Works by Campbell, Archie

Results: 99

Clinical and pharmacogenomic predictors of survival in tamoxifen treated breast cancer female patients: a real-world study.

Published in:

BMC Cancer, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12885-025-14162-4

By:

Al-Matrafi, Abdullah R.;
Bedair, Khaled F.;
Srinivasan, Sundararajan;
Palmer, Colin;
Campbell, Archie;
Hayward, Caroline;
Pearson, Ewan R.;
Petty, Russell D.

Publication type:

Article

General Framework for Meta-Analysis of Haplotype Association Tests.

Published in:

Genetic Epidemiology, 2016, v. 40, n. 3, p. 244, doi. 10.1002/gepi.21959

By:

Wang, Shuai;
Zhao, Jing Hua;
An, Ping;
Guo, Xiuqing;
Jensen, Richard A.;
Marten, Jonathan;
Huffman, Jennifer E.;
Meidtner, Karina;
Boeing, Heiner;
Campbell, Archie;
Rice, Kenneth M.;
Scott, Robert A.;
Yao, Jie;
Schulze, Matthias B.;
Wareham, Nicholas J.;
Borecki, Ingrid B.;
Province, Michael A.;
Rotter, Jerome I.;
Hayward, Caroline;
Goodarzi, Mark O.

Publication type:

Article

Blood-based epigenome-wide association study and prediction of alcohol consumption.

Published in:

Clinical Epigenetics, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13148-025-01818-y

By:

Bernabeu, Elena;
Chybowska, Aleksandra D.;
Kresovich, Jacob K.;
Suderman, Matthew;
McCartney, Daniel L.;
Hillary, Robert F.;
Corley, Janie;
Valdés-Hernández, Maria Del C.;
Maniega, Susana Muñoz;
Bastin, Mark E.;
Wardlaw, Joanna M.;
Xu, Zongli;
Sandler, Dale P.;
Campbell, Archie;
Harris, Sarah E.;
McIntosh, Andrew M.;
Taylor, Jack A.;
Yousefi, Paul;
Cox, Simon R.;
Evans, Kathryn L.

Publication type:

Article

Epigenetic scores of blood-based proteins as biomarkers of general cognitive function and brain health.

Published in:

Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-024-01661-7

By:

Smith, Hannah M.;
Moodie, Joanna E.;
Monterrubio-Gómez, Karla;
Gadd, Danni A.;
Hillary, Robert F.;
Chybowska, Aleksandra D.;
McCartney, Daniel L.;
Campbell, Archie;
Redmond, Paul;
Page, Danielle;
Taylor, Adele;
Corley, Janie;
Harris, Sarah E.;
Valdés Hernández, Maria;
Muñoz Maniega, Susana;
Bastin, Mark E.;
Wardlaw, Joanna M.;
Deary, Ian J.;
Boardman, James P.;
Mullin, Donncha S.

Publication type:

Article

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

A novel framework to build saliva‐based DNA methylation biomarkers: Quantifying systemic chronic inflammation as a case study.

Published in:

Aging Cell, 2025, v. 24, n. 4, p. 1, doi. 10.1111/acel.14444

By:

Schmunk, Lisa J.;
Call, Toby P.;
McCartney, Daniel L.;
Javaid, Hira;
Hastings, Waylon J.;
Jovicevic, Vanja;
Kojadinović, Dragoljub;
Tomkinson, Natacha;
Zlamalova, Eliska;
McGee, Kirsty C.;
Sullivan, Jack;
Campbell, Archie;
McIntosh, Andrew M.;
Óvári, Veronika;
Wishart, Karl;
Behrens, Christian E.;
Stone, Emma;
Gavrilov, Miloš;
Thompson, Rob;
Jackson, Thomas

Publication type:

Article

Correction: Association of low-frequency and rare coding variants with information processing speed.

Published in:

2022

By:

Bressler, Jan;
Davies, Gail;
Smith, Albert V.;
Saba, Yasaman;
Bis, Joshua C.;
Jian, Xueqiu;
Hayward, Caroline;
Yanek, Lisa;
Smith, Jennifer A.;
Mirza, Saira S.;
Wang, Ruiqi;
Adams, Hieab H. H.;
Becker, Diane;
Boerwinkle, Eric;
Campbell, Archie;
Cox, Simon R.;
Eiriksdottir, Gudny;
Fawns-Ritchie, Chloe;
Gottesman, Rebecca F.;
Grove, Megan L.

