David J. Porteous

Active 1981–2025

254
Papers
48,497
Citations
115
h-index
248
i10-index

Citations

Citations per year for David J. Porteous1978: 1 citations1979: 1 citations1982: 1 citations1984: 3 citations1985: 2 citations1986: 7 citations1987: 6 citations1988: 6 citations1989: 4 citations1990: 16 citations1991: 18 citations1992: 28 citations1993: 33 citations1994: 30 citations1995: 56 citations1996: 45 citations1997: 66 citations1998: 70 citations1999: 71 citations2000: 65 citations2001: 86 citations2002: 73 citations2003: 87 citations2004: 105 citations2005: 137 citations2006: 178 citations2007: 237 citations2008: 259 citations2009: 276 citations2010: 268 citations2011: 336 citations2012: 254 citations2013: 271 citations2014: 229 citations2015: 277 citations2016: 288 citations2017: 293 citations2018: 388 citations2019: 1,424 citations2020: 1,643 citations2021: 2,167 citations2022: 1,863 citations2023: 1,406 citations2024: 1,987 citations2025: 813 citations2026: 21 citations1980–1981: no citations, so these years are not shown1983: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,738 citing papers, 22% of this breakdownUnited Kingdom: 3,306 citing papers, 12.6% of this breakdownChina: 1,628 citing papers, 6.2% of this breakdownGermany: 1,479 citing papers, 5.7% of this breakdownNetherlands: 1,172 citing papers, 4.5% of this breakdownAustralia: 1,125 citing papers, 4.3% of this breakdownCanada: 1,036 citing papers, 4% of this breakdownSweden: 806 citing papers, 3.1% of this breakdownItaly: 776 citing papers, 3% of this breakdownFrance: 740 citing papers, 2.8% of this breakdownSpain: 603 citing papers, 2.3% of this breakdownNorway: 555 citing papers, 2.1% of this breakdown
0%22%Other 27.4%

Fields

  • Biochemistry, Genetics and Molecular Biology45.8%
  • Medicine32.9%
  • Neuroscience8.9%
  • Psychology4.4%
  • Immunology and Microbiology1.6%
  • Environmental Science1%
  • Other5.4%

Topics

  • Genetic Associations and Epidemiology7.8%
  • Epigenetics and DNA Methylation3.6%
  • Genetics and Neurodevelopmental Disorders2.1%
  • COVID-19 Clinical Research Studies1.8%
  • Bioinformatics and Genomic Networks1.7%
  • Tryptophan and brain disorders1.6%
  • Other81.4%

Coauthors

All papers

Open in search
  1. Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Enda M. Byrne, Stephan Ripke, Daniel J. Smıth, Patrick F. Sullivan, Naomi R. Wray, Gerome Breen, Cathryn M. Lewis, Andrew M. McIntosh - Nature Neuroscience 2019 cited by 2,796

  2. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joey W. Trampush, Shefali S. Verma, Yang Wu, Max Lam, Jing Hua Zhao, Zhili Zheng, Jason D. Boardman, Harry Campbell, Jeremy Freese, Kathleen Mullan Harris, Caroline Hayward, Pamela Herd, Meena Kumari, Todd Lencz, Jian’an Luan, Anil K. Malhotra, Andres Metspalu, Lili Milani, Ken K. Ong, John R. B. Perry, David J. Porteous, Marylyn D. Ritchie, Melissa Smart, Blair H. Smith, Joyce Y. Tung, Nicholas J. Wareham, James F. Wilson, Jonathan Beauchamp, Dalton Conley, Tõnu Esko, Steven F. Lehrer, Patrik K. E. Magnusson, Sven Oskarsson, Tune H. Pers, Matthew R. Robinson, Kevin Thom, Chelsea Watson, Christopher F. Chabris, Michelle N. Meyer, David Laibson, Jian Yang, Magnus Johannesson, Philipp Koellinger, Patrick Turley, Peter M. Visscher, Daniel J. Benjamin, David Cesarini - Nature Genetics 2018 cited by 2,846

