Works matching AU Marioni, Riccardo E.

Results: 108
    1

    Epigenetic markers of adverse lifestyle identified among evening and night shift workers in two UK population-based studies: Generation Scotland and Understanding Society.

    Published in:
    Chronobiology International: The Journal of Biological & Medical Rhythm Research, 2025, v. 42, n. 5, p. 561, doi. 10.1080/07420528.2025.2493208
    By:
    • Hulls, Paige M.;
    • McCartney, Daniel L.;
    • Bao, Yanchun;
    • Walker, Rosie M.;
    • de Vocht, Frank;
    • Martin, Richard M.;
    • Relton, Caroline L.;
    • Evans, Kathryn L.;
    • Kumari, Meena;
    • Marioni, Riccardo E.;
    • Richmond, Rebecca C.
    Publication type:
    Article
    2

    Identification of 55,000 Replicated DNA Methylation QTL.

    Published in:
    Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35871-w
    By:
    • McRae, Allan F.;
    • Marioni, Riccardo E.;
    • Shah, Sonia;
    • Yang, Jian;
    • Powell, Joseph E.;
    • Harris, Sarah E.;
    • Gibson, Jude;
    • Henders, Anjali K.;
    • Bowdler, Lisa;
    • Painter, Jodie N.;
    • Murphy, Lee;
    • Martin, Nicholas G.;
    • Starr, John M.;
    • Wray, Naomi R.;
    • Deary, Ian J.;
    • Visscher, Peter M.;
    • Montgomery, Grant W.
    Publication type:
    Article
    3

    Epigenetic scores derived in saliva are associated with gestational age at birth.

    Published in:
    Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-024-01701-2
    By:
    • Mckinnon, Katie;
    • Conole, Eleanor L. S.;
    • Vaher, Kadi;
    • Hillary, Robert F.;
    • Gadd, Danni A.;
    • Binkowska, Justyna;
    • Sullivan, Gemma;
    • Stevenson, Anna J.;
    • Corrigan, Amy;
    • Murphy, Lee;
    • Whalley, Heather C.;
    • Richardson, Hilary;
    • Marioni, Riccardo E.;
    • Cox, Simon R.;
    • Boardman, James P.
    Publication type:
    Article
    4
    5

    Blood-based epigenome-wide analyses of 19 common disease states: A longitudinal, population-based linked cohort study of 18,413 Scottish individuals.

    Published in:
    PLoS Medicine, 2023, v. 20, n. 7, p. 1, doi. 10.1371/journal.pmed.1004247
    By:
    • Hillary, Robert F.;
    • McCartney, Daniel L.;
    • Smith, Hannah M.;
    • Bernabeu, Elena;
    • Gadd, Danni A.;
    • Chybowska, Aleksandra D.;
    • Cheng, Yipeng;
    • Murphy, Lee;
    • Wrobel, Nicola;
    • Campbell, Archie;
    • Walker, Rosie M.;
    • Hayward, Caroline;
    • Evans, Kathryn L.;
    • McIntosh, Andrew M.;
    • Marioni, Riccardo E.
    Publication type:
    Article
    6

    Assessing the causal role of epigenetic clocks in the development of multiple cancers: a Mendelian randomization study.

    Published in:
    eLife, 2022, p. 1, doi. 10.7554/eLife.75374
    By:
    • Berstein, Fernanda Morales;
    • McCartney, Daniel L.;
    • Lu, Ake T.;
    • Tsilidis, Konstantinos K.;
    • Bouras, Emmanouil;
    • Haycock, Philip;
    • Burrows, Kimberley;
    • Phipps, Amanda I.;
    • Buchanan, Daniel D.;
    • Cheng, Iona;
    • Martin, Richard M.;
    • Smith, George Davey;
    • Relton, Caroline L.;
    • Horvath, Steve;
    • Marioni, Riccardo E.;
    • Richardson, Tom G.;
    • Richmond, Rebecca C.
    Publication type:
    Article
    7

    Assessing the causal role of epigenetic clocks in the development of multiple cancers: a Mendelian randomization study.

