A citation-based method for searching scientific literature

Fernando Riveros-Mckay, Michael E Weale, Rachel Moore, Saskia Selzam, Eva Krapohl, R Michael Sivley, William A Tarran, Peter Sørensen, Alexander S Lachapelle, Jonathan A Griffiths, Ayden Saffari, John Deanfield, Chris C A Spencer, Julia Hippisley-Cox, David J Hunter, Jack W O'Sullivan, Euan A Ashley, Vincent Plagnol, Peter Donnelly. Circ Genom Precis Med 2021
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention.
Michael Inouye, Gad Abraham, Christopher P Nelson, Angela M Wood, Michael J Sweeting, Frank Dudbridge, Florence Y Lai, Stephen Kaptoge, Marta Brozynska, Tingting Wang,[...]. J Am Coll Cardiol 2018
221
66

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
838
66

Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease.
Jonathan D Mosley, Deepak K Gupta, Jingyi Tan, Jie Yao, Quinn S Wells, Christian M Shaffer, Suman Kundu, Cassianne Robinson-Cohen, Bruce M Psaty, Stephen S Rich,[...]. JAMA 2020
84
55

Predictive Accuracy of a Polygenic Risk Score-Enhanced Prediction Model vs a Clinical Risk Score for Coronary Artery Disease.
Joshua Elliott, Barbara Bodinier, Tom A Bond, Marc Chadeau-Hyam, Evangelos Evangelou, Karel G M Moons, Abbas Dehghan, David C Muller, Paul Elliott, Ioanna Tzoulaki. JAMA 2020
89
55

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.
Amit V Khera, Connor A Emdin, Isabel Drake, Pradeep Natarajan, Alexander G Bick, Nancy R Cook, Daniel I Chasman, Usman Baber, Roxana Mehran, Daniel J Rader,[...]. N Engl J Med 2016
495
55

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
44

Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial.
Amy Damask, P Gabriel Steg, Gregory G Schwartz, Michael Szarek, Emil Hagström, Lina Badimon, M John Chapman, Catherine Boileau, Sotirios Tsimikas, Henry N Ginsberg,[...]. Circulation 2020
52
44

Predicting Benefit From Evolocumab Therapy in Patients With Atherosclerotic Disease Using a Genetic Risk Score: Results From the FOURIER Trial.
Nicholas A Marston, Frederick K Kamanu, Francesco Nordio, Yared Gurmu, Carolina Roselli, Peter S Sever, Terje R Pedersen, Anthony C Keech, Huei Wang, Armando Lira Pineda,[...]. Circulation 2020
54
44

Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
J L Mega, N O Stitziel, J G Smith, D I Chasman, M Caulfield, J J Devlin, F Nordio, C Hyde, C P Cannon, F Sacks,[...]. Lancet 2015
322
44

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
Majid Nikpay, Anuj Goel, Hong-Hee Won, Leanne M Hall, Christina Willenborg, Stavroula Kanoni, Danish Saleheen, Theodosios Kyriakou, Christopher P Nelson, Jemma C Hopewell,[...]. Nat Genet 2015
44

Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting.
Pradeep Natarajan, Robin Young, Nathan O Stitziel, Sandosh Padmanabhan, Usman Baber, Roxana Mehran, Samantha Sartori, Valentin Fuster, Dermot F Reilly, Adam Butterworth,[...]. Circulation 2017
201
44

Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers.
Nina Mars, Jukka T Koskela, Pietari Ripatti, Tuomo T J Kiiskinen, Aki S Havulinna, Joni V Lindbohm, Ari Ahola-Olli, Mitja Kurki, Juha Karjalainen, Priit Palta,[...]. Nat Med 2020
70
44

Combined Utility of 25 Disease and Risk Factor Polygenic Risk Scores for Stratifying Risk of All-Cause Mortality.
Allison Meisner, Prosenjit Kundu, Yan Dora Zhang, Lauren V Lan, Sungwon Kim, Disha Ghandwani, Parichoy Pal Choudhury, Sonja I Berndt, Neal D Freedman, Montserrat Garcia-Closas,[...]. Am J Hum Genet 2020
13
33

Discovery and refinement of loci associated with lipid levels.
Cristen J Willer, Ellen M Schmidt, Sebanti Sengupta, Gina M Peloso, Stefan Gustafsson, Stavroula Kanoni, Andrea Ganna, Jin Chen, Martin L Buchkovich, Samia Mora,[...]. Nat Genet 2013
33