  3. Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David A. Hinds, Karen E. Huber, Aaron Kleinman, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Joanna L. Mountain, Carrie A. M. Northover, Steven J. Pitts, J. Fah Sathirapongsasuti, Olga V. Sazonova, Janie F. Shelton, Suyash Shringarpure, Joyce Y. Tung, Vladimir Vacic, Catherine H. Wilson, Mark Alan Fontana, Tune H. Pers, Cornelius A. Rietveld, Guo‐Bo Chen, Valur Emilsson, S. Fleur W. Meddens, Joseph K. Pickrell, Kevin Thom, Pascal Timshel, Ronald de Vlaming, Abdel Abdellaoui, Tarunveer S. Ahluwalia, Jonas Bačelis, Clemens Baumbach, Gyða Björnsdóttir, J Brandsma, Maria Pina Concas, Jaime Derringer, Tessel E. Galesloot, Giorgia Girotto, Richa Gupta, Leanne M. Hall, Sarah E. Harris, Edith Hofer, Momoko Horikoshi, Jennifer E. Huffman, Kadri Kaasik, Ioanna Panagiota Kalafati, Robert Karlsson, Jari Lahti, Sven J. van der Lee, Christiaan de Leeuw, Penelope A. Lind, Karl‐Oskar Lindgren, Tian Liu, Massimo Mangino, Jonathan Marten, Evelin Mihailov, Michael Miller, Peter J. van der Most, Christopher Oldmeadow, Antony Payton, Natalia Pervjakova, Wouter J. Peyrot, Yong Qian, Olli T. Raitakari, Rico Rueedi, Erika Salvi, Börge Schmidt, Katharina E. Schraut, Jianxin Shi, Albert V. Smith, Raymond A. Poot, Beaté St Pourcain and 200 more - Nature Genetics 2022 cited by 689

  4. Long COVID burden and risk factors in 10 UK longitudinal studies and electronic health records

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Richard Croker, David Evans, Tom Ward, Jonathan Cockburn, Simon Davy, Krishnan Bhaskaran, Anna Schultze, Elizabeth Williamson, William Hulme, Helen McDonald, Laurie A. Tomlinson, Rohini Mathur, Rosalind M. Eggo, Kevin Wing, Angel Wong, Harriet Forbes, John Tazare, John Parry, Frank Hester, Sam Harper, Ian Douglas, Stephen Evans, Liam Smeeth, Ben Goldacre, Andrew Steptoe, David J. Porteous, Rosemary McEachan, Laurie A. Tomlinson, Ben Goldacre, Praveetha Patalay, George B. Ploubidis, Srinivasa Vittal Katikireddi, Kate Tilling, Christopher T. Rentsch, Nicholas J. Timpson, Nish Chaturvedi, Claire J. Steves - Nature Communications 2022 cited by 566

  5. Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ian J. Deary, Allan F. McRae, Peter M. Visscher - Genome Medicine 2019 cited by 512

  6. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Genetic mechanisms of critical illness in COVID-19

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chenqing Zheng, Graeme R. Grimes, Rupert Beale, Jonathan Millar, Barbara Shih, Seán Keating, Marie Zechner, Chris Haley, David J. Porteous, Caroline Hayward, Jian Yang, Julian C. Knight, Charlotte Summers, Manu Shankar‐Hari, Paul Klenerman, Lance Turtle, Antonia Ho, Shona C. Moore, Charles Hinds, Peter Horby, Alistair Nichol, David M. Maslove, Lowell Ling, Danny McAuley, Hugh Montgomery, Timothy Walsh, Alexandre C. Pereira, Alessandra Renieri, Xia Shen, Chris P. Ponting, Angie Fawkes, Albert Tenesa, Mark J. Caulfield, Richard H. Scott, Kathy Rowan, Lee Murphy, Peter Openshaw, Malcolm G. Semple, Andrew Law, Véronique Vitart, James F. Wilson, J. Kenneth Baillie, J. Kenneth Baillie - Nature 2020 cited by 1,509

  8. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  9. GWAS on family history of Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , - Translational Psychiatry 2018 cited by 620

