David J. Porteous
Active 1981–2025
- 254
- Papers
- 48,497
- Citations
- 115
- h-index
- 248
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.1%
- University of Edinburgh0.9%
- King's College London0.8%
- University College London0.7%
- Broad Institute0.6%
- Karolinska Institutet0.6%
- Other95.3%
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
- Archie Campbell86
- Andrew M. McIntosh78
- Caroline Hayward66
- Ian J. Deary59
- Kathryn L. Evans45
- Riccardo E. Marioni44
- Rosie M. Walker36
- Gail Davies34
- Mark J. Adams30
- Daniel L. McCartney24
- Heather C. Whalley23
- Stewart W. Morris23
- Sarah E. Harris22
- David M. Howard20
- Douglas Blackwood20
- J. Kirsty Millar20
- Pippa A. Thomson20
- Blair H. Smith18
- Chris Haley18
- Michelle Luciano18
- Toni‐Kim Clarke18
- Peter M. Visscher17
- David C. Liewald16
- John M. Starr16
All papers
- Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Authors: David M. Howard, Mark J. Adams, Toni‐Kim Clarke, Jonathan D. Hafferty, Jude Gibson, Masoud Shirali, Jonathan R. I. Coleman, Saskia P. Hagenaars, Joey Ward, Eleanor M. Wigmore, Clara Alloza, Xueyi Shen, Miruna C. Barbu, Eileen Y. Xu, Heather C. Whalley, Riccardo E. Marioni, David J. Porteous, Gail Davies, Ian J. Deary, Gibran Hemani, Klaus Berger, Henning Teismann, Rajesh Rawal, Volker Arolt, Bernhard T. Baune, Udo Dannlowski, Katharina Domschke, Chao Tian, David A. Hinds, Maciej Trzaskowski, 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
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Authors: James J. Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter N. Bowers, Julia Sidorenko, Richard Karlsson Linnér, Mark Alan Fontana, Tushar Kundu, Chan Wook Lee, Hui Li, Ruoxi Li, Rebecca Royer, Pascal Timshel, Raymond K. Walters, Emily A. Willoughby, Loïc Yengo, Maris Alver, Yanchun Bao, David W. Clark, Felix R. Day, Nicholas A. Furlotte, Peter K. Joshi, Kathryn E. Kemper, Aaron Kleinman, Claudia Langenberg, Reedik Mägi, 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
- Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Authors: Aysu Okbay, Yeda Wu, Nancy Wang, Hariharan Jayashankar, Michael Bennett, Seyed Moeen Nehzati, Julia Sidorenko, Hyeokmoon Kweon, Grant Goldman, Tamara Gjorgjieva, Yunxuan Jiang, Barry Hicks, Chao Tian, David A. Hinds, Rafael Ahlskog, Patrik K. E. Magnusson, Sven Oskarsson, Caroline Hayward, Archie Campbell, David J. Porteous, Jeremy Freese, Pamela Herd, Michelle Agee, Babak Alipanahi, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah L. Elson, Pierre Fontanillas, Nicholas A. Furlotte, 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
- Long COVID burden and risk factors in 10 UK longitudinal studies and electronic health records
Authors: Ellen J. Thompson, Dylan M. Williams, Alex J Walker, Ruth E. Mitchell, Claire L. Niedzwiedz, Tiffany Yang, Charlotte F. Huggins, Alex S. F. Kwong, Richard J. Silverwood, Giorgio Di Gessa, Ruth C. E. Bowyer, Kate Northstone, Bo Hou, Michael J. Green, Brian Dodgeon, Katie J. Doores, Emma L. Duncan, Frances M. K. Williams, OpenSAFELY Collaborative, Alex J Walker, Brian MacKenna, Peter Inglesby, Christopher T. Rentsch, Helen J Curtis, Caroline E Morton, Jessica Morley, Amir Mehrkar, Seb Bacon, George Hickman, Chris Bates, 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
- Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
Authors: Qian Zhang, Costanza L. Vallerga, Rosie M. Walker, Tian Lin, Anjali K. Henders, Grant W. Montgomery, Ji He, Dongsheng Fan, Javed Fowdar, Martin A. Kennedy, Toni L. Pitcher, John F. Pearson, Glenda M. Halliday, John B. Kwok, Ian B. Hickie, Simon J.G. Lewis, Tim Anderson, Peter A. Silburn, George D. Mellick, Sarah E. Harris, Paul Redmond, Alison D. Murray, David J. Porteous, Chris Haley, Kathryn L. Evans, Andrew M. McIntosh, Jian Yang, Jacob Gratten, Riccardo E. Marioni, Naomi R. Wray, Ian J. Deary, Allan F. McRae, Peter M. Visscher - Genome Medicine 2019 cited by 512
- 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
- Genetic mechanisms of critical illness in COVID-19