    Published in:
    eLife, 2022, p. 1, doi. 10.7554/eLife.75374
    By:
    • Berstein, Fernanda Morales;
    • McCartney, Daniel L.;
    • Lu, Ake T.;
    • Tsilidis, Konstantinos K.;
    • Bouras, Emmanouil;
    • Haycock, Philip;
    • Burrows, Kimberley;
    • Phipps, Amanda I.;
    • Buchanan, Daniel D.;
    • Iona Cheng;
    • Martin, Richard M.;
    • Smith, George Davey;
    • Relton, Caroline L.;
    • Horvath, Steve;
    • Marioni, Riccardo E.;
    • Richardson, Tom G.;
    • Richmond, Rebecca C.
    Publication type:
    Article
    8

    Exome Sequencing to Detect Rare Variants Associated With General Cognitive Ability: A Pilot Study.

    Published in:
    Twin Research & Human Genetics, 2015, v. 18, n. 2, p. 117, doi. 10.1017/thg.2015.10
    By:
    • Luciano, Michelle;
    • Svinti, Victoria;
    • Campbell, Archie;
    • Marioni, Riccardo E.;
    • Hayward, Caroline;
    • Wright, Alan F.;
    • Taylor, Martin S.;
    • Porteous, David J.;
    • Thomson, Pippa;
    • Prendergast, James G.D.;
    • Hastie, Nicholas D.;
    • Farrington, Susan M.;
    • Scotland, Generation;
    • Dunlop, Malcolm G.;
    • Deary, Ian J.
    Publication type:
    Article
    9

    DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29792-6
    By:
    • Wielscher, Matthias;
    • Mandaviya, Pooja R.;
    • Kuehnel, Brigitte;
    • Joehanes, Roby;
    • Mustafa, Rima;
    • Robinson, Oliver;
    • Zhang, Yan;
    • Bodinier, Barbara;
    • Walton, Esther;
    • Mishra, Pashupati P.;
    • Schlosser, Pascal;
    • Wilson, Rory;
    • Tsai, Pei-Chien;
    • Palaniswamy, Saranya;
    • Marioni, Riccardo E.;
    • Fiorito, Giovanni;
    • Cugliari, Giovanni;
    • Karhunen, Ville;
    • Ghanbari, Mohsen;
    • Psaty, Bruce M.
    Publication type:
    Article
    10
    11

    Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach.

    Published in:
    2017
    By:
    • Mendelson, Michael M.;
    • Marioni, Riccardo E.;
    • Joehanes, Roby;
    • Liu, Chunyu;
    • Hedman, Åsa K.;
    • Aslibekyan, Stella;
    • Demerath, Ellen W.;
    • Guan, Weihua;
    • Zhi, Degui;
    • Yao, Chen;
    • Huan, Tianxiao;
    • Willinger, Christine;
    • Chen, Brian;
    • Courchesne, Paul;
    • Multhaup, Michael;
    • Irvin, Marguerite R.;
    • Cohain, Ariella;
    • Schadt, Eric E.;
    • Grove, Megan L.;
    • Bressler, Jan
    Publication type:
    journal article
    12

    DNAmethylation in relation to gestational age and brain dysmaturation in preterm infants.

    Published in:
    Brain Communications, 2022, v. 4, n. 2, p. 1, doi. 10.1093/braincomms/fcac056
    By:
    • Wheater, Emily N. W.;
    • Galdi, Paola;
    • McCartney, Daniel L.;
    • Blesa, Manuel;
    • Sullivan, Gemma;
    • Stoye, David Q.;
    • Lamb, Gillian;
    • Sparrow, Sarah;
    • Murphy, Lee;
    • Wrobel, Nicola;
    • Quigley, Alan J.;
    • Semple, Scott;
    • Thrippleton, Michael J.;
    • Wardlaw, Joanna M.;
    • Bastin, Mark E.;
    • Marioni, Riccardo E.;
    • Cox, Simon R.;
    • Boardman, James P.
    Publication type:
    Article
    13

    Structural Brain MRI Trait Polygenic Score Prediction of Cognitive Abilities.

