Logo of plosmedPLoS MedicineSubmit to PLoSGet E-mail AlertsContact UsPublic Library of Science (PLoS)View this Article
PLoS Med. 2006 Dec; 3(12): e473.
Published online 2006 Dec 5. doi:  10.1371/journal.pmed.0030473
PMCID: PMC1762059

The Malaria Atlas Project: Developing Global Maps of Malaria Risk

In allocating public health resources, the guiding principle should be an evidence-based quantification of need. A significant effort to categorize diseases by their global morbidity and mortality impact has developed during the last decade, epitomized by the Global Burden of Diseases [1] and the Disease Control Priorities projects [2]. But despite these efforts, the evidence base for allocating resources for malaria control on a global scale is poor.

National reporting on malaria continues to be fanciful; Kenya, for example, reported only 135 malaria deaths in 2002 to the World Health Organization [3]. In addition, less than half (22/49) of the malaria-endemic countries in Africa provided information for the most-recent reporting year, 2003; the rest were older [3]. Information on the global burden of malaria remains the subject of best guesses rooted in national reporting systems [3], informed estimation based on epidemiological data linked to historical malaria distributions [4], or unvalidated models of malaria distribution in Africa [5–7]. As a corollary, resource allocations for malaria interventions remain driven by perceptions and politics, rather than an objective assessment of need. This status quo is untenable when global and national financial resources must be defined to meet needs for new, expensive antimalarial drugs and commodities to prevent infection, and to ensure that these interventions are optimally targeted.

It has been almost 40 years since the last global map of malaria endemicity was constructed [8], and a decade since the need for maps of malaria transmission in Africa was first advocated [9]. Although substantial progress has been made [10–21], an evidence-based map of malaria transmission intensity for Africa remains illusive, and there have been no recent efforts to construct a credible evidence-based global malaria map.

figure pmed.0030473.g002
MAP Logo

A New Mapping Project

The primary goal of the recently launched Malaria Atlas Project (MAP) is to develop the science of malaria cartography. Our approach will be first to define the global limits of contemporary malaria transmission; we have initiated this process [12,13], but will substantially refine these layers with additional medical intelligence in future years.

Within these limits, we plan to then model endemicity using a global evidence base of malaria parasite prevalence. This Health in Action concentrates mostly on how we intend to achieve this important goal. Once we have created these global endemicity maps, these will then provide a baseline to facilitate estimation of populations at risk of malaria and more-credible predictions of disease burden. These maps will also provide a platform to help target intervention needs, and may provide a means to measure progress toward national and international malaria public health goals at a global scale.

Why Do We Need Maps of Malaria Transmission?

Malaria parasite transmission intensity is spatially heterogeneous [6,2224]. This heterogeneity has important implications for risks and age patterns of progression from malaria infection to disease, disability, and death [5,25].

Endemicity is a measure of the level of malaria challenge in a human population, and determines the average age of first exposure, the rate of development of immunity, and thus, the expected clinical spectrum of disease [25,26]. Therefore, suites of relevant interventions should be tailored to these basic epidemiological foundations [9,2729].

This is obvious for malaria early warning systems, for example, that have a rationale only in epidemic-prone areas [30,31]. In addition, intermittent presumptive treatment of infants is likely to have little impact on the incidence of clinical malaria and anaemia in areas of exceptionally low transmission [32]. Moreover, where one should withhold iron supplementation in young children demands an understanding of the balanced risks of iron deficiency, malaria disease incidence, and intensity of transmission [33,34]. Furthermore, optimizing the introduction of diagnostics to rationalize the use of new, expensive therapies will require better tools to target where this is cost efficient and where presumptive treatment remains appropriate. We anticipate that other interventions are likely to have health impacts and cost-effectiveness balances that may vary under different endemicity conditions, and we propose to conduct a detailed systematic review of the evidence.

It is often not immediately apparent when reading guidelines for malaria control that there are many intervention options available, that these may need to be appropriately combined, and that the optimal mix could depend on the intensity of malaria transmission in a given area. This would be as true for Africa as it is for other malarious territories of the Old and New Worlds. Global maps of malaria endemicity should therefore be essential in every step, from selecting appropriate intervention options and identifying requirements and budgeting, to planning, implementing, and monitoring at subnational, national, and regional scales.

