A citation-based method for searching scientific literature

John L Slunecka, Matthijs D van der Zee, Jeffrey J Beck, Brandon N Johnson, Casey T Finnicum, René Pool, Jouke-Jan Hottenga, Eco J C de Geus, Erik A Ehli. Hum Genomics 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
66

Polygenic risk score predicts prevalence of cardiovascular disease in patients with familial hypercholesterolemia.
Martine Paquette, Michael Chong, Sébastien Thériault, Robert Dufour, Guillaume Paré, Alexis Baass. J Clin Lipidol 2017
60
33

Polygenic Contribution to Low-Density Lipoprotein Cholesterol Levels and Cardiovascular Risk in Monogenic Familial Hypercholesterolemia.
Mark Trinder, Martine Paquette, Lubomira Cermakova, Matthew R Ban, Robert A Hegele, Alexis Baass, Liam R Brunham. Circ Genom Precis Med 2020
14
33

Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries.
Michael E Weale, Fernando Riveros-Mckay, Saskia Selzam, Priyanka Seth, Rachel Moore, William A Tarran, Eva Gradovich, Carla Giner-Delgado, Duncan Palmer, Daniel Wells,[...]. Am J Cardiol 2021
9
33

How Do We Incorporate Polygenic Risk Scores in Cardiovascular Disease Risk Assessment and Management?
Trevor D Hadley, Ali M Agha, Christie M Ballantyne. Curr Atheroscler Rep 2021
1
100

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
36
33

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
113
33

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
128
33

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
565
33

Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia.
Mark Trinder, Xuan Li, Maria Liza DeCastro, Luba Cermakova, Singh Sadananda, Linda M Jackson, Hawmid Azizi, G B John Mancini, Gordon A Francis, Jiri Frohlich,[...]. J Am Coll Cardiol 2019
66
33

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
143
33

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
33

Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction.
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,[...]. Circ Genom Precis Med 2021
16
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

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
33

Polygenic risk score and coronary artery disease: A meta-analysis of 979,286 participant data.
Thomas A Agbaedeng, Jean Jacques Noubiap, Edith Pascale Mofo Mato, Derek P Chew, Gemma A Figtree, M Abdullah Said, Pim van der Harst. Atherosclerosis 2021
3
33

Robust relationship inference in genome-wide association studies.
Ani Manichaikul, Josyf C Mychaleckyj, Stephen S Rich, Kathy Daly, Michèle Sale, Wei-Min Chen. Bioinformatics 2010
33

African genetic diversity and adaptation inform a precision medicine agenda.
Luisa Pereira, Leon Mutesa, Paulina Tindana, Michèle Ramsay. Nat Rev Genet 2021
24
33

Could Polygenic Risk Scores Be Useful in Psychiatry?: A Review.
Graham K Murray, Tian Lin, Jehannine Austin, John J McGrath, Ian B Hickie, Naomi R Wray. JAMA Psychiatry 2021
47
33

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
288
33

Defining the role of common variation in the genomic and biological architecture of adult human height.
Andrew R Wood, Tonu Esko, Jian Yang, Sailaja Vedantam, Tune H Pers, Stefan Gustafsson, Audrey Y Chu, Karol Estrada, Jian'an Luan, Zoltán Kutalik,[...]. Nat Genet 2014
33

Biospecimens and the ABCD study: Rationale, methods of collection, measurement and early data.
Kristina A Uban, Megan K Horton, Joanna Jacobus, Charles Heyser, Wesley K Thompson, Susan F Tapert, Pamela A F Madden, Elizabeth R Sowell. Dev Cogn Neurosci 2018
35
33

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Anubha Mahajan, Jennifer Wessel, Sara M Willems, Wei Zhao, Neil R Robertson, Audrey Y Chu, Wei Gan, Hidetoshi Kitajima, Daniel Taliun, N William Rayner,[...]. Nat Genet 2018
192
33

Polygenic Scores for Height in Admixed Populations.
Bárbara D Bitarello, Iain Mathieson. G3 (Bethesda) 2020
26
33

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Alicia R Martin, Christopher R Gignoux, Raymond K Walters, Genevieve L Wojcik, Benjamin M Neale, Simon Gravel, Mark J Daly, Carlos D Bustamante, Eimear E Kenny. Am J Hum Genet 2017
519
33

Comparing distributions of polygenic risk scores of type 2 diabetes and coronary heart disease within different populations.
Sulev Reisberg, Tatjana Iljasenko, Kristi Läll, Krista Fischer, Jaak Vilo. PLoS One 2017
39
33

Systematic Review of Polygenic Risk Scores for Type 1 and Type 2 Diabetes.
Felipe Padilla-Martínez, Francois Collin, Miroslaw Kwasniewski, Adam Kretowski. Int J Mol Sci 2020
15
33

Genetic disease risks can be misestimated across global populations.
Michelle S Kim, Kane P Patel, Andrew K Teng, Ali J Berens, Joseph Lachance. Genome Biol 2018
72
33


