A citation-based method for searching scientific literature

Gibran Hemani, Jie Zheng, Benjamin Elsworth, Kaitlin H Wade, Valeriia Haberland, Denis Baird, Charles Laurin, Stephen Burgess, Jack Bowden, Ryan Langdon, Vanessa Y Tan, James Yarmolinsky, Hashem A Shihab, Nicholas J Timpson, David M Evans, Caroline Relton, Richard M Martin, George Davey Smith, Tom R Gaunt, Philip C Haycock. Elife 2018
Times Cited: 728







List of co-cited articles
438 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
938
42

Mendelian randomization analysis with multiple genetic variants using summarized data.
Stephen Burgess, Adam Butterworth, Simon G Thompson. Genet Epidemiol 2013
716
30



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
25

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
22

Reading Mendelian randomisation studies: a guide, glossary, and checklist for clinicians.
Neil M Davies, Michael V Holmes, George Davey Smith. BMJ 2018
386
20

Evaluating the potential role of pleiotropy in Mendelian randomization studies.
Gibran Hemani, Jack Bowden, George Davey Smith. Hum Mol Genet 2018
203
18

Bias due to participant overlap in two-sample Mendelian randomization.
Stephen Burgess, Neil M Davies, Simon G Thompson. Genet Epidemiol 2016
239
17

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
289
16

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
317
14



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
14

Orienting the causal relationship between imprecisely measured traits using GWAS summary data.
Gibran Hemani, Kate Tilling, George Davey Smith. PLoS Genet 2017
150
13

Calculating statistical power in Mendelian randomization studies.
Marie-Jo A Brion, Konstantin Shakhbazov, Peter M Visscher. Int J Epidemiol 2013
358
13

A review of instrumental variable estimators for Mendelian randomization.
Stephen Burgess, Dylan S Small, Simon G Thompson. Stat Methods Med Res 2017
199
13

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
214
12

Interpreting findings from Mendelian randomization using the MR-Egger method.
Stephen Burgess, Simon G Thompson. Eur J Epidemiol 2017
273
12

Triangulation in aetiological epidemiology.
Debbie A Lawlor, Kate Tilling, George Davey Smith. Int J Epidemiol 2016
318
11

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
264
11

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
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

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
11

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
11

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases.
Jie Zheng, Valeriia Haberland, Denis Baird, Venexia Walker, Philip C Haycock, Mark R Hurle, Alex Gutteridge, Pau Erola, Yi Liu, Shan Luo,[...]. Nat Genet 2020
37
29

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
332
10

Causal associations between risk factors and common diseases inferred from GWAS summary data.
Zhihong Zhu, Zhili Zheng, Futao Zhang, Yang Wu, Maciej Trzaskowski, Robert Maier, Matthew R Robinson, John J McGrath, Peter M Visscher, Naomi R Wray,[...]. Nat Commun 2018
229
10

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

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
865
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
453
10

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
343
10

Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
Sara L Pulit, Charli Stoneman, Andrew P Morris, Andrew R Wood, Craig A Glastonbury, Jessica Tyrrell, Loïc Yengo, Teresa Ferreira, Eirini Marouli, Yingjie Ji,[...]. Hum Mol Genet 2019
157
10

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
10


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
313
9

The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
Annalisa Buniello, Jacqueline A L MacArthur, Maria Cerezo, Laura W Harris, James Hayhurst, Cinzia Malangone, Aoife McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis,[...]. Nucleic Acids Res 2019
834
9

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
127
9

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
546
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
8


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
170
8

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Anubha Mahajan, Daniel Taliun, Matthias Thurner, Neil R Robertson, Jason M Torres, N William Rayner, Anthony J Payne, Valgerdur Steinthorsdottir, Robert A Scott, Niels Grarup,[...]. Nat Genet 2018
428
8


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
137
8

Guidelines for performing Mendelian randomization investigations.
Stephen Burgess, George Davey Smith, Neil M Davies, Frank Dudbridge, Dipender Gill, M Maria Glymour, Fernando P Hartwig, Michael V Holmes, Cosetta Minelli, Caroline L Relton,[...]. Wellcome Open Res 2020
65
12


Avoiding bias from weak instruments in Mendelian randomization studies.
Stephen Burgess, Simon G Thompson. Int J Epidemiol 2011
252
8

Genetic effects on gene expression across human tissues.
Alexis Battle, Christopher D Brown, Barbara E Engelhardt, Stephen B Montgomery. Nature 2017
8


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.