A citation-based method for searching scientific literature

Ryan S Dhindsa, Johan Mattsson, Abhishek Nag, Quanli Wang, Louise V Wain, Richard Allen, Eleanor M Wigmore, Kristina Ibanez, Dimitrios Vitsios, Sri V V Deevi, Sebastian Wasilewski, Maria Karlsson, Glenda Lassi, Henric Olsson, Daniel Muthas, Susan Monkley, Alex Mackay, Lynne Murray, Simon Young, Carolina Haefliger, Toby M Maher, Maria G Belvisi, Gisli Jenkins, Philip L Molyneaux, Adam Platt, Slavé Petrovski. Commun Biol 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Cristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman, Joshua D Hoffman, Daren Liu, Ashutosh K Pandey, Claudia Gonzaga-Jauregui, Shareef Khalid, Bin Ye, Nilanjana Banerjee,[...]. Nature 2020
80
100

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
100

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
100

Validating therapeutic targets through human genetics.
Robert M Plenge, Edward M Scolnick, David Altshuler. Nat Rev Drug Discov 2013
339
100


Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.
Keren J Carss, Anna A Baranowska, Javier Armisen, Tom R Webb, Stephen E Hamby, Diluka Premawardhana, Abtehale Al-Hussaini, Alice Wood, Quanli Wang, Sri V V Deevi,[...]. Circ Genom Precis Med 2020
8
100

The support of human genetic evidence for approved drug indications.
Matthew R Nelson, Hannah Tipney, Jeffery L Painter, Judong Shen, Paola Nicoletti, Yufeng Shen, Aris Floratos, Pak Chung Sham, Mulin Jun Li, Junwen Wang,[...]. Nat Genet 2015
541
100

Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
Mark I McCarthy, Gonçalo R Abecasis, Lon R Cardon, David B Goldstein, Julian Little, John P A Ioannidis, Joel N Hirschhorn. Nat Rev Genet 2008
50

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.
Paul Nioi, Asgeir Sigurdsson, Gudmar Thorleifsson, Hannes Helgason, Arna B Agustsdottir, Gudmundur L Norddahl, Anna Helgadottir, Audur Magnusdottir, Aslaug Jonasdottir, Solveig Gretarsdottir,[...]. N Engl J Med 2016
68
50

Lessons learned from the fate of AstraZeneca's drug pipeline: a five-dimensional framework.
David Cook, Dearg Brown, Robert Alexander, Ruth March, Paul Morgan, Gemma Satterthwaite, Menelas N Pangalos. Nat Rev Drug Discov 2014
641
50


Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.
Anna Fry, Thomas J Littlejohns, Cathie Sudlow, Nicola Doherty, Ligia Adamska, Tim Sprosen, Rory Collins, Naomi E Allen. Am J Epidemiol 2017
711
50

Evaluating drug targets through human loss-of-function genetic variation.
Eric Vallabh Minikel, Konrad J Karczewski, Hilary C Martin, Beryl B Cummings, Nicola Whiffin, Daniel Rhodes, Jessica Alföldi, Richard C Trembath, David A van Heel, Mark J Daly,[...]. Nature 2020
41
50

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
50

Proof of mechanism for the DGAT1 inhibitor AZD7687: results from a first-time-in-human single-dose study.
H Denison, C Nilsson, M Kujacic, L Löfgren, C Karlsson, M Knutsson, J W Eriksson. Diabetes Obes Metab 2013
37
50

A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.
Noura S Abul-Husn, Xiping Cheng, Alexander H Li, Yurong Xin, Claudia Schurmann, Panayiotis Stevis, Yashu Liu, Julia Kozlitina, Stefan Stender, G Craig Wood,[...]. N Engl J Med 2018
281
50



DGAT1 mutation is linked to a congenital diarrheal disorder.
Joel T Haas, Harland S Winter, Elaine Lim, Andrew Kirby, Brendan Blumenstiel, Matthew DeFelice, Stacey Gabriel, Chaim Jalas, David Branski, Carrie A Grueter,[...]. J Clin Invest 2012
88
50

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
50

Innovation in the pharmaceutical industry: New estimates of R&D costs.
Joseph A DiMasi, Henry G Grabowski, Ronald W Hansen. J Health Econ 2016
940
50

Effect of the DGAT1 inhibitor pradigastat on triglyceride and apoB48 levels in patients with familial chylomicronemia syndrome.
Charles Daniel Meyers, Karine Tremblay, Ahmed Amer, Jin Chen, Liewen Jiang, Daniel Gaudet. Lipids Health Dis 2015
60
50

Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome.
Gregory G Schwartz, P Gabriel Steg, Michael Szarek, Deepak L Bhatt, Vera A Bittner, Rafael Diaz, Jay M Edelberg, Shaun G Goodman, Corinne Hanotin, Robert A Harrington,[...]. N Engl J Med 2018
50

