Anna Helgadóttir

2004–2025 年に発表

別表記
Anna Helgadottir
68
論文数
20,255
被引用数
51
h 指数
65
i10 指数

被引用数

Anna Helgadóttir の年別被引用数1974 年: 被引用 1 件1982 年: 被引用 1 件1986 年: 被引用 1 件1998 年: 被引用 1 件2000 年: 被引用 1 件2002 年: 被引用 1 件2004 年: 被引用 18 件2005 年: 被引用 32 件2006 年: 被引用 86 件2007 年: 被引用 139 件2008 年: 被引用 178 件2009 年: 被引用 260 件2010 年: 被引用 289 件2011 年: 被引用 248 件2012 年: 被引用 255 件2013 年: 被引用 212 件2014 年: 被引用 175 件2015 年: 被引用 168 件2016 年: 被引用 138 件2017 年: 被引用 158 件2018 年: 被引用 119 件2019 年: 被引用 329 件2020 年: 被引用 401 件2021 年: 被引用 462 件2022 年: 被引用 460 件2023 年: 被引用 461 件2024 年: 被引用 772 件2025 年: 被引用 394 件2026 年: 被引用 40 件1975〜1981 年は被引用が無いため表示していません1983〜1985 年は被引用が無いため表示していません1987〜1997 年は被引用が無いため表示していません1999 年は被引用が無いため表示していません2001 年は被引用が無いため表示していません2003 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,562 件、この内訳の 21.4%イギリス: 引用元論文 1,166 件、この内訳の 9.8%中国: 引用元論文 843 件、この内訳の 7%ドイツ: 引用元論文 664 件、この内訳の 5.6%オランダ: 引用元論文 525 件、この内訳の 4.4%カナダ: 引用元論文 486 件、この内訳の 4.1%スウェーデン: 引用元論文 449 件、この内訳の 3.8%イタリア: 引用元論文 411 件、この内訳の 3.4%オーストラリア: 引用元論文 378 件、この内訳の 3.2%フランス: 引用元論文 338 件、この内訳の 2.8%デンマーク: 引用元論文 328 件、この内訳の 2.7%フィンランド: 引用元論文 299 件、この内訳の 2.5%
0%21.4%その他 29.3%

分野

  • Biochemistry, Genetics and Molecular Biology46.7%
  • Medicine42.4%
  • Immunology and Microbiology4.4%
  • Neuroscience2.3%
  • Nursing0.9%
  • Computer Science0.8%
  • その他2.5%

トピック

  • Genetic Associations and Epidemiology11.1%
  • Lipoproteins and Cardiovascular Health2.3%
  • Genetic Mapping and Diversity in Plants and Animals2.2%
  • Bioinformatics and Genomic Networks2.1%
  • Pancreatic function and diabetes1.9%
  • Epigenetics and DNA Methylation1.9%
  • その他78.5%

共著者

全論文

検索で開く
  1. The power of genetic diversity in genome-wide association studies of lipids

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Masato Akiyama, Saori Sakaue, Chikashi Terao, Masahiro Kanai, Wei Zhou, Ben Brumpton, Humaira Rasheed, Sanni Ruotsalainen, Aki S. Havulinna, Yogasudha Veturi, QiPing Feng, Elisabeth A. Rosenthal, Todd Lingren, Jennifer A. Pacheco, Sarah A. Pendergrass, Jeffrey Haessler, Franco Giulianini, Yuki Bradford, Jason E. Miller, Archie Campbell, Kuang Lin, Iona Y. Millwood, George Hindy, Asif Rasheed, Jessica D. Faul, Wei Zhao, David R. Weir, Constance Turman, Hongyan Huang, Mariaelisa Graff, Anubha Mahajan, Michael R. Brown, Weihua Zhang, Ketian Yu, Ellen M. Schmidt, Anita Pandit, Stefan Gustafsson, Xianyong Yin, Jian’an Luan, Jing-Hua Zhao, Fumihiko Matsuda, Hye-Mi Jang, Kyungheon Yoon, Carolina Medina‐Gómez, Achilleas Pitsillides, Jouke‐Jan Hottenga, Gonneke Willemsen, Andrew R. Wood, Yingji Ji, Zishan Gao, Simon Haworth, Ruth E. Mitchell, Jin Fang Chai, Mette Aadahl, Jie Yao, Ani Manichaikul, Helen R. Warren, Julia Ramírez, Jette Bork‐Jensen, Line Lund Kårhus, Anuj Goel, Maria Sabater‐Lleal, Raymond Noordam, Carlo Sidore, Edoardo Fiorillo, Aaron F. McDaid, Pedro Marques‐Vidal, Matthias Wielscher, Stella Trompet, Naveed Sattar ほか 427 名 - Nature 2021 被引用: 1,079