  10. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm, Deepika Dokuru, Luke M. Evans, Eco J. C. de Geus, Sudheer Giddaluru, Scott D. Gordon, K. Paige Harden, W. David Hill, Amanda Hughes, Shona M. Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Debbie A. Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K. E. Magnusson, Travis T. Mallard, Pekka Martikainen, Melinda C. Mills, Pål R. Njølstad, John D. Overton, Nancy L. Pedersen, David J. Porteous, Jeffrey G. Reid, Karri Silventoinen, Melissa C. Southey, Camilla Stoltenberg, Elliot M. Tucker–Drob, Margaret J. Wright, Hyeokmoon Kweon, Philipp Koellinger, Daniel J. Benjamin, Patrick Turley, Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm and 96 more - Nature Genetics 2022 cited by 393

  11. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zongli Xu, Jie Yao, Wei Zhao, Adolfo Correa, Eric Boerwinkle, Pierre‐Antoine Dugué, Peter Durda, Hannah R. Elliott, Christian Gieger, Eco J. C. de Geus, Sarah E. Harris, Gibran Hemani, Medea Imboden, Mika Kähönen, Sharon L. R. Kardia, Jacob K. Kresovich, Shengxu Li, Kathryn L. Lunetta, Massimo Mangino, Dan Mason, Andrew M. McIntosh, Jonas Mengel‐From, Ann Zenobia Moore, Joanne M. Murabito, Miina Ollikainen, James S. Pankow, Nancy L. Pedersen, Annette Peters, Silvia Polidoro, David J. Porteous, Olli T. Raitakari, Stephen S. Rich, Dale P. Sandler, Elina Sillanpää, Alicia K. Smith, Melissa C. Southey, Konstantin Strauch, Hemant K. Tiwari, Toshiko Tanaka, Therese Tillin, André G. Uitterlinden, David Van Den Berg, Jenny van Dongen, James G. Wilson, John Wright, İdil Yet, Donna K. Arnett, Stefania Bandinelli, Jordana T. Bell, Alexandra M. Binder, Dorret I. Boomsma, Wei Chen, Kaare Christensen, Karen N. Conneely, Paul Elliott, Luigi Ferrucci, Myriam Fornage, Sara Hägg, Caroline Hayward, Marguerite M Irvin, Jaakko Kaprio, Deborah A. Lawlor, Terho Lehtimäki, Falk W. Lohoff, Lili Milani, Roger L. Milne, Nicole Probst‐Hensch, Alex P. Reiner, Beate Ritz, Jerome I. Rotter and 9 more - Genome biology 2021 cited by 304

  12. Ultra-High-Throughput Clinical Proteomics Reveals Classifiers of COVID-19 Infection

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Florian Kurth, Leif Erik Sander, Markus Ralser - Cell Systems 2020 cited by 615

  13. Cardiac Troponin T and Troponin I in the General Population

    Authors: , , , , , , , , , , , , , , - Circulation 2019 cited by 327

  14. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Terho Lehtimäki, Richard J. Allen, Per Bakke, Terri H. Beaty, Eugene R. Bleecker, Yohan Bossé, Corry‐Anke Brandsma, Zhengming Chen, James D. Crapo, John Danesh, Dawn L. DeMeo, Frank Dudbridge, Ralf Ewert, Christian Gieger, Amund Gulsvik, Anna Hansell, Ke Hao, Joshua Hoffman, John E. Hokanson, Georg Homuth, Peter K. Joshi, Philippe Joubert, Claudia Langenberg, Xuan Li, Liming Li, Kuang Lin, Lars Lind, Nicholas Locantore, Jian’an Luan, Anubha Mahajan, Joseph Maranville, Alison D. Murray, David C. Nickle, Richard Packer, Margaret M. Parker, Megan L. Paynton, David J. Porteous, Dmitry Prokopenko, Dandi Qiao, Rajesh Rawal, Heiko Runz, Ian Sayers, Don D. Sin, Blair H. Smith, María Soler Artigas, David Sparrow, Ruth Tal‐Singer, Paul R. H. J. Timmers, Maarten van den Berge, John C. Whittaker, Prescott G. Woodruff, Laura M. Yerges-Armstrong, Olga G. Troyanskaya, Olli Raitakari, Mika Kähönen, Ozren Polašek, Ulf Gyllensten, Igor Rudan, Ian J. Deary, Nicole Probst‐Hensch, Holger Schulz, Alan L James, James F. Wilson, Beate Stubbe, Eleftheria Zeggini, Marjo‐Riitta Järvelin, Nick Wareham, Edwin K. Silverman, Caroline Hayward, Andrew P. Morris and 10 more - Nature Genetics 2019 cited by 599

