Ilja M. Nolte
Active 2002–2025
- Also published as
- Ilja M Nolte
- 154
- Papers
- 29,810
- Citations
- 89
- h-index
- 146
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.2%
- Broad Institute0.8%
- Massachusetts General Hospital0.8%
- Brigham and Women's Hospital0.6%
- University of Cambridge0.6%
- Karolinska Institutet0.6%
- Other95.4%
Fields
- Medicine40.8%
- Biochemistry, Genetics and Molecular Biology40.5%
- Neuroscience4.3%
- Psychology2.7%
- Immunology and Microbiology2.3%
- Agricultural and Biological Sciences1.5%
- Other7.9%
Topics
- Genetic Associations and Epidemiology9.7%
- Genetic Mapping and Diversity in Plants and Animals2.2%
- Epigenetics and DNA Methylation2%
- Genetic and phenotypic traits in livestock1.7%
- Diabetes, Cardiovascular Risks, and Lipoproteins1.6%
- Birth, Development, and Health1.3%
- Other81.5%
Coauthors
- Harold Snieder38
- Tõnu Esko20
- Albert V. Smith19
- Alexander Teumer18
- Mary F. Feitosa18
- Peter J. van der Most18
- Daniel I. Chasman17
- Lude Franke13
- Nora Franceschini13
- Aaron Isaacs12
- Ahmad Vaez12
- LifeLines Cohort Study12
- Reedik Mägi12
- Joshua C. Bis11
- Jouke‐Jan Hottenga11
- Pim van der Harst11
- Stephan J. L. Bakker11
- Tarunveer S. Ahluwalia11
- Thomas W. Winkler11
- Toby Johnson10
- Cisca Wijmenga9
- Jian Yang9
- Peter M. Visscher9
- Solomon K. Musani9
All papers
- Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project
Authors: Esteban A. Lopera-Maya, Alexander Kurilshikov, Adriaan van der Graaf, Shixian Hu, Sergio Andreu‐Sánchez, Lianmin Chen, Arnau Vich Vila, Ranko Gaćeša, Trishla Sinha, Valerie Collij, Marjiolein A. Y. Klaassen, Laura A. Bolte, Milla F. Brandao Gois, Pieter B. Neerincx, Morris A. Swertz, LifeLines Cohort Study, Raúl Aguirre‐Gamboa, Patrick Deelen, Lude Franke, Jan Albert Kuivenhoven, Esteban A. Lopera-Maya, Ilja M. Nolte, Serena Sanna, Harold Snieder, Morris A. Swertz, Judith M. Vonk, Cisca Wijmenga, Hermie J. M. Harmsen, Cisca Wijmenga, Jingyuan Fu, Rinse K. Weersma, Alexandra Zhernakova, Serena Sanna - Nature Genetics 2022 cited by 565
- The trans-ancestral genomic architecture of glycemic traits
Authors: Jihua Chen, Cassandra N. Spracklen, Gaëlle Marenne, Arushi Varshney, Laura J. Corbin, Jian’an Luan, Sara M. Willems, Ying Wu, Xiaoshuai Zhang, Momoko Horikoshi, Thibaud Boutin, Reedik Mägi, Johannes Waage, Ruifang Li‐Gao, Kei Hang Katie Chan, Jie Yao, Mila Desi Anasanti, Audrey Y. Chu, Annique Claringbould, Jani Heikkinen, Jaeyoung Hong, Jouke‐Jan Hottenga, Shaofeng Huo, Marika Kaakinen, Tin Louie, Winfried März, Hortensia Moreno-Macías, Anne Ndungu, Sarah C. Nelson, Ilja M. Nolte, Kari E. North, Chelsea K. Raulerson, Debashree Ray, Rebecca Rohde, Denis Rybin, Claudia Schurmann, Xueling Sim, Lorraine Southam, Isobel D. Stewart, Carol A. Wang, Yujie Wang, Peitao Wu, Weihua Zhang, Tarunveer S. Ahluwalia, Emil V. R. Appel, Lawrence F. Bielak, Jennifer A. Brody, Noël P. Burtt, Claudia Cabrera, Brian E. Cade, Jin Fang Chai, Xiaoran Chai, Li-Ching Chang, Chien-Hsiun