  2. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 706

  3. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Graciela E. Delgado, Spiros Denaxas, Alex S. F. Doney, Marcus Dörr, Samuel C. Dudley, Michael E. Dunn, Gunnar Engström, Tõnu Esko, Stephan B. Felix, Chris Finan, Ian Ford, Mohsen Ghanbari, Sahar Ghasemi, Vilmantas Giedraitis, Franco Giulianini, John S. Gottdiener, Stefan Groß, Daníel F. Guðbjartsson, Rebecca Gutmann, Christopher M. Haggerty, Pim van der Harst, Craig Hyde, Erik Ingelsson, J. Wouter Jukema, Maryam Kavousi, Kay‐Tee Khaw, Marcus E. Kleber, Lars Køber, Andrea Koekemoer, Claudia Langenberg, Lars Lind, Cecilia M. Lindgren, Barry London, Luca A. Lotta, Ruth C. Lovering, Jian’an Luan, Patrik K. E. Magnusson, Anubha Mahajan, Kenneth B. Margulies, Winfried März, Olle Melander, Ify Mordi, Thomas M. Morgan, Andrew D. Morris, Andrew P. Morris, Alanna C. Morrison, Michael W. Nagle, Christopher P. Nelson, Alexander Niessner, Teemu Niiranen, Michelle L. O’Donoghue, Anjali Owens, Colin N. A. Palmer, Helen Parry, Markus Perola, Eliana Portilla-Fernández, Bruce M. Psaty, Goncalo Abecasis, Joshua Backman, Xiaodong Bai, Suganthi Balasubramanian, Nilanjana Banerjee, Aris Baras, Leland Barnard, Christina Beechert, Andrew Blumenfeld, Michael Cantor, Yating Chai, Jonathan Chung, Giovanni Coppola ほか 103 名 - Nature Communications 2020 被引用: 929

  4. Multiomics study of nonalcoholic fatty liver disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 229

  5. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2006 被引用: 2,279

  6. Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alex Hørby Christensen, Susan Mikkelsen, Rikke Louise Jacobsen, Joseph Dowsett, Ole Birger Pedersen, Christian Erikstrup, Sisse Rye Ostrowski, Christopher J. O’Donnell, Matthew J. Budoff, Vilmundur Guðnason, Wendy S. Post, Jerome I. Rotter, Mark Lathrop, Henning Bundgaard, Bengt Johansson, Johan Ljungberg, Ulf Näslund, Thierry Le Tourneau, J. G. Smith, Quinn S. Wells, Stefan Söderberg, Kāri Stefánsson, Jean‐Jacques Schott, Daniel J. Rader, Robert Clarke, James C. Engert, George Thanassoulis - European Heart Journal 2023 被引用: 112

  7. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jessica D. Faul, Eric B. Fauman, Cristiano Fava, Teresa Ferreira, Christopher N. Foley, Nora Franceschini, He Gao, Olga Giannakopoulou, Franco Giulianini, Daníel F. Guðbjartsson, Xiuqing Guo, Sarah E. Harris, Aki S. Havulinna, Anna Helgadóttir, Jennifer E. Huffman, Shih‐Jen Hwang, Stavroula Kanoni, Jukka Kontto, Martin G. Larson, Ruifang Li‐Gao, Jaana Lindström, Luca A. Lotta, Yingchang Lu, Jian’an Luan, Anubha Mahajan, Giovanni Malerba, Nicholas G. D. Masca, Hao Mei, Cristina Menni, Dennis O. Mook‐Kanamori, David Mosén-Ansorena, Martina Müller‐Nurasyid, Guillaume Paré, Dirk S. Paul, Markus Perola, Alaitz Poveda, Rainer Rauramaa, Melissa A. Richard, Tom G. Richardson, Nuno Sepúlveda, Xueling Sim, Albert V. Smith, Jennifer A. Smith, James R Staley, Alena Stanáková, Patrick Sulem, Sébastien Thériault, Unnur Þorsteinsdóttir, Stella Trompet, Tibor V. Varga, Digna R. Velez Edwards, Giovanni Veronesi, Stefan Weiß, Sara M. Willems, Jie Yao, Robin Young, Bing Yu, Weihua Zhang, Jinghua Zhao, Wei Zhao, Wei Zhao, Εvangelos Εvangelou, Stefanie Aeschbacher, Eralda Asllanaj, Stefan Blankenberg, Lori L. Bonnycastle, Jette Bork‐Jensen, Ivan Brandslund, Peter S. Braund, Stephen Burgess ほか 212 名 - Nature Genetics 2020 被引用: 239

