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The University of Edinburgh

The University of Edinburgh | College of Medicine and Veterinary Medicine |
Deanery of Molecular, Genetic and Population Health Sciences | Usher Institute

Centre for Population Health Sciences

Strapline photo
Photo of Harry Campbell

Professor Harry Campbell

Professor of Genetic Epidemiology and Public Health

Tel: 0131 650 3218
Fax: (0131) 650 6909


  • Co-Director of Centre for Global Health Research, MBChB course
  • Co-Director WHO Collaborating Centre for Population Health Research and Training
  • Programme lead for public health, Research Governance Committee, NHS Lothian

Teaching Responsibilities

  • Co-ordinator social sciences and public health programme theme, MBChB course
  • MPH: Course leader - Global Health Epidemiology
  • MPH: Course lecturer Genetic Epidemiology; Epidemiology for Public Health; Epidemiology of non communicable diseases

Research Interests

  1. Genetic epidemiology studies
    • Colorectal cancer genetics
    • Mapping of complex disease QTL in genetic isolate populations
  2. Epidemiology of glycans in health and disease
  3. International Health
  4. Health Services Research

Current Research Involvement

  1. Genetic epidemiology studies
    1. Genetic isolate populations
      We have established cohort studies recruiting families / extended pedigrees and measuring a wide range of quantitative traits of public health importance in the Dalmatian islands, Croatia and in Orkney island, Scotland. We have also established a research collaboration linking 5 genetic isolate populations throughout Europe (EUROSPAN). Currently funded by 5 year MRC Programme grant (QTL in Health and Disease).

      Research areas
      • QTL mapping on wide variety of disease-related traits
      • Population genetics characterisation of isolate populations
      • Inbreeding depression effects on late-onset traits
    2. Contribution to other collaborative genetic epidemiology studies
      • Scottish Family Health Study (Generation Scotland)
      • Member of many international GWAS consortia
  2. Colorectal cancer genetics (together with Prof Malcolm Dunlop and colorectal cancer genetics group at MRC Human Genetics Unit)
    We have recruited about 4,000 patients with colorectal cancer in Scotland, 1,400 of these with early onset (under 55 years of age). We have also recruited population and family based controls and environmental exposure /survival / clinical data (SOCCS study)). Study funded by 5 year Programme grants from CRC and CRUK since 2003 (current Programme grant 2016 – 2020)

    Research areas include
    1. Epidemiology of mismatch repair gene mutations
      • Prevalence, penetrance, modifiers etc
    2. Identification of novel genetic variants
      • Candidate gene / association approach
      • Genome wide screen / association approach - Exome sequencing
      • Field synopses of colorectal adenoma / carcinoma genetics
  3. Glycomic epidemiology studies
    We have undertaken GWAS studies of plasma and IgG N-glycans and associated follow on studies in disease cohorts. - current EU funded projects include
    • IBD BIOM - inflammatory disease glycomics
    • MIMOmics -
    • High GLYCAN
  4. International Health
    I have long standing interests in several aspects of childhood respiratory infections in developing countries - epidemiology, prevention and treatment. - current funded projects include:

    • WHO / UNICEF Child Health Epidemiology Reference Group (now Maternal and Child health Estimation and Evaluation group
    • Improving Coverage Measurement in MNCH (ICM) Core Group
    • RSV Global Estimation Network
    • Optimal use of clinical signs for diagnosis and prognosis of childhood pneumonia

Other Responsibilities/Activities

Further Information

Work History

Previous Appointments
1986-1989 Epidemiologist / Research Clinician, MRC, The Gambia, West Africa
1989-1992 Medical Officer, World Health Organisation, Geneva, Switzerland
1992-1995 Consultant in Public Health Medicine, Fife Health Board, Scotland
1995-2004 Senior Lecturer then Reader in Genetic Epidemiology / Public Health, University of Edinburgh

