Kāri Stefánsson
Active 1980–2025
- Also published as
- Kari Stefansson · Kári Stefánsson · Kári Stefansson
- 512
- Papers
- 138,783
- Citations
- 191
- h-index
- 489
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.2%
- Broad Institute0.8%
- Massachusetts General Hospital0.7%
- University of Oxford0.6%
- King's College London0.6%
- Karolinska Institutet0.5%
- Other95.6%
Fields
- Medicine40.4%
- Biochemistry, Genetics and Molecular Biology40.3%
- Neuroscience10.2%
- Immunology and Microbiology2.4%
- Psychology1.7%
- Computer Science0.8%
- Other4.2%
Topics
- Genetic Associations and Epidemiology6.7%
- Alzheimer's disease research and treatments2.1%
- Epigenetics and DNA Methylation1.8%
- Genetics and Neurodevelopmental Disorders1.8%
- Genomics and Rare Diseases1.8%
- Genomic variations and chromosomal abnormalities1.7%
- Other84.1%
Coauthors
- Daníel F. Guðbjartsson164
- Guðmar Þorleifsson162
- Patrick Sulem125
- Unnur Þorsteinsdóttir105
- Hreinn Stefánsson101
- Augustine Kong83
- Gísli Másson72
- Hilma Hólm72
- Agnar Helgason71
- Ásgeir Sigurðsson63
- Þórunn Rafnar62
- Bjarni V. Halldórsson60
- Jeffrey R. Gulcher60
- Garðar Sveinbjörnsson58
- Ingileif Jónsdóttir56
- Sigurjón A. Guðjónsson54
- Anna Helgadóttir52
- Gísli H. Halldórsson52
- Valgerður Steinthórsdóttir51
- Áslaug Jónasdóttir50
- G. Bragi Walters49
- Simon Stacey49
- Sólveig Grétarsdóttir49
- Michael L. Frigge47
All papers
- Large-scale integration of the plasma proteome with genetics and disease
Authors: Egil Ferkingstad, Patrick Sulem, Bjarni A. Atlason, Garðar Sveinbjörnsson, Magnus I. Magnusson, Edda L. Styrmisdottir, Kristbjörg Gunnarsdóttir, Agnar Helgason, Ásmundur Oddsson, Bjarni V. Halldórsson, Brynjar Ö. Jensson, Florian Zink, Gísli H. Halldórsson, Gísli Másson, Gudny A. Arnadottir, Hildigunnur Katrínardóttir, Kristinn Juliusson, Magnús K. Magnússon, Ólafur Þ. Magnússon, Rún Friðriksdóttir, Saedís Saevarsdóttir, Sigurjón A. Guðjónsson, Simon Stacey, Sölvi Rögnvaldsson, Thjodbjorg Eiriksdottir, Thorunn A. Olafsdottir, Valgerður Steinthórsdóttir, Vinicius Tragante, Magnús Ö. Úlfarsson, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Páll Melsted, Jona Saemundsdottir, Gudmundur L. Norddahl, Sigrún H. Lund, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2021 cited by 1,668
- Identification of common genetic risk variants for autism spectrum disorder
Authors: Jakob Grove, BUPGEN, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 cited by 2,632
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk
Authors: Iris E. Jansen, Jeanne E. Savage, Kyoko Watanabe, Julien Bryois, Dylan M. Williams, Stacy Steinberg, Julia Sealock, Ida Karlsson, Sara Hägg, Lavinia Athanasiu, Nicola Voyle, Petroula Proitsi, Aree Witoelar, Sven Stringer, Dag Aarsland, Ina S. Almdahl, Fred Andersen, Sverre Bergh, Francesco Bettella, Sigurbjörn Björnsson, Anne Brækhus, Geir Bråthen, Christiaan de Leeuw, Rahul S. Desikan, Srdjan Djurovic, Logan Dumitrescu, Tormod Fladby, Timothy J. Hohman, Pálmi V. Jónsson, Steven J. Kiddle, Arvid Rongve, Ingvild Saltvedt, Sigrid Botne Sando, Geir Selbæk, Maryam Shoai, Nathan Skene, Jón Snædal, Eystein Stordal, Ingun Ulstein, Yunpeng Wang, Linda R. White, John Hardy, Jens Hjerling‐Leffler, Patrick F. Sullivan, Wiesje M. van der Flier, Richard Dobson, Lea K. Davis, Hreinn Stefánsson, Kāri Stefánsson, Nancy L. Pedersen, Stephan Ripke, Ole A. Andreassen, Daniëlle Posthuma - Nature Genetics 2019 cited by 2,526