Large Area Efforts to Map Malaria since the 1960s

The fuzzy climate-suitability map for stable Plasmodium falciparum malaria transmission was a milestone in the mapping of malaria in Africa [10]. It represented the first attempt for several decades to provide a map of P. falciparum transmission at a continental scale, and has been widely used and cited by scientists, international agencies, and national malaria control programmes [6,35,36].

However, it has also been widely misinterpreted, as it represents a measure of the likelihood that stable transmission can occur, rather than ranges of transmission intensity. Furthermore, it has never been formally evaluated against contemporary parasite rate (PR) data outside of Kenya [37]. What is required for defining both disease risks and intervention need is a spatial model that predicts levels of endemicity, defined and validated by empirical data and constructed at a global scale. This approach to assembling epidemiological “training” data, environmental “predictor” data, and a suite of statistical mapping techniques to relate the two is considered below.

An Archive of Parasite Prevalence

There are many ways to measure the abundance of malaria in a given location, and they all have their advantages and disadvantages that have been reviewed elsewhere [23,24,38]. Regardless of any epidemiological preferences, PR data indisputably constitute the bulk of the global information available on the distribution of malaria endemicity. The PR is the proportion of a sampled population that is confirmed positive for malaria parasites, canonically by identifying immature “ring stage” trophozoites in blood slides [39].

We have adopted a single and traditional classification of malaria endemicity based on the PR [40], to standardize our definition of risk globally. Endemicity is defined by the PR in the two- to ten-year age cohort (hypoendemic, less than 0.1; mesoendemic, 0.11–0.5; hyperendemic, 0.51–0.75), except for the holoendemic class (greater than 0.75) where the PR refers to the one-year age group [40]. This is important because “risk” is a geographically relative concept: nation states in Latin America identify areas of “high” risk that would be classified as low risk in sub-Saharan Africa.

To gather global data on PR surveys of a sufficient extent and density to generate endemicity surfaces at moderate spatial resolution requires combinations of traditional and nontraditional search strategies. This process has involved electronic searches of formal literature and grey literature databases, as well as using personal contacts with malaria research scientists and malaria control personnel. Most recently, we have developed a Web site to guide people in identifying additional data sources from areas where information is lacking (Box 1). As of September 10, 2006, our search has provided 3,036 spatially independent geopositioned PR surveys undertaken since January 1985 from an aggregate sample of 2,143,979 blood slides in 79 malaria-endemic countries. The data included 2,728 survey locations reporting P. falciparum prevalence (Figure 1) and 1,379 locations reporting P. vivax prevalence.

Box 1. The MAP Web Site

The MAP Web site (http://www.map.ox.ac.uk) was launched on May 1, 2006, to further the aims and ambitions of MAP. The Web site allows users to visualize the current distribution of the assembled PR data through static maps in Web browsers, or more interactively through “.kmz” files that enable the data to be displayed in Google Earth (http://earth.google.com). We are currently interested in gathering additional PR data from the public health community, and to facilitate communication we have translated the entire Web site into Spanish and French.

MAP is different than previous attempts at mapping malaria, primarily because it is a global initiative, but also because it aims to share data from the outset. Those supplying useful PR data will be provided with the full database for their country of interest, provided full permission is granted from the data owners for distribution. In addition, the entire database will be released in the public domain after component outputs have been peer reviewed. We have set a June 1, 2009, deadline for this release.

A second unique feature of MAP is that it operates with strict inclusion criteria for PR data: only random or complete community-sample surveys conducted post-1985, where parasite species and age groups are defined and the survey involves more than 50 persons to minimize sampling error [68]. Extensive details of these and additional inclusion rules are provided online in English, Spanish, French, Chinese, and Swahili.

Thirdly, the MAP project will collect data on P. falciparum malaria, as well as the often neglected P. vivax parasite. The Web site also allows formal acknowledgment of those interested individuals and institutions who contribute data. We encourage you to have a look and send us feedback at ku.ca.xo.ooz@pam.

Figure 1
Distribution of the n = 3,036 PR Data Points Collected and Geopositioned by September 10, 2006

In addition, the distribution of the main Anopheles malaria vectors and the frequency of the inherited haemoglobin disorders will constrain malaria infection risks and disease outcomes globally. Both will be subject to a similar intensity of data search and assembly, which will be described elsewhere.

