The overall goal for this Administrative Core (Core A) is to provide effective administrative and scientific management to facilitate Interdisciplinary integration of the research and training activities developed under this ICEMR program. Core A will provide support to Project 1 on epidemiology, Project 2 on transmission and Project 3 on pathogenesis and their articulation with the DM Core (Core B). Organizationally, the ICEMR will be administered by the Caucaseco Scientific Research Center (CAUCASECO SRC) under the direction of Dr. Socrates Herrera, who will have the responsibility to articulate and guarantee an efficient communication among the PLs and CLs for Core B and C. CAUCASECO SRC will be legally and financially accountable for the use of funds for this ICEMR and will be responsible for all necessary administrative functions. Core A will contribute to the activities assigned to the Program Director (PD), the PLs and the CLs, as well as to all training activities and the special projects, promoting effective administrative and scientific management for team building. This includes key elements that will help us meet the overall goal of this ICEMR for establishment of the Centro Latino Americano de Investigacion en Malaria-CLAIM that will provide the necessary knowledge, tools, and evidence-based strategies for use by the National Malaria Control Program (NMCP) of the partner countries in this project. Core A will ensure an efficient communication with a "common language" among scientists, experts in diverse disciplines and staff members ofthe NMCP, and with endemic communities. It will ensure the accomplishment of the project milestones within the proposed fimelines and promote creative interdisciplinary approaches to tackle critical features responsible for malaria transmission maintenance that cannot be solved through standard disciplinary approaches. Moreover, it will promote partnerships with government officials and stakeholders in the partner countries as a means for fast-tracking research results into translafional steps towards malaria eliminafion. Models emerging from CLAIM activifies will have broader regional and global applications for solving major malaria disease problems. Our emphasis on high-impact interdisciplinary science will have a direct impact on local, regional, and global policy related to the control of diseases. Accordingly these significant'goals, strategies, and outcomes require the full scope of activities described. Core A team has the necessary background and experience to provide effective leadership for this program project. Nevertheless, we will promote coordination and integration of Projects and Cores by working interactively with the NIAID program staff, and will remain fiexible enough to implement changes when needed to better serve the overall ICEMR team. As we have demonstrated in past NIH projects with significant internafional components, the design of our scientific management plan will promote a solid foundation for facilitafing interdisciplinary collaboration and scientific productivity.
This core will play a key role on effective administrative and scientific management to facilitate interdisciplinary integration ofthe research and training activities developed under this ICEMR program.
|Ahumada, Martha L; Orjuela, Lorena I; Pareja, Paula X et al. (2016) Spatial distributions of Anopheles species in relation to malaria incidence at 70 localities in the highly endemic Northwest and South Pacific coast regions of Colombia. Malar J 15:407|
|Vallejo, Andres F; Martinez, Nora L; Tobon, Alejandra et al. (2016) Global genetic diversity of the Plasmodium vivax transmission-blocking vaccine candidate Pvs48/45. Malar J 15:202|
|Vallejo, AndrÃ©s F; GarcÃa, Jhon; Amado-Garavito, AndrÃ©s B et al. (2016) Plasmodium vivax gametocyte infectivity in sub-microscopic infections. Malar J 15:48|
|Guo, Suqin; He, Lishan; Tisch, Daniel J et al. (2016) Pilot testing of dipsticks as point-of-care assays for rapid diagnosis of poor-quality artemisinin drugs in endemic settings. Trop Med Health 44:15|
|Chaurio, Ricardo A; Pacheco, M AndreÃna; Cornejo, Omar E et al. (2016) Evolution of the Transmission-Blocking Vaccine Candidates Pvs28 and Pvs25 in Plasmodium vivax: Geographic Differentiation and Evidence of Positive Selection. PLoS Negl Trop Dis 10:e0004786|
|VÃ¡squez-JimÃ©nez, Juan M; ArÃ©valo-Herrera, Myriam; Henao-Giraldo, Juliana et al. (2016) Consistent prevalence of asymptomatic infections in malaria endemic populations in Colombia over time. Malar J 15:70|
|Pacheco, M AndreÃna; Lopez-Perez, Mary; Vallejo, AndrÃ©s F et al. (2016) Multiplicity of Infection and Disease Severity in Plasmodium vivax. PLoS Negl Trop Dis 10:e0004355|
|Alimi, Temitope O; Fuller, Douglas O; Herrera, Socrates V et al. (2016) A multi-criteria decision analysis approach to assessing malaria risk in northern South America. BMC Public Health 16:221|
|Valencia, SÃ³crates Herrera; Ocampo, IvÃ¡n DarÃo; Arce-Plata, MarÃa Isabel et al. (2016) Glucose-6-phosphate dehydrogenase deficiency prevalence and genetic variants in malaria endemic areas of Colombia. Malar J 15:291|
|Lennon, Shirley Evelyn; Miranda, Adolfo; Henao, Juliana et al. (2016) Malaria elimination challenges in Mesoamerica: evidence of submicroscopic malaria reservoirs in Guatemala. Malar J 15:441|
Showing the most recent 10 out of 73 publications