Chen, Brian H. Chen, Kumaraswamy Naidu Chitrala, Yen‐Feng Chiu, Hugoline G. de Haan, Graciela E. Delgado, Ayşe Demirkan, Qing Duan, Jorgen Engmann, Segun Fatumo, Javier Gayán, Franco Giulianini, Jung Ho Gong, Stefan Gustafsson, Yang Hai, Fernando Pires Hartwig, Jing He, Yoriko Heianza, Tao Huang, Alicia Huerta‐Chagoya, Mi Yeong Hwang, Richard A. Jensen, Takahisa Kawaguchi, Katherine A. Kentistou, Young Jin Kim, Marcus E. Kleber, Ishminder K. Kooner, Shuiqing Lai, Leslie A. Lange, Carl D. Langefeld, Marie Lauzon, Man Li, Symen Ligthart, Jun Liu, Marie Loh, Jirong Long, Valeriya Lyssenko, Massimo Mangino, Carola Marzi, May E. Montasser, Abhishek Nag, Masahiro Nakatochi, Damia Noce, Raymond Noordam, Giorgio Pistis, Michael Preuß, Laura M. Raffield and 317 more - Nature Genetics 2021 cited by 886
- Meta-analysis of genome-wide association studies of anxiety disorders
Authors: Takeshi Otowa, Karin Hek, M Lee, Enda M. Byrne, S S Mirza, Michel G. Nivard, Tim B. Bigdeli, Steven H. Aggen, Daniel E. Adkins, Aaron R. Wolen, Ayman H. Fanous, Matthew C. Keller, Enrique Castelao, Zoltán Kutalik, Sandra Van der Auwera, Georg Homuth, Matthias Nauck, Alexander Teumer, Yuri Milaneschi, J-J Hottenga, Neşe Direk, Albert Hofman, André G. Uitterlinden, C.L. Mulder, Anjali K. Henders, Sarah E. Medland, Scott D. Gordon, Andrew C. Heath, Pamela A. F. Madden, Michele L. Pergadia, Peter J. van der Most, Ilja M. Nolte, Floor V. A. van Oort, Catharina A. Hartman, Albertine J. Oldehinkel, Martin Preisig, Hans J. Grabe, Christel M. Middeldorp, Brenda W.J.H. Penninx, Dorret I. Boomsma, Nicholas G. Martin, Grant W. Montgomery, Brion S. Maher, Edwin J. van den Oord, Naomi R. Wray, Henning Tiemeier, John M. Hettema - Molecular Psychiatry 2016 cited by 618
- Host genetic regulation of human gut microbial structural variation
Authors: Daria V. Zhernakova, Daoming Wang, Lei Liu, Sergio Andreu‐Sánchez, Yue Zhang, Angel J. Ruiz‐Moreno, Haoran Peng, Niels Plomp, Ángela del Castillo-Izquierdo, Ranko Gaćeša, Esteban A. Lopera-Maya, Godfrey S. Temba, Vesla Kullaya, Sander S. van Leeuwen, Lifelines Cohort Study, Raul Aguirre-Gamboa, Patrick Deelen, Lude Franke, Jan A. Kuivenhoven, Ilja M. Nolte, Serena Sanna, Harold Snieder, Morris A. Swertz, Peter M. Visscher, Judith M. Vonk, Ramnik J. Xavier, Quirijn de Mast, Leo A. B. Joosten, Niels P. Riksen, Joost H.W. Rutten, Mihai G. Netea, Serena Sanna, Cisca Wijmenga, Rinse K. Weersma, Alexandra Zhernakova, Hermie J. M. Harmsen, Jingyuan Fu - Nature 2024 cited by 165
- Validity of (Ultra-)Short Recordings for Heart Rate Variability Measurements
Authors: M. Loretto Muñoz, Arie van Roon, Harriëtte Riese, Chris H. L. Thio, Emma Oostenbroek, Iris G. Westrik, Eco J. C. de Geus, Ron T. Gansevoort, Joop D. Lefrandt, Ilja M. Nolte, Harold Snieder - PLoS ONE 2015 cited by 390
- Common variants associated with plasma triglycerides and risk for coronary artery disease