An Archive of Global Environmental Data

Malaria is a vector-borne disease and the culpable anopheline mosquitoes are very sensitive to climate. This has been exploited in many ways to predict the distribution of malaria in time [14,30,31,41,42] and space [15,20,43]. Mapping the distribution of malaria requires spatially referenced data (e.g., altitude, temperature, rainfall, and vegetation extent) to be matched to the PR-survey positions, to establish uni and/or multivariate statistical relationships between malaria endemicity and the environment. These relationships can then be applied to the environmental data, in more or less sophisticated ways (see below), to generate continuous global maps [20].

Our proclivities are for such information derived from Earth-observing satellites [44–48] because they are globally consistent measurements, often more contemporary and often of higher spatial resolution than interpolated climatologies [47]. Examples of these environmental data [47] have been made available in the public domain, and will be hosted on a MAP Web site when all necessary distribution rights have been negotiated. There is significant potential for improvement in these environmental themes through data collected by new generations of satellite sensors [48]. Continual improvement of these data will be part of the ongoing commitment of MAP.

First Steps to Maps of Force of Infection

As a cross-sectional measure of prevalence, the PR is a less direct measure of malaria transmission than the entomological inoculation rate (the number of infective bites per capita, often expressed annually for P. falciparum, hence APfEIR) [22,23], the vectorial capacity (canonically, C) or the basic reproductive number (canonically, R0) [38]. These “force of infection” metrics, however, are much less frequently measured, [6,22] and while not recorded at sufficient frequency to enable mapping, will be archived by the MAP as companion data to inform modelling.

Moreover, in high-endemicity areas, PR samples are often restricted to children, but in areas of low endemicity, surveys are usually extended to include all age groups. PR is therefore confounded by the interacting factors of the age of the population sampled, its immune status, and the “detectability” of peripheral parasitaemia [23,24]. It is necessary to transform PR into a measure of the force of infection of malaria controlling for these factors. This is because these interrelated measures are more closely related to the life-history characteristics and dynamics of the Anopheles vector populations that we will attempt to model with environmental data. Our goal is to generate APfEIR, C, and ultimately R0 surfaces from our PR data for mapping, and the modelling framework within which to perform these conversions has already been developed [23,24].

Those techniques required to standardize PR for age represent an ongoing challenge, although methods by which to achieve this have been suggested [11]. The models written to perform these conversions will be made freely available in the public domain pending peer review. R is the chosen MAP platform as it is a programming environment that is free to all (http://www.r-project.org).

Measuring Risk and Managing Uncertainty

Quantifying the uncertainty in prediction has been a neglected area in the field of malaria mapping and in ecology, more generally [49]. Our aim is to present all risk maps generated through MAP with uncertainty guides, companion maps that show the spatial variation in predictive accuracy. We also intend to evaluate the most-accurate procedures for achieving the basic mapping with appropriate robustness measures [11,5054]. There are alternative methods available to achieve mapping with error estimations: Bayesian [11,21,55], discriminant analyses [52], and logistic-regression [50,52] techniques, among others [53,54], and these will all be systematically tested as part of the MAP project. The code written to implement these techniques will again be written in R and distributed freely upon acceptance of its products through peer review.

Where People Live

Accurate population data are critical for the assessment of the effects of human population density on malaria risk and the attribution of risk to populations [56]. These databases are also becoming increasingly accessible [47,56,57]. Areas of the world for which we have a particularly poor understanding of human population distribution will limit the accuracy of MAP and other databases to derive population at-risk estimates. Countries of specific concern are highlighted in the ancillary data section of the MAP Web site. More contemporary or higher spatial resolution census data supplied to MAP will be forwarded with permission to collaborators developing the Gridded Population of the World, version 3 (GPWv3) and the Global Rural–Urban Mapping Project (GRUMP) (http://sedac.ciesin.columbia.edu).

Future Applications

These planned malaria-endemicity maps will provide the basis for increasing the fidelity of morbidity [4], mortality [5,6] and co-infection burden estimates [58,59]. These studies lead logically to more-accurate commodity demand and budget estimation. As we have argued, these maps may also provide a means to help determine the distribution of intervention types and mixes within countries. Companion maps of the global distribution of the main anopheline vector species will also be particularly important in helping inform the appropriate modes of control. At the very least, these map suites should augment the objective monitoring and evaluation of our interventions in the coming years. There are strong arguments for these exercises being conducted independently of international agencies responsible for the implementation and evaluation of interventions [60–62].