Genomics of disease risk in globally diverse populations.
Deepti Gurdasani, Inês Barroso, Eleftheria Zeggini, Manjinder S Sandhu. Nat Rev Genet 2019
77
50

Trends in clinical success rates and therapeutic focus.
Helen Dowden, Jamie Munro. Nat Rev Drug Discov 2019
83
50


Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
50


Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects.
Phuong A Nguyen, David A Born, Aimee M Deaton, Paul Nioi, Lucas D Ward. Nat Commun 2019
21
50

Resolving TYK2 locus genotype-to-phenotype differences in autoimmunity.
Calliope A Dendrou, Adrian Cortes, Lydia Shipman, Hayley G Evans, Kathrine E Attfield, Luke Jostins, Thomas Barber, Gurman Kaur, Subita Balaram Kuttikkatte, Oliver A Leach,[...]. Sci Transl Med 2016
96
50

The international serious adverse events consortium.
Arthur L Holden, Jorge L Contreras, Sally John, Matthew R Nelson. Nat Rev Drug Discov 2014
8
50

Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease.
Marc S Sabatine, Robert P Giugliano, Anthony C Keech, Narimon Honarpour, Stephen D Wiviott, Sabina A Murphy, Julia F Kuder, Huei Wang, Thomas Liu, Scott M Wasserman,[...]. N Engl J Med 2017
50

Diversity matters.
. Nat Rev Genet 2019
9
50

Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity.
Yoshiyuki Minegishi, Masako Saito, Tomohiro Morio, Ken Watanabe, Kazunaga Agematsu, Shigeru Tsuchiya, Hidetoshi Takada, Toshiro Hara, Nobuaki Kawamura, Tadashi Ariga,[...]. Immunity 2006
423
50

Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder.
Hyun Ji Noh, Ruqi Tang, Jason Flannick, Colm O'Dushlaine, Ross Swofford, Daniel Howrigan, Diane P Genereux, Jeremy Johnson, Gerard van Grootheest, Edna Grünblatt,[...]. Nat Commun 2017
28
50


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
50

TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits.
Dorothée Diogo, Lisa Bastarache, Katherine P Liao, Robert R Graham, Robert S Fulton, Jeffrey D Greenberg, Steve Eyre, John Bowes, Jing Cui, Annette Lee,[...]. PLoS One 2015
73
50

Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.
Gundula Povysil, Olympe Chazara, Keren J Carss, Sri V V Deevi, Quanli Wang, Javier Armisen, Dirk S Paul, Christopher B Granger, John Kjekshus, Vimla Aggarwal,[...]. JAMA Cardiol 2021
10
50

The impact of rare variation on gene expression across tissues.
Xin Li, Yungil Kim, Emily K Tsang, Joe R Davis, Farhan N Damani, Colby Chiang, Gaelen T Hess, Zachary Zappala, Benjamin J Strober, Alexandra J Scott,[...]. Nature 2017
108
50

Robust relationship inference in genome-wide association studies.
Ani Manichaikul, Josyf C Mychaleckyj, Stephen S Rich, Kathy Daly, Michèle Sale, Wei-Min Chen. Bioinformatics 2010
925
50

Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation.
Joshua Traynelis, Michael Silk, Quanli Wang, Samuel F Berkovic, Liping Liu, David B Ascher, David J Balding, Slavé Petrovski. Genome Res 2017
80
50

Discovery of rare variants for complex phenotypes.
Jack A Kosmicki, Claire L Churchhouse, Manuel A Rivas, Benjamin M Neale. Hum Genet 2016
28
50

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Elizabeth T Cirulli, Brittany N Lasseigne, Slavé Petrovski, Peter C Sapp, Patrick A Dion, Claire S Leblond, Julien Couthouis, Yi-Fan Lu, Quanli Wang, Brian J Krueger,[...]. Science 2015
572
50

Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.
Elizabeth T Cirulli, Simon White, Robert W Read, Gai Elhanan, William J Metcalf, Francisco Tanudjaja, Donna M Fath, Efren Sandoval, Magnus Isaksson, Karen A Schlauch,[...]. Nat Commun 2020
37
50

Genetics of 35 blood and urine biomarkers in the UK Biobank.
Nasa Sinnott-Armstrong, Yosuke Tanigawa, David Amar, Nina Mars, Christian Benner, Matthew Aguirre, Guhan Ram Venkataraman, Michael Wainberg, Hanna M Ollila, Tuomo Kiiskinen,[...]. Nat Genet 2021
28
50


REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi,[...]. Am J Hum Genet 2016
556
50

Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data.
Goo Jun, Matthew Flickinger, Kurt N Hetrick, Jane M Romm, Kimberly F Doheny, Gonçalo R Abecasis, Michael Boehnke, Hyun Min Kang. Am J Hum Genet 2012
210
50

ukbtools: An R package to manage and query UK Biobank data.
Ken B Hanscombe, Jonathan R I Coleman, Matthew Traylor, Cathryn M Lewis. PLoS One 2019
10
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.