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23andMe (United States)

InstitutionResearch output, impact & collaborations

23andMe (United States) is a institution indexed in ScholarIQ from OpenAlex.

What is known about 23andMe (United States)?

ScholarIQrecord summary

23andMe (United States) is a research organisation in Sunnyvale, US. OpenAlex records 900 works and 588,969 citations for it. 253 researchers list it as their most recent affiliation.

How many works does 23andMe (United States) have?

ScholarIQindexed works

23andMe (United States) has 900 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does 23andMe (United States) have?

ScholarIQcitation count

23andMe (United States) has 588,969 citations in the OpenAlex counts ScholarIQ stores.

How many researchers are at 23andMe (United States)?

ScholarIQresearcher count

23andMe (United States) has 253 researchers in the ScholarIQ index.

What is the average h-index at 23andMe (United States)?

ScholarIQavg h-index

23andMe (United States) has an average h-index of 65.7 in OpenAlex.

What is the ROR of 23andMe (United States)?

ScholarIQror

The ROR for 23andMe (United States) is on the source record.

What is the OpenAlex record for 23andMe (United States)?

ScholarIQopenalex

The OpenAlex for 23andMe (United States) is on the source record.

Who are the most-cited researchers behind 23andMe (United States)?

ScholarIQtop researchers by citations
1
Adam Auton · Genetic Associations and Epidemiology
182 works103,934 citations
2
David A. Hinds · Genetic Associations and Epidemiology
368 works61,796 citations
3
Suyash Shringarpure · Genetic Associations and Epidemiology
221 works51,146 citations
4
Joyce Y. Tung · Genetic Associations and Epidemiology
134 works22,819 citations
5
Alan Kwong · Genetic Associations and Epidemiology
54 works17,191 citations

What are the most-cited papers on 23andMe (United States)?