Publication type:

Correction Notice

Association of low-frequency and rare coding variants with information processing speed.

Published in:

Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01736-6

By:

Bressler, Jan;
Davies, Gail;
Smith, Albert V.;
Saba, Yasaman;
Bis, Joshua C.;
Jian, Xueqiu;
Hayward, Caroline;
Yanek, Lisa;
Smith, Jennifer A.;
Mirza, Saira S.;
Wang, Ruiqi;
Adams, Hieab H. H.;
Becker, Diane;
Boerwinkle, Eric;
Campbell, Archie;
Cox, Simon R.;
Eiriksdottir, Gudny;
Fawns-Ritchie, Chloe;
Gottesman, Rebecca F.;
Grove, Megan L.

Publication type:

Article

Hair glucocorticoids are associated with childhood adversity, depressive symptoms and reduced global and lobar grey matter in Generation Scotland.

Published in:

Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01644-9

By:

Green, Claire;
Stolicyn, Aleks;
Harris, Mathew A.;
Shen, Xueyi;
Romaniuk, Liana;
Barbu, Miruna C.;
Hawkins, Emma L.;
Wardlaw, Joanna M.;
Steele, J. Douglas;
Waiter, Gordon D.;
Sandu, Anca-Larisa;
Campbell, Archie;
Porteous, David J.;
Seckl, Jonathan R.;
Lawrie, Stephen M.;
Reynolds, Rebecca M.;
Cavanagh, Jonathan;
McIntosh, Andrew M.;
Whalley, Heather C.

Publication type:

Article

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

Integrated methylome and phenome study of the circulating proteome reveals markers pertinent to brain health.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32319-8

By:

Gadd, Danni A.;
Hillary, Robert F.;
McCartney, Daniel L.;
Shi, Liu;
Stolicyn, Aleks;
Robertson, Neil A.;
Walker, Rosie M.;
McGeachan, Robert I.;
Campbell, Archie;
Xueyi, Shen;
Barbu, Miruna C.;
Green, Claire;
Morris, Stewart W.;
Harris, Mathew A.;
Backhouse, Ellen V.;
Wardlaw, Joanna M.;
Steele, J. Douglas;
Oyarzún, Diego A.;
Muniz-Terrera, Graciela;
Ritchie, Craig

Publication type:

Article

Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans.

Published in:

Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-02953-6

By:

Gao, Chenhao;
Amador, Carmen;
Walker, Rosie M.;
Campbell, Archie;
Madden, Rebecca A.;
Adams, Mark J.;
Bai, Xiaomeng;
Liu, Ying;
Li, Miaoxin;
Hayward, Caroline;
Porteous, David J.;
Shen, Xueyi;
Evans, Kathryn L.;
Haley, Chris S.;
McIntosh, Andrew M.;
Navarro, Pau;
Zeng, Yanni

Publication type:

Article

Blood-based epigenome-wide analyses of cognitive abilities.

Published in:

Genome Biology, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s13059-021-02596-5

By:

McCartney, Daniel L.;
Hillary, Robert F.;
Conole, Eleanor L. S.;
Banos, Daniel Trejo;
Gadd, Danni A.;
Walker, Rosie M.;
Nangle, Cliff;
Flaig, Robin;
Campbell, Archie;
Murray, Alison D.;
Maniega, Susana Muñoz;
Valdés-Hernández, María del C.;
Harris, Mathew A.;
Bastin, Mark E.;
Wardlaw, Joanna M.;
Harris, Sarah E.;
Porteous, David J.;
Tucker-Drob, Elliot M.;
McIntosh, Andrew M.;
Evans, Kathryn L.

Publication type:

Article

Sex-Differences in the Metabolic Health of Offspring of Parents with Diabetes: A Record-Linkage Study.

Published in:

PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0134883

By:

Aldhous, Marian C.;
Reynolds, Rebecca M.;
Campbell, Archie;
Linksted, Pamela;
Lindsay, Robert S.;
Smith, Blair H.;
Seckl, Jonathan R.;
Porteous, David J.;
Norman, Jane E.;
null, null

Publication type:

Article

Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis.