- Variant of TREM2 Associated with the Risk of Alzheimer's Disease
Authors: Thorlákur Jónsson, Hreinn Stefánsson, Stacy Steinberg, Ingileif Jónsdóttir, Pálmi V. Jónsson, Jón Snædal, Sigurbjörn Björnsson, Johanna Huttenlocher, Allan I. Levey, James J. Lah, Dan Rujescu, Harald Hampel, Ina Giegling, Ole A. Andreassen, Knut Engedal, Ingun Ulstein, Srdjan Djurovic, Carla A. Ibrahim‐Verbaas, Albert Hofman, M. Arfan Ikram, Cornelia M. van Duijn, Unnur Þorsteinsdóttir, Augustine Kong, Kāri Stefánsson - New England Journal of Medicine 2012 cited by 2,620
- Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Authors: Krishna G. Aragam, Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri, E. Weeks, Minxian Wang, George Hindy, Wei Zhou, Christopher Grace, Carolina Roselli, Nicholas Marston, Frederick Kamanu, Ida Surakka, Loreto Muñoz Venegas, Paul Sherliker, Satoshi Koyama, Kazuyoshi Ishigaki, Bjørn Olav Åsvold, Michael R. Brown, Ben Brumpton, Paul S. de Vries, Olga Giannakopoulou, Tota Giardoglou, Daníel F. Guðbjartsson, Ulrich Güldener, Syed M. Ijlal Haider, Anna Helgadóttir, M Ibrahim, Adnan Kastrati, Thorsten Kessler, Theodosios Kyriakou, Tomasz Konopka, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Gavin R. Schnitzler, Damian Smedley, Guðmar Þorleifsson, Moritz von Scheidt, Jacob C. Ulirsch, Biobank Japan, EPIC-CVD, John Danesh, Davíð O. Arnar, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Kaoru Ito, Dongkeun Jang, Yoichiro Kamatani, Amit V. Khera, Issei Komuro, Iftikhar J. Kullo, Luca A. Lotta, Christopher P. Nelson, Robert Roberts, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Tom R. Webb, Aris Baras, Johan Björkegren, Eric Boerwinkle, George Dedoussis, Hilma Hólm, Kristian Hveem, Olle Melander, Alanna C. Morrison, Marju Orho‐Melander, Lοukianos S. Rallidis, Arno Ruusalepp, Marc S. Sabatine, Kāri Stefánsson, Pierre Zalloua, Patrick T. Ellinor, Martin Farrall, John Danesh, Christian T. Ruff, Hilary K. Finucane, Jemma C. Hopewell, Robert Clarke, Rajat M. Gupta, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth, Paul S. de Vries, Moritz von Scheidt - Nature Genetics 2022 cited by 706
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Authors: Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Katrina L. Grasby, Jakob Grove, Ólafur Ó. Guðmundsson, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Nicholas G. Martin, Jennifer L. Moran, Jonatan Pallesen, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Håkon Håkonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale - Nature Genetics 2018 cited by 2,320
- Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Authors: Ditte Demontis, G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen, Leila Farajzadeh, Georgios Voloudakis, Jaroslav Bendl, Biau Zeng, Wen Zhang, Jakob Grove, Thomas D. Als, Jinjie Duan, F. Kyle Satterstrom, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Ólafur Ó. Guðmundsson, Sigurður H. Magnússon, Gísli Baldursson, Katrín Davíðsdóttir, Gyða S. Haraldsdóttir, Esben Agerbo, Gabriel E. Hoffman, Søren Dalsgaard, Joanna Martin, Marta Ribasés, Dorret I. Boomsma, María Soler Artigas, Nina Roth Mota, Daniel P. Howrigan, Sarah E. Medland, Tetyana Zayats, Veera M. Rajagopal, Alexandra Havdahl, Alysa E. Doyle, Andreas Reif, Anita Thapar, Bru Cormand, Calwing Liao, Christie L. Burton, Claiton H.D. Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Henrik Larsson, Ian R. Gizer, Irwin D. Waldman, Isabell Brikell, Jan Haavik, Jennifer Crosbie, James J. McGough, Jonna Kuntsi, Joseph Glessner, K. Langley, Klaus‐Peter Lesch, Luís Augusto Rohde, Mara Helena Hutz, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Michael O‘Donovan, Ole A. Andreassen, Patrick W. L. Leung, Pedro Mário Pan, Ridha Joober, Russell Schachar, Sandra K. Loo, Stephanie H. Witt, Ted Reichborn‐Kjennerud, Tobias Banaschewski, Ziarih Hawi, Mark J. Daly, Ole Mors, Merete Nordentoft, Ole Mors, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Hreinn Stefánsson, Panos Roussos, Barbara Franke, Thomas Werge, Benjamin M. Neale, Kāri Stefánsson, Anders D. Børglum - Nature Genetics 2023 cited by 760
- Large-scale plasma proteomics comparisons through genetics and disease associations
Authors: Grímur Hjörleifsson Eldjárn, Egil Ferkingstad, Sigrún H. Lund, Hannes Helgason, Ólafur Þ. Magnússon, Kristbjörg Gunnarsdóttir, Thorunn A. Olafsdottir, Bjarni V. Halldórsson, Pall I. Olason, Florian Zink, Sigurjón A. Guðjónsson, Garðar Sveinbjörnsson, Magnus I. Magnusson, Agnar Helgason, Ásmundur Oddsson, Gísli H. Halldórsson, Magnús K. Magnússon, Saedís Saevarsdóttir, Thjodbjorg Eiriksdottir, Gísli Másson, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Páll Melsted, Jona Saemundsdottir, Gudmundur L. Norddahl, Guðmar Þorleifsson, Magnús Ö. Úlfarsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Patrick Sulem, Kāri Stefánsson - Nature 2023 cited by 520
- The sequences of 150,119 genomes in the UK Biobank
Authors: Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, Hannes Hauswedell, Ögmundur Eiríksson, Magnús Ö. Úlfarsson, Gunnar Pálsson, Marteinn T. Hardarson, Ásmundur Oddsson, Brynjar Ö. Jensson, Snædís Kristmundsdóttir, Brynja D. Sigurpalsdottir, Ólafur Andri Stefánsson, Doruk Beyter, Guillaume Holley, Vinicius Tragante, Arnaldur Gylfason, Pall I. Olason, Florian Zink, Margret Asgeirsdottir, Sverrir T. Sverrisson, Brynjar Sigurdsson, Sigurjón A. Guðjónsson, Gunnar Sigurðsson, Gísli H. Halldórsson, Garðar Sveinbjörnsson, Kristján Norland, Unnur Styrkársdóttir, Droplaug N. Magnúsdóttir, Steinunn Snorradóttir, Kári