I've worked in public health and education focusing on monitoring, evaluation, and research for over 15 years. I worked for UN agencies, donors, and non-governmental organizations while based in Cambodia, Indonesia, and France, and I am now in the US.
Affiliations
Department of Global Health and Development
Faculty of Public Health and Policy
Research
I have a keen interest in coordination of services and improved measurement for decision making and program improvement. My PhD project focuses on interfacility transfer systems to hospitals from primary health centres in Indonesia. I will use mixed-methods approaches to understand factors associated with acceptance of referrals from the family's perspective and from the health system's perspective.
Research Area
Child health
Health services research
Primary health care
Adolescent health
Global health
Neonatal health
Health outcomes
Health systems
Public health
Public health measure evaluation
Evaluation
Health services
Qualitative research
Health policy
Maternal health
Systematic reviews
Mixed methods research
Country
Indonesia
Cambodia
Region
East Asia & Pacific (all income levels)
Selected Publications
Characterization of an Aquaporin-2 Water Channel Gene Mutation Causing Partial Nephrogenic Diabetes Insipidus in a Mexican Family: Evidence of Increased Frequency of the Mutation in the Town of Origin
2004
Journal of the American Society of Nephrology
Assessing the interactions of people and policy-makers in social participation for health: an inventory of participatory governance measures from a rapid systematic literature review.
2023
International journal for equity in health
Prevalence of Diabetic Retinopathy and Blindness in Indonesian Adults With Type 2 Diabetes
2017
American Journal of Ophthalmology
Paucity of skeletal manifestations in Hispanic families with FBN1 mutations.
2009
European Journal of Medical Genetics
An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease
2008
Journal of Human Genetics
FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly
2004
Journal of Medical Genetics