While we strive to assemble data to define an endemicity baseline, the static maps we generate will represent a “snapshot” of a dynamic malaria epidemiology. It is important to establish this epidemiological baseline because history has shown that changes independent of planned interventions are inevitable [63]. These global environmental changes will affect the populations at risk of malaria. Land-use changes [64], such as deforestation [65], may modify vector population dynamics, for example. Population growth, urbanization [6], and climate change [66] will additionally affect human population dynamics. Other factors such as the progression of the HIV/AIDS pandemic and changes in undernutrition and socioeconomic status [66,67] will influence the ability of human population to cope with malaria infection. These changes will be significant over the time span of international development goals and targets. MAP aims to develop plausible scenarios for many of these influences and techniques to model their potential impact, as they will be confounders in our ability to evaluate critically interventions at scale.


The distribution of populations exposed to the risk of P. falciparum and P. vivax malaria is poorly understood at the global level. Considerable effort as part of MAP is required to improve our basic maps of malaria transmission intensity and help identify the global distribution of populations at risk of malaria. This will involve assembling the largest-ever collection of PR data and a significant parallel investment in establishing the required environmental, population, and malaria vector data.

A very considerable research effort is also required to evaluate those statistical techniques needed to relate the PR and environmental data for extensive map predictions with confidence intervals. This will take time and succeed only with the cooperation of the malaria control community. To encourage interaction, MAP will be connected with the philosophy of open access, so that all data collected and techniques developed can be made available in the public domain rapidly after peer review.


We thank Drs. Carlos Guerra and Andrew Tatem for commenting on the manuscript.


MAPMalaria Atlas Project
PRparasite rate


Simon I. Hay and Robert W. Snow are in the Malaria Public Health and Epidemiology Group, Centre for Geographic Medicine, Kenya Medical Research Institute, Nairobi, Kenya. Simon I. Hay is also in the Spatial Ecology and Epidemiology Group, Department of Zoology, University of Oxford, Oxford, United Kingdom. Robert W. Snow is also at the Centre for Tropical Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.

Funding: SIH is funded by a senior research fellowship from the Wellcome Trust (no. 079091). RWS is a Wellcome Trust principal research fellow (no. 079080), and acknowledges the support of the Kenyan Medical Research Institute. This Health in Action is published with the permission of the director of the Kenyan Medical Research Institute. This work forms part of the output of the Malaria Atlas Project (http://www.map.ox.ac.uk), principally funded by the Wellcome Trust, London, United Kingdom.

Competing Interests: The authors have declared that no competing interests exist.


  • Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJ. Global and regional burden of disease and risk factors, 2001: Systematic analysis of population health data. Lancet. 2006;367:1747–1757. [PubMed]
  • Jamison DT, Breman JG, Measham AR, Alleyne G, Claeson M, et al. Washington (D. C.): World Bank Publications; 2006. Disease control priorities in developing countries.1352 p. editors.
  • The World Health Organization. Geneva: World Health Organization; 2005. The world malaria report 2005. Available: http://www.rbm.who.int/wmr2005. Accessed 10 September 2006.
  • Snow RW, Guerra CA, Noor AM, Myint HY, Hay SI. The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature. 2005;434:214–217. [PMC free article] [PubMed]
  • Snow RW, Craig M, Deichmann U, Marsh K. Estimating mortality, morbidity and disability due to malaria among Africa's non-pregnant population. Bull World Health Organ. 1999;77:624–640. [PMC free article] [PubMed]
  • Hay SI, Guerra CA, Tatem AJ, Atkinson PM, Snow RW. Urbanization, malaria transmission and disease burden in Africa. Nat Rev Microbiology. 2005;3:81–90. [PMC free article] [PubMed]
  • Rowe AK, Rowe SY, Snow RW, Korenromp EL, Armstrong Schellenberg JR, et al. The burden of malaria mortality among African children in the year 2000. Int J Epidemiol. 2006;35:691–704. [PMC free article] [PubMed]
  • Lysenko AY, Semashko IN. [Geography of malaria: A medico-geographic profile of an ancient disease] In: Lebedew AW, editor. Medicinskaja Geografija. Moscow: Academy of Sciences; 1968. pp. 25–146. editor.
  • Snow RW, Marsh K, le Sueur D. The need for maps of transmission intensity to guide malaria control in Africa. Parasitol Today. 1996;12:455–457.
  • Craig MH, Snow RW, le Sueur D. A climate-based distribution model of malaria transmission in sub-Saharan Africa. Parasitol Today. 1999;15:105–111. [PubMed]
  • Gemperli A, Vounatsou P, Sogoba N, Smith T. Malaria mapping using transmission models: Application to survey data from Mali. Am J Trop Med Hyg. 2006;163:289–297. [PubMed]
  • Guerra CA, Snow RW, Hay SI. Defining the global spatial limits of malaria transmission in 2005. Adv Parasitol. 2006;62:157–179. [PMC free article] [PubMed]
  • Guerra CA, Snow RW, Hay SI. Mapping the global extent of malaria in 2005. Trends Parasitol. 2006;22:353–358. [PMC free article] [PubMed]
  • Hay SI, Snow RW, Rogers DJ. Predicting malaria seasons in Kenya using multitemporal meteorological satellite sensor data. Trans R Soc Trop Med Hyg. 1998;92:12–20. [PubMed]
  • Hay SI, Omumbo JA, Craig MH, Snow RW. Earth observation, geographic information systems and Plasmodium falciparum malaria in sub-Saharan Africa. Adv Parasitol. 2000;47:173–215. [PMC free article] [PubMed]
  • Kleinschmidt I, Bagayoko M, Clarke GPY, Craig M, Le Sueur D. A spatial statistical approach to malaria mapping. Int J Epidemiol. 2000;29:355–361. [PubMed]
  • Kleinschmidt I, Omumbo J, Briet O, van de Giesen N, Sogoba N, et al. An empirical malaria distribution map for West Africa. Trop Med Int Health. 2001;6:779–786. [PubMed]
  • Omumbo JA, Hay SI, Goetz SJ, Snow RW, Rogers DJ. Updating historical maps of malaria transmission intensity in East Africa using remote sensing. Photogrammetric Eng Remote Sens. 2002;68:161–166. [PMC free article] [PubMed]
  • Omumbo JA, Hay SI, Snow RW, Tatem AJ, Rogers DJ. Modelling malaria risk in East Africa at high-spatial resolution. Trop Med Int Health. 2005;10:557–566. [PMC free article] [PubMed]
  • Rogers DJ, Randolph SE, Snow RW, Hay SI. Satellite imagery in the study and forecast of malaria. Nature. 2002;415:710–715. [PMC free article] [PubMed]
  • Gemperli A, Sogoba N, Fondjo E, Mabaso M, Bagayoko M, et al. Mapping malaria transmission in West and Central Africa. Trop Med Int Health. 2006;11:1032–1046. [PubMed]
  • Hay SI, Rogers DJ, Toomer JF, Snow RW. Annual Plasmodium falciparum entomological inoculation rates (EIR) across Africa: literature survey, Internet access and review. Trans R Soc Trop Med Hyg. 2000;94:113–127. [PMC free article] [PubMed]
  • Smith DL, Dushoff J, Snow RW, Hay SI. The entomological inoculation rate and Plasmodium falciparum infection in African children. Nature. 2005;438:492–495. [PMC free article] [PubMed]
  • Smith DL, McKenzie FE, Snow RW, Hay SI. Revisiting the basic reproductive number for malaria and its implications for malaria control. PLoS Biol. 2007. In press. [PMC free article] [PubMed]
