A citation-based method for searching scientific literature

Laura M Schultz, Alison K Merikangas, Kosha Ruparel, Sébastien Jacquemont, David C Glahn, Raquel E Gur, Ran Barzilay, Laura Almasy. HGG Adv 2022
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
562
50

Polygenic Scores for Height in Admixed Populations.
Bárbara D Bitarello, Iain Mathieson. G3 (Bethesda) 2020
31
50

Variable prediction accuracy of polygenic scores within an ancestry group.
Hakhamanesh Mostafavi, Arbel Harpak, Ipsita Agarwal, Dalton Conley, Jonathan K Pritchard, Molly Przeworski. Elife 2020
124
33

Common SNPs explain a large proportion of the heritability for human height.
Jian Yang, Beben Benyamin, Brian P McEvoy, Scott Gordon, Anjali K Henders, Dale R Nyholt, Pamela A Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery,[...]. Nat Genet 2010
33

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
509
33

Hidden heritability due to heterogeneity across seven populations.
Felix C Tropf, S Hong Lee, Renske M Verweij, Gert Stulp, Peter J van der Most, Ronald de Vlaming, Andrew Bakshi, Daniel A Briley, Charles Rahal, Robert Hellpap,[...]. Nat Hum Behav 2017
54
33

Using Genetic Distance to Infer the Accuracy of Genomic Prediction.
Marco Scutari, Ian Mackay, David Balding. PLoS Genet 2016
54
33

MultiBLUP: improved SNP-based prediction for complex traits.
Doug Speed, David J Balding. Genome Res 2014
148
33

Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals.
Davide Marnetto, Katri Pärna, Kristi Läll, Ludovica Molinaro, Francesco Montinaro, Toomas Haller, Mait Metspalu, Reedik Mägi, Krista Fischer, Luca Pagani. Nat Commun 2020
31
33

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
33

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
65
33

Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data.
Huwenbo Shi, Kathryn S Burch, Ruth Johnson, Malika K Freund, Gleb Kichaev, Nicholas Mancuso, Astrid M Manuel, Natalie Dong, Bogdan Pasaniuc. Am J Hum Genet 2020
19
33

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
594
33

Multiethnic polygenic risk scores improve risk prediction in diverse populations.
Carla Márquez-Luna, Po-Ru Loh, Alkes L Price. Genet Epidemiol 2017
129
33

Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease.
Jessica K Dennis, Julia M Sealock, Peter Straub, Younga H Lee, Donald Hucks, Ky'Era Actkins, Annika Faucon, Yen-Chen Anne Feng, Tian Ge, Slavina B Goleva,[...]. Genome Med 2021
15
33

Theoretical and empirical quantification of the accuracy of polygenic scores in ancestry divergent populations.
Ying Wang, Jing Guo, Guiyan Ni, Jian Yang, Peter M Visscher, Loic Yengo. Nat Commun 2020
54
33


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
243
33

Tutorial: a guide to performing polygenic risk score analyses.
Shing Wan Choi, Timothy Shin-Heng Mak, Paul F O'Reilly. Nat Protoc 2020
318
33

A unified framework for cross-population trait prediction by leveraging the genetic correlation of polygenic traits.
Mingxuan Cai, Jiashun Xiao, Shunkang Zhang, Xiang Wan, Hongyu Zhao, Gang Chen, Can Yang. Am J Hum Genet 2021
17
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
596
33

Analysis of polygenic risk score usage and performance in diverse human populations.
L Duncan, H Shen, B Gelaye, J Meijsen, K Ressler, M Feldman, R Peterson, B Domingue. Nat Commun 2019
331
33

Improving the trans-ancestry portability of polygenic risk scores by prioritizing variants in predicted cell-type-specific regulatory elements.
Tiffany Amariuta, Kazuyoshi Ishigaki, Hiroki Sugishita, Tazro Ohta, Masaru Koido, Kushal K Dey, Koichi Matsuda, Yoshinori Murakami, Alkes L Price, Eiryo Kawakami,[...]. Nat Genet 2020
44
33