A classical twin study of PTSD symptoms and resilience: Evidence for a single spectrum of vulnerability to traumatic stress.
Erika J Wolf, Mark W Miller, Danielle R Sullivan, Ananda B Amstadter, Karen S Mitchell, Jack Goldberg, Kathryn M Magruder. Depress Anxiety 2018
37
33

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores.
Julian R Homburger, Cynthia L Neben, Gilad Mishne, Alicia Y Zhou, Sekar Kathiresan, Amit V Khera. Genome Med 2019
23
33


Contributions of PTSD polygenic risk and environmental stress to suicidality in preadolescents.
Nikolaos P Daskalakis, Laura M Schultz, Elina Visoki, Tyler M Moore, Stirling T Argabright, Nathaniel G Harnett, Grace E DiDomenico, Varun Warrier, Laura Almasy, Ran Barzilay. Neurobiol Stress 2021
3
33

Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts.
Rebecca E Graff, Taylor B Cavazos, Khanh K Thai, Linda Kachuri, Sara R Rashkin, Joshua D Hoffman, Stacey E Alexeeff, Maruta Blatchins, Travis J Meyers, Lancelote Leong,[...]. Nat Commun 2021
15
33

Second-generation PLINK: rising to the challenge of larger and richer datasets.
Christopher C Chang, Carson C Chow, Laurent Cam Tellier, Shashaank Vattikuti, Shaun M Purcell, James J Lee. Gigascience 2015
33

Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.
Roseann E Peterson, Karoline Kuchenbaecker, Raymond K Walters, Chia-Yen Chen, Alice B Popejoy, Sathish Periyasamy, Max Lam, Conrad Iyegbe, Rona J Strawbridge, Leslie Brick,[...]. Cell 2019
142
33

Generalizing polygenic risk scores from Europeans to Hispanics/Latinos.
Kelsey E Grinde, Qibin Qi, Timothy A Thornton, Simin Liu, Aladdin H Shadyab, Kei Hang K Chan, Alexander P Reiner, Tamar Sofer. Genet Epidemiol 2019
37
33

Tutorial: a guide to performing polygenic risk score analyses.
Shing Wan Choi, Timothy Shin-Heng Mak, Paul F O'Reilly. Nat Protoc 2020
239
33

Improved polygenic prediction by Bayesian multiple regression on summary statistics.
Luke R Lloyd-Jones, Jian Zeng, Julia Sidorenko, Loïc Yengo, Gerhard Moser, Kathryn E Kemper, Huanwei Wang, Zhili Zheng, Reedik Magi, Tõnu Esko,[...]. Nat Commun 2019
96
33

Rare and low-frequency coding variants alter human adult height.
Eirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, Ken Sin Lo, Andrew R Wood, Troels R Kjaer, Rebecca S Fine, Yingchang Lu, Claudia Schurmann, Heather M Highland,[...]. Nature 2017
317
33

Mixed-model association for biobank-scale datasets.
Po-Ru Loh, Gleb Kichaev, Steven Gazal, Armin P Schoech, Alkes L Price. Nat Genet 2018
224
33

Next-generation genotype imputation service and methods.
Sayantan Das, Lukas Forer, Sebastian Schönherr, Carlo Sidore, Adam E Locke, Alan Kwong, Scott I Vrieze, Emily Y Chew, Shawn Levy, Matt McGue,[...]. Nat Genet 2016
33

Polygenic risk scores: a biased prediction?
Francisco M De La Vega, Carlos D Bustamante. Genome Med 2018
46
33

Genome-wide association study of type 2 diabetes in Africa.
Ji Chen, Meng Sun, Adebowale Adeyemo, Fraser Pirie, Tommy Carstensen, Cristina Pomilla, Ayo P Doumatey, Guanjie Chen, Elizabeth H Young, Manjinder Sandhu,[...]. Diabetologia 2019
30
33

The use of polygenic risk scores to identify phenotypes associated with genetic risk of bipolar disorder and depression: A systematic review.
Sumit Mistry, Judith R Harrison, Daniel J Smith, Valentina Escott-Price, Stanley Zammit. J Affect Disord 2018
52
33

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.
Caroline M Nievergelt, Adam X Maihofer, Torsten Klengel, Elizabeth G Atkinson, Chia-Yen Chen, Karmel W Choi, Jonathan R I Coleman, Shareefa Dalvie, Laramie E Duncan, Joel Gelernter,[...]. Nat Commun 2019
136
33

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
33

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Robert A Scott, Laura J Scott, Reedik Mägi, Letizia Marullo, Kyle J Gaulton, Marika Kaakinen, Natalia Pervjakova, Tune H Pers, Andrew D Johnson, John D Eicher,[...]. Diabetes 2017
367
33

Polygenic Score Models for Alzheimer's Disease: From Research to Clinical Applications.
Xiaopu Zhou, Yolanda Y T Li, Amy K Y Fu, Nancy Y Ip. Front Neurosci 2021
4
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
539
33


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.