Kristinsson, Emilia Sobech, Helgi Jónsson, Árni Jón Geirsson, Ísleifur Ólafsson, Pálmi V. Jónsson, Ole Birger Pedersen, Christian Erikstrup, Søren Brunak, Sisse Rye Ostrowski, Steffen Andersen, Karina Banasik, Kristoffer Sølvsten Burgdorf, Maria Didriksen, Khoa Manh Dinh, Christian Erikstrup, Daníel F. Guðbjartsson, Thomas Folkmann Hansen, Henrik Hjalgrim, Gregor B. E. Jemec, Poul Jennum, Pär I. Johansson, Margit Anita Hørup Larsen, Susan Mikkelsen, Kasper Nielsen, Mette Nyegaard, Sisse Rye Ostrowski, Susanne Gjørup Sækmose, Erik Sørensen, Unnur Þorsteinsdóttir, Mie Topholm Brun, Henrik Ullum, Thomas Werge, Guðmar Þorleifsson, Frosti Jónsson, Páll Melsted, Ingileif Jónsdóttir, Þórunn Rafnar, Hilma Hólm, Hreinn Stefánsson, Jona Saemundsdottir, Daníel F. Guðbjartsson, Ólafur Þ. Magnússon, Gísli Másson, Unnur Þorsteinsdóttir, Agnar Helgason, Hákon Jónsson, Patrick Sulem, Kāri Stefánsson - Nature 2022 cited by 490
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Authors: Jonas B. Nielsen, Rósa B. Þórólfsdóttir, Lars G. Fritsche, Wei Zhou, Morten W. Skov, Sarah E. Graham, Todd J. Herron, Shane McCarthy, Ellen M. Schmidt, Garðar Sveinbjörnsson, Ida Surakka, Michael R. Mathis, Masatoshi Yamazaki, Ryan Crawford, Maiken E. Gabrielsen, Anne Heidi Skogholt, Oddgeir L. Holmen, Maoxuan Lin, Brooke N. Wolford, Rounak Dey, Håvard Dalen, Patrick Sulem, Jonathan H. Chung, Joshua Backman, Davíð O. Arnar, Unnur Þorsteinsdóttir, Aris Baras, Colm O’Dushlaine, Anders G. Holst, Xiaoquan Wen, Whitney Hornsby, Frederick E. Dewey, Michael Boehnke, Sachin Kheterpal, Bhramar Mukherjee, Seunggeun Lee, Hyun Min Kang, Hilma Hólm, Jacob O. Kitzman, Jordan A. Shavit, José Jalife, Chad M. Brummett, Tanya M. Teslovich, David J. Carey, Daníel F. Guðbjartsson, Kāri Stefánsson, Gonçalo R. Abecasis, Kristian Hveem, Cristen J. Willer - Nature Genetics 2018 cited by 936
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Authors: Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, Valentina Escott‐Price, Stephan Ripke, Noa Carrera, Sophie E. Legge, Sophie Bishop, Darren Cameron, Marian L. Hamshere, Jun Han, Leon Hubbard, Amy Lynham, Kiran K. Mantripragada, Elliott Rees, James H. MacCabe, Steven A. McCarroll, Bernhard T. Baune, Gerome Breen, Enda M. Byrne, Udo Dannlowski, Thalia C. Eley, Caroline Hayward, Nicholas G. Martin, Andrew M. McIntosh, Robert Plomin, David J. Porteous, Naomi R. Wray, Armando Caballero, Daniel H. Geschwind, Laura M. Huckins, Douglas M. Ruderfer, Enrique Santiago, Pamela Sklar, Eli A. Stahl, Hyejung Won, Esben Agerbo, Thomas D. Als, Ole A. Andreassen, Marie Bækvad‐Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D. Børglum, Jonas Bybjerg‐Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, В. Е. Голимбет, Jakob Grove, David M. Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejović-Milovančević, Engilbert Sigurðsson, Teimuraz Silagadze, Christine Søholm Hansen, Kāri Stefánsson, Hreinn Stefánsson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David Collier, Dan Rujescu, George Kirov, Michael J. Owen, Michael O‘Donovan, James Walters - Nature Genetics 2018 cited by 1,728
- Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Authors: Thomas D. Als, Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko, Trine Tollerup Nielsen, Joonas Naamanka, Kumar Veerapen, Daniel F. Levey, Jaroslav Bendl, Jonas Bybjerg‐Grauholm, Biao Zeng, Ditte Demontis, Anders Rosengren, Georgios Athanasiadis, Marie Bækved-Hansen, Per Qvist, G. Bragi Walters, Thorgeir E. Thorgeirsson, Hreinn Stefánsson, Katherine L. Musliner, Veera M. Rajagopal, Leila Farajzadeh, Janne Pia Thirstrup, Bjarni J. Vilhjálmsson, John J. McGrath, Manuel Mattheisen, Sandra Meier, Esben Agerbo, Kāri Stefánsson, Merete Nordentoft, Thomas Werge, David M. Hougaard, Preben Bo Mortensen, Murray B. Stein, Joel Gelernter, Iiris Hovatta, Panos Roussos, Mark J. Daly, Ole Mors, Aarno Palotie, Anders D. Børglum - Nature Medicine 2023 cited by 305
- Brain age prediction using deep learning uncovers associated sequence variants
Authors: Benedikt A. Jónsson, Gyða Björnsdóttir, Thorgeir E. Thorgeirsson, Lotta M. Ellingsen, G. Bragi Walters, Daníel F. Guðbjartsson, Hreinn Stefánsson, Kāri Stefánsson, Magnús Ö. Úlfarsson - Nature Communications 2019 cited by 413
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Authors: Mike A. Nalls, 23andMe, GenePD, The Ashkenazi Jewish Dataset Investigator, Alzheimer Genetic Analysis Group, Nathan Pankratz, Christina M. Lill, Chuong B Do, Dena G. Hernandez, Mohamad Saad, Anita L. DeStefano, Eleanna Kara, José Brás, Manu Sharma, Claudia Schulte, Margaux F. Keller, Sampath Arepalli, Christopher T. Letson, Connor Edsall, Hreinn Stefánsson, Xinmin Liu, Hannah A. Pliner, Joseph H. Lee, Rong Cheng, M. Arfan Ikram, John P. A. Ioannidis, Georgios M. Hadjigeorgiou, Joshua C Bis, María Martínez, Joel S. Perlmutter, Alison Goate, Karen Marder, Brian Fiske, Margaret Sutherland, Georgia Xiromerisiou, Richard H. Myers, Lorraine N. Clark, Kāri Stefánsson, John Hardy, Peter Heutink, Honglei Chen, Nicholas Wood, Henry Houlden, Haydeh Payami, Alexis Brice, William K. Scott, Thomas Gasser, Lars Bertram, Nicholas Eriksson, Tatiana Foroud, Andrew Singleton - Nature Genetics 2014 cited by 1,964
- The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Authors: Nilüfer Rahmioğlu, Sally Mortlock, Marzieh Ghiasi, Peter Möller, Lilja Stefánsdóttir, Geneviève Galarneau, Constance Turman, Rebecca Danning, Matthew H. Law, Yadav Sapkota, Paraskevi Christofidou, Sini Skarp, Ayush Giri, Karina Banasik, Michał Krassowski, Maarja Lepamets, Błażej Marciniak, Margit Nõukas, Danielle Perro, Eeva Sliz, Marta Sobalska‐Kwapis, Guðmar Þorleifsson, Nura F. Topbas-Selcuki, Allison F. Vitonis, David Westergaard, Ragnheidur Arnadottir, Kristoffer Sølvsten Burgdorf, Archie Campbell, Cecilia S. K. Cheuk, Caterina Clementi, James P. Cook, Immaculata De Vivo, Amy D. DiVasta, O Dorien, Jacqueline F. Donoghue, Todd L. Edwards, Pierre Fontanillas, Jenny N. Fung, Reynir