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
Bjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, Alexander Gusev, Sara Lindström, Stephan Ripke, Giulio Genovese, Po-Ru Loh, Gaurav Bhatia, Ron Do,[...]. Am J Hum Genet 2015
464
33

Tutorial: a guide to performing polygenic risk score analyses.
Shing Wan Choi, Timothy Shin-Heng Mak, Paul F O'Reilly. Nat Protoc 2020
119
33

Improving reporting standards for polygenic scores in risk prediction studies.
Hannah Wand, Samuel A Lambert, Cecelia Tamburro, Michael A Iacocca, Jack W O'Sullivan, Catherine Sillari, Iftikhar J Kullo, Robb Rowley, Jacqueline S Dron, Deanna Brockman,[...]. Nature 2021
36
33

Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.
Ozan Dikilitas, Daniel J Schaid, Matthew L Kosel, Robert J Carroll, Christopher G Chute, Joshua A Denny, Alex Fedotov, QiPing Feng, Hakon Hakonarson, Gail P Jarvik,[...]. Am J Hum Genet 2020
21
33

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
33

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
33

Statins in Familial Hypercholesterolemia: Consequences for Coronary Artery Disease and All-Cause Mortality.
Joost Besseling, G Kees Hovingh, Roeland Huijgen, John J P Kastelein, Barbara A Hutten. J Am Coll Cardiol 2016
102
33

Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease.
George Hindy, Krishna G Aragam, Kenney Ng, Mark Chaffin, Luca A Lotta, Aris Baras, Isabel Drake, Marju Orho-Melander, Olle Melander, Sekar Kathiresan,[...]. Arterioscler Thromb Vasc Biol 2020
14
33

Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history.
Hayato Tada, Olle Melander, Judy Z Louie, Joseph J Catanese, Charles M Rowland, James J Devlin, Sekar Kathiresan, Dov Shiffman. Eur Heart J 2016
134
33

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus.
Kiran Musunuru, Alanna Strong, Maria Frank-Kamenetsky, Noemi E Lee, Tim Ahfeldt, Katherine V Sachs, Xiaoyu Li, Hui Li, Nicolas Kuperwasser, Vera M Ruda,[...]. Nature 2010
717
22

Biological, clinical and population relevance of 95 loci for blood lipids.
Tanya M Teslovich, Kiran Musunuru, Albert V Smith, Andrew C Edmondson, Ioannis M Stylianou, Masahiro Koseki, James P Pirruccello, Samuli Ripatti, Daniel I Chasman, Cristen J Willer,[...]. Nature 2010
22

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
814
22

A decade of genome-wide association studies for coronary artery disease: the challenges ahead.
Jeanette Erdmann, Thorsten Kessler, Loreto Munoz Venegas, Heribert Schunkert. Cardiovasc Res 2018
110
22


Polygenic scores via penalized regression on summary statistics.
Timothy Shin Heng Mak, Robert Milan Porsch, Shing Wan Choi, Xueya Zhou, Pak Chung Sham. Genet Epidemiol 2017
61
22

Genome-wide association studies for common diseases and complex traits.
Joel N Hirschhorn, Mark J Daly. Nat Rev Genet 2005
22

Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South Asians.
Minxian Wang, Ramesh Menon, Sanghamitra Mishra, Aniruddh P Patel, Mark Chaffin, Deepak Tanneeru, Manjari Deshmukh, Oshin Mathew, Sanika Apte, Christina S Devanboo,[...]. J Am Coll Cardiol 2020
13
22

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
22

Genomic prediction of coronary heart disease.
Gad Abraham, Aki S Havulinna, Oneil G Bhalala, Sean G Byars, Alysha M De Livera, Laxman Yetukuri, Emmi Tikkanen, Markus Perola, Heribert Schunkert, Eric J Sijbrands,[...]. Eur Heart J 2016
147
22

Estimating the prevalence of heterozygous familial hypercholesterolaemia: a systematic review and meta-analysis.
Leo E Akioyamen, Jacques Genest, Shubham D Shan, Rachel L Reel, Jordan M Albaum, Anna Chu, Jack V Tu. BMJ Open 2017
150
22

