A citation-based method for searching scientific literature

Sanjay Shete, Fay J Hosking, Lindsay B Robertson, Sara E Dobbins, Marc Sanson, Beatrice Malmer, Matthias Simon, Yannick Marie, Blandine Boisselier, Jean-Yves Delattre, Khe Hoang-Xuan, Soufiane El Hallani, Ahmed Idbaih, Diana Zelenika, Ulrika Andersson, Roger Henriksson, A Tommy Bergenheim, Maria Feychting, Stefan Lönn, Anders Ahlbom, Johannes Schramm, Michael Linnebank, Kari Hemminki, Rajiv Kumar, Sarah J Hepworth, Amy Price, Georgina Armstrong, Yanhong Liu, Xiangjun Gu, Robert Yu, Ching Lau, Minouk Schoemaker, Kenneth Muir, Anthony Swerdlow, Mark Lathrop, Melissa Bondy, Richard S Houlston. Nat Genet 2009
Times Cited: 587







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



Times Cited
  Times     Co-cited
Similarity


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
361
42

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Beatrice S Melin, Jill S Barnholtz-Sloan, Margaret R Wrensch, Christoffer Johansen, Dora Il'yasova, Ben Kinnersley, Quinn T Ostrom, Karim Labreche, Yanwen Chen, Georgina Armstrong,[...]. Nat Genet 2017
127
36

Genome-wide association study of glioma and meta-analysis.
Preetha Rajaraman, Beatrice S Melin, Zhaoming Wang, Roberta McKean-Cowdin, Dominique S Michaud, Sophia S Wang, Melissa Bondy, Richard Houlston, Robert B Jenkins, Margaret Wrensch,[...]. Hum Genet 2012
171
32

Genome-wide association study identifies multiple susceptibility loci for glioma.
Ben Kinnersley, Marianne Labussière, Amy Holroyd, Anna-Luisa Di Stefano, Peter Broderick, Jayaram Vijayakrishnan, Karima Mokhtari, Jean-Yves Delattre, Konstantinos Gousias, Johannes Schramm,[...]. Nat Commun 2015
62
45

Chromosome 7p11.2 (EGFR) variation influences glioma risk.
Marc Sanson, Fay J Hosking, Sanjay Shete, Diana Zelenika, Sara E Dobbins, Yussanne Ma, Victor Enciso-Mora, Ahmed Idbaih, Jean-Yves Delattre, Khe Hoang-Xuan,[...]. Hum Mol Genet 2011
111
20

Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.
Kyle M Walsh, Veryan Codd, Ivan V Smirnov, Terri Rice, Paul A Decker, Helen M Hansen, Thomas Kollmeyer, Matthew L Kosel, Annette M Molinaro, Lucie S McCoy,[...]. Nat Genet 2014
120
19

A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation.
Robert B Jenkins, Yuanyuan Xiao, Hugues Sicotte, Paul A Decker, Thomas M Kollmeyer, Helen M Hansen, Matthew L Kosel, Shichun Zheng, Kyle M Walsh, Terri Rice,[...]. Nat Genet 2012
94
18

The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.
David N Louis, Arie Perry, Guido Reifenberger, Andreas von Deimling, Dominique Figarella-Branger, Webster K Cavenee, Hiroko Ohgaki, Otmar D Wiestler, Paul Kleihues, David W Ellison. Acta Neuropathol 2016
17

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.
Simon N Stacey, Patrick Sulem, Aslaug Jonasdottir, Gisli Masson, Julius Gudmundsson, Daniel F Gudbjartsson, Olafur T Magnusson, Sigurjon A Gudjonsson, Bardur Sigurgeirsson, Kristin Thorisdottir,[...]. Nat Genet 2011
179
17

The epidemiology of glioma in adults: a "state of the science" review.
Quinn T Ostrom, Luc Bauchet, Faith G Davis, Isabelle Deltour, James L Fisher, Chelsea Eastman Langer, Melike Pekmezci, Judith A Schwartzbaum, Michelle C Turner, Kyle M Walsh,[...]. Neuro Oncol 2014
785
17

Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.
Jeanette E Eckel-Passow, Daniel H Lachance, Annette M Molinaro, Kyle M Walsh, Paul A Decker, Hugues Sicotte, Melike Pekmezci, Terri Rice, Matt L Kosel, Ivan V Smirnov,[...]. N Engl J Med 2015
945
14

Brain tumor epidemiology: consensus from the Brain Tumor Epidemiology Consortium.
Melissa L Bondy, Michael E Scheurer, Beatrice Malmer, Jill S Barnholtz-Sloan, Faith G Davis, Dora Il'yasova, Carol Kruchko, Bridget J McCarthy, Preetha Rajaraman, Judith A Schwartzbaum,[...]. Cancer 2008
490
14