Tómas Geirsson, Jane E. Girling, Paivi Harkki, Holly R. Harris, Martin Healey, Oskari Heikinheimo, Sarah J. Holdsworth‐Carson, Isabel C. Hostettler, Henry Houlden, Sahar Houshdaran, Juan C. Irwin, Marjo‐Riitta Järvelin, Yoichiro Kamatani, Stephen Kennedy, Ewa Kępka, Johannes Kettunen, Michiaki Kubo, Bartosz Kulig, Venla Kurra, Hannele Laivuori, Marc R. Laufer, Cecilia M. Lindgren, Stuart MacGregor, Massimo Mangino, Nicholas G. Martin, Charoula Matalliotaki, Michail Matalliotakis, Alison D. Murray, Anne Ndungu, Camran Nezhat, Catherine M. Olsen, Jessica Opoku‐Anane, Sandosh Padmanabhan, Manish Paranjpe, Maire Peters, Grzegorz Polak, David J. Porteous, Joseph T. Rabban, Kathryn M. Rexrode, Hanna Romanowicz, Merli Saare, Liisu Saavalainen, Andrew J. Schork, Sushmita Sen, Amy L. Shafrir, Anna Siewierska-Górska, Marcin Słomka, Blair H. Smith, Beata Smolarz, Tomasz Szaflik, Krzysztof Szyłło, Atsushi Takahashi, Kathryn L. Terry, Carla Tomassetti, Susan A. Treloar, Arne Vanhie, Katy Vincent, Kim Chi Vo, David J. Werring, Eleftheria Zeggini, Maria I. Zervou, Kāri Stefánsson and 48 more - Nature Genetics 2023 cited by 287
- Rate of de novo mutations and the importance of father’s age to disease risk
Authors: Augustine Kong, Michael L. Frigge, Gísli Másson, Søren Besenbacher, Patrick Sulem, Gísli Magnússon, Sigurjón A. Guðjónsson, Ásgeir Sigurðsson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Wendy S.W. Wong, Gunnar Sigurðsson, G. Bragi Walters, Stacy Steinberg, Hannes Helgason, Guðmar Þorleifsson, Daníel F. Guðbjartsson, Agnar Helgason, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature 2012 cited by 2,273
- Multiomics study of nonalcoholic fatty liver disease
Authors: Garðar Sveinbjörnsson, Magnús Ö. Úlfarsson, Rósa B. Þórólfsdóttir, Benedikt A. Jónsson, Eyþór Einarsson, Gylfi Gunnlaugsson, Sölvi Rögnvaldsson, Davíð O. Arnar, Magnús Baldvinsson, Ragnar Bjarnason, Thjodbjorg Eiriksdottir, Christian Erikstrup, Egil Ferkingstad, Gísli H. Halldórsson, Hannes Helgason, Anna Helgadóttir, Lotte Hindhede, Grimur Hjörleifsson, David A. Jones, Kirk U. Knowlton, Sigrún H. Lund, Páll Melsted, Kristján Norland, Ísleifur Ólafsson, Sigurður Ólafsson, Gudjon R. Oskarsson, Sisse Rye Ostrowski, Ole Birger Pedersen, Auðunn Skúta Snæbjarnarson, Emil Sigurdsson, Valgerður Steinthórsdóttir, Michael Schwinn, Guðmundur Þorgeirsson, Guðmar Þorleifsson, Ingileif Jónsdóttir, Henning Bundgaard, Lincoln Nadauld, Einar S. Björnsson, Ingrid C. Rulifson, Þórunn Rafnar, Gudmundur L. Norddahl, Unnur Þorsteinsdóttir, Patrick Sulem, Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson - Nature Genetics 2022 cited by 229
- Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly
Authors: Florian Zink, Simon Stacey, Gudmundur L. Norddahl, Michael L. Frigge, Ólafur Þ. Magnússon, Ingileif Jónsdóttir, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Sigurjón A. Guðjónsson, Jūlı́us Guðmundsson, Jón G. Jónasson, Laufey Tryggvadóttír, Þorvaldur Jónsson, Agnar Helgason, Arnaldur Gylfason, Patrick Sulem, Þórunn Rafnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Gísli Másson, Augustine Kong, Kāri Stefánsson - Blood 2017 cited by 789