ScholarIQmost cited works
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, Felix Graßmann, Sebanti Sengupta, Jennifer L. Bragg‐Gresham, Kathryn P. Burdon, Scott J. Hebbring, Cindy Wen, Mathias Gorski, Ivana K. Kim, David Cho, Donald J. Zack, Eric H. Souied, Hendrik P. N. Scholl, Elisa Bala, Kristine E Lee, David J. Hunter, Rebecca J. Sardell, Paul Mitchell, Joanna E. Merriam, Valentina Cipriani, Joshua Hoffman, Tina Schick, Yara Lechanteur, Robyn H. Guymer, Matthew P. Johnson, Yingda Jiang, Chloë M. Stanton, Gabriëlle H.S. Buitendijk, Xiaowei Zhan, Alan Kwong, Alexis Boleda, Matthew Brooks, Linn Gieser, Rinki Ratnapriya, Kari Branham, Johanna R. Foerster, John R. Heckenlively, Mohammad Othman, Brendan J. Vote, Helena H. Liang, Emmanuelle Souzeau, Ian L. McAllister, Timothy Isaacs, Janette M. Hall, Stewart Lake, David A. Mackey, Ian J. Constable, Jamie E. Craig, Terrie Kitchner, Zhenglin Yang, Zhiguang Su, Hongrong Luo, Daniel Chen, Hong Ouyang, Ken Flagg, Danni Lin, Guanping Mao, Henry Ferreyra, Klaus Stark, Claudia N. von Strachwitz, Armin Wolf, Caroline Brandl, Guenther Rudolph, Matthias Olden, Margaux A. Morrison, Denise J. Morgan, Matthew Schu, Jeeyun Ahn, Giuliana Silvestri, Evangelia E. Tsironi, Kyu Hyung Park, Lindsay A. Farrer, Anton Orlin, Alexander J. Brucker, Mingyao Li, Christine A. Curcio, Saddek Mohand‐Saïd, José‐Alain Sahel, Isabelle Audo, Mustapha Benchaboune, Angela J. Cree, Christina Rennie, Srinivas Goverdhan, Michelle Grunin, Shira Hagbi-Levi, Peter A. Campochiaro, Nicholas Katsanis, Frank G. Holz, Frédéric Blond, Hélène Blanché, Jean‐François Deleuze, Robert P. Igo, Barbara Truitt, Neal S. Peachey, Stacy M. Meuer, Chelsea E. Myers, Emily Moore, Ronald Klein
Nature Genetics. 20151,631 CitationsOPEN ACCESS
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
Philip R. Jansen, Kyoko Watanabe, Sven Stringer, Nathan Skene, Julien Bryois, Anke R. Hammerschlag, Christiaan de Leeuw, Jeroen S. Benjamins, Ana B. Muñoz‐Manchado, Mats Nagel, Jeanne E. Savage, Henning Tiemeier, Tonya White, Joyce Y. Tung, David A. Hinds, Vladimir Vacic, Xin Wang, Patrick F. Sullivan, Sophie van der Sluis, Tinca J. C. Polderman, August B. Smit, Jens Hjerling‐Leffler, Eus J.W. Van Someren, Daniëlle Posthuma
Nature Genetics. 2019948 CitationsOPEN ACCESS
An atlas of genetic influences on osteoporosis in humans and mice
John Morris, John P. Kemp, Scott E. Youlten, Lætitia Laurent, John G. Logan, Ryan C. Chai, Nicholas A. Vulpescu, Vincenzo Forgetta, Aaron Kleinman, Sindhu T. Mohanty, C. Marcelo Sergio, Julian M.W. Quinn, Loan Nguyen‐Yamamoto, Aimée-Lee Luco, Jinchu Vijay, Marie-Michelle Simon, Albéna Pramatarova, Carolina Medina‐Gómez, Katerina Trajanoska, Elena J. Ghirardello, Natalie C. Butterfield, Katharine F. Curry, Victoria D. Leitch, Penny C. Sparkes, Anne‐Tounsia Adoum, Naila S. Mannan, Davide Komla‐Ebri, Andrea S. Pollard, Hannah F. Dewhurst, Thomas Hassall, Michael-John G. Beltejar, Douglas J. Adams, Suzanne M. Vaillancourt, Stephen Kaptoge, Paul A. Baldock, Cyrus Cooper, J. Reeve, Evangelia Ntzani, Evangelos Evangelou, Claes Ohlsson, David Karasik, Fernando Rivadeneira, Douglas P. Kiel, Jonathan H. Tobias, Celia L. Gregson, Nicholas C. Harvey, Elin Grundberg, David Goltzman, David J. Adams, Christopher J. Lelliott, David A. Hinds, Cheryl L. Ackert‐Bicknell, Yi‐Hsiang Hsu, Matthew T. Maurano, Peter I. Croucher, Graham R. Williams, J. H. Duncan Bassett, David M. Evans, J. Brent Richards
Nature Genetics. 2018844 CitationsOPEN ACCESS
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Manuel A. R. Ferreira, AAGC collaborators, LifeLines Cohort Study, Judith M. Vonk, Hansjörg Baurecht, Ingo Marenholz, Chao Tian, Joshua Hoffman, Quinta Helmer, Annika Tillander, Vilhelmina Ullemar, Jenny van Dongen, Yi Lu, Franz Rüschendorf, Jorge Esparza-Gordillo, Chris Medway, Edward Mountjoy, Kimberley Burrows, Oliver Hummel, Sarah Grosche, Ben Brumpton, John S. Witte, Jouke‐Jan Hottenga, Gonneke Willemsen, Jie Zheng, Elke Rodríguez, Melanie Hotze, André Franke, Joana Revez, Jonathan Beesley, Melanie C. Matheson, Shyamali C. Dharmage, Lisa Bain, Lars G. Fritsche, Maiken E. Gabrielsen, Brunilda Balliu, Jonas B. Nielsen, Wei Zhou, Kristian Hveem, Arnulf Langhammer, Oddgeir L. Holmen, Mari Løset, Gonçalo R. Abecasis, Cristen J. Willer, Andreas Arnold, Georg Homuth, Carsten Oliver Schmidt, Philip J. Thompson, Nicholas G. Martin, David L Duffy, Natalija Novak, Holger Schulz, Stefan Karrasch, Christian Gieger, Konstantin Strauch, Ronald B. Melles, David A. Hinds, Norbert Hübner, Stephan Weidinger, Patrik K. E. Magnusson, Rick Jansen, Eric Jorgenson, Young‐Ae Lee, Dorret I. Boomsma, Catarina Almqvist, Robert Karlsson, Gerard H. Koppelman, Lavinia Paternoster
Nature Genetics. 2017578 CitationsOPEN ACCESS
Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior
Andrea Ganna, Karin J. H. Verweij, Michel G. Nivard, Robert Maier, Robbee Wedow, Alexander S. Busch, Abdel Abdellaoui, Shengru Guo, J. Fah Sathirapongsasuti, Paul Lichtenstein, Sebastian Lundström, Niklas Långström, Adam Auton, Kathleen Mullan Harris, Gary W. Beecham, Eden R. Martin, Alan R. Sanders, John R. B. Perry, Benjamin M. Neale, Brendan P. Zietsch
Science. 2019419 CitationsOPEN ACCESS

How much of the research on 23andMe (United States) is open access?

ScholarIQopen access share
100%OPEN ACCESS
Gold
0%
Green
56%
Hybrid
22%
Bronze
22%
Closed
0%

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