Selected grants

  • Investigating validity of maternal recall of care-seeking location (India) (Bill and Melinda Gates Foundation, 2014-2016) Nair H, Campbell H
  • Systematic literature review of Clostridium difficile disease burden (Sanofi Pasteur, 2014-2015) Nair H, Campbell H
  • Systematic literature review in multiple language databases to identify studies reporting data (by gender) on hospitalisations and mortality for the three leading causes of child mortality (UNICEF, 2014-2014) Nair H, Campbell H, Rudan I
  • Maternal and Child Epidemiology (Johns Hopkins University, 2014-2016) Rudan I, Campbell H, Nair H
  • Optimal use of clinical signs for diagnosis and prognosis of childhood pneumonia (World Health Organization, 2014-2015) Nair H, Campbell H
  • Improving current global estimates of morbidity and mortality due to RSV - associated acute lower respiratory infections in young children through acquisition of novel data and disease burden modelling (Bill and Melinda Gates Foundation, 2013-2015) Nair H, Campbell H, Rudan I, McAllister DA
  • Cost of treatment of childhood pneumonia under the revised WHO guidelines and the cost projection for management in 2015 (World Health Organization, 2013-2013) Nair H, Campbell H, Zhang S
  • Improving coverage measurement for MNCH: linking household survey data to assessments of service provision (Johns Hopkins University, 2013-2013) Campbell H, Nair H, Brondi L
  • Systematic literature review of relative risks / odds ratio for pneumonia in children associated with HIV infection (World Health Organization, 2013-2013) Campbell H, Nair H
  • Estimating the annual number of deaths from multidrug-resistant TB in the world (WHO, 2013-2013) Nair H, Brondi L, Campbell H
  • WHO Manual on Influenza Burden of Disease (Global Influenza Program, World Health Organization, Geneva, 2011-2012) Nair H, Campbell H
  • Analysis of landscape and potential impact of diagnostics for neonatal sepsis. (Bill and Melinda Gates Foundation, 2010-2012) Rudan I., Campbell H.
  • A mendelian randomisation study of vitamin D on colorectal cancer risk (Chief Scientist Office, 2009-2011) Campbell H, Theodoratou E, Dunlop M, McKeigue P, Davey Smith G, Farrington SM
  • Identifying susceptibility loci for osteoporosis by genome wide scan in the UK population isolate of Orkney. (Arthritis Research Council, 2007-2010) Ralston S, Wilson J, Wright A ,Campbell H, Albagha O, Wild S
  • EUROpean Special Populations reseArch Network (EUROSPAN): quantifying and harnessing genetic variation for gene discovery. : MRC Human Genetics Unit, Erasmus University (N), Zagreb University (Cr), National Research Center for Environment and Health Munich (G), Uppsala University (Sw), European Research Academy (It), IntegraGen (Fr). (European Union (FP6), 2006-2009) Campbell H et al
  • The Genetic Analysis of Ocular Morphometric Traits Related to Primary Open Angle Glaucoma Susceptibility in the Population Isolate of Orkney (The Glaucoma Inheritance Study of Orkney, GISO). (Chief Scientist Office, Scottish Executive, 2006-2008) Karunaratne V, Wright A, Wilson J, Fleck B, Campbell H
  • The Role of Base Excision Repair defects in predisposition to colorectal cancer. (Chief Scientist Office, Scottish Executive, 2006-2008) Melton D, Campbell H et al
  • Mapping genes underlying complex quantitative traits in isolate populations - Phase III. (Medical Research Council UK, 2005-2008) Rudan I, Wright A, Campbell H, Carothers A
  • Scottish Family Heart Study (Genetics and Healthcare Initiative). (Scottish Executive, 2005-2008) Morris A, Campbell H et al (CI University of Dundee)
  • Genome Scan To Identify Common Low Penetrance Alleles Contributing to Colorectal Cancer Aetiology. (CRUK, 2005-2007) Dunlop M, Campbell H
  • Statistical methods for describing gene-environment interactions in cardiovascular disease risk factors (Health Services Research studentship). (Chief Scientist Office, 2005-2008) Anderson N, Wild S, Campbell H
  • Investigating the effects of inbreeding on human quantitative traits. (National Institutes of Health, 2004-2006) Rudan I, Campbell H et al
  • Genetic dissection of high myopia using threshold-defined case and control subjects from a Scottish isolate sub-population, the Western Isles. (Chief Scientist Office, Scottish Executive, 2004-2007) Vitart V, Wright A, Campbell H et al (CI MRC Human Genetics)
  • The importance of cell cycle control and DNA repair gene polymorphisms in genetic predisposition to melanoma. (Chief Scientist Office, 2004-2007) Melton D W, Anderson N, Campbell H, Doherty V, Kavanagh G, Rees J
  • Genetic analysis of cardiovascular disease-related traits in Orkney. (Chief Scientist Office, 2004-2007) Wilson J, Campbell H, Wright A, Wild S, Visscher P, Carothers A et al
  • Genetics of Complex Traits and Diseases in Croatian genetic isolate. (The Royal Society, 2003-2005) Rudan I, Campbell H
  • An investigation of genetic determinants of susceptibility and disease behaviour in early inflammatory bowel disease. (Wellcome Trust Programme Grant, 2003-2008) Satsangi J, Campbell H et al
  • National Translational Cancer Research Network. (Department of Health, 2003-2008) Dunlop M, Campbell H et al
  • Utilising genetics to combat colorectal cancer. (Cancer Research UK Programme Grant, 2003-2008) Dunlop M, Campbell H
  • Associations of mutations in the human homolog of the MutY gene with early onset colorectal cancer. (Chief Scientist Office, Scottish Executive, 2003-2006) Farrington S, Dunlop M, Campbell H et al
  • Mapping genes underlying complex quantitative traits in Croatian isolate population - Phase I. (Medical Research Council, 2002-2002) Wright A, Hayward C, Hastie N, Rudan I, Campbell H et al (CI MRC Human Genetics)
  • Mapping genes underlying complex quantitative traits in Croatian isolate population - Phase II. (Medical Research Council, 2002-2005) Wright A, Hayward C, Hastie N, Rudan I, Campbell H (CI MRC Human Genetics)
  • Centre for colorectal cancer research. (Digestive Disorders Foundation, 2002-2007) Campbell H, Dunlop M, Satsangi J, Jodrell D


