A citation-based method for searching scientific literature

Donna K Arnett, Alison E Baird, Ruth A Barkley, Craig T Basson, Eric Boerwinkle, Santhi K Ganesh, David M Herrington, Yuling Hong, Cashell Jaquish, Deborah A McDermott, Christopher J O'Donnell. Circulation 2007
Times Cited: 140







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



Times Cited
  Times     Co-cited
Similarity


Genomewide association analysis of coronary artery disease.
Nilesh J Samani, Jeanette Erdmann, Alistair S Hall, Christian Hengstenberg, Massimo Mangino, Bjoern Mayer, Richard J Dixon, Thomas Meitinger, Peter Braund, H-Erich Wichmann,[...]. N Engl J Med 2007
19


A common allele on chromosome 9 associated with coronary heart disease.
Ruth McPherson, Alexander Pertsemlidis, Nihan Kavaslar, Alexandre Stewart, Robert Roberts, David R Cox, David A Hinds, Len A Pennacchio, Anne Tybjaerg-Hansen, Aaron R Folsom,[...]. Science 2007
18

A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Anna Helgadottir, Gudmar Thorleifsson, Andrei Manolescu, Solveig Gretarsdottir, Thorarinn Blondal, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Asgeir Sigurdsson, Adam Baker, Arnar Palsson,[...]. Science 2007
17

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
Heribert Schunkert, Anika Götz, Peter Braund, Ralph McGinnis, David-Alexandre Tregouet, Massimo Mangino, Patrick Linsel-Nitschke, Francois Cambien, Christian Hengstenberg, Klaus Stark,[...]. Circulation 2008
288
8

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.
Helen M Broadbent, John F Peden, Stefan Lorkowski, Anuj Goel, Halit Ongen, Fiona Green, Robert Clarke, Rory Collins, Maria Grazia Franzosi, Gianni Tognoni,[...]. Hum Mol Genet 2008
368
8

New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Jeanette Erdmann, Anika Grosshennig, Peter S Braund, Inke R König, Christian Hengstenberg, Alistair S Hall, Patrick Linsel-Nitschke, Sekar Kathiresan, Ben Wright, David-Alexandre Trégouët,[...]. Nat Genet 2009
363
8

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Sekar Kathiresan, Benjamin F Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C Engert, Nilesh J Samani, Heribert Schunkert,[...]. Nat Genet 2009
823
8

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
537
7

Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Cristen J Willer, Serena Sanna, Anne U Jackson, Angelo Scuteri, Lori L Bonnycastle, Robert Clarke, Simon C Heath, Nicholas J Timpson, Samer S Najjar, Heather M Stringham,[...]. Nat Genet 2008
7

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study.
Salim Yusuf, Steven Hawken, Stephanie Ounpuu, Tony Dans, Alvaro Avezum, Fernando Lanas, Matthew McQueen, Andrzej Budaj, Prem Pais, John Varigos,[...]. Lancet 2004
7

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease.
Jonathan C Cohen, Eric Boerwinkle, Thomas H Mosley, Helen H Hobbs. N Engl J Med 2006
6

Prediction of coronary heart disease using risk factor categories.
P W Wilson, R B D'Agostino, D Levy, A M Belanger, H Silbershatz, W B Kannel. Circulation 1998
6

Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring.
Donald M Lloyd-Jones, Byung-Ho Nam, Ralph B D'Agostino, Daniel Levy, Joanne M Murabito, Thomas J Wang, Peter W F Wilson, Christopher J O'Donnell. JAMA 2004
459
6



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
6

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.
Anna Helgadottir, Andrei Manolescu, Gudmar Thorleifsson, Solveig Gretarsdottir, Helga Jonsdottir, Unnur Thorsteinsdottir, Nilesh J Samani, Gudmundur Gudmundsson, Struan F A Grant, Gudmundur Thorgeirsson,[...]. Nat Genet 2004
691
5

Mechanisms of disease: The genetic basis of coronary heart disease.
Iftikhar J Kullo, Keyue Ding. Nat Clin Pract Cardiovasc Med 2007
53
9

Genomewide association studies of stroke.
M Arfan Ikram, Sudha Seshadri, Joshua C Bis, Myriam Fornage, Anita L DeStefano, Yurii S Aulchenko, Stephanie Debette, Thomas Lumley, Aaron R Folsom, Evita G van den Herik,[...]. N Engl J Med 2009
342
5

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.
Ying Wang, Jeffrey R O'Connell, Patrick F McArdle, James B Wade, Sarah E Dorff, Sanjiv J Shah, Xiaolian Shi, Lin Pan, Evadnie Rampersaud, Haiqing Shen,[...]. Proc Natl Acad Sci U S A 2009
221
5

Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond.
Michael J Pencina, Ralph B D'Agostino, Ralph B D'Agostino, Ramachandran S Vasan. Stat Med 2008
5

Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3.
Nina P Paynter, Daniel I Chasman, Julie E Buring, Dov Shiffman, Nancy R Cook, Paul M Ridker. Ann Intern Med 2009
172
5

Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.
Andreas Gschwendtner, Steve Bevan, John W Cole, Anna Plourde, Mar Matarin, Helen Ross-Adams, Thomas Meitinger, Erich Wichmann, Braxton D Mitchell, Karen Furie,[...]. Ann Neurol 2009
162
5

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.
Solveig Gretarsdottir, Gudmar Thorleifsson, Andrei Manolescu, Unnur Styrkarsdottir, Anna Helgadottir, Andreas Gschwendtner, Konstantinos Kostulas, Gregor Kuhlenbäumer, Steve Bevan, Thorbjorg Jonsdottir,[...]. Ann Neurol 2008
204
5