- A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
Authors: Thorlákur Jónsson, Jasvinder K. Atwal, Stacy Steinberg, Jón Snædal, Pálmi V. Jónsson, Sigurbjörn Björnsson, Hreinn Stefánsson, Patrick Sulem, Daníel F. Guðbjartsson, Janice Maloney, Kwame Hoyte, Amy Gustafson, Yichin Liu, Yanmei Lu, Tushar Bhangale, Robert Graham, Johanna Huttenlocher, Gyða Björnsdóttir, Ole A. Andreassen, Erik G. Jönsson, Aarno Palotie, Timothy W. Behrens, Ólafur Þ. Magnússon, Augustine Kong, Unnur Þorsteinsdóttir, Ryan J. Watts, Kāri Stefánsson - Nature 2012 cited by 1,745
- Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Authors: Heidi Hautakangas, Bendik S. Winsvold, Sanni Ruotsalainen, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman, Laurent F. Thomas, Raymond Noordam, Christian Benner, Padhraig Gormley, Ville Artto, Karina Banasik, Anna Bjornsdottir, Dorret I. Boomsma, Ben Brumpton, Kristoffer Sølvsten Burgdorf, Julie E. Buring, Mona Ameri Chalmer, Irene de Boer, Martin Dichgans, Christian Erikstrup, Markus Färkkilä, Maiken Elvestad Garbrielsen, Mohsen Ghanbari, Knut Hagen, Paavo Häppölä, Jouke‐Jan Hottenga, Maria Gudlaug Hrafnsdottir, Kristian Hveem, Marianne Bakke Johnsen, Mika Kähönen, Espen Saxhaug Kristoffersen, Tobias Kurth, Terho Lehtimäki, Lannie Lighart, Sigurður H. Magnússon, Rainer Malik, Ole Birger Pedersen, Nadine Pelzer, Brenda W.J.H. Penninx, Caroline Ran, Paul M. Ridker, Frits R. Rosendaal, Gudrun R. Sigurdardottir, Anne Heidi Skogholt, Ólafur Sveinsson, Thorgeir E. Thorgeirsson, Henrik Ullum, Lisanne S. Vijfhuizen, Elisabeth Widén, Ko Willems van Dijk, Irene de Boer, Arn M. J. M. van den Maagdenberg, HUNT All-in Headache, Danish Blood Donor Study Genomic Cohort, Arpo Aromaa, Andrea Carmine Belin, Tobias Freilinger, M. Arfan Ikram, Marjo‐Riitta Järvelin, Olli T. Raitakari, Gisela M. Terwindt, Mikko Kallela, Maija Wessman, Jes Olesen, Daniel I. Chasman, Dale R. Nyholt, Hreinn Stefánsson, Kāri Stefánsson, Arn M. J. M. van den Maagdenberg, Thomas Folkmann Hansen, Samuli Ripatti, John‐Anker Zwart, Aarno Palotie, Matti Pirinen - Nature Genetics 2022 cited by 395
- Parental influence on human germline de novo mutations in 1,548 trios from Iceland
Authors: Hákon Jónsson, Patrick Sulem, Birte Kehr, Snædís Kristmundsdóttir, Florian Zink, Eirikur Hjartarson, Marteinn T. Hardarson, Kristján Eldjárn Hjörleifsson, Hannes P. Eggertsson, Sigurjón A. Guðjónsson, Lucas D. Ward, Gudny A. Arnadottir, Einar A. Helgason, Hannes Helgason, Arnaldur Gylfason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Þórunn Rafnar, Mike Frigge, Simon Stacey, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Bjarni V. Halldórsson, Agnar Helgason, Daníel F. Guðbjartsson, Kāri Stefánsson - Nature 2017 cited by 670
- Characterizing mutagenic effects of recombination through a sequence-level genetic map