  8. Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hrefna Johannsdottir, Ingileif Jónsdóttir, Thorhildur Juliusdottir, Noor Kalsheker, A. K. Kasimov, John P. Kemp, Katja Kivinen, Kari Klungsøyr, Wai Lee, Mads Melbye, Zosia Miedzybrodska, Ashley Moffett, Dilbar Najmutdinova, Firuza Nishanova, Thorunn A. Olafsdottir, Markus Perola, Fiona Broughton Pipkin, Lucilla Poston, Gordon Prescott, Saedís Saevarsdóttir, Damilya Salimbayeva, Paula J. Scaife, Line Skotte, Eleonora Staines-Urias, Ólafur Andri Stefánsson, Karina Meden Sørensen, Liv Cecilie Vestrheim Thomsen, Vinicius Tragante, Lill Trogstad, Nigel Simpson, Hannele Laivuori, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Linda Morgan, Fiona Broughton Pipkin, Noor Kalsheker, James J. Walker, Sheila Macphail, Mark D. Kilby, Marwan Habiba, Catherine Williamson, Kevin M. O’Shaughnessy, Shaughn O’Brien, Alan C. Cameron, Christopher W.G. Redman, Martin Farrall, Mark J. Caulfield, Anna F. Dominiczak, Tamara Aripova, Juan P. Casas, Anna F. Dominiczak, James J. Walker, Unnur Þorsteinsdóttir, Ann‐Charlotte Iversen, Bjarke Feenstra, Debbie A. Lawlor, Heather A. Boyd, Per Magnus, Hannele Laivuori, Nodira Zakhidova, Gulnara Svyatova, Kāri Stefánsson, Linda Morgan - Nature Communications 2020 被引用: 193

  9. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Patrick Sulem, Unnur Þorsteinsdóttir, Hilma Hólm, Daníel F. Guðbjartsson, Kāri Stefánsson - JAMA 2023 被引用: 114

  10. Variants conferring risk of atrial fibrillation on chromosome 4q25

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eric E. Smith, Jonathan Rosand, Jan Hillert, Ronald C.W., Patrick T. Ellinor, Guðmundur Þorgeirsson, Jeffrey R. Gulcher, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature 2007 被引用: 960

  11. Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kāri Stefánsson - Nature Genetics 2023 被引用: 69

  12. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Daníel F. Guðbjartsson, Hilma Hólm, Kāri Stefánsson - Nature Genetics 2016 被引用: 265

  13. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hilma Hólm, Kāri Stefánsson - Journal of the American College of Cardiology 2019 被引用: 221

  14. VariantASGR1Associated with a Reduced Risk of Coronary Artery Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Williams, André M. van Rij, Gregory T. Jones, Riyaz Patel, Allan I. Levey, Salim S. Hayek, Svati H. Shah, Muredach P. Reilly, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ísleifur Ólafsson, Lambertus A. Kiemeney, Arshed A. Quyyumi, Daniel J. Rader, William E. Kraus, Nilesh J. Samani, Oluf Pedersen, Guðmundur Þorgeirsson, Gísli Másson, Hilma Hólm, Daníel F. Guðbjartsson, Patrick Sulem, Unnur Þorsteinsdóttir, Kāri Stefánsson - New England Journal of Medicine 2016 被引用: 191

  15. Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lambertus A. Kiemeney, Oluf Pedersen, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2008 被引用: 1,405

  16. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thorsten Kessler, Ling Li, Lijiang Ma, Thomas Meitinger, Sören Mucha, Matthias Munz, Federico Murgia, Jonas B. Nielsen, Markus M. Nöthen, Shichao Pang, Tobias Reinberger, Guðmar Þorleifsson, Moritz von Scheidt, Jacob K Ulirsch, Biobank Japan, Davíð O. Arnar, Deepak Atri, Noël P. Burtt, Maria C. Costanzo, Jason Flannick, Rajat M. Gupta, 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, Jeanette Erdmann, Nilesh J. Samani, Heribert Schunkert, Hugh Watkins, Cristen J. Willer, Panos Deloukas, Sekar Kathiresan, Adam S. Butterworth - medRxiv 2021 被引用: 69

