ScholarIQanswers from OpenAlex & ORCID
Juha Karjalainen
ResearcherPublications, citations & collaboration network
Juha Karjalainen is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Juha Karjalainen have?
ScholarIQindexed works
Juha Karjalainen has 214 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Juha Karjalainen have?
ScholarIQcitation count
Juha Karjalainen has 40,728 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Juha Karjalainen?
ScholarIQh-index
Juha Karjalainen has an h-index of 58 in OpenAlex.
What is the i10-index of Juha Karjalainen?
ScholarIQi10-index
Juha Karjalainen has an i10-index of 117 in OpenAlex.
What is the OpenAlex record for Juha Karjalainen?
ScholarIQopenalex
The OpenAlex for Juha Karjalainen is on the source record.
What are the most-cited papers on Juha Karjalainen?
ScholarIQmost cited works
Genetic studies of body mass index yield new insights for obesity biology
The LifeLines Cohort Study, Adam E. Locke, The AGEN-BMI Working Group, The GLGC, The ICBP, The MAGIC Investigators, Bratati Kahali, Sonja I. Berndt, Anne E. Justice, Tune H. Pers, Felix R. Day, C. E. Powell, Sailaja Vedantam, Martin L. Buchkovich, Jian Yang, Damien C. Croteau‐Chonka, Tõnu Esko, Tove Fall, Teresa Ferreira, Stefan Gustafsson, Zoltán Kutalik, Jian’an Luan, Reedik Mägi, Joshua C. Randall, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Jessica D. Faul, Jennifer A. Smith, Wei Zhao, Wei Zhao, Jin Chen, Rudolf S.N. Fehrmann, Åsa K. Hedman, Juha Karjalainen, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bolton, Jennifer L. Bragg‐Gresham, Steven Buyske, Ayşe Demirkan, Guohong Deng, Georg Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Anuj Goel, Jian Gong, Anne Jackson, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Sarah E. Medland, Michael A. Nalls, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. van Vliet‐Ostaptchouk, Zhaoming Wang, Loïc Yengo, Weihua Zhang, Aaron Isaacs, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Antony Attwood, Stefania Bandinelli, Amy Barrett, Isabelita Bas, Claire Bellis, Amanda J. Bennett, Christian Berne, Roza Blagieva, Matthias Blüher, Stefan Böhringer, Lori L. Bonnycastle, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Ida Henriette Caspersen, Yii‐Der Ida Chen
FinnGen provides genetic insights from a well-phenotyped isolated population
Mitja Kurki, Juha Karjalainen, Priit Palta, Timo P. Sipilä, Kati Kristiansson, Kati Donner, Mary Pat Reeve, Hannele Laivuori, Mervi Aavikko, Mari Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Päivi Laiho, Pietro Della Briotta Parolo, Arto Lehistö, Masahiro Kanai, Nina Mars, Joel Rämö, Tuomo Kiiskinen, Henrike Heyne, Kumar Veerapen, Sina Rüeger, Susanna Lemmelä, Wei Zhou, Sanni Ruotsalainen, Kalle Pärn, Tero Hiekkalinna, Sami Koskelainen, Teemu Paajanen, Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, FinnGen, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja
A cross-population atlas of genetic associations for 220 human phenotypes
Saori Sakaue, Masahiro Kanai, Yosuke Tanigawa, Juha Karjalainen, Mitja Kurki, S. Koshiba, Akira Narita, Takahiro Konuma, Kenichi Yamamoto, Masato Akiyama, Kazuyoshi Ishigaki, Akari Suzuki, Ken Suzuki, Wataru Obara, Ken Yamaji, Kazuhisa Takahashi, Satoshi Asai, Yasuo Takahashi, Takao Suzuki, Nobuaki Shinozaki, Hiroki Yamaguchi, Shiro Minami, Shigeo Murayama, Kozo Yoshimori, Satoshi Nagayama, Daisuke Obata, Masahiko Higashiyama, Akihide Masumoto, Yukihiro Koretsune, FinnGen, Kaoru Ito, Chikashi Terao, Toshimasa Yamauchi, Issei Komuro, Takashi Kadowaki, Gen Tamiya, Masayuki Yamamoto, Yusuke Nakamura, Michiaki Kubo, Yoshinori Murakami, Kazuhiko Yamamoto, Yoichiro Kamatani, Aarno Palotie, Manuel A. Rivas, Mark J. Daly, Koichi Matsuda, Yukinori Okada
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood, The LifeLines Cohort Study, Tõnu Esko, Jian Yang, Sailaja Vedantam, Tune H. Pers, Stefan Gustafsson, Audrey Y. Chu, Karol Estrada, Jian’an Luan, Zoltán Kutalik, Najaf Amin, Martin L. Buchkovich, Damien C. Croteau‐Chonka, Felix R. Day, Yanan Duan, Tove Fall, Rudolf S.N. Fehrmann, Teresa Ferreira, Anne Jackson, Juha Karjalainen, Ken Sin Lo, Adam E. Locke, Reedik Mägi, Evelin Mihailov, Eleonora Porcu, Joshua C. Randall, André Scherag, Anna A. E. Vinkhuyzen, Harm-Jan Westra, Thomas W. Winkler, Tsegaselassie Workalemahu, Wei Zhao, Devin Absher, Eva Albrecht, Denise Anderson, Jeffrey Baron, Marian Beekman, Ayşe Demirkan, Georg Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Ross M. Fraser, Anuj Goel, Jian Gong, Anne E. Justice, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Julian C. Lui, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Michael A. Nalls, Dale R. Nyholt, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Inga Prokopenko, Janina S. Ried, Stephan Ripke, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. van Vliet‐Ostaptchouk, Zhaoming Wang, Loïc Yengo, Weihua Zhang, Uzma Afzal, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Jennifer L. Bolton, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Brendan M. Buckley, Steven Buyske, Ida Henriette Caspersen, Peter S. Chines, Robert Clarke, Simone Claudi-Boehm, Matthew N. Cooper, E. Warwick Daw, Pim A. de Jong, Joris Deelen
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra, Marjolein J. Peters, Tõnu Esko, Hanieh Yaghootkar, Claudia Schurmann, Johannes Kettunen, Mark Christiansen, Benjamin P. Fairfax, Katharina Schramm, Joseph E. Powell, Alexandra Zhernakova, Daria V. Zhernakova, Jan H. Veldink, Leonard H. van den Berg, Juha Karjalainen, Sebo Withoff, André G. Uitterlinden, Albert Hofman, Fernando Rivadeneira, Peter A.C. ’t Hoen, Eva Reinmaa, Krista Fischer, Mari Nelis, Lili Milani, David Melzer, Luigi Ferrucci, Andrew Singleton, Dena Hernández, Michael A. Nalls, Georg Homuth, Matthias Nauck, Dörte Radke, Uwe Völker, Markus Perola, Veikko Salomaa, Jennifer A. Brody, Astrid M. Suchy‐Dicey, Sina A. Gharib, Daniel A. Enquobahrie, Thomas Lumley, Grant W. Montgomery, Seiko Makino, Holger Prokisch, Christian Herder, Michael Roden, Harald Grallert, Thomas Meitinger, Konstantin Strauch, Yang Li, Ritsert C. Jansen, Peter M. Visscher, Julian C. Knight, Bruce M. Psaty, Samuli Ripatti, Alexander Teumer, Timothy M. Frayling, Andres Metspalu, Joyce B. J. van Meurs, Lude Franke