Published in:

2016

By:

McIntosh, Andrew M.;
Hall, Lynsey S.;
Zeng, Yanni;
Adams, Mark J.;
Gibson, Jude;
Wigmore, Eleanor;
Hagenaars, Saskia P.;
Davies, Gail;
Fernandez-Pujals, Ana Maria;
Campbell, Archie I.;
Clarke, Toni-Kim;
Hayward, Caroline;
Haley, Chris S.;
Porteous, David J.;
Deary, Ian J.;
Smith, Daniel J.;
Nicholl, Barbara I.;
Hinds, David A.;
Jones, Amy V.;
Scollen, Serena

Publication type:

journal article

Methylome-wide association study of early life stressors and adult mental health.

Published in:

Human Molecular Genetics, 2022, v. 31, n. 4, p. 651, doi. 10.1093/hmg/ddab274

By:

Howard, David M;
Pain, Oliver;
Arathimos, Ryan;
Barbu, Miruna C;
Amador, Carmen;
Walker, Rosie M;
Jermy, Bradley;
Adams, Mark J;
Deary, Ian J;
Porteous, David;
Campbell, Archie;
Sullivan, Patrick F;
Evans, Kathryn L;
Arseneault, Louise;
Wray, Naomi R;
Meaney, Michael;
McIntosh, Andrew M;
Lewis, Cathryn M

Publication type:

Article

Genome-wide association study of cardiac troponin I in the general population.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 21, p. 2027, doi. 10.1093/hmg/ddab124

By:

Moksnes, Marta R;
Røsjø, Helge;
Richmond, Anne;
Lyngbakken, Magnus N;
Graham, Sarah E;
Hansen, Ailin Falkmo;
Wolford, Brooke N;
Taliun, Sarah A Gagliano;
LeFaive, Jonathon;
Rasheed, Humaira;
Thomas, Laurent F;
Zhou, Wei;
Aung, Nay;
Surakka, Ida;
Douville, Nicholas J;
Campbell, Archie;
Porteous, David J;
Petersen, Steffen E;
Munroe, Patricia B;
Welsh, Paul

Publication type:

Article

A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank.

Published in:

Human Molecular Genetics, 2020, v. 29, n. 8, p. 1396, doi. 10.1093/hmg/ddaa058

By:

Meng, Weihua;
Chan, Brian W;
Harris, Cameron;
Freidin, Maxim B;
Hebert, Harry L;
Adams, Mark J;
Campbell, Archie;
Hayward, Caroline;
Zheng, Hua;
Zhang, Xianwei;
Colvin, Lesley A;
Hales, Tim G;
Palmer, Colin N A;
Williams, Frances M K;
McIntosh, Andrew;
Smith, Blair H

Publication type:

Article

Insights into the genetic basis of retinal detachment.

Published in:

Human Molecular Genetics, 2020, v. 29, n. 4, p. 689, doi. 10.1093/hmg/ddz294

By:

Boutin, Thibaud S;
Charteris, David G;
Chandra, Aman;
Campbell, Susan;
Hayward, Caroline;
Campbell, Archie;
Consortium, UK Biobank Eye & Vision;
Nandakumar, Priyanka;
Hinds, David;
Team, 23andMe Research;
Mitry, Danny;
Vitart, Veronique

Publication type:

Article

Quantifying the extent to which index event biases influence large genetic association studies.

Published in:

Human Molecular Genetics, 2017, v. 26, n. 5, p. 1018, doi. 10.1093/hmg/ddw433

By:

Yaghootkar, Hanieh;
Bancks, Michael P.;
Jones, Sam E.;
McDaid, Aaron;
Beaumont, Robin;
Donnelly, Louise;
Wood, Andrew R.;
Campbell, Archie;
Tyrrell, Jessica;
Hocking, Lynne J.;
Tuke, Marcus A.;
Ruth, Katherine S.;
Pearson, Ewan R.;
Murray, Anna;
Freathy, Rachel M.;
Munroe, Patricia B.;
Hayward, Caroline;
Palmer, Colin;
Weedon, Michael N.;
Pankow, James S.