Authors: Ron Do, Cristen J. Willer, Ellen M. Schmidt, Sebanti Sengupta, Chi Gao, Gina M. Peloso, Stefan Gustafsson, Stavroula Kanoni, Andrea Ganna, Jin Chen, Martin L. Buchkovich, Samia Mora, J. Beckmann, Jennifer L. Bragg‐Gresham, Hsing‐Yi Chang, Ayşe Demirkan, Heleen M. den Hertog, Louise A. Donnelly, Georg Ehret, Tõnu Esko, Mary F. Feitosa, Teresa Ferreira, Krista Fischer, Pierre Fontanillas, Ross M. Fraser, Daniel F. Freitag, Deepti Gurdasani, Kauko Heikkilä, Elina Hyppönen, Aaron Isaacs, Anne Jackson, Åsa Johansson, Toby Johnson, Marika Kaakinen, Johannes Kettunen, Marcus E. Kleber, Xiaohui Li, Jian’an Luan, Leo‐Pekka Lyytikäinen, Patrik K. E. Magnusson, Massimo Mangino, Evelin Mihailov, May E. Montasser, Martina Müller‐Nurasyid, Ilja M. Nolte, Jeffrey R. O’Connell, Cameron D Palmer, Markus Perola, Ann-Kristin Petersen, Serena Sanna, Richa Saxena, Susan K. Service, Sonia Shah, Dmitry Shungin, Carlo Sidore, Ci Song, Rona J. Strawbridge, Ida Surakka, Toshiko Tanaka, Tanya M. Teslovich, Guðmar Þorleifsson, Evita G. van den Herik, Benjamin F. Voight, Kelly A. Volcik, Lindsay L. Waite, Andrew Wong, Ying Wu, Weihua Zhang, Devin Absher, Gershim Asiki, Inês Barroso, Latonya Been, Jennifer L. Bolton, Lori L. Bonnycastle, Paolo Brambilla, Mary Susan Burnett, Giancarlo Cesana, Maria Dimitriou, Alex S. F. Doney, Angela Döring, Paul Elliott, Stephen E. Epstein, Guðmundur I. Eyjólfsson, Bruna Gigante, Mark O. Goodarzi, Harald Grallert, Martha L. Gravito, Christopher J. Groves, Göran Hallmans, Anna-Liisa Hartikainen, Caroline Hayward, Dena Hernandez, Andrew A. Hicks, Hilma Hólm, Yi-Jen Hung, Thomas Illig, Michelle R. Jones, Pontiano Kaleebu, John J.P. Kastelein, Kay‐Tee Khaw and 163 more - Nature Genetics 2013 cited by 906
- Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
Authors: The LifeLines Cohort Study, Jian Yang, Andrew Bakshi, Zhihong Zhu, Gibran Hemani, Anna A. E. Vinkhuyzen, Sang Lee, Matthew R. Robinson, John R. B. Perry, Ilja M. Nolte, Jana V. van Vliet‐Ostaptchouk, Harold Snieder, Tõnu Esko, Lili Milani, Reedik Mägi, Andres Metspalu, Anders Hamsten, Patrik K. E. Magnusson, Nancy L. Pedersen, Erik Ingelsson, Nicole Soranzo, Matthew C. Keller, Naomi R. Wray, Michael E. Goddard, Peter M. Visscher - Nature Genetics 2015 cited by 883
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Authors: LifeLines Cohort Study, Anna Köttgen, Eva Albrecht, Alexander Teumer, Véronique Vitart, Jan Krumsiek, Claudia Hundertmark, Giorgio Pistis, Daniela Ruggiero, Conall M. O’Seaghdha, Toomas Haller, Qiong Yang, Toshiko Tanaka, Andrew D. Johnson, Zoltán Kutalik, Albert V. Smith, Julia Shi, Maksim Struchalin, Rita P. S. Middelberg, Morris J Brown, Angelo Gaffo, Nicola Pirastu, Li Guo, Caroline Hayward, Tatijana Zemunik, Jennifer E. Huffman, Loïc Yengo, Jing Hua Zhao, Ayşe Demirkan, Mary F. Feitosa, Xuan Liu, Giovanni Malerba, Lorna M. Lopez, Pim van der Harst, Man Li, Marcus E. Kleber, Andrew A. Hicks, Ilja M. Nolte, Åsa Johansson, Federico Murgia, Sarah H. Wild, Stephan J. L. Bakker, John F. Peden, Abbas Dehghan, Maristella Steri, Albert Tenesa, Vasiliki