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Adam S. Butterworth
ResearcherPublications, citations & collaboration network
Adam S. Butterworth is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 427 works, 65,555 citations, an h-index of 107 and an i10-index of 242.
427
Works
65,555
Citations
107
h-index
242
i10-index
How has Adam S. Butterworth's publication output changed over time?
ScholarIQpublication output · 2013–2022
Output grew0% over the shown period — from 1 works in 2013 to 1 in 2022.
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1
3
2
2
1
1
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20132014201620182019202020212022
What are the most-cited papers on Adam S. Butterworth?
ScholarIQmost cited works
Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data
Stephen Burgess, Adam S. Butterworth, Simon G. Thompson
S136352176. 20136,536 CitationsOPEN ACCESS
Genomic atlas of the human plasma proteome
Benjamin B. Sun, Joseph Maranville, James E. Peters, David Stacey, James R Staley, James Blackshaw, Stephen Burgess, Tao Jiang, Ellie Paige, Praveen Surendran, Clare Oliver‐Williams, Mihir Kamat, Bram P. Prins, Sheri K. Wilcox, Erik S. Zimmerman, An Chi, Narinder Bansal, Sarah L. Spain, Angela Wood, Nicholas W. Morrell, John R. Bradley, Nebojša Janjić, David J. Roberts, Willem H. Ouwehand, John A. Todd, Nicole Soranzo, Karsten Suhre, Dirk S. Paul, Caroline S. Fox, Robert M. Plenge, John Danesh, Heiko Runz, Adam S. Butterworth
Nature. 20182,462 CitationsOPEN ACCESS
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
Mihir Kamat, James Blackshaw, Robin Young, Praveen Surendran, Stephen Burgess, John Danesh, Adam S. Butterworth, James R Staley
S52395412. 20192,451 CitationsOPEN ACCESS
SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe
Steven H J Hageman, Lisa Pennells, Francisco Ojeda, Stephen Kaptoge, Kari Kuulasmaa, Tamar I. de Vries, Zhe Xu, Frank Kee, Ryan Chung, Angela Wood, John W. McEvoy, Giovanni Veronesi, Thomas Bolton, Stephan Achenbach, Krasimira Aleksandrova, Pilar Amiano, Donostia-San Sebastián, Philippe Amouyel, Jonas Andersson, Stephan J. L. Bakker, Rui Bebiano Da Providencia Costa, Joline W. J. Beulens, Michael J. Blaha, Martin Bobák, Jolanda M.A. Boer, Catalina Bonet, Fabrice Bonnet, Marie‐Christine Boutron‐Ruault, Tonje Braaten, Hermann Brenner, Fabian J. Brunner, Eric J. Brunner, Mattias Brunström, Julie E. Buring, Adam S. Butterworth, Naděžda Čapková, Giancarlo Cesana, Christina Chrysohoou, Sandra M. Colorado‐Yohar, Nancy R. Cook, Cyrus Cooper, Christina C. Dahm, Karina W. Davidson, Elaine Dennison, Augusto Di Castelnuovo, Chiara Donfrancesco, Marcus Dörr, Agnieszka Doryńska, Mats Eliasson, Gunnar Engström, Pietro Ferrari, Maurizio Ferrario, Ian Ford, Michael Fu, Ron T. Gansevoort, Simona Giampaoli, Richard F. Gillum, Agustı́n Gómez de la Cámara, Guıdo Grassı, Per‐Olof Hansson, Radu Huculeci, Kristian Hveem, Licia Iacoviello, M. Kamran Ikram, Torben Jørgensen, Bijoy Joseph, Pekka Jousilahti, J. Wouter Jukema, Rudolf Kaaks, Verena Katzke, Maryam Kavousi, Stefan Kiechl, Jens Klotsche, Wolfgang König, Richard A. Kronmal, Růžena Kubínová, Anna Kucharska‐Newton, Kristi Läll, Nils Lehmann, David M. Leistner, Allan Linneberg, David Lora Pablos, Thiess Lorenz, Wentian Lu, Dalia Lukšienė, Magnus Nakrem Lyngbakken, Christina Magnussen, Sofia Malyutina, Alejandro Marín Ibañez, Giovanna Masala, Ellisiv B. Mathiesen, Kuni Matsushita, Tom Meade, Olle Melander, Helmut E. Meyer, Karel G.M. Moons, Conchi Moreno‐Iribas, David C. Muller, Thomas Münzel, Y.P. Nikitin
European Heart Journal. 20211,705 CitationsOPEN ACCESS
PhenoScanner: a database of human genotype–phenotype associations
James R Staley, James Blackshaw, Mihir Kamat, Steve Ellis, Praveen Surendran, Benjamin B. Sun, Dirk S. Paul, Daniel Freitag, Stephen Burgess, John Danesh, Robin Young, Adam S. Butterworth
S52395412. 20161,678 CitationsOPEN ACCESS
Related on ScholarIQ
University of Cambridge
Institution
Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data
Paper
Genomic atlas of the human plasma proteome
Paper
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
Paper
SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe
Paper
PhenoScanner: a database of human genotype–phenotype associations
Paper