    Published in:
    2015
    By:
    • Luciano, Michelle;
    • Marioni, Riccardo E.;
    • Valdés Hernández, Maria;
    • Muñoz Maniega, Susana;
    • Hamilton, Iona F.;
    • Royle, Natalie A.;
    • Chauhan, Ganesh;
    • Bis, Joshua C.;
    • Debette, Stephanie;
    • DeCarli, Charles;
    • Fornage, Myriam;
    • Schmidt, Reinhold;
    • Ikram, M. Arfan;
    • Launer, Lenore J.;
    • Seshadri, Sudha;
    • Bastin, Mark E.;
    • Porteous, David J.;
    • Wardlaw, Joanna;
    • Deary, Ian J.;
    • Valdés Hernández, Maria
    Publication type:
    journal article
    14
    15

    A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 2, p. 358, doi. 10.1093/hmg/ddv454
    By:
    • de Vries, Paul S.;
    • Chasman, Daniel I.;
    • Sabater-Lleal, Maria;
    • Ming-Huei Chen;
    • Huffman, Jennifer E.;
    • Steri, Maristella;
    • Weihong Tang;
    • Teumer, Alexander;
    • Marioni, Riccardo E.;
    • Grossmann, Vera;
    • Hottenga, Jouke J.;
    • Trompet, Stella;
    • Müller-Nurasyid, Martina;
    • Jing Hua Zhao;
    • Brody, Jennifer A.;
    • Kleber, Marcus E.;
    • Xiuqing Guo;
    • Jie Jin Wang;
    • Auer, Paul L.;
    • Attia, John R.
    Publication type:
    Article
    16

    Prospective study design and data analysis in UK Biobank.

    Published in:
    Science Translational Medicine, 2024, v. 16, n. 729, p. 1, doi. 10.1126/scitranslmed.adf4428
    By:
    • Allen, Naomi E.;
    • Lacey, Ben;
    • Lawlor, Deborah A.;
    • Pell, Jill P.;
    • Gallacher, John;
    • Smeeth, Liam;
    • Elliott, Paul;
    • Matthews, Paul M.;
    • Lyons, Ronan A.;
    • Whetton, Anthony D.;
    • Lucassen, Anneke;
    • Hurles, Matthew E.;
    • Chapman, Michael;
    • Roddam, Andrew W.;
    • Fitzpatrick, Natalie K.;
    • Hansell, Anna L.;
    • Hardy, Rebecca;
    • Marioni, Riccardo E.;
    • O'Donnell, Valerie B.;
    • Williams, Julie
    Publication type:
    Article
    17
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    Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.

    Published in:
    Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00754-1
    By:
    • Hillary, Robert F.;
    • Trejo-Banos, Daniel;
    • Kousathanas, Athanasios;
    • McCartney, Daniel L.;
    • Harris, Sarah E.;
    • Stevenson, Anna J.;
    • Patxot, Marion;
    • Ojavee, Sven Erik;
    • Zhang, Qian;
    • Liewald, David C.;
    • Ritchie, Craig W.;
    • Evans, Kathryn L.;
    • Tucker-Drob, Elliot M.;
    • Wray, Naomi R.;
    • McRae, Allan F.;
    • Visscher, Peter M.;
    • Deary, Ian J.;
    • Robinson, Matthew R.;
    • Marioni, Riccardo E.
    Publication type:
    Article
    21
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    Alzheimer's disease genetic pathways impact cerebrospinal fluid biomarkers and imaging endophenotypes in non‐demented individuals.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 9, p. 6146, doi. 10.1002/alz.14096
    By:
    • Lorenzini, Luigi;
    • Collij, Lyduine E.;
    • Tesi, Niccoló;
    • Vilor‐Tejedor, Natàlia;
    • Ingala, Silvia;
    • Blennow, Kaj;
    • Foley, Christopher;
    • Frisoni, Giovanni B.;
    • Haller, Sven;
    • Holstege, Henne;
    • van der van der Lee, Sven;
    • Martinez‐Lage, Pablo;
    • Marioni, Riccardo E.;
    • McCartney, Daniel L.;
    • O' Brien, John;
    • Oliveira, Tiago Gil;
    • Payoux, Pierre;
    • Reinders, Marcel;
    • Ritchie, Craig;
    • Scheltens, Philip
    Publication type:
    Article
    24
    25

    Genetic prediction of male pattern baldness.