Publication type:

Article

Homozygous loss-of-function variants in European cosmopolitan and isolate populations.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 19, p. 5464, doi. 10.1093/hmg/ddv272

By:

Kaiser, Vera B.;
Svinti, Victoria;
Prendergast, James G.;
You-Ying Chau;
Campbell, Archie;
Patarcic, Inga;
Barroso, Inês;
Joshi, Peter K.;
Hastie, Nicholas D.;
Miljkovic, Ana;
Taylor, Martin S.;
Scotland, Generation;
Enroth, Stefan;
Memari, Yasin;
Kolb-Kokocinski, Anja;
Wright, Alan F.;
Gyllensten, Ulf;
Durbin, Richard;
Rudan, Igor;
Campbell, Harry

Publication type:

Article

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Published in:

Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0

By:

Sherwood, Kitty;
Ward, Joseph C.;
Soriano, Ignacio;
Martin, Lynn;
Campbell, Archie;
Rahbari, Raheleh;
Kafetzopoulos, Ioannis;
Sproul, Duncan;
Green, Andrew;
Sampson, Julian R.;
Donaldson, Alan;
Ong, Kai-Ren;
Heinimann, Karl;
Nielsen, Maartje;
Thomas, Huw;
Latchford, Andrew;
Palles, Claire;
Tomlinson, Ian

Publication type:

Article

Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Published in:

2023

By:

Sherwood, Kitty;
Ward, Joseph C.;
Soriano, Ignacio;
Martin, Lynn;
Campbell, Archie;
Rahbari, Raheleh;
Kafetzopoulos, Ioannis;
Sproul, Duncan;
Green, Andrew;
Sampson, Julian R.;
Donaldson, Alan;
Ong, Kai-Ren;
Heinimann, Karl;
Nielsen, Maartje;
Thomas, Huw;
Latchford, Andrew;
Palles, Claire;
Tomlinson, Ian

Publication type:

Correction Notice

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Published in:

Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0

By:

Sherwood, Kitty;
Ward, Joseph C.;
Soriano, Ignacio;
Martin, Lynn;
Campbell, Archie;
Rahbari, Raheleh;
Kafetzopoulos, Ioannis;
Sproul, Duncan;
Green, Andrew;
Sampson, Julian R.;
Donaldson, Alan;
Ong, Kai-Ren;
Heinimann, Karl;
Nielsen, Maartje;
Thomas, Huw;
Latchford, Andrew;
Palles, Claire;
Tomlinson, Ian

Publication type:

Article

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.

Published in:

Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0

By:

Sherwood, Kitty;
Ward, Joseph C.;
Soriano, Ignacio;
Martin, Lynn;
Campbell, Archie;
Rahbari, Raheleh;
Kafetzopoulos, Ioannis;
Sproul, Duncan;
Green, Andrew;
Sampson, Julian R.;
Donaldson, Alan;
Ong, Kai-Ren;
Heinimann, Karl;
Nielsen, Maartje;
Thomas, Huw;
Latchford, Andrew;
Palles, Claire;
Tomlinson, Ian

Publication type:

Article

Identification of epigenome-wide DNA methylation differences between carriers of APOE ε4 and APOE ε2 alleles.

Published in:

Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-020-00808-4

By:

Walker, Rosie M.;
Vaher, Kadi;
Bermingham, Mairead L.;
Morris, Stewart W.;
Bretherick, Andrew D.;
Zeng, Yanni;
Rawlik, Konrad;
Amador, Carmen;
Campbell, Archie;
Haley, Chris S.;
Hayward, Caroline;
Porteous, David J.;
McIntosh, Andrew M.;
Marioni, Riccardo E.;
Evans, Kathryn L.

Publication type:

Article

An epigenome-wide association study of sex-specific chronological ageing.

Published in:

Genome Medicine, 2019, v. 12, n. 1, p. 1, doi. 10.1186/s13073-019-0693-z

By:

McCartney, Daniel L.;
Zhang, Futao;
Hillary, Robert F.;
Zhang, Qian;
Stevenson, Anna J.;
Walker, Rosie M.;
Bermingham, Mairead L.;
Boutin, Thibaud;
Morris, Stewart W.;
Campbell, Archie;
Murray, Alison D.;
Whalley, Heather C.;
Porteous, David J.;
Hayward, Caroline;
Evans, Kathryn L.;
Chandra, Tamir;
Deary, Ian J.;
McIntosh, Andrew M.;
Yang, Jian;
Visscher, Peter M.

Publication type:

Article

Early life predictors of late life cerebral small vessel disease in four prospective cohort studies.

