sarek, Simon J Boulton. Trends Cell Biol 2014
68
22

Homologous recombination generates T-loop-sized deletions at human telomeres.
Richard C Wang, Agata Smogorzewska, Titia de Lange. Cell 2004
396
16

How shelterin protects mammalian telomeres.
Wilhelm Palm, Titia de Lange. Annu Rev Genet 2008
16

Defective telomere lagging strand synthesis in cells lacking WRN helicase activity.
Laure Crabbe, Ramiro E Verdun, Candy I Haggblom, Jan Karlseder. Science 2004
440
14

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Marieke Levitus, Quinten Waisfisz, Barbara C Godthelp, Yne de Vries, Shobbir Hussain, Wouter W Wiegant, Elhaam Elghalbzouri-Maghrani, Jûrgen Steltenpool, Martin A Rooimans, Gerard Pals,[...]. Nat Genet 2005
317
14

The C-terminal extension of human RTEL1, mutated in Hoyeraal-Hreidarsson syndrome, contains harmonin-N-like domains.
Guilhem Faure, Patrick Revy, Michael Schertzer, Arturo Londono-Vallejo, Isabelle Callebaut. Proteins 2014
25
44

Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival.
Yanhong Liu, Sanjay Shete, Carol J Etzel, Michael Scheurer, George Alexiou, Georgina Armstrong, Spyros Tsavachidis, Fu-Wen Liang, Mark Gilbert, Ken Aldape,[...]. J Clin Oncol 2010
82
13

RTEL1 tagging SNPs and haplotypes were associated with glioma development.
Gang Li, Tianbo Jin, Hongjuan Liang, Zhiguo Zhang, Shiming He, Yanyang Tu, Haixia Yang, Tingting Geng, Guangbin Cui, Chao Chen,[...]. Diagn Pathol 2013
25
40


TRF2 protects human telomeres from end-to-end fusions.
B van Steensel, A Smogorzewska, T de Lange. Cell 1998
12

Overexpression of M68/DcR3 in human gastrointestinal tract tumors independent of gene amplification and its location in a four-gene cluster.
C Bai, B Connolly, M L Metzker, C A Hilliard, X Liu, V Sandig, A Soderman, S M Galloway, Q Liu, C P Austin,[...]. Proc Natl Acad Sci U S A 2000
189
12

Super-resolution fluorescence imaging of telomeres reveals TRF2-dependent T-loop formation.
Ylli Doksani, John Y Wu, Titia de Lange, Xiaowei Zhuang. Cell 2013
260
12

Telomere protection by TPP1/POT1 requires tethering to TIN2.
Kaori K Takai, Tatsuya Kibe, Jill R Donigian, David Frescas, Titia de Lange. Mol Cell 2011
137
10

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
10


Control of telomere length by a trimming mechanism that involves generation of t-circles.
Hilda A Pickett, Anthony J Cesare, Rebecca L Johnston, Axel A Neumann, Roger R Reddel. EMBO J 2009
138
10

Structure and mechanism of helicases and nucleic acid translocases.
Martin R Singleton, Mark S Dillingham, Dale B Wigley. Annu Rev Biochem 2007
804
10

Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1.
Petra van der Lelij, Krystyna H Chrzanowska, Barbara C Godthelp, Martin A Rooimans, Anneke B Oostra, Markus Stumm, Małgorzata Z Zdzienicka, Hans Joenje, Johan P de Winter. Am J Hum Genet 2010
125
10

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
Orna Levran, Claire Attwooll, Rashida T Henry, Kelly L Milton, Kornelia Neveling, Paula Rio, Sat Dev Batish, Reinhard Kalb, Eunike Velleuer, Sandra Barral,[...]. Nat Genet 2005
267
10

BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ.
Rachel Litman, Min Peng, Zhe Jin, Fan Zhang, Junran Zhang, Simon Powell, Paul R Andreassen, Sharon B Cantor. Cancer Cell 2005
283
10

Cancer susceptibility variants and the risk of adult glioma in a US case-control study.
Kathleen M Egan, Reid C Thompson, L B Nabors, Jeffrey J Olson, Daniel J Brat, Renato V Larocca, Steven Brem, Paul L Moots, Melissa H Madden, James E Browning,[...]. J Neurooncol 2011
65
12

Generation of a mouse model for studying the role of upregulated RTEL1 activity in tumorigenesis.
Xiaoli Wu, Sumit Sandhu, Zinnatun Nabi, Hao Ding. Transgenic Res 2012
16
50

Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNA.
Iris Cheung, Michael Schertzer, Ann Rose, Peter M Lansdorp. Nat Genet 2002
191
10



DNA damage foci at dysfunctional telomeres.
Hiroyuki Takai, Agata Smogorzewska, Titia de Lange. Curr Biol 2003
963
9

Increased telomere fragility and fusions resulting from TRF1 deficiency lead to degenerative pathologies and increased cancer in mice.
Paula Martínez, Maria Thanasoula, Purificación Muñoz, Chunyan Liao, Agueda Tejera, Carolyn McNees, Juana M Flores, Oscar Fernández-Capetillo, Madalena Tarsounas, Maria A Blasco. Genes Dev 2009
264
9

MMS19 links cytoplasmic iron-sulfur cluster assembly to DNA metabolism.
Kerstin Gari, Ana María León Ortiz, Valérie Borel, Helen Flynn, J Mark Skehel, Simon J Boulton. Science 2012
138
9


Crystal structure of the FeS cluster-containing nucleotide excision repair helicase XPD.
Stefanie C Wolski, Jochen Kuper, Petra Hänzelmann, James J Truglio, Deborah L Croteau, Bennett Van Houten, Caroline Kisker. PLoS Biol 2008
159
9

The DNA repair helicases XPD and FancJ have essential iron-sulfur domains.
Jana Rudolf, Vasso Makrantoni, W John Ingledew, Michael J R Stark, Malcolm F White. Mol Cell 2006
239
9

The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2.
Patricia L Opresko, Marit Otterlei, Jesper Graakjaer, Per Bruheim, Lale Dawut, Steen Kølvraa, Alfred May, Michael M Seidman, Vilhem A Bohr. Mol Cell 2004
242
9

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
9


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.