    Published in:
    PLoS Genetics, 2017, v. 13, n. 2, p. 1, doi. 10.1371/journal.pgen.1006594
    By:
    • Hagenaars, Saskia P.;
    • Hill, W. David;
    • Harris, Sarah E.;
    • Ritchie, Stuart J.;
    • Davies, Gail;
    • Liewald, David C.;
    • Gale, Catharine R.;
    • Porteous, David J.;
    • Deary, Ian J.;
    • Marioni, Riccardo E.
    Publication type:
    Article
    26

    Creating and Validating a DNA Methylation-Based Proxy for Interleukin-6.

    Published in:
    2021
    By:
    • Stevenson, Anna J;
    • Gadd, Danni A;
    • Hillary, Robert F;
    • McCartney, Daniel L;
    • Campbell, Archie;
    • Walker, Rosie M;
    • Evans, Kathryn L;
    • Harris, Sarah E;
    • Spires-Jones, Tara L;
    • McRae, Allan F;
    • Visscher, Peter M;
    • McIntosh, Andrew M;
    • Deary, Ian J;
    • Marioni, Riccardo E
    Publication type:
    journal article
    27
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    31

    Epigenome-Wide Association Study Reveals CpG Sites Associated with Thyroid Function and Regulatory Effects on KLF9.

    Published in:
    Thyroid, 2023, v. 33, n. 3, p. 301, doi. 10.1089/thy.2022.0373
    By:
    • Weihs, Antoine;
    • Chaker, Layal;
    • Martin, Tiphaine C.;
    • Braun, Kim V.E.;
    • Campbell, Purdey J.;
    • Cox, Simon R.;
    • Fornage, Myriam;
    • Gieger, Christian;
    • Grabe, Hans J.;
    • Grallert, Harald;
    • Harris, Sarah E.;
    • Kühnel, Brigitte;
    • Marioni, Riccardo E.;
    • Martin, Nicholas G.;
    • McCartney, Daniel L.;
    • McRae, Allan F.;
    • Meisinger, Christa;
    • van Meurs, Joyce B.J.;
    • Nano, Jana;
    • Nauck, Matthias
    Publication type:
    Article
    32
    33

    Addendum: Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05310-5
    By:
    • Howard, David M.;
    • Adams, Mark J.;
    • Shirali, Masoud;
    • Clarke, Toni-Kim;
    • Marioni, Riccardo E.;
    • Davies, Gail;
    • Coleman, Jonathan R. I.;
    • Alloza, Clara;
    • Shen, Xueyi;
    • Barbu, Miruna C.;
    • Wigmore, Eleanor M.;
    • Gibson, Jude;
    • Hagenaars, Saskia P.;
    • Lewis, Cathryn M.;
    • Ward, Joey;
    • Smith, Daniel J.;
    • Sullivan, Patrick F.;
    • Haley, Chris S.;
    • Breen, Gerome;
    • Deary, Ian J.
    Publication type:
    Article
    34
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    Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41467-018-04362-x
    By:
    • Davies, Gail;
    • Lam, Max;
    • Harris, Sarah E.;
    • Trampush, Joey W.;
    • Luciano, Michelle;
    • Hill, W. David;
    • Hagenaars, Saskia P.;
    • Ritchie, Stuart J.;
    • Marioni, Riccardo E.;
    • Fawns-Ritchie, Chloe;
    • Liewald, David C. M.;
    • Okely, Judith A.;
    • Ahola-Olli, Ari V.;
    • Barnes, Catriona L. K.;
    • Bertram, Lars;
    • Bis, Joshua C.;
    • Burdick, Katherine E.;
    • Christoforou, Andrea;
    • DeRosse, Pamela;
    • Djurovic, Srdjan
    Publication type:
    Article
    37

    Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03819-3
    By:
    • Howard, David M.;
    • Adams, Mark J.;
    • Shirali, Masoud;
    • Clarke, Toni-Kim;
    • Marioni, Riccardo E.;
    • Davies, Gail;
    • Coleman, Jonathan R. I.;
    • Alloza, Clara;
    • Shen, Xueyi;
    • Barbu, Miruna C.;
    • Wigmore, Eleanor M.;
    • Gibson, Jude;
    • Agee, Michelle;
    • Alipanahi, Babak;
    • Auton, Adam;
    • Bell, Robert K.;
    • Bryc, Katarzyna;
    • Elson, Sarah L.;
    • Fontanillas, Pierre;
    • Furlotte, Nicholas A.
    Publication type:
    Article
    38

    Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05310-5
    By:
    • Howard, David M.;
    • Adams, Mark J.;
    • Shirali, Masoud;
    • Clarke, Toni-Kim;
    • Marioni, Riccardo E.;
    • Davies, Gail;
    • Coleman, Jonathan R. I.;
    • Alloza, Clara;
    • Shen, Xueyi;
    • Barbu, Miruna C.;
    • Wigmore, Eleanor M.;
    • Gibson, Jude;
    • 23andMe Research Team;
    • Hagenaars, Saskia P.;
    • Lewis, Cathryn M.;
    • Ward, Joey;
    • Smith, Daniel J.;
    • Sullivan, Patrick F.;
    • Haley, Chris S.;
    • Breen, Gerome
    Publication type:
    Article
    39
    40

    GWAS of epigenetic aging rates in blood reveals a critical role for TERT.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02697-5
    By:
    • Lu, Ake T.;
    • Luting Xue;
    • Salfati, Elias L.;
    • Chen, Brian H.;
    • Ferrucci, Luigi;
    • Levy, Daniel;
    • Joehanes, Roby;
    • Murabito, Joanne M.;
    • Kiel, Douglas P.;
    • Pei-Chien Tsai;
    • Yet, Idil;
    • Bell, Jordana T.;
    • Mangino, Massimo;
    • Toshiko Tanaka;
    • McRae, Allan F.;
    • Marioni, Riccardo E.;
    • Visscher, Peter M.;
    • Wray, Naomi R.;
    • Deary, Ian J.;
    • Levine, Morgan E.
    Publication type:
    Article
    41

    Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes.

    Published in:
    PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0182472
    By:
    • Mandaviya, Pooja R.;
    • Joehanes, Roby;
    • Aïssi, Dylan;
    • Kühnel, Brigitte;
    • Marioni, Riccardo E.;
    • Truong, Vinh;
    • Stolk, Lisette;
    • Beekman, Marian;
    • Bonder, Marc Jan;
    • Franke, Lude;
    • Gieger, Christian;
    • Huan, Tianxiao;
    • Ikram, M. Arfan;
    • Kunze, Sonja;
    • Liang, Liming;
    • Lindemans, Jan;
    • Liu, Chunyu;
    • McRae, Allan F.;
    • Mendelson, Michael M.;
    • Müller-Nurasyid, Martina
    Publication type:
    Article
    42

    Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.

