ScholarIQanswers from OpenAlex & ORCID
David A. Hinds
ResearcherPublications, citations & collaboration network
David A. Hinds is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does David A. Hinds have?
ScholarIQindexed works
David A. Hinds has 368 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does David A. Hinds have?
ScholarIQcitation count
David A. Hinds has 61,796 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of David A. Hinds?
ScholarIQh-index
David A. Hinds has an h-index of 105 in OpenAlex.
What is the i10-index of David A. Hinds?
ScholarIQi10-index
David A. Hinds has an i10-index of 225 in OpenAlex.
What is the ORCID of David A. Hinds?
ScholarIQorcid
The ORCID for David A. Hinds is on the source record.
What is the OpenAlex record for David A. Hinds?
ScholarIQopenalex
The OpenAlex for David A. Hinds is on the source record.
What are the most-cited papers on David A. Hinds?
ScholarIQmost cited works
A second generation human haplotype map of over 3.1 million SNPs
Sarah S. Murray, Dennis G. Ballinger, David R. Cox, David A. Hinds, Laura L. Stuvé, John W. Belmont, Suzanne M. Leal, David A. Wheeler, Donna M. Muzny, Lynne Nazareth, E Södergren, George M. Weinstock, Imtaz Yakub, Andrew Boudreau, T. D. Willis, Jean-François Olivier, Paul Hardenbol, Shiran Pasternak, Lalitha Krishnan, Albert V. Smith, Marcela K. Tello-Ruiz, Fuli Yu, Rachel Barry, Brendan Blumenstiel, Amy Camargo, Matthew DeFelice, Maura Faggart, Mary Goyette, Supriya Gupta, Jamie Moore, Huy Nguyen, Robert C. Onofrio, Melissa Parkin, Jessica Roy, Erich Stahl, Ellen Winchester, Liuda Ziaugra, Paul I. W. de Bakker, Jeff Barrett, Yves Chrétien, Julian Maller, Steve McCarroll, Nick Patterson, Alkes L. Price, Daniel J. Richter, Pardis C. Sabeti, Richa Saxena, S. F. Schaffner, Patrick Varilly, Chris Spencer, Bruce W. Birren, Mark J. Daly, Yang Gao, Haoran Hu, Weitao Hu, Chaohua Li, Wei Lin, Siqi Liu, Hao Pan, Xiaoli Tang, Jian Wang, Wei Wang, Jun Yu, Bo Zhang, Qingrun Zhang, Hongbin Zhao, Hui Zhao, Jun Zhou, Changqing Zeng, Shaun Purcell, Zhijian Yao, Xun Chu, Yungang He, Yangfan Liu, Yayun Shen, Weiwei Sun, Haifeng Wang, Yi Wang, Ying Wang, Xiaoyan Xiong, Liang Xu, Jin Li, Stephen Kwok‐Wing Tsui, J. Tze‐Fei Wong, Jian-Bing Fan, Kevin L. Gunderson, Stéphanie Roumy, Arthur L. Holden, Arnold Oliphant, Mark S. Chee, Fanny Chagnon, Vincent Ferretti, Martin Leboeuf, Michael Phillips, Andrei Verner, Clémentine Sallée, Bartha Maria Knoppers, Dongmei Cai, Ludmila Pawlikowska, Ming Xiao
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, Karl Heilbron, Sara Bandrés‐Ciga, Diana Chang, Manuela Tan, Demis A. Kia, Alastair J. Noyce, Angli Xue, José Brás, Emily Young, Rainer von Coelln, Javier Simón-Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Lasse Pihlstrøm, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Faraz Faghri, J Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Juan A. Botía, María Martínez, Jean‐Christophe Corvol, Suzanne Lesage, Joseph Jankovic, Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Ole A. Andreassen, Tushar Bangale, Alexis Brice, Jian Yang, Ziv Gan‐Or, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, David A. Hinds, John Hardy, Huw R Morris, Jacob Gratten, Peter M. Visscher, Robert Graham, Andrew B Singleton, Astrid Adarmes‐Gómez, Miquel Aguilar, Akbota Aitkulova, Vadim Akhmetzhanov, Roy N. Alcalay, Ignacio Álvarez, Victoria Álvarez, Sara Bandrés‐Ciga, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Kimberley J. Billingsley, Cornelis Blauwendraat, Marta Blazquez, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, José Brás, Alexis Brice, Kathrin Brockmann, Vivien J. Bubb, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Viorica Chelban, Jordi Clarimón, Carl E Clarke, Yaroslau Compta, Mark Cookson, Jean‐Christophe Corvol, David W. Craig, Fabrice Danjou, Mónica Díez-Fairén, Oriol Dols‐Icardo, J. Duarte, Raquel Durán, Francisco Escamilla‐Sevilla, Valentina Escott‐Price, Mario Ezquerra, Faraz Faghri, Cici Feliz, Manel Fernández, Rubén Fernández‐Santiago, Steven Finkbeiner, Thomas Foltynie, Ziv Gan‐Or, Ciara García
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
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
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Lavinia Paternoster, John P. Kemp, Jie Zheng, George Davey Smith, Caroline L. Relton, David M. Evans, Wendy L. McArdle, A John Henderson, Marie Standl, Carla M T Tiesler, Elisabeth Thiering, Joachim Heinrich, Johannes Waage, Klaus Bønnelykke, Eskil Kreiner‐Møller, Hans Bisgaard, Hansjörg Baurecht, Melanie Hotze, Elke Rodríguez, Regina Fölster‐Holst, Stephan Weidinger, David P. Strachan, John A. Curtin, Adnan Čustović, Angela Simpson, Chao Tian, Joyce Y. Tung, David A. Hinds, Atsushi Takahashi, Jorge Esparza-Gordillo, Ingo Marenholz, Birgit Kalb, Anja Matanovic, Franz Rüschendorf, Anja Bauerfeind, Norbert Hübner, Young‐Ae Lee, Alexessander Couto Alves, Jacob P. Thyssen, Herman T. den Dekker, de Jongste Jc, Vincent W. V. Jaddoe, L Duijts, F Rivadeneira, Albert Hofman, André G. Uitterlinden, Niels J. Elbert, Manuel A. R. Ferreira, Nuria Martín, Elisabeth Altmaier, Christian Gieger, Annette Peters, Janina S. Ried, Patrick M A Sleiman, J LI, Hakon Hakonarson, Feng Xiao, Xian Bo Zuo, Xiao Zheng, Xian Yin, Liang Sun, Xue Jun Zhang, Juan R González, Mariona Bustamante, Natàlia Vilor‐Tejedor, J. Oriol Sunyer, S Lau, Maria Pino‐Yanes, Donglei Hu, Celeste Eng, Scott Huntsman, E R Burchard, Cheng‐Jian Xu, Dirkje S. Postma, Lisbeth Carstensen, Bjarke Feenstra, Frank Geller, Mads Melbye, Maria M. Groen‐Blokhuis, Jouke Jan Hottenga, Christel M. Middeldorp, Dorret I. Boomsma, Cristina Venturini, Pirro G. Hysi, Véronique Bataille, Spector TD, Daniel Glass, Craig E. Pennell, Carol A. Wang, Sheila J. Barton, Godfrey KM, Albert M. Levin, Ivan Curjuric, Ashish Kumar, Medea Imboden, Nicole M Probst-Hensch, Gabrielle A. Lockett, John W. Holloway, Jonas Bačelis, Bo Jacobsson