Published in:

2021

By:

Backhouse, Ellen V;
Shenkin, Susan D;
McIntosh, Andrew M;
Bastin, Mark E;
Whalley, Heather C;
Hernandez, Maria Valdez;
Maniega, Susana Muñoz;
Harris, Mathew A;
Stolicyn, Aleks;
Campbell, Archie;
Steele, Douglas;
Waiter, Gordon D;
Sandu, Anca-Larisa;
Waymont, Jennifer M J;
Murray, Alison D;
Cox, Simon R;
Rooij, Susanne R de;
Roseboom, Tessa J;
Wardlaw, Joanna M;
Valdez Hernandez, Maria

Publication type:

journal article

Blunted medial prefrontal cortico-limbic reward-related effective connectivity and depression.

Published in:

2020

By:

Rupprechter, Samuel;
Romaniuk, Liana;
Series, Peggy;
Hirose, Yoriko;
Hawkins, Emma;
Sandu, Anca-Larisa;
Waiter, Gordon D;
McNeil, Christopher J;
Shen, Xueyi;
Harris, Mathew A;
Campbell, Archie;
Porteous, David;
Macfarlane, Jennifer A;
Lawrie, Stephen M;
Murray, Alison D;
Delgado, Mauricio R;
McIntosh, Andrew M;
Whalley, Heather C;
Steele, J Douglas

Publication type:

journal article

Identification and validation of plasma proteome signatures associated with MRI measurements in healthy individuals.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.052512

By:

Shi, Liu;
Hillary, Robert Francis;
Marioni, Riccardo E.;
Campbell, Archie;
Hayward, Caroline;
Stolicyn, Aleks;
Whalley, Heather C.;
Buckley, Noel;
Nevado‐Holgado, Alejo J

Publication type:

Article

Correction: Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation.

Published in:

2017

By:

Xia, Charley;
Amador, Carmen;
Huffman, Jennifer;
Trochet, Holly;
Campbell, Archie;
Porteous, David;
Scotland, Generation;
Hastie, Nicholas D.;
Hayward, Caroline;
Vitart, Veronique;
Navarro, Pau;
Haley, Chris S.

Publication type:

Correction Notice

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation.

Published in:

PLoS Genetics, 2016, v. 12, n. 2, p. 1, doi. 10.1371/journal.pgen.1005804

By:

Xia, Charley;
Amador, Carmen;
Huffman, Jennifer;
Trochet, Holly;
Campbell, Archie;
Porteous, David;
null, null;
Hastie, Nicholas D.;
Hayward, Caroline;
Vitart, Veronique;
Navarro, Pau;
Haley, Chris S.

Publication type:

Article

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

SNP and Haplotype Regional Heritability Mapping (SNHap-RHM): Joint Mapping of Common and Rare Variation Affecting Complex Traits.

Published in:

Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.791712

By:

Oppong, Richard F.;
Boutin, Thibaud;
Campbell, Archie;
McIntosh, Andrew M.;
Porteous, David;
Hayward, Caroline;
Haley, Chris S.;
Navarro, Pau;
Knott, Sara

Publication type:

Article

Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2020, v. 183, n. 6, p. 309, doi. 10.1002/ajmg.b.32807

By:

Hagenaars, Saskia P.;
Coleman, Jonathan R. I.;
Choi, Shing Wan;
Gaspar, Héléna;
Adams, Mark J.;
Howard, David M.;
Hodgson, Karen;
Traylor, Matthew;
Air, Tracy M.;
Andlauer, Till F. M.;
Arolt, Volker;
Baune, Bernhard T.;
Binder, Elisabeth B.;
Blackwood, Douglas H. R.;
Boomsma, Dorret I.;
Campbell, Archie;
Cearns, Micah;
Czamara, Darina;
Dannlowski, Udo;
Domschke, Katharina

Publication type:

Article

Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study.

Published in:

PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0170653

By:

van Hecke, Oliver;
Hocking, Lynne J.;
Torrance, Nicola;
Campbell, Archie;
Padmanabhan, Sandosh;
Porteous, David J.;
McIntosh, Andrew M.;
Burri, Andrea V.;
Tanaka, Haruka;
Williams, Frances M. K.;
Smith, Blair H.

Publication type:

Article

Associations of negative affective biases and depressive symptoms in a community-based sample.