Association between 9p21 genomic markers and heart disease: a meta-analysis.
Glenn E Palomaki, Stephanie Melillo, Linda A Bradley. JAMA 2010
114
5

Large-scale association analysis identifies new risk loci for coronary artery disease.
Panos Deloukas, Stavroula Kanoni, Christina Willenborg, Martin Farrall, Themistocles L Assimes, John R Thompson, Erik Ingelsson, Danish Saleheen, Jeanette Erdmann, Benjamin A Goldstein,[...]. Nat Genet 2013
5

Heart disease and stroke statistics--2015 update: a report from the American Heart Association.
Dariush Mozaffarian, Emelia J Benjamin, Alan S Go, Donna K Arnett, Michael J Blaha, Mary Cushman, Sarah de Ferranti, Jean-Pierre Després, Heather J Fullerton, Virginia J Howard,[...]. Circulation 2015
5


Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Sekar Kathiresan, Olle Melander, Candace Guiducci, Aarti Surti, Noël P Burtt, Mark J Rieder, Gregory M Cooper, Charlotta Roos, Benjamin F Voight, Aki S Havulinna,[...]. Nat Genet 2008
4

Meta-analysis: apolipoprotein E genotypes and risk for coronary heart disease.
Yiqing Song, Meir J Stampfer, Simin Liu. Ann Intern Med 2004
390
4

Apolipoprotein E alleles and risk of coronary disease. A meta-analysis.
P W Wilson, E J Schaefer, M G Larson, J M Ordovas. Arterioscler Thromb Vasc Biol 1996
458
4

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
Kouichi Ozaki, Yozo Ohnishi, Aritoshi Iida, Akihiko Sekine, Ryo Yamada, Tatsuhiko Tsunoda, Hiroshi Sato, Hideyuki Sato, Masatsugu Hori, Yusuke Nakamura,[...]. Nat Genet 2002
648
4

Prediction of the risk of myocardial infarction from polymorphisms in candidate genes.
Yoshiji Yamada, Hideo Izawa, Sahoko Ichihara, Fumimaro Takatsu, Hitoshi Ishihara, Haruo Hirayama, Takahito Sone, Masashi Tanaka, Mitsuhiro Yokota. N Engl J Med 2002
523
4

Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility.
Xiaosong Wang, Massimiliano Ria, Peter M Kelmenson, Per Eriksson, David C Higgins, Ann Samnegård, Christina Petros, Jarod Rollins, Anna M Bennet, Björn Wiman,[...]. Nat Genet 2005
227
4

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
4


Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
Eleftheria Zeggini, Michael N Weedon, Cecilia M Lindgren, Timothy M Frayling, Katherine S Elliott, Hana Lango, Nicholas J Timpson, John R B Perry, Nigel W Rayner, Rachel M Freathy,[...]. Science 2007
4


Angiotensin I-converting enzyme insertion/deletion polymorphism and cardiac mortality and morbidity after coronary artery bypass graft surgery.
Henry Völzke, Julia Engel, Volker Kleine, Christian Schwahn, Johannes B Dahm, Lothar Eckel, Rainer Rettig. Chest 2002
33
12

High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population.
Yoshiki Itoh, Nobuhisa Mizuki, Tsuyako Shimada, Fumihiro Azuma, Mitsuo Itakura, Koichi Kashiwase, Eri Kikkawa, Jerzy K Kulski, Masahiro Satake, Hidetoshi Inoko. Immunogenetics 2005
238
4


The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.
Juha Karvanen, Kaisa Silander, Frank Kee, Laurence Tiret, Veikko Salomaa, Kari Kuulasmaa, Per-Gunnar Wiklund, Jarmo Virtamo, Olli Saarela, Claire Perret,[...]. Genet Epidemiol 2009
72
5

Genome-wide association study identifies eight loci associated with blood pressure.
Christopher Newton-Cheh, Toby Johnson, Vesela Gateva, Martin D Tobin, Murielle Bochud, Lachlan Coin, Samer S Najjar, Jing Hua Zhao, Simon C Heath, Susana Eyheramendy,[...]. Nat Genet 2009
880
4

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.
Axel Visel, Yiwen Zhu, Dalit May, Veena Afzal, Elaine Gong, Catia Attanasio, Matthew J Blow, Jonathan C Cohen, Edward M Rubin, Len A Pennacchio. Nature 2010
338
4

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
David-Alexandre Trégouët, Inke R König, Jeanette Erdmann, Alexandru Munteanu, Peter S Braund, Alistair S Hall, Anika Grosshennig, Patrick Linsel-Nitschke, Claire Perret, Maylis DeSuremain,[...]. Nat Genet 2009
334
4

Common variants at 30 loci contribute to polygenic dyslipidemia.
Sekar Kathiresan, Cristen J Willer, Gina M Peloso, Serkalem Demissie, Kiran Musunuru, Eric E Schadt, Lee Kaplan, Derrick Bennett, Yun Li, Toshiko Tanaka,[...]. Nat Genet 2009
4

Molecular genetics of atherosclerosis.
Himadri Roy, Shalini Bhardwaj, Seppo Yla-Herttuala. Hum Genet 2009
37
10

Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study.
Ariel Brautbar, Christie M Ballantyne, Kim Lawson, Vijay Nambi, Lloyd Chambless, Aaron R Folsom, James T Willerson, Eric Boerwinkle. Circ Cardiovasc Genet 2009
68
5



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.