Link to Edinburgh Research Explorer for full publications list

Selected publications

Global Health
  • Evropi Theodoratou, David A McAllister, Craig Reed, Davies O Adeloye, Igor Rudan, Lulu M Muhe, Shabir A Madhi, Harry Campbell, Harish Nair. Global, regional, and national estimates of pneumonia burden in HIV-infected children in 2010: a meta-analysis and modelling study. Lancet Infect Dis 2014;14:1250–58. DOI Link
  • Bhutta ZA, Das JK, Walker N, Rizvi A, Campbell H, Rudan I, Black RE. Interventions to address diarrhoea and pneumonia deaths equitably: what works and at what cost? Lancet. 2013; 381: 1417 – 29 DOI Link
  • Chopra M, Mason E, Borrazzo J, Campbell H, Rudan I, Liu L, Black RE, Bhutta Z. Ending preventable deaths from pneumonia and diarrhoea – an achievable goal. Lancet. 2013; 381: 1499 – 1506 DOI Link
  • Hazir T, Begum K, El Arifeen S, Khan AM, Huque MH, Kazmi N, Roy S, Abbasi S, Rahman QS, Theodoratou E, Khorshed MS, Rahman KM, Bari S, Kaiser MM, Saha SK, Ahmed AS, Rudan I, Bryce J, Qazi SA, Campbell H. Measuring Coverage in MNCH: A Prospective Validation Study in Pakistan and Bangladesh on Measuring Correct Treatment of Childhood Pneumonia. PLoS Med. 2013 10: e1001422 DOI Link
  • Walker CL, Rudan I, Liu L, Nair H, Theodoratou E, Bhutta ZA, O'Brien KL, Campbell H, Black RE. Global burden of childhood pneumonia and diarrhoea. Lancet 2013; 381(9875):1405-16 DOI Link
  • Nair H, Simões EA, Rudan I, Gessner BD, Azziz-Baumgartner E, Zhang JS, Feikin DR, Mackenzie GA, Moïsi JC, Roca A, Baggett HC, Zaman SM, Singleton RJ, Lucero MG, Chandran A, Gentile A, Cohen C, Krishnan A, Bhutta ZA, Arguedas A, Clara AW, Andrade AL, Ope M, Ruvinsky RO, Hortal M, McCracken JP, Madhi SA, Bruce N, Qazi SA, Morris SS, El Arifeen S, Weber MW, Scott JA, Brooks WA, Breiman RF, Campbell H. Global and regional burden of hospital admissions for severe acute lower respiratory infections in young children in 2010: a systematic analysis. Lancet 2013; 381(9875):1380-90 DOI Link
  • Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, Rudan I, Campbell H, Cibulskis R, Li M, Mathers C, Black RE, for the Child Health Epidemiology Reference Group of WHO and UNICEF (including Theodoratou E) Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet 2012; 379: 2151-61 DOI Link
  • Nair H, Brooks WA, Katz M, Roca A, Berkley JA, Madhi SA et al. Global burden of respiratory infections due to seasonal influenza in young children: a systematic review and meta-analysis. Lancet. 2011; 378(9807): 1917-30 DOI Link
  • Rudan I, Chan KY, Zhang JSF, Theodoratou E, Feng XL, Salomon J, Lawn JE, Cousens S, Black RE, Guo Y, Campbell H on behalf of WHO/UNICEF’s Child Health Epidemiology Reference Group (CHERG). Causes of deaths in children younger than five years in China in 2008. The Lancet. 2010; 375:1083–89 DOI Link
  • Black RE, Cousens S, Johnson HL, Lawn JE, Rudan I, Bassani DG, Jha P, Campbell H, Walker CF, Cibulskis R, Eisele T, Liu L, Mathers C, Child Health Epidemiology Reference Group of WHO and UNICEF (including Theodoratou E). Global, regional, and national causes of child mortality in 2008: a systematic analysis. Lancet 2010; 375: 1969-87 DOI Link
