A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Effect of telomere proximity on telomere position effect, chromosome healing, and sensitivity to DNA double-strand breaks in a human tumor cell line.
Avanti Kulkarni, Oliver Zschenker, Gloria Reynolds, Douglas Miller, John P Murnane. Mol Cell Biol 2010
31
40

The epigenetic regulation of mammalian telomeres.
María A Blasco. Nat Rev Genet 2007
466
40

DNA damage and repair in telomeres: relation to aging.
P A Kruk, N J Rampino, V A Bohr. Proc Natl Acad Sci U S A 1995
246
40

Oxidative stress shortens telomeres.
Thomas von Zglinicki. Trends Biochem Sci 2002
40




Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.
Manoj Raghavan, Debra M Lillington, Spyros Skoulakis, Silvana Debernardi, Tracy Chaplin, Nicola J Foot, T Andrew Lister, Bryan D Young. Cancer Res 2005
222
40

Human papillomavirus and rising oropharyngeal cancer incidence in the United States.
Anil K Chaturvedi, Eric A Engels, Ruth M Pfeiffer, Brenda Y Hernandez, Weihong Xiao, Esther Kim, Bo Jiang, Marc T Goodman, Maria Sibug-Saber, Wendy Cozen,[...]. J Clin Oncol 2011
40

Cancer statistics, 2015.
Rebecca L Siegel, Kimberly D Miller, Ahmedin Jemal. CA Cancer J Clin 2015
40

Increasing incidence of oral tongue squamous cell carcinoma in young white women, age 18 to 44 years.
Sagar C Patel, William R Carpenter, Seth Tyree, Marion Everett Couch, Mark Weissler, Trevor Hackman, D Neil Hayes, Carol Shores, Bhishamjit S Chera. J Clin Oncol 2011
218
40

Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors.
Alex Martin-Trujillo, Enrique Vidal, Ana Monteagudo-Sánchez, Marta Sanchez-Delgado, Sebastian Moran, Jose Ramon Hernandez Mora, Holger Heyn, Miriam Guitart, Manel Esteller, David Monk. Nat Commun 2017
16
40

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays.
Go Yamamoto, Yasuhito Nannya, Motohiro Kato, Masashi Sanada, Ross L Levine, Norihiko Kawamata, Akira Hangaishi, Mineo Kurokawa, Shigeru Chiba, D Gary Gilliland,[...]. Am J Hum Genet 2007
216
40

Involvement of homologous recombination in carcinogenesis.
Ramune Reliene, Alexander J R Bishop, Robert H Schiestl. Adv Genet 2007
52
40

Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies.
Karen Stephens, Molly Weaver, Kathleen A Leppig, Kyoko Maruyama, Peter D Emanuel, Michelle M Le Beau, Kevin M Shannon. Blood 2006
50
40

Characterizing Genetic Transitions of Copy Number Alterations and Allelic Imbalances in Oral Tongue Carcinoma Metastasis.
Takuma Morita, Narikazu Uzawa, Kaoru Mogushi, Jun Sumino, Chieko Michikawa, Ken-Ichiro Takahashi, Kunihiro Myo, Toshiyuki Izumo, Kiyoshi Harada. Genes Chromosomes Cancer 2016
7
40


Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain.
Anneke C Blackburn, S Christine McLary, Rizwan Naeem, Jason Luszcz, David W Stockton, Lawrence A Donehower, Mansoor Mohammed, John B Mailhes, Tamar Soferr, Stephen P Naber,[...]. Cancer Res 2004
35
40

Prognostic relevance of acquired uniparental disomy in serous ovarian cancer.
Musaffe Tuna, Zhenlin Ju, Marcel Smid, Christopher I Amos, Gordon B Mills. Mol Cancer 2015
12
40


Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma.
Maria Sebastiana Marescalco, Carmela Capizzi, Daniele Filippo Condorelli, Vincenza Barresi. J Oral Pathol Med 2014
22
40

The telomerase database.
Joshua D Podlevsky, Christopher J Bley, Rebecca V Omana, Xiaodong Qi, Julian J-L Chen. Nucleic Acids Res 2008
141
20

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases.
Ivona Aksentijevich, Miroslawa Nowak, Mustapha Mallah, Jae Jin Chae, Wendy T Watford, Sigrun R Hofmann, Leonard Stein, Ricardo Russo, Donald Goldsmith, Peter Dent,[...]. Arthritis Rheum 2002
520
20

Digenic inheritance in medical genetics.
Alejandro A Schäffer. J Med Genet 2013
110
20