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
13

Lung cancer susceptibility locus at 5p15.33.
James D McKay, Rayjean J Hung, Valerie Gaborieau, Paolo Boffetta, Amelie Chabrier, Graham Byrnes, David Zaridze, Anush Mukeria, Neonilia Szeszenia-Dabrowska, Jolanta Lissowska,[...]. Nat Genet 2008
430
12

Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population.
Hongyan Chen, Yuanyuan Chen, Yao Zhao, Weiwei Fan, Keke Zhou, Yanhong Liu, Liangfu Zhou, Ying Mao, Qingyi Wei, Jianfeng Xu,[...]. Am J Epidemiol 2011
73
15

Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
Daniel J Brat, Roel G W Verhaak, Kenneth D Aldape, W K Alfred Yung, Sofie R Salama, Lee A D Cooper, Esther Rheinbay, C Ryan Miller, Mark Vitucci, Olena Morozova,[...]. N Engl J Med 2015
11

Common 5p15.33 and 6p21.33 variants influence lung cancer risk.
Yufei Wang, Peter Broderick, Emily Webb, Xifeng Wu, Jayaram Vijayakrishnan, Athena Matakidou, Mobshra Qureshi, Qiong Dong, Xiangjun Gu, Wei Vivien Chen,[...]. Nat Genet 2008
420
10

Deciphering the 8q24.21 association for glioma.
Victor Enciso-Mora, Fay J Hosking, Ben Kinnersley, Yufei Wang, Sanjay Shete, Diana Zelenika, Peter Broderick, Ahmed Idbaih, Jean-Yves Delattre, Khe Hoang-Xuan,[...]. Hum Mol Genet 2013
34
29

Genome-wide association study identifies three loci associated with melanoma risk.
D Timothy Bishop, Florence Demenais, Mark M Iles, Mark Harland, John C Taylor, Eve Corda, Juliette Randerson-Moor, Joanne F Aitken, Marie-Francoise Avril, Esther Azizi,[...]. Nat Genet 2009
326
9

The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium.
E Susan Amirian, Georgina N Armstrong, Renke Zhou, Ching C Lau, Elizabeth B Claus, Jill S Barnholtz-Sloan, Dora Il'yasova, Joellen Schildkraut, Francis Ali-Osman, Siegal Sadetzki,[...]. Am J Epidemiol 2016
30
30

Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk.
Kyle M Walsh, Veryan Codd, Terri Rice, Christopher P Nelson, Ivan V Smirnov, Lucie S McCoy, Helen M Hansen, Edward Elhauge, Juhi Ojha, Stephen S Francis,[...]. Oncotarget 2015
60
15

Identification of seven loci affecting mean telomere length and their association with disease.
Veryan Codd, Christopher P Nelson, Eva Albrecht, Massimo Mangino, Joris Deelen, Jessica L Buxton, Jouke Jan Hottenga, Krista Fischer, Tõnu Esko, Ida Surakka,[...]. Nat Genet 2013
564
9

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
Michael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, John Burn, Bernard Keavney. PLoS Genet 2010
274
8

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
Philip C Haycock, Stephen Burgess, Aayah Nounu, Jie Zheng, George N Okoli, Jack Bowden, Kaitlin Hazel Wade, Nicholas J Timpson, David M Evans, Peter Willeit,[...]. JAMA Oncol 2017
189
8

Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222.
V Enciso-Mora, F J Hosking, A L Di Stefano, D Zelenika, S Shete, P Broderick, A Idbaih, J-Y Delattre, K Hoang-Xuan, Y Marie,[...]. Br J Cancer 2013
39
20

IDH1 and IDH2 mutations in gliomas.
Hai Yan, D Williams Parsons, Genglin Jin, Roger McLendon, B Ahmed Rasheed, Weishi Yuan, Ivan Kos, Ines Batinic-Haberle, Siân Jones, Gregory J Riggins,[...]. N Engl J Med 2009
8

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.
Gloria M Petersen, Laufey Amundadottir, Charles S Fuchs, Peter Kraft, Rachael Z Stolzenberg-Solomon, Kevin B Jacobs, Alan A Arslan, H Bas Bueno-de-Mesquita, Steven Gallinger, Myron Gross,[...]. Nat Genet 2010
428
8

Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma.
Michele Ceccarelli, Floris P Barthel, Tathiane M Malta, Thais S Sabedot, Sofie R Salama, Bradley A Murray, Olena Morozova, Yulia Newton, Amie Radenbaugh, Stefano M Pagnotta,[...]. Cell 2016
922
8

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Maria Teresa Landi, Nilanjan Chatterjee, Kai Yu, Lynn R Goldin, Alisa M Goldstein, Melissa Rotunno, Lisa Mirabello, Kevin Jacobs, William Wheeler, Meredith Yeager,[...]. Am J Hum Genet 2009
406
7

Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene.
Y Kotake, T Nakagawa, K Kitagawa, S Suzuki, N Liu, M Kitagawa, Y Xiong. Oncogene 2011
711
7

Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a.
Kyoko L Yap, Side Li, Ana M Muñoz-Cabello, Selina Raguz, Lei Zeng, Shiraz Mujtaba, Jesús Gil, Martin J Walsh, Ming-Ming Zhou. Mol Cell 2010
951
7

Quantifying the heritability of glioma using genome-wide complex trait analysis.
Ben Kinnersley, Jonathan S Mitchell, Konstantinos Gousias, Johannes Schramm, Ahmed Idbaih, Marianne Labussière, Yannick Marie, Amithys Rahimian, H-Erich Wichmann, Stefan Schreiber,[...]. Sci Rep 2015
21
33

Principal components analysis corrects for stratification in genome-wide association studies.
Alkes L Price, Nick J Patterson, Robert M Plenge, Michael E Weinblatt, Nancy A Shadick, David Reich. Nat Genet 2006
7

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
10

TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal.
Patrick J Killela, Zachary J Reitman, Yuchen Jiao, Chetan Bettegowda, Nishant Agrawal, Luis A Diaz, Allan H Friedman, Henry Friedman, Gary L Gallia, Beppino C Giovanella,[...]. Proc Natl Acad Sci U S A 2013
854
7

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
7

Familial and personal medical history of cancer and nervous system conditions among adults with glioma and controls.
M Wrensch, M Lee, R Miike, B Newman, G Barger, R Davis, J Wiencke, J Neuhaus. Am J Epidemiol 1997
136
7

Distinct germ line polymorphisms underlie glioma morphologic heterogeneity.
Robert B Jenkins, Margaret R Wrensch, Derek Johnson, Brooke L Fridley, Paul A Decker, Yuanyuan Xiao, Thomas M Kollmeyer, Amanda L Rynearson, Stephanie Fink, Terri Rice,[...]. Cancer Genet 2011
58
12

Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk loci.
Karim Labreche, Ben Kinnersley, Giulia Berzero, Anna Luisa Di Stefano, Amithys Rahimian, Ines Detrait, Yannick Marie, Benjamin Grenier-Boley, Khe Hoang-Xuan, Jean-Yves Delattre,[...]. Acta Neuropathol 2018
22
31


Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
Rosalind A Eeles, Ali Amin Al Olama, Sara Benlloch, Edward J Saunders, Daniel A Leongamornlert, Malgorzata Tymrakiewicz, Maya Ghoussaini, Craig Luccarini, Joe Dennis, Sarah Jugurnauth-Little,[...]. Nat Genet 2013
396
6

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
Anna Helgadottir, Gudmar Thorleifsson, Kristinn P Magnusson, Solveig Grétarsdottir, Valgerdur Steinthorsdottir, Andrei Manolescu, Gregory T Jones, Gabriel J E Rinkel, Jan D Blankensteijn, Antti Ronkainen,[...]. Nat Genet 2008
526
6

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Laura J Scott, Karen L Mohlke, Lori L Bonnycastle, Cristen J Willer, Yun Li, William L Duren, Michael R Erdos, Heather M Stringham, Peter S Chines, Anne U Jackson,[...]. Science 2007
6

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
Kathryn P Burdon, Stuart Macgregor, Alex W Hewitt, Shiwani Sharma, Glyn Chidlow, Richard A Mills, Patrick Danoy, Robert Casson, Ananth C Viswanathan, Jimmy Z Liu,[...]. Nat Genet 2011
292
6

ANRIL expression is associated with atherosclerosis risk at chromosome 9p21.
Lesca M Holdt, Frank Beutner, Markus Scholz, Stephan Gielen, Gábor Gäbel, Hendrik Bergert, Gerhard Schuler, Joachim Thiery, Daniel Teupser. Arterioscler Thromb Vasc Biol 2010
302
6

Telomere maintenance and the etiology of adult glioma.
Kyle M Walsh, John K Wiencke, Daniel H Lachance, Joseph L Wiemels, Annette M Molinaro, Jeanette E Eckel-Passow, Robert B Jenkins, Margaret R Wrensch. Neuro Oncol 2015
41
14

Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies.
Kyle M Walsh, Erik Anderson, Helen M Hansen, Paul A Decker, Matt L Kosel, Thomas Kollmeyer, Terri Rice, Shichun Zheng, Yuanyuan Xiao, Jeffrey S Chang,[...]. Genet Epidemiol 2013
37
16

The somatic genomic landscape of glioblastoma.
Cameron W Brennan, Roel G W Verhaak, Aaron McKenna, Benito Campos, Houtan Noushmehr, Sofie R Salama, Siyuan Zheng, Debyani Chakravarty, J Zachary Sanborn, Samuel H Berman,[...]. Cell 2013
6

A new multipoint method for genome-wide association studies by imputation of genotypes.
Jonathan Marchini, Bryan Howie, Simon Myers, Gil McVean, Peter Donnelly. Nat Genet 2007
6



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.