    Published in:
    PLoS ONE, 2017, v. 12, n. 1, p. 1, doi. 10.1371/journal.pone.0167742
    By:
    • de Vries, Paul S.;
    • Sabater-Lleal, Maria;
    • Chasman, Daniel I.;
    • Trompet, Stella;
    • Ahluwalia, Tarunveer S.;
    • Teumer, Alexander;
    • Kleber, Marcus E.;
    • Chen, Ming-Huei;
    • Wang, Jie Jin;
    • Attia, John R.;
    • Marioni, Riccardo E.;
    • Steri, Maristella;
    • Weng, Lu-Chen;
    • Pool, Rene;
    • Grossmann, Vera;
    • Brody, Jennifer A.;
    • Venturini, Cristina;
    • Tanaka, Toshiko;
    • Rose, Lynda M.;
    • Oldmeadow, Christopher
    Publication type:
    Article
    43
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    45

    Genetic Variants Associated With Altered Plasma Levels of C-Reactive Protein are not Associated With Late-Life Cognitive Ability in Four Scottish Samples.

    Published in:
    Behavior Genetics, 2010, v. 40, n. 1, p. 3, doi. 10.1007/s10519-009-9302-z
    By:
    • Marioni, Riccardo E.;
    • Deary, Ian J.;
    • Murray, Gordon D.;
    • Lowe, Gordon D. O.;
    • Rafnsson, Snorri B.;
    • Strachan, Mark W. J.;
    • Luciano, Michelle;
    • Houlihan, Lorna M.;
    • Gow, Alan J.;
    • Harris, Sarah E.;
    • Stewart, Marlene C.;
    • Rumley, Ann;
    • Fowkes, F. Gerrry R.;
    • Price, Jackie F.
    Publication type:
    Article
    46

    No Association Between Cholinergic Muscarinic Receptor 2 ( CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples.

    Published in:
    Behavior Genetics, 2009, v. 39, n. 5, p. 513, doi. 10.1007/s10519-009-9274-z
    By:
    • Lind, Penelope A.;
    • Luciano, Michelle;
    • Horan, Michael A.;
    • Marioni, Riccardo E.;
    • Wright, Margaret J.;
    • Bates, Timothy C.;
    • Rabbitt, Patrick;
    • Harris, Sarah E.;
    • Davidson, Yvonne;
    • Deary, Ian J.;
    • Gibbons, Linda;
    • Pickles, Andrew;
    • Ollier, William;
    • Pendleton, Neil;
    • Price, Jackie F.;
    • Payton, Antony;
    • Martin, Nicholas G.
    Publication type:
    Article
    47

    ASSOCIATION OF LOW-FREQUENCY AND RARE CODING VARIANTS WITH INFORMATION PROCESSING SPEED.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P448, doi. 10.1016/j.jalz.2016.06.866
    By:
    • Bressler, Jan;
    • Davies, Gail;
    • Fawns-Ritchie, Chloe;
    • Smith, Albert V.;
    • Bis, Joshua C.;
    • Smith, Jennifer A.;
    • Yanek, Lisa R.;
    • Marioni, Riccardo E.;
    • Huffman, Jennifer E.;
    • Polasek, Ozren;
    • Mirza, Saira S.;
    • van der Lee, Sven J.;
    • Grove, Megan L.;
    • Boerwinkle, Eric;
    • Launer, Lenore J.;
    • Fitzpatrick, Annette L.;
    • Fornage, Myriam;
    • Turner, Stephen T.;
    • Kardia, Sharon L.R.;
    • Nyquist, Paul
    Publication type:
    Article
    48
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    Molecular genetic contributions to self-rated health.

    Published in:
    2017
    By:
    • Harris, Sarah E.;
    • Hagenaars, Saskia P.;
    • Davies, Gail;
    • Hill, W. David;
    • Liewald, David C. M.;
    • Ritchie, Stuart J.;
    • Marioni, Riccardo E.;
    • Sudlow, Cathie L. M.;
    • Wardlaw, Joanna M.;
    • McIntosh, Andrew M.;
    • Gale, Catharine R.;
    • Deary, Ian J.;
    • David Hill, W;
    • METASTROKE Consortium, International Consortium for Blood Pressure Genome-Wide Association Studies;
    • International Consortium for Blood Pressure Genome-Wide Association Studies;
    • CHARGE Consortium Aging and Longevity Group;
    • CHARGE Consortium Cognitive Group
    Publication type:
    journal article
    50