  • Snow RW, Omumbo JA, Lowe B, Molyneux CS, Obiero JO, et al. Relation between severe malaria morbidity in children and level of Plasmodium falciparum transmission in Africa. Lancet. 1997;349:1650–1654. [PubMed]
  • Snow RW, Marsh K. The consequences of reducing transmission of Plasmodium falciparum in Africa. Adv Parasitol. 2002;52:235–264. [PubMed]
  • Greenwood BM, Bojang K, Whitty CJM, Targett GAT. Malaria. Lancet. 2005;365:1487–1498. [PubMed]
  • Shiff C. Integrated approach to malaria control. Clin Microbiology Rev. 2002;15:278–293. [PMC free article] [PubMed]
  • The World Health Organization. Geneva: World Health Organization; 2006. Malaria vector control and personal protection: Report of a WHO study group.62 p. WHO technical report series, No. 936.
  • Hay SI, Rogers DJ, Shanks GD, Myers MF, Snow RW. Malaria early warning in Kenya. Trends Parasitol. 2001;17:95–99. [PMC free article] [PubMed]
  • Hay SI, Were EC, Renshaw M, Noor AM, Ochola SA, et al. Forecasting, warning, and detection of malaria epidemics: A case study. Lancet. 2003;361:1705–1706. [PMC free article] [PubMed]
  • Schellenberg D, Cisse B, Menedez C. The IPTi Consortium: Research for policy and action. Trends Parasitol. 2006;22:296–300. [PubMed]
  • English M, Snow RW. Iron and folic acid supplementation and malaria risk. Lancet. 2006;367:90–91. [PubMed]
  • Sazawal S, Black RE, Ramsan M, Chwaya HM, Stoltzfus RJ, et al. Effects of routine prophylactic supplementation with iron and folic acid on admission to hospital and mortality in preschool children in a high malaria transmission setting: Community-based, randomised, placebo-controlled trial. Lancet. 2006;367:133–143. [PubMed]
  • Small J, Goetz SJ, Hay SI. Climatic suitability for malaria transmission in Africa, 1911–1995. Proc Natl Acad Sci U S A. 2003;100:15341–15345. [PMC free article] [PubMed]
  • Thomas CJ, Davies G, Dunn CE. Mixed picture for changes in stable malaria distribution with future climate in Africa. Trends Parasitol. 2004;20:216–220. [PubMed]
  • Omumbo JA, Hay SI, Guerra CA, Snow RW. The relationship between the Plasmodium falciparum parasite ratio in childhood and climate estimates of malaria transmission in Kenya. Malaria J. 2004;3:17. [PMC free article] [PubMed]
  • Smith DL, McKenzie FE. Statics and dynamics of malaria infection in Anopheles mosquitoes. Malaria J. 2004;3:13. [PMC free article] [PubMed]
  • Gilles HM. The malaria parasites. In: Gilles HM, Warrel DA, . Bruce-Chwatt's essential malariology. 3rd ed. London: Arnold; 1993. pp. 12–34. editors.
  • Metselaar D, Van Thiel PH. Classification of malaria. Trop Geogr Med. 1959;11:157–161.
  • Hay SI, Renshaw M, Ochola SA, Noor AM, Snow RW. Performance of forecasting, warning and detection of malaria epidemics in the highlands of western Kenya. Trends Parasitol. 2003;19:394–399. [PMC free article] [PubMed]
  • Hay SI, Snow RW, Rogers DJ. From predicting mosquito habitat to malaria seasons using remotely sensed data: Practice, problems and perspectives. Parasitol Today. 1998;14:306–313. [PubMed]
  • Hay SI, Packer MJ, Rogers DJ. The impact of remote sensing on the study and control of invertebrate intermediate host and vectors for disease. Int J Remote Sens. 1997;18:2899–2930.
  • Hay SI. An overview of remote sensing and geodesy for epidemiology and public health application. Adv Parasitol. 2000;47:1–35. [PMC free article] [PubMed]
  • Hay SI, Lennon JJ. Deriving meteorological variables across Africa for the study and control of vector-borne disease: A comparison of remote sensing and spatial interpolation of climate. Trop Med Int Health. 1999;4:58–71. [PMC free article] [PubMed]
  • Hay SI, Tucker CJ, Rogers DJ, Packer MJ. Remotely sensed surrogates of meteorological data for the study of the distribution and abundance of arthropod vectors of disease. Ann Trop Med Parasitol. 1996;90:1–19. [PubMed]
  • Hay SI, Tatem AJ, Graham AJ, Goetz SJ, Rogers DJ. Global environmental data for mapping infectious disease distribution. Adv Parasitol. 2006;62:37–77. [PMC free article] [PubMed]
  • Tatem AJ, Goetz SJ, Hay SI. Terra and Aqua: New data for epidemiology and public health. Int J Appl Earth Obs Geoinform. 2004;6:33–46. [PMC free article] [PubMed]
  • Clark JS. Uncertainty in ecological inference and forecasting. Ecology. 2003;84:1349–1350.