Genetic susceptibility to death from coronary heart disease in a study of twins.
M E Marenberg, N Risch, L F Berkman, B Floderus, U de Faire. N Engl J Med 1994
890
22

Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Satoshi Koyama, Kaoru Ito, Chikashi Terao, Masato Akiyama, Momoko Horikoshi, Yukihide Momozawa, Hiroshi Matsunaga, Hirotaka Ieki, Kouichi Ozaki, Yoshihiro Onouchi,[...]. Nat Genet 2020
27
22

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society.
Børge G Nordestgaard, M John Chapman, Steve E Humphries, Henry N Ginsberg, Luis Masana, Olivier S Descamps, Olov Wiklund, Robert A Hegele, Frederick J Raal, Joep C Defesche,[...]. Eur Heart J 2013
22

Developing and evaluating polygenic risk prediction models for stratified disease prevention.
Nilanjan Chatterjee, Jianxin Shi, Montserrat García-Closas. Nat Rev Genet 2016
290
22

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
422
22

2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines.
Donna K Arnett, Roger S Blumenthal, Michelle A Albert, Andrew B Buroker, Zachary D Goldberger, Ellen J Hahn, Cheryl Dennison Himmelfarb, Amit Khera, Donald Lloyd-Jones, J William McEvoy,[...]. J Am Coll Cardiol 2019
429
22

Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease.
Krishna G Aragam, Amanda Dobbyn, Renae Judy, Mark Chaffin, Kumardeep Chaudhary, George Hindy, Andrew Cagan, Phoebe Finneran, Lu-Chen Weng, Ruth J F Loos,[...]. J Am Coll Cardiol 2020
26
22

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Daniel Taliun, Daniel N Harris, Michael D Kessler, Jedidiah Carlson, Zachary A Szpiech, Raul Torres, Sarah A Gagliano Taliun, André Corvelo, Stephanie M Gogarten, Hyun Min Kang,[...]. Nature 2021
140
22

Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial).
Iftikhar J Kullo, Hayan Jouni, Erin E Austin, Sherry-Ann Brown, Teresa M Kruisselbrink, Iyad N Isseh, Raad A Haddad, Tariq S Marroush, Khader Shameer, Janet E Olson,[...]. Circulation 2016
121
22

Interactions Between Enhanced Polygenic Risk Scores and Lifestyle for Cardiovascular Disease, Diabetes, and Lipid Levels.
Yixuan Ye, Xi Chen, James Han, Wei Jiang, Pradeep Natarajan, Hongyu Zhao. Circ Genom Precis Med 2021
8
25

Association analyses based on false discovery rate implicate new loci for coronary artery disease.
Christopher P Nelson, Anuj Goel, Adam S Butterworth, Stavroula Kanoni, Tom R Webb, Eirini Marouli, Lingyao Zeng, Ioanna Ntalla, Florence Y Lai, Jemma C Hopewell,[...]. Nat Genet 2017
293
22

Genetic identification of familial hypercholesterolemia within a single U.S. health care system.
Noura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, Eric A Wright, Dustin N Hartzel, Claudia Gonzaga-Jauregui, Colm O'Dushlaine, Joseph B Leader, H Lester Kirchner, D'Andra M Lindbuchler,[...]. Science 2016
209
22

Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study.
Philippa J Talmud, Sonia Shah, Ros Whittall, Marta Futema, Philip Howard, Jackie A Cooper, Seamus C Harrison, Kawah Li, Fotios Drenos, Frederik Karpe,[...]. Lancet 2013
352
22

Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.
Joshua W Knowles, Shirin Zarafshar, Aleksandra Pavlovic, Benjamin A Goldstein, Sandra Tsai, Jin Li, Michael V McConnell, Devin Absher, Euan A Ashley, Michaela Kiernan,[...]. Front Cardiovasc Med 2017
23
22

Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.
Akl C Fahed, Minxian Wang, Julian R Homburger, Aniruddh P Patel, Alexander G Bick, Cynthia L Neben, Carmen Lai, Deanna Brockman, Anthony Philippakis, Patrick T Ellinor,[...]. Nat Commun 2020
59
22

Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel.
Amy C Sturm, Joshua W Knowles, Samuel S Gidding, Zahid S Ahmad, Catherine D Ahmed, Christie M Ballantyne, Seth J Baum, Mafalda Bourbon, Alain Carrié, Marina Cuchel,[...]. J Am Coll Cardiol 2018
171
22


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.