  15. Timing, rates and spectra of human germline mutation

    Authors: , , , , , , , , , , , - Nature Genetics 2015 cited by 729

  16. Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip

    Authors: , , , , , - Genomics Data 2016 cited by 433

  17. Epigenetic measures of ageing predict the prevalence and incidence of leading causes of death and disease burden

    Authors: , , , , , , , , , , , , , - Clinical Epigenetics 2020 cited by 277

  18. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Elizabeth C. Oelsner, Stephen S. Rich, R. Graham Barr, Shona M. Kerr, Véronique Vitart, Michael R. Brown, Matthias Wielscher, Medea Imboden, Ayoung Jeong, Traci M. Bartz, Sina A. Gharib, Claudia Flexeder, Stefan Karrasch, Christian Gieger, Annette Peters, Beate Stubbe, Xiaowei Hu, Victor E. Ortega, Deborah A. Meyers, Eugene R. Bleecker, Stacey Gabriel, Namrata Gupta, Albert V. Smith, Jian’an Luan, Jinghua Zhao, Ailin Falkmo Hansen, Arnulf Langhammer, Cristen J. Willer, Laxmi Bhatta, David J. Porteous, Blair H. Smith, Archie Campbell, Tamar Sofer, Jiwon Lee, Martha L. Daviglus, Bing Yu, Elise Lim, Hanfei Xu, George O'connor, Gaurav Thareja, Omar Albagha, Said I. Ismail, Wadha Al‐Muftah, Radja Badji, Hamdi Mbarek, Dima Darwish, Tasnim Fadl, Heba Yasin, Maryem Ennaifar, Rania G. Abdel‐latif, Fatima Alkuwari, Muhammad Arshad Alvi, Yasser Al‐Sarraj, Chadi Saad, Asmaa Althani, Biobank and Sample Preparation, Eleni Fethnou, Fatima Qafoud, Eiman Alkhayat, Nahla Afifi, Sequencing and Genotyping group, Sara Tomei, Wei Liu, Stephan Lorenz, Applied Bioinformatics Core, Najeeb Syed, Hakeem Almabrazi, Fazulur Rehaman Vempalli, Ramzi Temanni, Data Management and Computing Infrastructure group and 95 more - Nature Genetics 2023 cited by 186

  19. Identifying the Common Genetic Basis of Antidepressant Response

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eleanor M. Wigmore, Wolfgang Maier, Naomi R. Wray, Katherine J. Aitchison, Volker Arolt, Bernhard T. Baune, Joanna M. Biernacka, Guido Bondolfi, Katharina Domschke, Masaki Kato, Qingqin S. Li, Yu‐Li Liu, Alessandro Serretti, Shih‐Jen Tsai, Gustavo Turecki, Richard M. Weinshilboum, Siegfried Kasper, Joseph Zohar, Daniel Souery, Stuart Montgomery, Diego Albani, Gianluigi Forloni, Panagiotis Ferentinos, Dan Rujescu, Julien Mendlewicz, Naomi R. Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M. Byrne, Abdel Abdellaoui, Mark J. Adams, Esben Agerbo, Tracy Air, Till F. M. Andlauer, Silviu‐Alin Bacanu, Marie Bækvad‐Hansen, Aartjan T.F. Beekman, Tim B. Bigdeli, Elisabeth B. Binder, Julien Bryois, Henriette N. Buttenschøn, Jonas Bybjerg‐Grauholm, Na Cai, Enrique Castelao, Jane Christensen, Toni‐Kim Clarke, Jonathan R. I. Coleman, Lucía Colodro‐Conde, Baptiste Couvy‐Duchesne, Nick Craddock, Gregory E. Crawford, Gail Davies, Ian J. Deary, Franziska Degenhardt, Eske M. Derks, Neşe Direk, Conor V. Dolan, Erin C. Dunn, Thalia C. Eley, Valentina Escott‐Price, Farnush Farhadi Hassan Kiadeh, Hilary K. Finucane, Jerome C. Foo, Andreas J. Forstner, Josef Frank, Héléna A. Gaspar, Michael Gill, Fernando S. Goes, Scott D. Gordon and 155 more - Biological Psychiatry Global Open Science 2021 cited by 133