  • Theodoratou E, Campbell H, Ventham NT, Kolarich D, Pučić-Baković M, Zoldoš V, Fernandes D, Pemberton IK, Rudan I, Kennedy NA, Wuhrer M, Nimmo E, Annese V, McGovern DP, Satsangi J, Lauc G. The role of glycosylation in IBD. Nat Rev Gastroenterol Hepatol. 2014 Oct;11(10):588-600 DOI Link
  • Dunlop MG, Tenesa A, Farrington SM, Ballereau S, Brewster DH, Koessler T, Pharoah P, Schafmayer C, Hampe J, Völzke H, Chang-Claude J, Hoffmeister M, Brenner H, von Holst S, Picelli S, Lindblom A, Jenkins MA, Hopper JL, Casey G, Duggan D, Newcomb PA, Abulí A, Bessa X, Ruiz-Ponte C, Castellví-Bel S, Niittymäki I, Tuupanen S, Karhu A, Aaltonen L, Zanke B, Hudson T, Gallinger S, Barclay E, Martin L, Gorman M, Carvajal-Carmona L, Walther A, Kerr D, Lubbe S, Broderick P, Chandler I, Pittman A, Penegar S, Campbell H, Tomlinson I, Houlston RS. Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals. Gut. 2013 Jun;62(6):871-81. Epub 2012 Apr 5. DOI Link
  • Theodoratou E*, Montazeri Z*, Hawken S, Allum GCdL, Gong J, Tait V, Kirac I, Tazari M, Farrington SM, Demarsh A, Zgaga L, Landry D, Benson HE, Read SH, Rudan I, Tenesa A, Dunlop MG, Campbell H*, Little J*. Systematic meta-analyses and field synopsis of genetic association studies in colorectal cancer. J Natl Cancer Inst 2012: 1433-1457 DOI Link
  • Dunlop MG, Dobbins SE, ..., Theodoratou E,..., Tomlinson IP, Houlston R. Common variation at 6p21 (CDKN1A), 11q13.4 (POLD3) and Xp22.2 influences colorectal cancer risk. Nat Gen 2012; 44: 770-776 DOI Link
  • Din FVN*, Theodoratou E*, Farrington SM, Tenesa A, Barnetson RA, Cetnarskyj R, Stark LA, Porteous ME, Campbell H, Dunlop MG. Effect of aspirin and NSAIDs on risk and survival from colorectal cancer. Gut 2010; 59: 1670-9 DOI Link
  • Houlston RS, Cheadle J, Dobbins SE, Tenesa A, Jones AM, Howarth K, Spain SL, Broderick P, Domingo E, Farrington S, Prendergast JG, Pittman AM, Theodoratou E, ..., Tomlinson IP. Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat Genet 2010; 42: 973-7 DOI Link
  • COGENT Study, Houlston RS, Webb E, Broderick P, Pittman AM, Di Bernardo MC, Lubbe S, Chandler I, Vijayakrishnan J, Sullivan K, Penegar S; Colorectal Cancer Association Study Consortium, Carvajal-Carmona L, Howarth K, Jaeger E, Spain SL, Walther A, Barclay E, Martin L, Gorman M, Domingo E, Teixeira AS; CoRGI Consortium, Kerr D, Cazier JB, Niittymäki I, Tuupanen S, Karhu A, Aaltonen LA, Tomlinson IP, Farrington SM, Tenesa A, Prendergast JG, Barnetson RA, Cetnarskyj R, Porteous ME, Pharoah PD, Koessler T, Hampe J, Buch S, Schafmayer C, Tepel J, Schreiber S, Völzke H, Chang-Claude J, Hoffmeister M, Brenner H, Zanke BW, Montpetit A, Hudson TJ, Gallinger S; International Colorectal Cancer Genetic Association Consortium, Campbell H, Dunlop MG. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet. 2008; 40: 1426 - 35. DOI Link