Authors: Bjarni V. Halldórsson, Gunnar Pálsson, Ólafur Andri Stefánsson, Hákon Jónsson, Marteinn T. Hardarson, Hannes P. Eggertsson, Bjarni Gunnarsson, Ásmundur Oddsson, Gísli H. Halldórsson, Florian Zink, Sigurjón A. Guðjónsson, Michael L. Frigge, Guðmar Þorleifsson, Ásgeir Sigurðsson, Simon Stacey, Patrick Sulem, Gísli Másson, Agnar Helgason, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Kāri Stefánsson - Science 2019 cited by 423
- Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
Authors: Dongmei Yu, Jae Hoon Sul, Fotis Tsetsos, Muhammad Sulaman Nawaz, Alden Y. Huang, Ivette Zelaya, Cornelia Illmann, Lisa Osiecki, Sabrina M. Darrow, Matthew E. Hirschtritt, Erica Greenberg, Kirsten Müller‐Vahl, Manfred Stuhrmann, Yves Dion, Guy A. Rouleau, H.N. Aschauer, M. Stamenković, Monika Schlögelhofer, Paul Sandor, Cathy L. Barr, Marco A. Grados, Harvey S. Singer, Markus M. Nöthen, Johannes Hebebrand, Anke Hinney, Robert A. King, Thomas Fernandez, Csaba Barta, Zsanett Tárnok, Péter Nagy, Christel Depienne, Yulia Worbe, Andreas Hartmann, Cathy L. Budman, Renata Rizzo, Gholson J. Lyon, William M. McMahon, James R. Batterson, Daniëlle C. Cath, Irene A. Malaty, Michael S. Okun, Cheston M. Berlin, Douglas W. Woods, Paul C. Lee, Joseph Jankovic, Mary M. Robertson, Donald L. Gilbert, Lawrence W. Brown, Barbara Coffey, Andrea Dietrich, Pieter J. Hoekstra, Samuel Kuperman, Samuel H. Zinner, Pétur Lúðvígsson, Evald Sæmundsen, Ólafur Thorarensen, Gil Atzmon, Nir Barzilai, Michael Wagner, Rainald Moessner, Roel A. Ophoff, Carlos N. Pato, Michele T. Pato, James A. Knowles, Joshua L. Roffman, Jordan W. Smoller, Randy L. Buckner, A. Jeremy Willsey, Jay A. Tischfield, Gary A. Heiman, Hreinn Stefánsson, Kāri Stefánsson, Daniëlle Posthuma, Nancy J. Cox, David L. Pauls, Nelson B. Freimer, Benjamin M. Neale, Lea K. Davis, Peristera Paschou, Giovanni Coppola, Carol A. Mathews, Jeremiah M. Scharf - American Journal of Psychiatry 2019 cited by 443
- Genetic predisposition to mosaic Y chromosome loss in blood
Authors: Deborah J. Thompson, The Kidney Cancer GWAS Meta-Analysis Project, Giulio Genovese, Jonatan Halvardson, Jacob C. Ulirsch, Daniel J. Wright, Chikashi Terao, Olafur B. Davidsson, Felix R. Day, Patrick Sulem, Yunxuan Jiang, Marcus Danielsson, Hanna Davies, Joe Dennis, Malcolm G. Dunlop, Douglas F. Easton, Victoria A. Fisher, Florian Zink, Richard S. Houlston, Martin Ingelsson, Siddhartha Kar, Nicola D. Kerrison, Ben Kinnersley, Ragnar P. Kristjansson, Philip Law, Rong Li, Chey Loveday, Jonas Mattisson, Steven A. McCarroll, Yoshinori Murakami, Anna Murray, Paweł Olszewski, Edyta Rychlicka-Buniowska, Robert A. Scott, Unnur Þorsteinsdóttir, Ian Tomlinson, Behrooz Torabi Moghadam, Clare Turnbull, Nicholas J. Wareham, Daníel F. Guðbjartsson, Yoichiro Kamatani, Eva R. Hoffmann, Steve P. Jackson, Kāri Stefánsson, Adam Auton, Ken K. Ong, Mitchell J. Machiela, Po‐Ru Loh, Jan P. Dumanski, Stephen J. Chanock, Lars A. Forsberg, John R. B. Perry - Nature 2019 cited by 342