Published in:

Psychological Medicine, 2023, v. 53, n. 12, p. 5518, doi. 10.1017/S0033291722002720

By:

de Nooij, Laura;
Adams, Mark J.;
Hawkins, Emma L.;
Romaniuk, Liana;
Munafò, Marcus R.;
Penton-Voak, Ian S.;
Elliott, Rebecca;
Bland, Amy R.;
Waiter, Gordon D.;
Sandu, Anca-Larisa;
Habota, Tina;
Steele, J. Douglas;
Murray, Alison D.;
Campbell, Archie;
Porteous, David J.;
McIntosh, Andrew M.;
Whalley, Heather C.

Publication type:

Article

Common Genetic Variants Explain the Majority of the Correlation Between Height and Intelligence: The Generation Scotland Study.

Published in:

Behavior Genetics, 2014, v. 44, n. 2, p. 91, doi. 10.1007/s10519-014-9644-z

By:

Marioni, Riccardo;
Batty, G.;
Hayward, Caroline;
Kerr, Shona;
Campbell, Archie;
Hocking, Lynne;
Porteous, David;
Visscher, Peter;
Deary, Ian

Publication type:

Article

Pharmaco-epidemiology of antidepressant exposure in a UK cohort record-linkage study.

Published in:

2019

By:

Hafferty, Jonathan D.;
Wigmore, Eleanor M.;
Howard, David M.;
Adams, Mark J.;
Clarke, Toni-Kim;
Campbell, Archie I.;
MacIntyre, Donald J.;
Nicodemus, Kristin K.;
Lawrie, Stephen M.;
Porteous, David J.;
McIntosh, Andrew M.

Publication type:

journal article

Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations.

Published in:

International Journal of Epidemiology, 2022, v. 51, n. 3, p. e108, doi. 10.1093/ije/dyab234

By:

Unnarsdóttir, Anna Bára;
Lovik, Anikó;
Fawns-Ritchie, Chloe;
Ask, Helga;
Kõiv, Kadri;
Hagen, Kristen;
Didriksen, Maria;
Christoffersen, Lea Arregui Nordahl;
Garðarsson, Alexander Berg;
McIntosh, Andrew;
Kähler, Anna K;
Campbell, Archie;
Hauksdóttir, Arna;
Erikstrup, Christian;
Mikkelsen, Dorte Helenius;
Altschul, Drew;
Thordardottir, Edda Bjork;
Frans, Emma Maria;
Kvale, Gerd;
Tómasson, Gunnar

Publication type:

Article

Factors associated with sharing e-mail information and mental health survey participation in large population cohorts.

Published in:

2020

By:

Adams, Mark J;
Hill, W David;
Howard, David M;
Dashti, Hassan S;
Davis, Katrina A S;
Campbell, Archie;
Clarke, Toni-Kim;
Deary, Ian J;
Hayward, Caroline;
Porteous, David;
Hotopf, Matthew;
McIntosh, Andrew M

Publication type:

journal article

Evidence for large-scale gene-by-smoking interaction effects on pulmonary function.

Published in:

2017

By:

Aschard, Hugues;
Tobin, Martin D.;
Hancock, Dana B.;
Skurnik, David;
Sood, Akshay;
James, Alan;
Smith, Albert Vernon;
Manichaikul, Ani W.;
Campbell, Archie;
Prins, Bram P.;
Hayward, Caroline;
Loth, Daan W.;
Porteous, David J.;
Strachan, David P.;
Zeggini, Eleftheria;
O'Connor, George T.;
Brusselle, Guy G.;
Boezen, H. Marike;
Schulz, Holger;
Deary, Ian J.

Publication type:

journal article

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

Published in:

International Journal of Epidemiology, 2013, v. 42, n. 3, p. 689, doi. 10.1093/ije/dys084

By:

Smith, Blair H;
Campbell, Archie;
Linksted, Pamela;
Fitzpatrick, Bridie;
Jackson, Cathy;
Kerr, Shona M;
Deary, Ian J;
MacIntyre, Donald J;
Campbell, Harry;
McGilchrist, Mark;
Hocking, Lynne J;
Wisely, Lucy;
Ford, Ian;
Lindsay, Robert S;
Morton, Robin;
Palmer, Colin N A;
Dominiczak, Anna F;
Porteous, David J;
Morris, Andrew D

Publication type:

Article

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits.