Evaluation of polygenic prediction methodology within a reference-standardized framework.
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,[...]. PLoS Genet 2021
33
33

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
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

Improving polygenic prediction in ancestrally diverse populations.
Yunfeng Ruan, Yen-Feng Lin, Yen-Chen Anne Feng, Chia-Yen Chen, Max Lam, Zhenglin Guo, Lin He, Akira Sawa, Alicia R Martin, Shengying Qin,[...]. Nat Genet 2022
31
33

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
Pierrick Wainschtein, Deepti Jain, Zhili Zheng, L Adrienne Cupples, Aladdin H Shadyab, Barbara McKnight, Benjamin M Shoemaker, Braxton D Mitchell, Bruce M Psaty, Charles Kooperberg,[...]. Nat Genet 2022
31
16

Finding the sources of missing heritability in a yeast cross.
Joshua S Bloom, Ian M Ehrenreich, Wesley T Loo, Thúy-Lan Võ Lite, Leonid Kruglyak. Nature 2013
266
16

The mystery of missing heritability: Genetic interactions create phantom heritability.
Or Zuk, Eliana Hechter, Shamil R Sunyaev, Eric S Lander. Proc Natl Acad Sci U S A 2012
933
16

Missing heritability and strategies for finding the underlying causes of complex disease.
Evan E Eichler, Jonathan Flint, Greg Gibson, Augustine Kong, Suzanne M Leal, Jason H Moore, Joseph H Nadeau. Nat Rev Genet 2010
16

The new genetics of intelligence.
Robert Plomin, Sophie von Stumm. Nat Rev Genet 2018
112
16

Predicting educational achievement from genomic measures and socioeconomic status.
Sophie von Stumm, Emily Smith-Woolley, Ziada Ayorech, Andrew McMillan, Kaili Rimfeld, Philip S Dale, Robert Plomin. Dev Sci 2020
28
16

The genetic attributable risk of breast and ovarian cancer.
E B Claus, J M Schildkraut, W D Thompson, N J Risch. Cancer 1996
515
16

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
16


Nature-via-nurture and unravelling causality in evolutionary genetics.
Kathleen E Lynch, Darrell J Kemp. Trends Ecol Evol 2014
15
16

Genetic Prediction.
Eric Turkheimer. Hastings Cent Rep 2015
9
16

Predicting educational achievement from DNA.
S Selzam, E Krapohl, S von Stumm, P F O'Reilly, K Rimfeld, Y Kovas, P S Dale, J J Lee, R Plomin. Mol Psychiatry 2018
3
33

Polygenic scores: prediction versus explanation.
Robert Plomin, Sophie von Stumm. Mol Psychiatry 2022
4
25

A test of the equal-environment assumption in twin studies of psychiatric illness.
K S Kendler, M C Neale, R C Kessler, A C Heath, L J Eaves. Behav Genet 1993
232
16

General epistatic models of the risk of complex diseases.
Yun S Song, Fulton Wang, Montgomery Slatkin. Genetics 2010
10
16

Searching for missing heritability: designing rare variant association studies.
Or Zuk, Stephen F Schaffner, Kaitlin Samocha, Ron Do, Eliana Hechter, Sekar Kathiresan, Mark J Daly, Benjamin M Neale, Shamil R Sunyaev, Eric S Lander. Proc Natl Acad Sci U S A 2014
376
16

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
674
16

A Polygenic Risk Score to Predict Future Adult Short Stature Among Children.
Tianyuan Lu, Vincenzo Forgetta, Haoyu Wu, John R B Perry, Ken K Ong, Celia M T Greenwood, Nicholas J Timpson, Despoina Manousaki, J Brent Richards. J Clin Endocrinol Metab 2021
9
16

Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
16

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
James J Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter Bowers, Julia Sidorenko, Richard Karlsson Linnér,[...]. Nat Genet 2018
790
16


Genotypic Context and Epistasis in Individuals and Populations.
Timothy B Sackton, Daniel L Hartl. Cell 2016
70
16

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
741
16


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.