  17. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Unnur Unnsteinsdóttir, G. Bragi Walters, Florian Zink, Linn Rødevand, Ole A. Andreassen, Jannicke Igland, Rolv T. Lie, Jan Haavik, Karina Banasik, Søren Brunak, Maria Didriksen, Mie Topholm Bruun, Christian Erikstrup, Lisette J. A. Kogelman, Kaspar René Nielsen, Erik Sørensen, Ole Birger Pedersen, Henrik Ullum, Jakob Thaning Bay, Jens Kjærgaard Boldsen, Thorsten Brodersen, Kristoffer Sølvsten Burgdorf, Khoa Manh Dinh, Joseph Dowsett, Bjarke Feenstra, Frank Geller, Lotte Hindhede, Henrik Hjalgrim, Rikke Louise Jacobsen, Gregor B. E. Jemec, Katrine Kaspersen, Bertram D. Kjerulf, Margit Anita Hørup Larsen, Ioannis Louloudis, Agnete Troen Lundgaard, Susan Mikkelsen, Christina Mikkelsen, Janna Nissen, Mette Nyegaard, Alexander Pil Henriksen, Palle Duun Rohde, Klaus Rostgaard, Michael Swinn, Lise Wegner Thørner, Mie Topholm Bruun, Thomas Werge, David Westergaard, Gísli Másson, Unnur Þorsteinsdóttir, Jes Olesen, Pétur Lúðvígsson, Ólafur Thorarensen, Anna Bjornsdottir, Gudrun R. Sigurdardottir, Ólafur Sveinsson, Sisse Rye Ostrowski, Hilma Hólm, Daníel F. Guðbjartsson, Guðmar Þorleifsson, Patrick Sulem, Hreinn Stefánsson, Thorgeir E. Thorgeirsson, Thomas Folkmann Hansen, Kāri Stefánsson - Nature Genetics 2023 被引用: 55

  18. Genetics of gene expression and its effect on disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jeffrey R. Gulcher, Marc L. Reitman, Augustine Kong, Eric E. Schadt, Kāri Stefánsson - Nature 2008 被引用: 1,347

  19. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maria Samuel, John Danesh, Danish Saleheen, John C Chambers, Paul Elliott, Weihua Zhang, Weihua Zhang, John C Chambers, Jaspal S. Kooner, Mark Lathrop, Jörg Hager, Simon Heath, Marc Délepine, Kathy Stirrups, Leena Peltonen, Nicole Soranzo, Panos Deloukas, Muhammed Murtaza, Paul Elliott, John Öhrvik, Lasse Folkersen, Angela Silveira, Ferdinand M van 't Hooft, Rona J. Strawbridge, Anders Mälarstig, Per Eriksson, Anders Hamsten, John Öhrvik, Lasse Folkersen, Angela Silveira, Ferdinand M. van’t Hooft, Rona J. Strawbridge, Anders Mälarstig, Per Eriksson, Anders Hamsten, James Scott, Jaspal S. Kooner, Joban Sehmi, Rhian Gwilliam, Sarah Hunt, Sarah Edkins, Emma Gray, Suzannah Bumpstead, Simon Potter, Ann‐Christine Syvänen, Tomas Axelsson, Anders Franco-Cereceda, Anders Gabrielsen, Udo Seedorf, Stephan Rust, Gerd Assmann, Gonçalo R. Abecasis, Nabeel Ahmed, Angad S. Kooner, Mark J. Caulfield, Mark I. McCarthy, Peter Donnelly, Peter Donnelly, Philippe Froguel, Mark I McCarthy, Mark I McCarthy, N. J. Samani, N. J. Samani, Mai‐Lis Hellénius, Gunnar Olsson, Gunnar Olsson, Gianni Tognoni, Simona Barlera, Maria Grazia Franzosi, F. Gori ほか 32 名 - Nature Genetics 2011 被引用: 686

