A citation-based method for searching scientific literature

Stephen Burgess, Adam Butterworth, Simon G Thompson. Genet Epidemiol 2013
Times Cited: 940







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



Times Cited
  Times     Co-cited
Similarity



Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator.
Jack Bowden, George Davey Smith, Philip C Haycock, Stephen Burgess. Genet Epidemiol 2016
67


The MR-Base platform supports systematic causal inference across the human phenome.
Gibran Hemani, Jie Zheng, Benjamin Elsworth, Kaitlin H Wade, Valeriia Haberland, Denis Baird, Charles Laurin, Stephen Burgess, Jack Bowden, Ryan Langdon,[...]. Elife 2018
32


Mendelian randomization: using genes as instruments for making causal inferences in epidemiology.
Debbie A Lawlor, Roger M Harbord, Jonathan A C Sterne, Nic Timpson, George Davey Smith. Stat Med 2008
29

Robust inference in summary data Mendelian randomization via the zero modal pleiotropy assumption.
Fernando Pires Hartwig, George Davey Smith, Jack Bowden. Int J Epidemiol 2017
426
24


Interpreting findings from Mendelian randomization using the MR-Egger method.
Stephen Burgess, Simon G Thompson. Eur J Epidemiol 2017
425
17

Calculating statistical power in Mendelian randomization studies.
Marie-Jo A Brion, Konstantin Shakhbazov, Peter M Visscher. Int J Epidemiol 2013
468
17

A framework for the investigation of pleiotropy in two-sample summary data Mendelian randomization.
Jack Bowden, Fabiola Del Greco M, Cosetta Minelli, George Davey Smith, Nuala Sheehan, John Thompson. Stat Med 2017
297
15

Avoiding bias from weak instruments in Mendelian randomization studies.
Stephen Burgess, Simon G Thompson. Int J Epidemiol 2011
363
15

Assessing the suitability of summary data for two-sample Mendelian randomization analyses using MR-Egger regression: the role of the I2 statistic.
Jack Bowden, Fabiola Del Greco M, Cosetta Minelli, George Davey Smith, Nuala A Sheehan, John R Thompson. Int J Epidemiol 2016
377
15


An examination of multivariable Mendelian randomization in the single-sample and two-sample summary data settings.
Eleanor Sanderson, George Davey Smith, Frank Windmeijer, Jack Bowden. Int J Epidemiol 2019
218
13

Reading Mendelian randomisation studies: a guide, glossary, and checklist for clinicians.
Neil M Davies, Michael V Holmes, George Davey Smith. BMJ 2018
581
13

A review of instrumental variable estimators for Mendelian randomization.
Stephen Burgess, Dylan S Small, Simon G Thompson. Stat Methods Med Res 2017
276
12

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
12

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Mengzhen Liu, Yu Jiang, Robbee Wedow, Yue Li, David M Brazel, Fang Chen, Gargi Datta, Jose Davila-Velderrain, Daniel McGuire, Chao Tian,[...]. Nat Genet 2019
490
12

Bias due to participant overlap in two-sample Mendelian randomization.
Stephen Burgess, Neil M Davies, Simon G Thompson. Genet Epidemiol 2016
342
12

Mendelian Randomization.
Connor A Emdin, Amit V Khera, Sekar Kathiresan. JAMA 2017
237
12

Genomic atlas of the human plasma proteome.
Benjamin B Sun, Joseph C Maranville, James E Peters, David Stacey, James R Staley, James Blackshaw, Stephen Burgess, Tao Jiang, Ellie Paige, Praveen Surendran,[...]. Nature 2018
474
11

Orienting the causal relationship between imprecisely measured traits using GWAS summary data.
Gibran Hemani, Kate Tilling, George Davey Smith. PLoS Genet 2017
254
11

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
11


Using published data in Mendelian randomization: a blueprint for efficient identification of causal risk factors.
Stephen Burgess, Robert A Scott, Nicholas J Timpson, George Davey Smith, Simon G Thompson. Eur J Epidemiol 2015
389
11

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015
11


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
10

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
10

Recent Developments in Mendelian Randomization Studies.
Jie Zheng, Denis Baird, Maria-Carolina Borges, Jack Bowden, Gibran Hemani, Philip Haycock, David M Evans, George Davey Smith. Curr Epidemiol Rep 2017
200
10

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry.
Loic Yengo, Julia Sidorenko, Kathryn E Kemper, Zhili Zheng, Andrew R Wood, Michael N Weedon, Timothy M Frayling, Joel Hirschhorn, Jian Yang, Peter M Visscher. Hum Mol Genet 2018
635
10

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
10



PhenoScanner V2: an expanded tool for searching human genotype-phenotype associations.
Mihir A Kamat, James A Blackshaw, Robin Young, Praveen Surendran, Stephen Burgess, John Danesh, Adam S Butterworth, James R Staley. Bioinformatics 2019
246
9

PhenoScanner: a database of human genotype-phenotype associations.
James R Staley, James Blackshaw, Mihir A Kamat, Steve Ellis, Praveen Surendran, Benjamin B Sun, Dirk S Paul, Daniel Freitag, Stephen Burgess, John Danesh,[...]. Bioinformatics 2016
408
9

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
9


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
9

Two-sample Mendelian randomization: avoiding the downsides of a powerful, widely applicable but potentially fallible technique.
Fernando Pires Hartwig, Neil Martin Davies, Gibran Hemani, George Davey Smith. Int J Epidemiol 2016
175
8

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Rainer Malik, Ganesh Chauhan, Matthew Traylor, Muralidharan Sargurupremraj, Yukinori Okada, Aniket Mishra, Loes Rutten-Jacobs, Anne-Katrin Giese, Sander W van der Laan, Solveig Gretarsdottir,[...]. Nat Genet 2018
504
8

Bayesian test for colocalisation between pairs of genetic association studies using summary statistics.
Claudia Giambartolomei, Damjan Vukcevic, Eric E Schadt, Lude Franke, Aroon D Hingorani, Chris Wallace, Vincent Plagnol. PLoS Genet 2014
747
8

Detecting pleiotropy in Mendelian randomisation studies with summary data and a continuous outcome.
Fabiola Del Greco M, Cosetta Minelli, Nuala A Sheehan, John R Thompson. Stat Med 2015
196
8

Evaluating the potential role of pleiotropy in Mendelian randomization studies.
Gibran Hemani, Jack Bowden, George Davey Smith. Hum Mol Genet 2018
294
7

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
678
7

Best (but oft-forgotten) practices: the design, analysis, and interpretation of Mendelian randomization studies.
Philip C Haycock, Stephen Burgess, Kaitlin H Wade, Jack Bowden, Caroline Relton, George Davey Smith. Am J Clin Nutr 2016
212
7


A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
7

Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption.
Jack Bowden, Fabiola Del Greco M, Cosetta Minelli, Qingyuan Zhao, Debbie A Lawlor, Nuala A Sheehan, John Thompson, George Davey Smith. Int J Epidemiol 2019
90
6


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.