Published in:

2020

By:

Banos, Daniel Trejo;
McCartney, Daniel L.;
Patxot, Marion;
Anchieri, Lucas;
Battram, Thomas;
Christiansen, Colette;
Costeira, Ricardo;
Walker, Rosie M.;
Morris, Stewart W.;
Campbell, Archie;
Zhang, Qian;
Porteous, David J.;
McRae, Allan F.;
Wray, Naomi R.;
Visscher, Peter M.;
Haley, Chris S.;
Evans, Kathryn L.;
Deary, Ian J.;
McIntosh, Andrew M.;
Hemani, Gibran

Publication type:

Correction Notice

Bayesian reassessment of the epigenetic architecture of complex traits.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16520-1

By:

Trejo Banos, Daniel;
McCartney, Daniel L.;
Patxot, Marion;
Anchieri, Lucas;
Battram, Thomas;
Christiansen, Colette;
Costeira, Ricardo;
Walker, Rosie M.;
Morris, Stewart W.;
Campbell, Archie;
Zhang, Qian;
Porteous, David J.;
McRae, Allan F.;
Wray, Naomi R.;
Visscher, Peter M.;
Haley, Chris S.;
Evans, Kathryn L.;
Deary, Ian J.;
McIntosh, Andrew M.;
Hemani, Gibran

Publication type:

Article

Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases.

Published in:

Cancers, 2023, v. 15, n. 13, p. 3313, doi. 10.3390/cancers15133313

By:

Figlioli, Gisella;
Billaud, Amandine;
Wang, Qin;
Bolla, Manjeet K.;
Dennis, Joe;
Lush, Michael;
Kvist, Anders;
Adank, Muriel A.;
Ahearn, Thomas U.;
Antonenkova, Natalia N.;
Auvinen, Päivi;
Behrens, Sabine;
Bermisheva, Marina;
Bogdanova, Natalia V.;
Bojesen, Stig E.;
Bonanni, Bernardo;
Brüning, Thomas;
Camp, Nicola J.;
Campbell, Archie;
Castelao, Jose E.

Publication type:

Article

The Impact of Acute Nutritional Interventions on the Plasma Proteome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 8, p. 2087, doi. 10.1210/clinem/dgad031

By:

Vernardis, Spyros I.;
Demichev, Vadim;
Lemke, Oliver;
Grüning, Nana-Maria;
Messner, Christoph;
White, Matt;
Pietzner, Maik;
Peluso, Alina;
Collet, Tinh-Hai;
Henning, Elana;
Gille, Christoph;
Campbell, Archie;
Hayward, Caroline;
Porteous, David J.;
Marioni, Riccardo E.;
Mülleder, Michael;
Zelezniak, Aleksej;
Wareham, Nicholas J.;
Langenberg, Claudia;
Farooqi, I. Sadaf

Publication type:

Article

Recent genomic heritage in Scotland.

Published in:

BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1605-2

By:

Amador, Carmen;
Huffman, Jennifer;
Trochet, Holly;
Campbell, Archie;
Porteous, David;
Wilson, James F.;
Hastie, Nick;
Vitart, Veronique;
Hayward, Caroline;
Navarro, Pau;
Haley, Chris S.

Publication type:

Article

Genome-wide methylation data improves dissection of the effect of smoking on body mass index.

Published in:

PLoS Genetics, 2021, v. 17, n. 9, p. 1, doi. 10.1371/journal.pgen.1009750

By:

Amador, Carmen;
Zeng, Yanni;
Barber, Michael;
Walker, Rosie M.;
Campbell, Archie;
McIntosh, Andrew M.;
Evans, Kathryn L.;
Porteous, David J.;
Hayward, Caroline;
Wilson, James F.;
Navarro, Pau;
Haley, Chris S.

Publication type:

Article

Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure.

Published in:

2017

By:

Zhang, Zhen‐Yu;
Ravassa, Susana;
Nkuipou‐Kenfack, Esther;
Yang, Wen‐Yi;
Kerr, Shona M.;
Koeck, Thomas;
Campbell, Archie;
Kuznetsova, Tatiana;
Mischak, Harald;
Padmanabhan, Sandosh;
Dominiczak, Anna F.;
Delles, Christian;
Staessen, Jan A.;
Zhang, Zhen-Yu;
Nkuipou-Kenfack, Esther;
Yang, Wen-Yi

Publication type:

journal article