  • Tomlinson I, Webb E, Carvajal-Carmona L, Broderick P, Howarth K, Pittman A, Spain S, Lubbe S, Walther A, Sullivan K, Jaeger E, Rowan A, Vijayakrishnan J, Domingo E, Chandler I, Kemp Z, Qureshi M, Farrington S, Tenesa A, Prendergast JGD, Barnetson RA, Penegar S, Barclay E, Wood W, Martin L, Gorman M, Thomas H, Peto J, Bishop T, Gray R, Maher E, Lucassen A, Kerr D, Evans G, Schafmayer C, Buch S, Volzke H, Hampe J, Schreiber S, John U, Koessler T, Pharoah PDP, van Wezel T, Morreau H, Wijnen J, Lipton L, Hopper JL, Southey M, Giles G, Severi G, Castellvi-Bel S, Ruiz-Ponte C, Carracedo A, Castells A, Forsti A, Hemminki K, Vodicka P, Naccarati A, Lipton L, Ho J, Cheng K, Sham P, Luk J, Agundez J, Ladero J, de la Hoya M, Caldes T, Niittymaki I, Tuupanene S, Karhu A, Aaltonen L, Cazier J, Campbell Hǂ, Dunlop MGǂ, Houlston RSǂ [ǂ joint senior authors] A genome-wide association study identifies novel colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet 2008; 40: 623-30. DOI Link
  • Tenesa A, Farrington SM, Prendergast JDG, Porteous ME, Walker M, Haq N, Barnetson RA, Theodoratou E, Cetnarskyj R, Cartwright N, Semple C, Clark AJ, Reid FJL, Smith LA, Kavoussanakis K, Koessler T, Pharoah PDP, Buch S, Schafmayer C, Tepel J, Schreiber S, Völzke H, Schmidt CO, Hampe J, Wilkening S, Canzian F, Chang-Claude J, Hoffmeister M, Brenner H, Capella G, Moreno V, Deary IJ, Starr JM, Tomlinson IM, Kemp Z, Carvajal-Carmona L, Webb E, Broderick P, Vijayakrishnan J, Houlston RS, Rennert G, Ballinger D, Rozek L, Gruber SB, Matsuda K, Kidokoro T, Nakamura Y, Zanke BW, Greenwood CMT, Rangrej J, Kustra R, Montpetit A, Hudson TJ, Gallinger S, Campbell H, Dunlop MG. A genome-wide association scan identifies a new colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet 2008; 40: 631-7. DOI Link
Molecular Epidemiology
  • Joshi PK, Esko T, ... Strachan DP, Campbell H, Hirschhorn JN, Perola M, Polašek O, Wilson JF. Directional dominance on stature and cognition in diverse human populations. Nature. 2015 Jul 23;523(7561):459-62. DOI Link
  • Thanabalasingham G, Huffman JE, Kattla JJ, Novokmet M, Rudan I, Gloyn AL, Hayward C, Adamczyk B, Reynolds RM, Muzinic A, Hassanali N, Pucic M, Bennett AJ, Essafi A, Polasek O, Mughal SA, Redzic I, Primorac D, Zgaga L, Kolcic I, Hansen T, Gasperikova D, Tjora E, Strachan MW, Nielsen T, Stanik J, Klimes I, Pedersen OB, Njølstad PR, Wild SH, Gyllensten U, Gornik O, Wilson JF, Hastie ND, Campbell H, McCarthy MI, Rudd PM, Owen KR, Lauc G, Wright AF. Mutations in HNF1A result in marked alterations of plasma glycan profile. Diabetes. 2013 Apr;62(4):1329-37 DOI Link
  • Lauc G, Huffman JE, Pučić M, Zgaga L, Adamczyk B, Mužinić A, Novokmet M, Polašek O, Gornik O, Krištić J, Keser T, Vitart V, Scheijen B, Uh HW, Molokhia M, Patrick AL, McKeigue P, Kolčić I, Lukić IK, Swann O, van Leeuwen FN, Ruhaak LR, Houwing-Duistermaat JJ, Slagboom PE, Beekman M, de Craen AJ, Deelder AM, Zeng Q, Wang W, Hastie ND, Gyllensten U, Wilson JF, Wuhrer M, Wright AF, Rudd PM, Hayward C, Aulchenko Y, Campbell H, Rudan I. Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. PLoS Genet. 2013;9(1):e1003225 DOI Link
