A citation-based method for searching scientific literature

Oliver Pain, Kylie P Glanville, Saskia P Hagenaars, Saskia Selzam, Anna E Fürtjes, Héléna A Gaspar, Jonathan R I Coleman, Kaili Rimfeld, Gerome Breen, Robert Plomin, Lasse Folkersen, Cathryn M Lewis. PLoS Genet 2021
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


Polygenic prediction via Bayesian regression and continuous shrinkage priors.
Tian Ge, Chia-Yen Chen, Yang Ni, Yen-Chen Anne Feng, Jordan W Smoller. Nat Commun 2019
153
57

Tutorial: a guide to performing polygenic risk score analyses.
Shing Wan Choi, Timothy Shin-Heng Mak, Paul F O'Reilly. Nat Protoc 2020
190
42

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
86
42

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
511
36

The UK Biobank resource with deep phenotyping and genomic data.
Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O'Connell,[...]. Nature 2018
36

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
946
36

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
572
36

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
31


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
87
31

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
31

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
31

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
488
31

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
31

Leveraging functional annotations in genetic risk prediction for human complex diseases.
Yiming Hu, Qiongshi Lu, Ryan Powles, Xinwei Yao, Can Yang, Fang Fang, Xinran Xu, Hongyu Zhao. PLoS Comput Biol 2017
51
26

PRSice-2: Polygenic Risk Score software for biobank-scale data.
Shing Wan Choi, Paul F O'Reilly. Gigascience 2019
247
26

From Basic Science to Clinical Application of Polygenic Risk Scores: A Primer.
Naomi R Wray, Tian Lin, Jehannine Austin, John J McGrath, Ian B Hickie, Graham K Murray, Peter M Visscher. JAMA Psychiatry 2021
52
26

Making the Most of Clumping and Thresholding for Polygenic Scores.
Florian Privé, Bjarni J Vilhjálmsson, Hugues Aschard, Michael G B Blum. Am J Hum Genet 2019
32
26

A reference panel of 64,976 haplotypes for genotype imputation.
Shane McCarthy, Sayantan Das, Warren Kretzschmar, Olivier Delaneau, Andrew R Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp,[...]. Nat Genet 2016
21

Integrative approaches for large-scale transcriptome-wide association studies.
Alexander Gusev, Arthur Ko, Huwenbo Shi, Gaurav Bhatia, Wonil Chung, Brenda W J H Penninx, Rick Jansen, Eco J C de Geus, Dorret I Boomsma, Fred A Wright,[...]. Nat Genet 2016
680
21

A better coefficient of determination for genetic profile analysis.
Sang Hong Lee, Michael E Goddard, Naomi R Wray, Peter M Visscher. Genet Epidemiol 2012
128
21

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
21

GCTA: a tool for genome-wide complex trait analysis.
Jian Yang, S Hong Lee, Michael E Goddard, Peter M Visscher. Am J Hum Genet 2011
21

Improving genetic prediction by leveraging genetic correlations among human diseases and traits.
Robert M Maier, Zhihong Zhu, Sang Hong Lee, Maciej Trzaskowski, Douglas M Ruderfer, Eli A Stahl, Stephan Ripke, Naomi R Wray, Jian Yang, Peter M Visscher,[...]. Nat Commun 2018
63
21

The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation.
Samuel A Lambert, Laurent Gil, Simon Jupp, Scott C Ritchie, Yu Xu, Annalisa Buniello, Aoife McMahon, Gad Abraham, Michael Chapman, Helen Parkinson,[...]. Nat Genet 2021
52
21

Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics.
Sung Chun, Maxim Imakaev, Daniel Hui, Nikolaos A Patsopoulos, Benjamin M Neale, Sekar Kathiresan, Nathan O Stitziel, Shamil R Sunyaev. Am J Hum Genet 2020
14
28