  20. Epigenetic scores for the circulating proteome as tools for disease prediction

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - eLife 2022 cited by 138

  21. Epigenetic prediction of complex traits and death

    Authors: , , , , , , , , , , , , , , , , , , , , - Genome biology 2018 cited by 295

  22. Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David A. Lomas, Stephanie J. London, Deborah A. Meyers, George O'connor, Stephen I. Rennard, David A. Schwartz, Paweł Śliwiński, David Sparrow, David P. Strachan, Ruth Tal‐Singer, Yohannes Tesfaigzi, Jørgen Vestbo, Judith M. Vonk, Jae‐Joon Yim, Xiaobo Zhou, Yohan Bossé, Ani Manichaikul, Lies Lahousse, Edwin K. Silverman, H. Marike Boezen, Louise V. Wain, Martin D. Tobin, Brian D. Hobbs, Michael H. Cho, Nick Shrine, Anna L. Guyatt, Chiara Batini, Jing Hua Zhao, Matthias Wielscher, Understanding Society Scientific Group, Stefan Weiß, Katherine A. Kentistou, James P. Cook, Jennie Hui, Stefan Karrasch, Medea Imboden, Sarah E. Harris, Jonathan Marten, Stefan Enroth, Shona M. Kerr, Ida Surakka, Véronique Vitart, Terho Lehtimäki, Ralf Ewert, Christian Gieger, Georg Homuth, Peter K. Joshi, Claudia Langenberg, Lars Lind, Jian’an Luan, Anubha Mahajan, Alison D. Murray, David J. Porteous, Rajesh Rawal, Blair H. Smith, Paul R. H. J. Timmers, Olli Raitakari, Mika Kähönen, Ozren Polašek, Ulf Gyllensten, Igor Rudan, Ian J. Deary, Nicole Probst‐Hensch, Holger Schulz, Alan L. James, James F. Wilson, Beate Stubbe, Eleftheria Zeggini, Marjo‐Riitta Järvelin, Nick Wareham and 89 more - Nature Genetics 2019 cited by 423

  23. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Reedik Mägi, Alice Stanton, John Connell, Stephan J. L. Bakker, Andres Metspalu, Denis C. Shields, Simon Thom, Morris J. Brown, Peter Sever, Tõnu Esko, Caroline Hayward, Pim van der Harst, Danish Saleheen, Rajiv Chowdhury, John C. Chambers, Daniel I. Chasman, Aravinda Chakravarti, Christopher Newton‐Cheh, Cecilia M. Lindgren, Daniel Levy, Jaspal S. Kooner, Bernard Keavney, Maciej Tomaszewski, Nilesh J. Samani, Joanna M. M. Howson, Martin D. Tobin, Patricia B. Munroe, Georg Ehret, Louise V. Wain, Louise V Wain, Ahmad Vaez, Rick Jansen, Roby Joehanes, Peter J van der Most, A Mesut Erzurumluoglu, Paul O'Reilly, Claudia P Cabrera, Helen R Warren, Lynda M Rose, Germaine C Verwoert, Jouke-Jan Hottenga, Rona J Strawbridge, Tonu Esko, Dan E Arking, Shih-Jen Hwang, Xiuqing Guo, Zoltan Kutalik, Stella Trompet, Nick Shrine, Alexander Teumer, Janina S Ried, Joshua C Bis, Albert V Smith, Najaf Amin, Ilja M Nolte, Leo-Pekka Lyytikäinen, Anubha Mahajan, Nicholas J Wareham, Edith Hofer, Peter K Joshi, Kati Kristiansson, Michela Traglia, Aki S Havulinna, Anuj Goel, Mike A Nalls, Siim Sõber, Dragana Vuckovic, Jian'an Luan, Fabiola Del Greco M, Kristin L Ayers and 206 more - Nature Genetics 2017 cited by 589

  24. Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness

    Authors: , , , , , , , , , , , , , , , , , , - International Journal of Epidemiology 2012 cited by 485