Frédéric B. Piel
occupation: researcher
Articles 44
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Small-area methods for investigation of environment and health
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Availability, access, analysis and dissemination of small-area data
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Advances in spatiotemporal models for non-communicable disease surveillance
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Advances in mapping population and demographic characteristics at small-area levels
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Using large and complex datasets for small-area environment-health studies: from theory to practice
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Software application profile: the Rapid Inquiry Facility 4.0: an open access tool for environmental public health tracking
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Estimating the burden of α-thalassaemia in Thailand using a comprehensive prevalence database for Southeast Asia
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Access to emergency departments for acute events and identification of sickle cell disease in refugees
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Sickle cell disease.
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The challenge of opt-outs from NHS data: a small-area perspective
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Estimating the burden of α-thalassaemia in Thailand using a comprehensive prevalence database for Southeast Asia
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Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference
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The spatial epidemiology of sickle-cell anaemia in India
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Sickle Cell Disease
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Real-life experience with hydroxyurea in sickle cell disease: A multicenter study in a cohort of patients with heterogeneous descent.
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Subphenotypes of sickle cell disease in Africa.
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Global and National Burden of Diseases and Injuries Among Children and Adolescents Between 1990 and 2013: Findings From the Global Burden of Disease 2013 Study
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Observed and expected frequencies of structural hemoglobin variants in newborn screening surveys in Africa and the Middle East: deviations from Hardy-Weinberg equilibrium
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Associations between environmental factors and hospital admissions for sickle cell disease.
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The Present and Future Global Burden of the Inherited Disorders of Hemoglobin
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The evolutionary and clinical implications of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances
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Erratum: Observed and expected frequencies of structural hemoglobin variants in newborn screening surveys in Africa and the Middle East: deviations from Hardy-Weinberg equilibrium
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Global, regional, and national disability-adjusted life years (DALYs) for 306 diseases and injuries and healthy life expectancy (HALE) for 188 countries, 1990-2013: quantifying the epidemiological transition
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Environmental determinants of severity in sickle cell disease
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Changes in health in England, with analysis by English regions and areas of deprivation, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013
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Understanding the contrasting spatial haplotype patterns of malaria-protective β-globin polymorphisms
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Comparative multilocus phylogeography of two Palaearctic spruce bark beetles: influence of contrasting ecological strategies on genetic variation
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Sickle-cell disease: a call to action
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Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000.
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Vitamin A supplements, routine immunization, and the subsequent risk of Plasmodium infection among children under 5 years in sub-Saharan Africa
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The α-thalassemias
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Managing the burden of sickle-cell disease in Africa.
Human - wd:Q42305841