Multi-polygenic score approach to trait prediction.
E Krapohl, H Patel, S Newhouse, C J Curtis, S von Stumm, P S Dale, D Zabaneh, G Breen, P F O'Reilly, R Plomin. Mol Psychiatry 2018
69
21


Developing and evaluating polygenic risk prediction models for stratified disease prevention.
Nilanjan Chatterjee, Jianxin Shi, Montserrat García-Closas. Nat Rev Genet 2016
316
21

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
19
21

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
638
21

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
21

Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data.
Jianxin Shi, Ju-Hyun Park, Jubao Duan, Sonja T Berndt, Winton Moy, Kai Yu, Lei Song, William Wheeler, Xing Hua, Debra Silverman,[...]. PLoS Genet 2016
51
15

Twins Early Development Study: A Genetically Sensitive Investigation into Behavioral and Cognitive Development from Infancy to Emerging Adulthood.
Kaili Rimfeld, Margherita Malanchini, Thomas Spargo, Gemma Spickernell, Saskia Selzam, Andrew McMillan, Philip S Dale, Thalia C Eley, Robert Plomin. Twin Res Hum Genet 2019
33
15

Evidence for gene-environment correlation in child feeding: Links between common genetic variation for BMI in children and parental feeding practices.
Saskia Selzam, Tom A McAdams, Jonathan R I Coleman, Susan Carnell, Paul F O'Reilly, Robert Plomin, Clare H Llewellyn. PLoS Genet 2018
27
15

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
668
15

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
255
15

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
15

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.
C B Pedersen, J Bybjerg-Grauholm, M G Pedersen, J Grove, E Agerbo, M Bækvad-Hansen, J B Poulsen, C S Hansen, J J McGrath, T D Als,[...]. Mol Psychiatry 2018
117
15

LDpred2: better, faster, stronger.
Florian Privé, Julyan Arbel, Bjarni J Vilhjálmsson. Bioinformatics 2020
34
15

Genetic studies of body mass index yield new insights for obesity biology.
Adam E Locke, Bratati Kahali, Sonja I Berndt, Anne E Justice, Tune H Pers, Felix R Day, Corey Powell, Sailaja Vedantam, Martin L Buchkovich, Jian Yang,[...]. Nature 2015
15

PRSice: Polygenic Risk Score software.
Jack Euesden, Cathryn M Lewis, Paul F O'Reilly. Bioinformatics 2015
622
15

Estimating missing heritability for disease from genome-wide association studies.
Sang Hong Lee, Naomi R Wray, Michael E Goddard, Peter M Visscher. Am J Hum Genet 2011
649
15

Polygenic modeling with bayesian sparse linear mixed models.
Xiang Zhou, Peter Carbonetto, Matthew Stephens. PLoS Genet 2013
366
15

Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits.
Andrew D Grotzinger, Mijke Rhemtulla, Ronald de Vlaming, Stuart J Ritchie, Travis T Mallard, W David Hill, Hill F Ip, Riccardo E Marioni, Andrew M McIntosh, Ian J Deary,[...]. Nat Hum Behav 2019
157
15

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
15

Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Vassily Trubetskoy, Manuel Mattheisen, Yunpeng Wang, Jonathan R I Coleman, Héléna A Gaspar,[...]. Nat Genet 2019
546
15

MAGMA: generalized gene-set analysis of GWAS data.
Christiaan A de Leeuw, Joris M Mooij, Tom Heskes, Danielle Posthuma. PLoS Comput Biol 2015
932
15

A global overview of pleiotropy and genetic architecture in complex traits.
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, Maša Umićević Mirkov, Christiaan de Leeuw, Tinca J C Polderman, Sophie van der Sluis, Ole A Andreassen, Benjamin M Neale, Danielle Posthuma. Nat Genet 2019
256
15

Prediction of individual genetic risk to disease from genome-wide association studies.
Naomi R Wray, Michael E Goddard, Peter M Visscher. Genome Res 2007
387
15


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.