Lagou, Perttu Salo, Massimo Mangino, Lynda M. Rose, Terho Lehtimäki, Owen M. Woodward, Yukinori Okada, Adrienne Tin, Christian Müller, Christopher Oldmeadow, Margus Putku, Darina Czamara, Peter Kraft, Laura Frogheri, Gian Andri Thun, Anne Grotevendt, Gauti Kjartan Gíslason, Tamara B. Harris, Lenore J. Launer, Patrick F. McArdle, Alan R. Shuldiner, Eric Boerwinkle, Josef Coresh, Helena Schmidt, Michael Schallert, Nicholas G. Martin, Grant W. Montgomery, Michiaki Kubo, Yusuke Nakamura, Toshihiro Tanaka, Patricia B. Munroe, Nilesh J. Samani, David R. Jacobs, Kiang Liu, Pio D’Adamo, Sheila Ulivi, Jerome I. Rotter, Bruce M. Psaty, Péter Vollenweider, Gérard Waeber, Susan Campbell, Olivier Devuyst, Pau Navarro, Ivana Kolčić, Nicholas D. Hastie, Beverley Balkau, Philippe Froguel, Tõnu Esko, Andres Salumets, Kay‐Tee Khaw, Claudia Langenberg, Nicholas J. Wareham, Aaron Isaacs, Aldi T. Kraja and 126 more - Nature Genetics 2012 cited by 878
- Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Authors: Alexander Teumer, Layal Chaker, Stefan Groeneweg, Yong Li, Celia Di Munno, Caterina Barbieri, Ulla T. Schultheiß, Michela Traglia, Tarunveer S. Ahluwalia, Masato Akiyama, Emil V. R. Appel, Dan E. Arking, Alice M. Arnold, Arne Astrup, Marian Beekman, John Beilby, Sofie Bekaert, Eric Boerwinkle, Suzanne J. Brown, Marc De Buyzere, Purdey J. Campbell, Graziano Ceresini, Charlotte Cerqueira, Francesco Cucca, Ian J. Deary, Joris Deelen, Kai‐Uwe Eckardt, Arif B. Ekici, Johan G. Eriksson, Luigi Ferrrucci, Tom Fiers, Edoardo Fiorillo, Ian Ford, Caroline S. Fox, Christian Fuchsberger, Tessel E. Galesloot, Christian Gieger, Martin Gögele, Alessandro De Grandi, Niels Grarup, Karin Halina Greiser, Kadri Haljas, Torben Hansen, Sarah E. Harris, Diana van Heemst, Martin den Heijer, Andrew A. Hicks, Wouter den Hollander, Georg Homuth, Jennie Hui, M. Arfan Ikram, Till Ittermann, Richard A. Jensen, Jiaojiao Jing, J. Wouter Jukema, Eero Kajantie, Yoichiro Kamatani, Elisa Kasbohm, Jean‐Marc Kaufman, Lambertus A. Kiemeney, M. Kloppenburg, Florian Kronenberg, Michiaki Kubo, Jari Lahti, Bruno Lapauw, Shuo Li, David C. Liewald, Lifelines Cohort Study, Behrooz Z. Alizadeh, H. Marike Boezen, Lude Franke, Pim van der Harst, Gerjan Navis, Marianne G. Rots, Harold Snieder, Morris A. Swertz, Cisca Wijmenga, Ee Mun Lim, Allan Linneberg, Michela Marina, Deborah Mascalzoni, Koichi Matsuda, Daniel Medenwald, Christa Meisinger, Ingrid Meulenbelt, Tim De Meyer, Henriette E. Meyer zu Schwabedissen, Rafael Mikolajczyk, Matthijs Moed, Romana T. Netea‐Maier, Ilja M. Nolte, Yukinori Okada, Mauro Pala, Cristian Pattaro, Oluf Pedersen, Astrid Petersmann, Eleonora Porcu, Iris Postmus, Peter P. Pramstaller, Bruce M. Psaty and 38 more - Nature Communications 2018 cited by 289
- Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