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
Lina Shao, Chad A Shaw, Xin-Yan Lu, Trilochan Sahoo, Carlos A Bacino, Seema R Lalani, Pawel Stankiewicz, Svetlana A Yatsenko, Yinfeng Li, Sarah Neill,[...]. Am J Med Genet A 2008
88
20

Hypercholesterolemia and reduced HDL-C promote hematopoietic stem cell proliferation and monocytosis: studies in mice and FH children.
Sonia Tolani, Tamara A Pagler, Andrew J Murphy, Andrea E Bochem, Sandra Abramowicz, Carrie Welch, Prabhakara R Nagareddy, Steve Holleran, G K Hovingh, Jan Albert Kuivenhoven,[...]. Atherosclerosis 2013
67
20


Hypercholesterolemia-induced priming of hematopoietic stem and progenitor cells aggravates atherosclerosis.
Tom Seijkens, Marten A Hoeksema, Linda Beckers, Esther Smeets, Svenja Meiler, Johannes Levels, Marc Tjwa, Menno P J de Winther, Esther Lutgens. FASEB J 2014
66
20

Live Cell Imaging Reveals the Dynamics of Telomerase Recruitment to Telomeres.
Jens C Schmidt, Arthur J Zaug, Thomas R Cech. Cell 2016
87
20

Telomere position effect: regulation of gene expression with progressive telomere shortening over long distances.
Jérôme D Robin, Andrew T Ludlow, Kimberly Batten, Frédérique Magdinier, Guido Stadler, Kathyrin R Wagner, Jerry W Shay, Woodring E Wright. Genes Dev 2014
147
20

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
562
20

Understanding TERT Promoter Mutations: A Common Path to Immortality.
Robert J A Bell, H Tomas Rube, Ana Xavier-Magalhães, Bruno M Costa, Andrew Mancini, Jun S Song, Joseph F Costello. Mol Cancer Res 2016
118
20

The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients.
Camille Leroy, Emilie Landais, Sylvain Briault, Albert David, Olivier Tassy, Nicolas Gruchy, Bruno Delobel, Marie-José Grégoire, Bruno Leheup, Laurence Taine,[...]. Eur J Hum Genet 2013
54
20

Familial autoinflammatory diseases: genetics, pathogenesis and treatment.
Silvia Stojanov, Daniel L Kastner. Curr Opin Rheumatol 2005
247
20


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
831
20



MAD2L2 controls DNA repair at telomeres and DNA breaks by inhibiting 5' end resection.
Vera Boersma, Nathalie Moatti, Sandra Segura-Bayona, Marieke H Peuscher, Jaco van der Torre, Brigitte A Wevers, Alexandre Orthwein, Daniel Durocher, Jacqueline J L Jacobs. Nature 2015
166
20


53BP1 links DNA damage-response pathways to immunoglobulin heavy chain class-switch recombination.
John P Manis, Julio C Morales, Zhenfang Xia, Jeffery L Kutok, Frederick W Alt, Phillip B Carpenter. Nat Immunol 2004
251
20

The serial cultivation of human diploid cell strains.
L HAYFLICK, P S MOORHEAD. Exp Cell Res 1961
20

Role of mammalian Mre11 in classical and alternative nonhomologous end joining.
Anyong Xie, Amy Kwok, Ralph Scully. Nat Struct Mol Biol 2009
235
20

RNF168 binds and amplifies ubiquitin conjugates on damaged chromosomes to allow accumulation of repair proteins.
Carsten Doil, Niels Mailand, Simon Bekker-Jensen, Patrice Menard, Dorthe Helena Larsen, Rainer Pepperkok, Jan Ellenberg, Stephanie Panier, Daniel Durocher, Jiri Bartek,[...]. Cell 2009
637
20

The RIDDLE syndrome protein mediates a ubiquitin-dependent signaling cascade at sites of DNA damage.
Grant S Stewart, Stephanie Panier, Kelly Townsend, Abdallah K Al-Hakim, Nadine K Kolas, Edward S Miller, Shinichiro Nakada, Jarkko Ylanko, Signe Olivarius, Megan Mendez,[...]. Cell 2009
533
20

Increased sensitivity of subtelomeric regions to DNA double-strand breaks in a human cancer cell line.
Oliver Zschenker, Avanti Kulkarni, Douglas Miller, Gloria E Reynolds, Marine Granger-Locatelli, Géraldine Pottier, Laure Sabatier, John P Murnane. DNA Repair (Amst) 2009
29
20



Apollo contributes to G overhang maintenance and protects leading-end telomeres.
Peng Wu, Megan van Overbeek, Sean Rooney, Titia de Lange. Mol Cell 2010
98
20



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.