  20. Actionable Genotypes and Their Association with Life Span in Iceland

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jona Saemundsdottir, Ólafur Þ. Magnússon, Gísli Másson, Bjarni V. Halldórsson, Agnar Helgason, Hreinn Stefánsson, Ingileif Jónsdóttir, Hilma Hólm, Þórunn Rafnar, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson, Patrick Sulem - New England Journal of Medicine 2023 被引用: 56

  21. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Boonen, Dorota Włoch-Kopeć, Valerie Valant, Julia Slark, Karen L. Furie, Hossein Delavaran, Cordelia Langford, Panos Deloukas, Sarah Edkins, Sarah Hunt, Emma Gray, Serge Dronov, Leena Peltonen, Sólveig Grétarsdóttir, Gudmar Thorleifsson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Giorgio B. Boncoraglio, Eugenio Parati, John Attia, Elizabeth Holliday, Christopher Levi, Maria-Grazia Franzosi, Anuj Goel, Anna Helgadóttir, Jenefer M. Blackwell, Elvira Bramon, Matthew A. Brown, Juan P. Casas, Aiden Corvin, Audrey Duncanson, Janusz Jankowski, Christopher G. Mathew, Colin N A Palmer, Robert Plomin, Anna Rautanen, Stephen Sawcer, Richard C. Trembath, Ananth C. Viswanathan, Nicholas Wood, Bradford B. Worrall, Steven J. Kittner, Braxton D. Mitchell, Brett Kissela, James F. Meschia, Vincent Thijs, Arne Lindgren, Mary Joan MacLeod, Agnieszka Słowik, James Walters, Jonathan Rosand, Pankaj Sharma, Martin Farrall, Cathie Sudlow, Peter M. Rothwell, Martin Dichgans, Peter Donnelly, Hugh S. Markus - Nature Genetics 2012 被引用: 420

  22. Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2018 被引用: 155

  23. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jakob Werner Hansen, Vibeke Backer, Thomas Werge, Christer Janson, Ulla‐Britt Jönsson, Maggie Ng, Juliana C.N. Chan, Wing Yee So, Ronald C.W., Svati H. Shah, Christopher B. Granger, Arshed A. Quyyumi, Allan I. Levey, Viola Vaccarino, Muredach P. Reilly, Daniel J. Rader, Michael Williams, André M. van Rij, Gregory T. Jones, Elisabetta Trabetti, Giovanni Malerba, Pier Franco Pignatti, Attilio Boner, Lydia Pescollderungg, Domenico Girelli, Oliviero Olivieri, Nicola Martinelli, Björn R. Lúdvíksson, Dóra Lúðvíksdóttir, Guðmundur I. Eyjólfsson, Davíð O. Arnar, Guðmundur Þorgeirsson, Klaus A. Deichmann, Philip J. Thompson, Matthias Wjst, Ian P. Hall, Dirkje S. Postma, Þórarinn Gíslason, Jeffrey R. Gulcher, Augustine Kong, Ingileif Jónsdóttir, Unnur Þorsteinsdóttir, Kāri Stefánsson - Nature Genetics 2009 被引用: 762

  24. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Weang-Kee Ho, Joanna Pera, Robin Lemmens, Bo Norrving, Peter Higgins, Marianne Benn, Michèle M. Sale, Gregor Kuhlenbäumer, Alex S. F. Doney, Astrid M. Vicente, Hossein Delavaran, Ale Algra, Gail Davies, Sofia A. Oliveira, Colin N A Palmer, Ian J. Deary, Helena Schmidt, Massimo Pandolfo, Joan Montaner, Cara L. Carty, Paul I. W. de Bakker, Konstantinos Kostulas, José M. Ferro, Natalie R. van Zuydam, Einar Már Valdimarsson, Børge G. Nordestgaard, Arne Lindgren, Vincent Thijs, Agnieszka Słowik, Danish Saleheen, Guillaume Paré, Klaus Berger, Guðmar Þorleifsson, Albert Hofman, Thomas H. Mosley, Braxton D. Mitchell, Karen L. Furie, Robert Clarke, Christopher Levi, Sudha Seshadri, Andreas Gschwendtner, Giorgio B. Boncoraglio, Pankaj Sharma, Joshua C Bis, Sólveig Grétarsdóttir, Bruce M. Psaty, Peter M. Rothwell, Jonathan Rosand, James F. Meschia, Kāri Stefánsson, Martin Dichgans, Hugh S. Markus - The Lancet Neurology 2012 被引用: 487