Authors: Paolo Zanoni, Sumeet A. Khetarpal, Daniel B. Larach, William Hancock‐Cerutti, John S. Millar, Marina Cuchel, Stephanie DerOhannessian, Anatol Kontush, Praveen Surendran, Danish Saleheen, Stella Trompet, J. Wouter Jukema, Anton de Craen, Panos Deloukas, Naveed Sattar, Ian Ford, Chris J. Packard, Abdullah Al Shafi Majumder, Dewan S Alam, Emanuele Di Angelantonio, Gonçalo R. Abecasis, Rajiv Chowdhury, Jeanette Erdmann, Børge G. Nordestgaard, Sune F. Nielsen, Anne Tybjærg‐Hansen, Ruth Frikke‐Schmidt, Kari Kuulasmaa, Dajiang J. Liu, Markus Perola, Stefan Blankenberg, Veikko Salomaa, Satu Männistö, Philippe Amouyel, Dominique Arveiler, Jean Ferrières, Martina Müller‐Nurasyid, Maurizio Ferrario, Frank Kee, Cristen J. Willer, Nilesh J. Samani, Heribert Schunkert, Adam S. Butterworth, Joanna M. M. Howson, Gina M. Peloso, Nathan O. Stitziel, John Danesh, Sekar Kathiresan, Daniel J. Rader, Sarah Watson, Ellen M. Schmidt, Sebanti Sengupta, Stefan Gustafsson, Stavroula Kanoni, Andrea Ganna, Jin Chen, Martin L. Buchkovich, Samia Mora, J. Beckmann, Jennifer L. Bragg‐Gresham, Hsing‐Yi Chang, Ayşe Demirkan, Heleen M. den Hertog, Ron Do, Louise A. Donnelly, Georg Ehret, Tõnu Esko, Mary F. Feitosa, Teresa Ferreira, Krista Fischer, Pierre Fontanillas, Ross M. Fraser, Daniel F. Freitag, Deepti Gurdasani, Kauko Heikkilä, Elina Hyppönen, Aaron Isaacs, Anne Jackson, Åsa Johansson, Toby Johnson, Marika Kaakinen, Johannes Kettunen, Marcus E. Kleber, Xiaohui Li, Jian’an Luan, Leo‐Pekka Lyytikäinen, Patrik K. E. Magnusson, Massimo Mangino, Evelin Mihailov, May E. Montasser, Ilja M. Nolte, Jeffrey R. O’Connell, Cameron D. Palmer, Ann-Kristin Petersen, Serena Sanna, Richa Saxena, Susan K. Service, Sonia Shah, Dmitry Shungin, Carlo Sidore and 211 more - Science 2016 cited by 551
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Authors: Cristian Pattaro, Alexander Teumer, Mathias Gorski, Audrey Y. Chu, Man Li, Vladan Mijatovic, Maija Garnaas, Adrienne Tin, Rossella Sorice, Yong Li, Daniel Taliun, Matthias Olden, Meredith C. Foster, Qiong Yang, Ming‐Huei Chen, Tune H. Pers, Andrew D. Johnson, Yi-An Ko, Christian Fuchsberger, Bamidele O. Tayo, Michael A. Nalls, Mary F. Feitosa, Aaron Isaacs, Abbas Dehghan, Pio D’Adamo, Adebowale Adeyemo, Aida Karina Dieffenbach, Alan B. Zonderman, Ilja M. Nolte, Peter J. van der Most, Alan F. Wright, Alan R. Shuldiner, Alanna C. Morrison, Albert Hofman, Albert V. Smith, Albert W. Dreisbach, André Franke, André G. Uitterlinden, Andres Metspalu, Anke Tönjes, Antonio Lupo, Antonietta Robino, Åsa Johansson, Ayşe Demirkan, Barbara Kollerits, Barry I. Freedman, Belén Ponte, Ben A. Oostra, Bernhard Paulweber, Bernhard K. Krämer, Braxton D. Mitchell, Brendan M. Buckley, Carmen A. Peralta, Caroline Hayward, Catherine Helmer, Charles N. Rotimi, Christian M. Shaffer, Christian Müller, Cinzia Sala, Cornelia M. van Duijn, Aude Saint-Pierre, Daniel Ackermann, Daniel Shriner, Daniela Ruggiero, Daniela Toniolo, Yingchang Lu, Daniele Cusi, Darina Czamara, David Ellinghaus, David S. Siscovick, Douglas M. Ruderfer, Christian Gieger, Harald Grallert, Elena Rochtchina, Elizabeth J. Atkinson, Elizabeth G. Holliday, Eric Boerwinkle, Erika Salvi, Erwin P. Böttinger, Federico Murgia, Fernando Rivadeneira, Florian Ernst, Florian Kronenberg, Frank B. Hu, Gerjan Navis, Gary C. Curhan, G. Ehret, Georg Homuth, Stefan Coassin, Gian Andri Thun, Giorgio Pistis, Giovanni Gambaro, Giovanni Malerba, Grant W. Montgomery, Guðný Eiríksdóttir, Gunnar Jacobs, Li Guo, H-Erich Wichmann, Harry Campbell, Helena Schmidt and 600 more - Nature Communications 2016 cited by 536
- Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
Authors: Symen Ligthart, Ahmad Vaez, Urmo Võsa, Maria G. Stathopoulou, Paul S. de Vries, Bram P. Prins, Peter J. van der Most, Toshiko Tanaka, Elnaz Naderi, Lynda M. Rose, Ying Wu, Robert Karlsson, Maja Barbalić, Honghuang Lin, René Pool, Gu Zhu, Aurélien Macé, Carlo Sidore, Stella Trompet, Massimo Mangino, Maria Sabater‐Lleal, John P. Kemp, Ali Abbasi, Tim Kacprowski, Niek Verweij, Albert V. Smith, Tao Huang, Carola Marzi, Mary F. Feitosa, Kurt K. Lohman, Marcus E. Kleber, Yuri Milaneschi, Christian Mueller, Mahmudul Huq, Efthymia Vlachopoulou, Leo-Pekka Lyytikäinen, Christopher Oldmeadow, Joris Deelen, Markus Perola, Jing Hua Zhao, Bjarke Feenstra, Behrooz Z. Alizadeh, H. Marike Boezen, Lude Franke, Pim van der Harst, Gerjan Navis, Marianne G. Rots, Harold Snieder, Morris Swertz, Bruce H. R. Wolffenbuttel, Cisca Wijmenga, Marzyeh Amini, Emelia J. Benjamin, Daniel I. Chasman, Abbas Dehghan, Tarunveer S. Ahluwalia, James B. Meigs, Russell P. Tracy, Behrooz Z. Alizadeh, Symen Ligthart, Josh Bis, Gudny Eiriksdottir, Nathan Pankratz, Myron Gross, Alex Rainer, Harold Snieder, James Wilson, Bruce M. Psaty, Josée Dupuis, Bram P. Prins, Urmo Vaso, Maria G. Stathopoulou, Lude Franke, Terho Lehtimäki, Wolfgang Köenig, Yalda Jamshidi, Sophie Siest, Ali Abbasi, André G. Uitterlinden, Mohammadreza Abdollahi, Renate B. Schnabel, Ursula M. Schick, Ilja M. Nolte, Aldi T. Kraja, Yi‐Hsiang Hsu, Daniel S. Tylee, Alyson Zwicker, Rudolf Uher, George Davey-Smith, Alanna C. Morrison, Andrew A. Hicks, Cornelia M. van Duijn, Cavin Ward‐Caviness, Eric Boerwinkle, Jerome I. Rotter, Kenneth Rice, Leslie A. Lange, Markus Perola, Eco J. C. de Geus, Andrew P. Morris and 249 more - The American Journal of Human Genetics 2018 cited by 453
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Authors: The LifeLines Cohort Study, Felix R. Day, kConFab/AOCS Investigators, Deborah J. Thompson, Hannes Helgason, Daniel I. Chasman, Hilary K. Finucane, Patrick Sulem, Katherine S. Ruth, Sean Whalen, Abhishek Sarkar, Eva Albrecht, Elisabeth Altmaier, Marzyeh Amini, Caterina Barbieri, Thibaud Boutin, Archie Campbell, Ellen W. Demerath, Ayush Giri, Chunyan He, Jouke‐Jan Hottenga, Robert Karlsson, Ivana Kolčić, Po‐Ru Loh, Kathryn L. Lunetta, Massimo Mangino, Marco Brumat, George McMahon, Sarah E. Medland, Ilja M. Nolte, Raymond Noordam, Teresa Nutile, Lavinia Paternoster, Natalia Perjakova, Eleonora Porcu, Lynda M. Rose, Katharina E. Schraut, Ayellet V. Segrè, Albert V. Smith, Lisette Stolk, Alexander Teumer, Irene