about
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritabilitySystematic meta-analyses and field synopsis of genetic association studies in colorectal cancerGenome-wide association and large-scale follow up identifies 16 new loci influencing lung function.Chromatin structure and evolution in the human genome.Invasive meningococcal disease in Scotland, 1994 to 1999, with emphasis on group B meningococcal disease.High-throughput IgG Fc N-glycosylation profiling by mass spectrometry of glycopeptides.Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.Abundant pleiotropy in human complex diseases and traits.TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres.Prevalence of autistic spectrum disorders in Lothian, Scotland: an estimate using the "capture-recapture" technique.Is it acceptable to approach colorectal cancer patients at diagnosis to discuss genetic testing? A pilot studyReferrals of women with a family history of breast cancer from primary care to cancer genetics services in South East ScotlandPatient satisfaction with two different models of cancer genetic services in south-east Scotland.Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.The fellow eye in retinal detachment: findings from the Scottish Retinal Detachment Study.SNP mistyping in genotyping arrays--an important cause of spurious association in case-control studies.Influenza and pneumococcal vaccine distribution and use in primary care and hospital settings in Scotland: coverage, practice and policies.Referrals of patients to colorectal cancer genetics services in south-east Scotland.Population-based estimate of the sibling recurrence risk ratio for rhegmatogenous retinal detachment.3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia.Prevalence of penicillin non-susceptible invasive pneumococcal disease in the elderly in Scotland, 1992-99.Non-invasive pneumococcal disease and antimicrobial resistance: vaccine implications.Association of Medication with the Human Plasma N-GlycomeDoes inbreeding affect N-glycosylation of human plasma proteins?Dietary Flavonoids and the Risk of Colorectal CancerGermline mutation prevalence in the base excision repair gene,MYH, in patients with endometrial cancerPrevalence of family history of colorectal cancer in the general populationHospital Care for Children in Developing Countries: Clinical Guidelines and the Need for EvidenceLong-term visual acuity and the duration of macular detachment: findings from a prospective population-based studySurgical outcome and risk stratification for primary retinal detachment repair: results from the Scottish Retinal Detachment studyThe Predisposing Pathology and Clinical Characteristics in the Scottish Retinal Detachment StudyGlycomics meets lipidomics—associations of N-glycans with classical lipids, glycerophospholipids, and sphingolipids in three European populationsEvaluation of severe infection and survival after splenectomyThe changing epidemiology of bacterial meningitis and invasive non-meningitic bacterial disease in scotland during the period 1983-99DNA repair gene polymorphisms and genetic predisposition to cutaneous melanomaCommentary: rare alleles, modest genetic effects and the need for collaborationUptake of testing for BRCA1/2 mutations in South East ScotlandKetosis and bipolar disorder: controlled analytic study of online reportsMapping ICD-10 and ICD-10-CM Codes to Phecodes: Workflow Development and Initial EvaluationGenetically determined serum urate levels and cardiovascular and other diseases in UK Biobank cohort: A phenome-wide mendelian randomization study
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P50
description
researcher
@en
wetenschapper
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name
Harry Campbell
@en
Harry Campbell
@nl
type
label
Harry Campbell
@en
Harry Campbell
@nl
prefLabel
Harry Campbell
@en
Harry Campbell
@nl
P106
P31
P496
0000-0002-6169-6262