  • Augustin NH, Mugglestone MA, Buckland ST. An autologistic model for the spatial distribution of wildlife. J Appl Ecol. 1996;33:339–347.
  • Brooker S, Hay SI, Bundy DAP. Tools from ecology: Useful for evaluating infection risk models? Trends Parasitol. 2002;18:70–74. [PMC free article] [PubMed]
  • Rogers DJ. Models for vectors and vector-borne diseases. Adv Parasitol. 2006;62:1–35. [PubMed]
  • Elith J, Graham CH, Anderson RP, Dudik M, Ferrier S, et al. Novel methods improve prediction of species' distributions from occurrence data. Ecography. 2006;29:129–151.
  • Segurado P, Araujo MB. An evaluation of methods for modelling species distributions. J Biogeography. 2004;31:1555–1568.
  • Gemperli A, Vounatsou P. Strategies for fitting large, geostatistical data in MCMC simulation. Commun Stat Simul Comput. 2006;35:331–345.
  • Balk DL, Deichmann U, Yetman G, Pozzi F, Hay SI, et al. Determining global population distribution: Methods, applications and data. Adv Parasitol. 2006;62:119–156. [PMC free article] [PubMed]
  • Hay SI, Noor AM, Nelson A, Tatem AJ. The accuracy of human population maps for public health application. Trop Med Int Health. 2005;10:1073–1086. [PMC free article] [PubMed]
  • Korenromp EL, Williams BG, de Vlas SJ, Gouws E, Gilks CF, et al. Malaria attributable to the HIV-1 epidemic, sub-Saharan Africa. Emerg Infect Dis. 2005;11:1410–1419. [PMC free article] [PubMed]
  • Mwangi TW, Bethony J, Brooker S. Worms and malaria interactions: An epidemiological viewpoint. Ann Trop Med Parasitol. 2006;100:551–570. [PMC free article] [PubMed]
  • Murray CJL, Lopez AD, Wibulpolprasert S. Monitoring global health: Time for new solutions. BMJ. 2004;329:1096–1100. [PMC free article] [PubMed]
  • Attaran A. An immeasurable crisis? A criticism of the millennium development goals and why they cannot be measured. PLoS Med. 2005;2:e318. [PMC free article] [PubMed]
  • Horton R. The Ellison Institute: Monitoring health, challenging WHO. Lancet. 2005;366:179–181. [PubMed]
  • Hay SI, Guerra CA, Tatem AJ, Noor AM, Snow RW. The global distribution and population at risk of malaria: Past, present, and future. Lancet Infect Dis. 2004;4:327–336. [PMC free article] [PubMed]
  • Feddema JJ, Oleson KW, Bonan GB, Mearns LO, Buja LE, et al. The importance of land-cover change in simulating future climates. Science. 2005;310:1674–1678. [PubMed]
  • Guerra CA, Snow RW, Hay SI. A global assessment of closed forests, deforestation and malaria risk. Ann Trop Med Parasitol. 2006;100:189–204. [PMC free article] [PubMed]
  • Hay SI, Tatem AJ, Guerra CA, Snow RW. London: Department of Trade and Industry; 2006. Infectious diseases: Preparing for the future. Report T8.2: Population at malaria risk in Africa: 2005, 2015 and 2030. Available: http://www.foresight.gov.uk/Previous_Projects/Detection_and_Identification_of_Infectious_Diseases/Reports_and_Publications/Final_Reports/T/T8_2.pdf. Accessed 10 September 2006.
  • Snow RW, Hay SI, Marsh K. London: Department of Trade and Industry; 2006. Infectious diseases: Preparing for the future. Report T5.8: Malaria in Africa: Sources, risks, drivers and disease burden: 2005–2030. http://www.foresight.gov.uk/Previous_Projects/Detection_and_Identification_of_Infectious_Diseases/Reports_and_Publications/Final_Reports/T/t5_8.pdf. Accessed 10 September 2006.
  • Jovani R, Tella JL. Parasite prevalence and sample size: Misconceptions and solutions. Trends Parasitol. 2006;22:214–218. [PubMed]

Articles from PLoS Medicine are provided here courtesy of Public Library of Science
PubReader format: click here to try


Save items

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...


  • Cited in Books
    Cited in Books
    NCBI Bookshelf books that cite the current articles.
  • Compound
    PubChem chemical compound records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records. Multiple substance records may contribute to the PubChem compound record.
  • PubMed
    PubMed citations for these articles
  • Substance
    PubChem chemical substance records that cite the current articles. These references are taken from those provided on submitted PubChem chemical substance records.
  • Taxonomy
    Taxonomy records associated with the current articles through taxonomic information on related molecular database records (Nucleotide, Protein, Gene, SNP, Structure).
  • Taxonomy Tree
    Taxonomy Tree

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...