Authors: The GenOMICC Investigators, Erola Pairo‐Castineira, The ISARIC4C Investigators, The COVID-19 Human Genetics Initiative, 23andMe Investigators, BRACOVID Investigators, Gen-COVID Investigators, Sara Clohisey, Lucija Klarić, Andrew D. Bretherick, Konrad Rawlik, Dorota Pasko, Susan Walker, Nick Parkinson, Max Head Fourman, Clark D Russell, James Furniss, Anne Richmond, Viktoria‐Eleni Gountouna, Nicola Wrobel, David A Harrison, Bo Wang, Yang Wu, Alison Meynert, Fiona Griffiths, Wilna Oosthuyzen, Athanasios Kousathanas, Loukas Moutsianas, Zhijian Yang, Ranran Zhai, 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
- 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
- GWAS on family history of Alzheimer’s disease
Authors: Riccardo E. Marioni, Sarah E. Harris, Qian Zhang, Allan F. McRae, Saskia P. Hagenaars, W. David Hill, Gail Davies, Craig Ritchie, Catharine R. Galé, John M. Starr, Alison Goate, David J. Porteous, Jian Yang, Kathryn L. Evans, Ian J. Deary, Naomi R. Wray, Peter M. Visscher - Translational Psychiatry 2018 cited by 620
- Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Authors: 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, Aris Baras, Christopher R. Bauer, Dorret I. Boomsma, Archie Campbell, Harry Campbell, 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
- Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Authors: Daniel L. McCartney, Josine L. Min, Rebecca C. Richmond, Ake T. Lu, Maria Sobczyk, Gail Davies, Linda Broer, Xiuqing Guo, Ayoung Jeong, Jeesun Jung, Silva Kasela, Şeyma Katrinli, Pei‐Lun Kuo, Pamela R. Matías‐García, Pashupati P. Mishra, Marianne Nygaard, Teemu Palviainen, Amit Patki, Laura M. Raffield, Scott M. Ratliff, Tom G. Richardson, Oliver Robinson, Mette Soerensen, Dianjianyi Sun, Pei-Chien Tsai, Matthijs D. van der Zee, Rosie M. Walker, Xiaochuan Wang, Yunzhang Wang, Rui Xia, 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
- Ultra-High-Throughput Clinical Proteomics Reveals Classifiers of COVID-19 Infection
Authors: Christoph B. Messner, Vadim Demichev, Daniel Wendisch, Laura Michalick, Matthew White, Anja Freiwald, Kathrin Textoris‐Taube, Spyros I. Vernardis, Anna-Sophia Egger, Marco Kreidl, Daniela Ludwig, Christiane Kilian, Federica Agostini, Aleksej Zelezniak, Charlotte Thibeault, Moritz Pfeiffer, Stefan Hippenstiel, Andreas C. Hocke, Christof von Kalle, Archie Campbell, Caroline Hayward, David J. Porteous, Riccardo E. Marioni, Claudia Langenberg, Kathryn S. Lilley, Wolfgang M. Kuebler, Michael Mülleder, Christian Drosten, Norbert Suttorp, Martin Witzenrath, Florian Kurth, Leif Erik Sander, Markus Ralser - Cell Systems 2020 cited by 615
- Cardiac Troponin T and Troponin I in the General Population
Authors: Paul Welsh, David Preiss, Caroline Hayward, Anoop Shah, David McAllister, Andrew Briggs, Charles Boachie, Alex McConnachie, Sandosh Padmanabhan, Claire Welsh, Mark Woodward, Archie Campbell, David J. Porteous, Nicholas L. Mills, Naveed Sattar - Circulation 2019 cited by 327
- New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Authors: Nick Shrine, Anna L. Guyatt, A. Mesut Erzurumluoglu, Victoria E. Jackson, Brian D. Hobbs, Carl Melbourne, Chiara Batini, Katherine A. Fawcett, Kijoung Song, Phuwanat Sakornsakolpat, Xingnan Li, Ruth Boxall, Nicola Reeve, Ma’en Obeidat, Jing Hua Zhao, Matthias Wielscher, Stefan Weiß, Katherine A. Kentistou, James P. Cook, Benjamin B. Sun, Jian Zhou, Jennie Hui, Stefan Karrasch, Medea Imboden, Sarah E. Harris, Jonathan Marten, Stefan Enroth, Shona M. Kerr, Ida Surakka, Véronique Vitart, 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
- Timing, rates and spectra of human germline mutation
Authors: Raheleh Rahbari, Arthur Wüster, Sarah Lindsay, Robert J. Hardwick, Ludmil B. Alexandrov, Saeed Al Turki, Anna F. Dominiczak, Andrew D. Morris, David J. Porteous, Blair H. Smith, Michael R. Stratton, Matthew E. Hurles - Nature Genetics 2015 cited by 729
- Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChip
Authors: Daniel L. McCartney, Rosie M. Walker, Stewart W. Morris, Andrew M. McIntosh, David J. Porteous, Kathryn L. Evans - Genomics Data 2016 cited by 433
- Epigenetic measures of ageing predict the prevalence and incidence of leading causes of death and disease burden