L. Andrulis, Stefania Bandinelli, Matthias W. Beckmann, Javier Benı́tez, Sven Bergmann, Murielle Bochud, Eric Boerwinkle, Stig E. Bojesen, Manjeet K. Bolla, Judith S. Brand, Hiltrud Brauch, Hermann Brenner, Linda Broer, Thomas Brüning, Julie E. Buring, Harry Campbell, Eulalia Catamo, Stephen J. Chanock, Georgia Chenevix‐Trench, Tanguy Corre, Fergus J. Couch, Diana L. Cousminer, Angela Cox, Laura Crisponi, Kamila Czene, George Davey Smith, Eco J. C. de Geus, Renée de Mutsert, Immaculata De Vivo, Joe Dennis, Peter Devilee, Isabel dos‐Santos‐Silva, Alison M. Dunning, Johan G. Eriksson, Peter A. Fasching, Lindsay Fernández‐Rhodes, Luigi Ferrucci, Dieter Flesch‐Janys, Lude Franke, Marike Gabrielson, Ilaria Gandin, Graham G. Giles, Harald Grallert, Daníel F. Guðbjartsson, Pascal Guénel, Per Hall, Emily Hallberg, Ute Hamann, Tamara B. Harris, Catharina A. Hartman, Gerardo Heiss, Maartje J. Hooning, John L. Hopper, Frank B. Hu, David J. Hunter, M. Arfan Ikram, Hae Kyung Im, Marjo‐Riitta Järvelin, Peter K. Joshi and 118 more - Nature Genetics 2017 cited by 646
- Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Authors: LifeLines Cohort Study, Aysu Okbay, Bart M. L. Baselmans, Jan-Emmanuel De Neve, Patrick Turley, Michel G. Nivard, Mark Alan Fontana, S Fleur W Meddens, Richard Karlsson Linnér, Cornelius A. Rietveld, Jaime Derringer, Jacob Gratten, James J. Lee, Jimmy Z. Liu, Ronald de Vlaming, Tarunveer S. Ahluwalia, Jadwiga Buchwald, Alana Cavadino, Alexis C. Wood, Nicholas A. Furlotte, Victoria Garfield, Marie Henrike Geisel, Juan R Gonzalez, Saskia Haitjema, Robert Karlsson, Sander W. van der Laan, Karl-Heinz Ladwig, Jari Lahti, Sven J. van der Lee, Penelope A. Lind, Tian Liu, Lindsay Matteson, Evelin Mihailov, Michael Miller, Camelia C. Minică, Ilja M. Nolte, Dennis O. Mook‐Kanamori, Peter J. van der Most, Christopher Oldmeadow, Yong Qian, Olli Raitakari, Rajesh Rawal, Anu Realo, Rico Rueedi, Börge Schmidt, Albert V. Smith, Evie Stergiakouli, Toshiko Tanaka, Kent D. Taylor, Gudmar Thorleifsson, Juho Wedenoja, Juergen Wellmann, Harm-Jan Westra, Sara M. Willems, Wei Zhao, Najaf Amin, Andrew Bakshi, Sven Bergmann, Gyða Björnsdóttir, Patricia A. Boyle, Samantha Cherney, Simon R Cox, Gail Davies, Oliver S. P. Davis, Jun Ding, Neşe Direk, Peter Eibich, Rebecca T. Emeny, Ghazaleh Fatemifar, Jessica D. Faul, Luigi Ferrucci, Andreas J. Forstner, Christian Gieger, Richa Gupta, Tamara B Harris, Juliette Harris, Elizabeth G Holliday, Jouke-Jan Hottenga, Philip L De Jager, Marika Kaakinen, Eero Kajantie, Ville Karhunen, Ivana Kolčić, Meena Kumari, Lenore J Launer, Lude Franke, Ruifang Li‐Gao, David C. Liewald, Marisa Koini, Anu Loukola, Pedro Marques‐Vidal, Grant W. Montgomery, Miriam A. Mosing, Lavinia Paternoster, Alison Pattie, Katja Petrovic, Laura Pulkki-Råback, Lydia Quaye, Katri Räikkönen, Igor Rudan and 88 more - Nature Genetics 2016 cited by 1,129
- Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
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