  • Demirkan A, van Duijn CM, Ugocsai P, Isaacs A, Pramstaller PP, Liebisch G, Wilson JF, Johansson Å, Rudan I, Aulchenko YS, Kirichenko AV, Janssens AC, Jansen RC, Gnewuch C, Domingues FS, Pattaro C, Wild SH, Jonasson I, Polasek O, Zorkoltseva IV, Hofman A, Karssen LC, Struchalin M, Floyd J, Igl W, Biloglav Z, Broer L, Pfeufer A, Pichler I, Campbell S, Zaboli G, Kolcic I, Rivadeneira F, Huffman J, Hastie ND, Uitterlinden A, Franke L, Franklin CS, Vitart V; DIAGRAM Consortium, Nelson CP, Preuss M; CARDIoGRAM Consortium, Bis JC, O'Donnell CJ, Franceschini N; CHARGE Consortium, Witteman JC, Axenovich T, Oostra BA, Meitinger T, Hicks AA, Hayward C, Wright AF, Gyllensten U, Campbell H, Schmitz G; EUROSPAN consortium. Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. PLoS Genet. 2012;8(2):e1002490 DOI Link
  • Ameur A, Enroth S, Johansson A, Zaboli G, Igl W, Johansson AC, Rivas MA, Daly MJ, Schmitz G, Hicks AA, Meitinger T, Feuk L, van Duijn C, Oostra B, Pramstaller PP, Rudan I, Wright AF, Wilson JF, Campbell H, Gyllensten U. Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids. Am J Hum Genet. 2012 May 4;90(5):809-20 DOI Link
  • Igl W, Polašek O, Gornik O, Knežević A, Pučić M, Novokmet M, Huffman J, Gnewuch C, Liebisch G, Rudd PM, Campbell H, Wilson JF, Rudan I, Gyllensten U, Schmitz G, Lauc G. Glycomics meets lipidomics--associations of N-glycans with classical lipids, glycerophospholipids, and sphingolipids in three European populations. Mol Biosyst. 2011 Jun;7(6):1852-62 DOI Link
  • Sivakumaran S*, Agakov F*, Theodoratou E*, Prendergast JG, Zgaga L, Manolio T, Rudan I, McKeigue P, Wilson JF, Campbell H. Abundant pleiotropy in human complex diseases and traits. AJHG 2011; 89: 607-18 DOI Link
  • Igl W, Johansson A, Wilson JF, Wild SH, Polasek O, Hayward C, Vitart V, Hastie N, Rudan P, Gnewuch C, Schmitz G, Meitinger T, Pramstaller PP, Hicks AA, Oostra BA, van Duijn CM, Rudan I, Wright A, Campbell H, Gyllensten U; EUROSPAN Consortium. Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. PLoS Genet. 2010 Jan;6(1):e1000798 DOI Link
  • Lauc G, Essafi A, Huffman JE, Hayward C, Knežević A, Kattla JJ, Polašek O, Gornik O, Vitart V, Abrahams JL, Pučić M, Novokmet M, Redžić I, Campbell S, Wild SH, Borovečki F, Wang W, Kolčić I, Zgaga L, Gyllensten U, Wilson JF, Wright AF, Hastie ND, Campbell H, Rudd PM, Rudan I. Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. PLoS Genet. 2010 Dec 23;6(12):e1001256 DOI Link
  • Hicks AA, Pramstaller PP, Johansson A, Vitart V, Rudan I, Ugocsai P, Aulchenko Y, Franklin CS, Liebisch G, Jonasson I, Pattaro C, Hayward C, Isaacs A, Huffman J, Gnewuch C, Marroni F, Polasek O, Demirkan A, Kolcic I, Schweinbacher C, Igl W, Biloglav Z, Witteman JCM, Pichler I, Zaboli G, Hastie N, Oostra BA, Wild SH, Meitinger T, Gyllensten U, van Duijn CM, Wilson JF, Wright AF, Schmitz G, Campbell H. Genetic determinants of circulating sphingolipid concentrations PLoSGenetics 2009: in press DOI Link

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