Authors: Robert F. Hillary, Anna J. Stevenson, Daniel L. McCartney, Archie Campbell, Rosie M. Walker, David M. Howard, Craig Ritchie, Steve Horvath, Caroline Hayward, Andrew M. McIntosh, David J. Porteous, Ian J. Deary, Kathryn L. Evans, Riccardo E. Marioni - Clinical Epigenetics 2020 cited by 277
- Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Authors: Nick Shrine, Abril G. Izquierdo, Jing Chen, Richard Packer, Robert J. Hall, Anna L. Guyatt, Chiara Batini, Rebecca Thompson, Chandan Pavuluri, Vidhi Malik, Brian D. Hobbs, Matthew Moll, Wonji Kim, Ruth Tal‐Singer, Per Bakke, Katherine A. Fawcett, Catherine John, Kayesha Coley, Noemi Nicole Piga, Alfred Pozarickij, Kuang Lin, Iona Y. Millwood, Zhengming Chen, Liming Li, China Kadoorie Biobank Collaborative Group, Sara Wijnant, Lies Lahousse, Guy Brusselle, André G. Uitterlinden, Ani Manichaikul, 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
- Identifying the Common Genetic Basis of Antidepressant Response
Authors: Oliver Pain, Karen Hodgson, Vassily Trubetskoy, Stephan Ripke, Victoria Marshe, Mark J. Adams, Enda M. Byrne, Adrián I. Campos, Tania Carrillo‐Roa, Annamaria Cattaneo, Thomas D. Als, Daniel Souery, Mojca Zvezdana Dernovšek, Chiara Fabbri, Caroline Hayward, Neven Henigsberg, Joanna Hauser, James L. Kennedy, Eric J. Lenze, Glyn Lewis, Daniel J. Müller, Nicholas G. Martin, Benoit H. Mulsant, Ole Mors, Nader Perroud, David J. Porteous, Miguel E. Rentería, Charles F. Reynolds, Marcella Rietschel, Rudolf Uher, 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
- Epigenetic scores for the circulating proteome as tools for disease prediction
Authors: Danni A. Gadd, Robert F. Hillary, Daniel L. McCartney, Shaza B. Zaghlool, Anna J. Stevenson, Yipeng Cheng, Chloe Fawns‐Ritchie, Clifford Nangle, Archie Campbell, Robin Flaig, Sarah E. Harris, Rosie M. Walker, Liu Shi, Elliot M. Tucker–Drob, Christian Gieger, Annette Peters, Mélanie Waldenberger, Johannes Graumann, Allan F. McRae, Ian J. Deary, David J. Porteous, Caroline Hayward, Peter M. Visscher, Simon R Cox, Kathryn L. Evans, Andrew M. McIntosh, Karsten Suhre, Riccardo E. Marioni - eLife 2022 cited by 138
- Epigenetic prediction of complex traits and death
Authors: Daniel L. McCartney, Robert F. Hillary, Anna J. Stevenson, Stuart J. Ritchie, Rosie M. Walker, Qian Zhang, Stewart W. Morris, Mairead L. Bermingham, Archie Campbell, Alison D. Murray, Heather C. Whalley, Catharine R. Galé, David J. Porteous, Chris Haley, Allan F. McRae, Naomi R. Wray, Peter M. Visscher, Andrew M. McIntosh, Kathryn L. Evans, Ian J. Deary, Riccardo E. Marioni - Genome biology 2018 cited by 295
- Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Authors: Phuwanat Sakornsakolpat, Dmitry Prokopenko, Maxime Lamontagne, Nicola Reeve, Anna L. Guyatt, Victoria E. Jackson, Nick Shrine, Dandi Qiao, Traci M. Bartz, Deog Kyeom Kim, Mi Kyeong Lee, Jeanne C. Latourelle, Xingnan Li, Jarrett D. Morrow, Ma’en Obeidat, Annah B. Wyss, Per Bakke, R. Graham Barr, Terri H. Beaty, Steven A. Belinsky, Guy Brusselle, James D. Crapo, Kim de Jong, Dawn L. DeMeo, Tasha E. Fingerlin, Sina A. Gharib, Amund Gulsvik, Ian P. Hall, John E. Hokanson, Woo Jin Kim, 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
- Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Authors: Helen R. Warren, Εvangelos Εvangelou, Claudia P. Cabrera, He Gao, Meixia Ren, Borbála Mifsud, Ioanna Ntalla, Praveen Surendran, Chunyu Liu, James P. Cook, Aldi T. Kraja, Fotios Drenos, Marie Loh, Niek Verweij, Jonathan Marten, İbrahim Karaman, Marcelo P Segura Lepe, Paul F. O’Reilly, Jo Knight, Harold Snieder, Norihiro Kato, Jiang He, E Shyong Tai, M. Abdullah Said, David J. Porteous, Maris Alver, Neil R Poulter, Martin Farrall, Ron T. Gansevoort, Sandosh Padmanabhan, 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
- 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: Blair H. Smith, Archie Campbell, Pamela Linksted, Bridie Fitzpatrick, Cathy Jackson, Shona M. Kerr, Ian J. Deary, Donald J. MacIntyre, Harry Campbell, Mark McGilchrist, Lynne J. Hocking, Lucy Wisely, Ian Ford, Robert S. Lindsay, Robin A. Morton, Colin N A Palmer, Anna F. Dominiczak, David J. Porteous, Andrew D. Morris - International Journal of Epidemiology 2012 cited by 485
