A citation-based method for searching scientific literature

Eleonora Porcu, Jennifer Sjaarda, Kaido Lepik, Cristian Carmeli, Liza Darrous, Jonathan Sulc, Ninon Mounier, Zoltán Kutalik. Cold Spring Harb Perspect Med 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Using genetic data to strengthen causal inference in observational research.
Jean-Baptiste Pingault, Paul F O'Reilly, Tabea Schoeler, George B Ploubidis, Frühling Rijsdijk, Frank Dudbridge. Nat Rev Genet 2018
120
100

Robust research needs many lines of evidence.
Marcus R Munafò, George Davey Smith. Nature 2018
56
100

Prioritizing putative influential genes in cardiovascular disease susceptibility by applying tissue-specific Mendelian randomization.
Kurt Taylor, George Davey Smith, Caroline L Relton, Tom R Gaunt, Tom G Richardson. Genome Med 2019
14
100


Integrating Family-Based and Mendelian Randomization Designs.
Liang-Dar Hwang, Neil M Davies, Nicole M Warrington, David M Evans. Cold Spring Harb Perspect Med 2021
7
100

SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
50

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
260
50

Reevaluation of SNP heritability in complex human traits.
Doug Speed, Na Cai, Michael R Johnson, Sergey Nejentsev, David J Balding. Nat Genet 2017
186
50

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
50


Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models.
Hashem A Shihab, Julian Gough, David N Cooper, Peter D Stenson, Gary L A Barker, Keith J Edwards, Ian N M Day, Tom R Gaunt. Hum Mutat 2013
616
50

Lessons from 1 million genomes.
Michelle Trenkmann. Nat Rev Genet 2018
2
50

Alcohol intake and blood pressure: a systematic review implementing a Mendelian randomization approach.
Lina Chen, George Davey Smith, Roger M Harbord, Sarah J Lewis. PLoS Med 2008
200
50

GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
Nora Franceschini, Claudia Giambartolomei, Paul S de Vries, Chris Finan, Joshua C Bis, Rachael P Huntley, Ruth C Lovering, Salman M Tajuddin, Thomas W Winkler, Misa Graff,[...]. Nat Commun 2018
49
50

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
50

Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization.
Suzanne H Gage, Hannah J Jones, Amy E Taylor, Stephen Burgess, Stanley Zammit, Marcus R Munafò. Sci Rep 2017
33
50

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
50

A transcriptome-wide Mendelian randomization study to uncover tissue-dependent regulatory mechanisms across the human phenome.
Tom G Richardson, Gibran Hemani, Tom R Gaunt, Caroline L Relton, George Davey Smith. Nat Commun 2020
19
50


ClinVar at five years: Delivering on the promise.
Melissa J Landrum, Brandi L Kattman. Hum Mutat 2018
78
50

Ensembl 2018.
Daniel R Zerbino, Premanand Achuthan, Wasiu Akanni, M Ridwan Amode, Daniel Barrell, Jyothish Bhai, Konstantinos Billis, Carla Cummins, Astrid Gall, Carlos García Girón,[...]. Nucleic Acids Res 2018
50

An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
50

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
50

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
838
50

Colocalization of GWAS and eQTL Signals Detects Target Genes.
Farhad Hormozdiari, Martijn van de Bunt, Ayellet V Segrè, Xiao Li, Jong Wha J Joo, Michael Bilow, Jae Hoon Sul, Sriram Sankararaman, Bogdan Pasaniuc, Eleazar Eskin. Am J Hum Genet 2016
222
50

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
847
50

The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.
Gil Stelzer, Naomi Rosen, Inbar Plaschkes, Shahar Zimmerman, Michal Twik, Simon Fishilevich, Tsippi Iny Stein, Ron Nudel, Iris Lieder, Yaron Mazor,[...]. Curr Protoc Bioinformatics 2016
801
50

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
50

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
50

Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses.
Ben Brumpton, Eleanor Sanderson, Karl Heilbron, Fernando Pires Hartwig, Sean Harrison, Gunnhild Åberge Vie, Yoonsu Cho, Laura D Howe, Amanda Hughes, Dorret I Boomsma,[...]. Nat Commun 2020
54
50

Conventional and genetic evidence on alcohol and vascular disease aetiology: a prospective study of 500 000 men and women in China.
Iona Y Millwood, Robin G Walters, Xue W Mei, Yu Guo, Ling Yang, Zheng Bian, Derrick A Bennett, Yiping Chen, Caixia Dong, Ruying Hu,[...]. Lancet 2019
128
50

PRSice: Polygenic Risk Score software.
Jack Euesden, Cathryn M Lewis, Paul F O'Reilly. Bioinformatics 2015
586
50

Alcohol intake and cardiovascular risk factors: A Mendelian randomisation study.
Yoonsu Cho, So-Youn Shin, Sungho Won, Caroline L Relton, George Davey Smith, Min-Jeong Shin. Sci Rep 2015
50
50

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
52
50

A Bayesian framework for multiple trait colocalization from summary association statistics.
Claudia Giambartolomei, Jimmy Zhenli Liu, Wen Zhang, Mads Hauberg, Huwenbo Shi, James Boocock, Joe Pickrell, Andrew E Jaffe, Bogdan Pasaniuc, Panos Roussos. Bioinformatics 2018
65
50

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
339
50


Calculating statistical power in Mendelian randomization studies.
Marie-Jo A Brion, Konstantin Shakhbazov, Peter M Visscher. Int J Epidemiol 2013
394
50

An integrative approach to detect epigenetic mechanisms that putatively mediate the influence of lifestyle exposures on disease susceptibility.
Tom G Richardson, Rebecca C Richmond, Teri-Louise North, Gibran Hemani, George Davey Smith, Gemma C Sharp, Caroline L Relton. Int J Epidemiol 2019
6
50

An atlas of genetic associations in UK Biobank.
Oriol Canela-Xandri, Konrad Rawlik, Albert Tenesa. Nat Genet 2018
212
50

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
50

Orienting the causal relationship between imprecisely measured traits using GWAS summary data.
Gibran Hemani, Kate Tilling, George Davey Smith. PLoS Genet 2017
185
50

Integrating functional data to prioritize causal variants in statistical fine-mapping studies.
Gleb Kichaev, Wen-Yun Yang, Sara Lindstrom, Farhad Hormozdiari, Eleazar Eskin, Alkes L Price, Peter Kraft, Bogdan Pasaniuc. PLoS Genet 2014
224
50

Toward genome-wide SNP genotyping.
Ann-Christine Syvänen. Nat Genet 2005
250
50

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
338
50

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
134
50

Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework.
Yoonsu Cho, Philip C Haycock, Eleanor Sanderson, Tom R Gaunt, Jie Zheng, Andrew P Morris, George Davey Smith, Gibran Hemani. Nat Commun 2020
15
50

10 Years of GWAS Discovery: Biology, Function, and Translation.
Peter M Visscher, Naomi R Wray, Qian Zhang, Pamela Sklar, Mark I McCarthy, Matthew A Brown, Jian Yang. Am J Hum Genet 2017
50

Mining the human phenome using allelic scores that index biological intermediates.
David M Evans, Marie Jo A Brion, Lavinia Paternoster, John P Kemp, George McMahon, Marcus Munafò, John B Whitfield, Sarah E Medland, Grant W Montgomery, Nicholas J Timpson,[...]. PLoS Genet 2013
52
50

Triangulating Evidence through the Inclusion of Genetically Informed Designs.
Marcus R Munafò, Julian P T Higgins, George Davey Smith. Cold Spring Harb Perspect Med 2021
4
50


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.