Yoong Khean Khoo

Dr. Yoong Khean Khoo

orcid

Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 December 2023 in Drug Safety
Verified
Journal Article
Closed access
PDF file
YKYoong Khean Khoo
Yoong Khean Khoo
JLJohn CW Lim
John CW Lim
WTWei Chuen Tan-Koi
Wei Chuen Tan-Koi
NKNokuthula Sikhethiwe Kitikiti
Nokuthula Sikhethiwe Kitikiti
ASAi Ling Sim-Devadas
Ai Ling Sim-Devadas

27 February 2025 in Cell Genomics
Verified
Journal Article
Open access
YKYoong Khean Khoo
Yoong Khean Khoo
SWSuci Wulandari
Suci Wulandari
MGMarya Getchell
Marya Getchell
LMLa Moe
La Moe
SKShurendar Selva Kumar
Shurendar Selva Kumar
PPPaul Michael Pronyk
Paul Michael Pronyk
Sustaining and expanding genomic surveillance capacity requires broader investment in genomics that target both novel and pandemic pathogens. Currently, there is no standardized methodology to evaluate the cost and benefit of a multi-pathogen surveillance system. We propose a framework for pathogen genomic surveillance that links public health and systems considerations to a stepwise approach.

6 February 2026 in BMJ Global Health
Verified
Journal Article
Open access
ASAnne-Claire Stona
Anne-Claire Stona
YKYoong Khean Khoo
Yoong Khean Khoo
LMLa Moe
La Moe
SWSuci Wulandari
Suci Wulandari
SAShreya Agoramurthy
Shreya Agoramurthy
PPPaul M Pronyk
Paul M Pronyk
Introduction: While pathogen genomics using next-generation sequencing (NGS) has been recommended by the WHO as an essential tool for national communicable disease surveillance programmes, procurement and supply chain management (PSM) systems for this new technology are still evolving. To assess the status of PSM systems for pathogen genomics, we examined perspectives from end-users and manufacturers across South and Southeast Asia. Methods: Between 2022 and 2023, a cross-sectional survey was conducted among institutional partners supporting pathogen genomics among primarily low- and middle-income countries in South and Southeast Asia. This was complemented by qualitative interviews with the major regional NGS manufacturers. A PSM framework was employed to assess sales, procurement, production, distribution and post-sales support. Analyses are expressed as proportions and means or medians for continuous variables. Results: A total of 42 partners across 13 countries, 3 genomics manufacturers and 22 laboratory personnel contributed data to this assessment. PSM challenges were reported by all countries and for all sequencing platforms. High costs of equipment and consumables were identified by 85% of respondents. Long equipment purchasing lead times and reagent re-supply times were reported by 69% and 77% of countries, respectively, with reagent resupply times averaging 8 weeks (IQR 6.2–9.0). Additional barriers included customs clearance, variability of import procedures, taxes and duties. Manufacturers reported a range of strategies to respond to PSM bottlenecks, including establishing regional hubs, distributor networks and financing schemes. Conclusion: Coordinated national and regional efforts are required to improve PSM systems for pathogen genomic sequencing to enhance timely early disease detection and response capacity in South and Southeast Asia.

4 September 2026 in npj Digital Medicine
Verified
Journal Article
Open access
PDF file
MGMarya Getchell
Marya Getchell
MBMichael Barber
Michael Barber
TCThomas Carpino
Thomas Carpino
CSCarl J. E. Suster
Carl J. E. Suster
VSVitali Sintchenko
Vitali Sintchenko
PPPaul M. Pronyk
Paul M. Pronyk
Artificial intelligence (AI)-enabled infectious disease surveillance platforms are expanding rapidly, but their roles within health systems remain poorly characterized. This review examined 20 platforms according to primary data inputs, surveillance function, AI methods, data privacy, geographic scope and pathogen focus. Three archetypes emerged: Early Warning Networks, Situational Awareness Platforms and Integrated Surveillance Platforms. Their comparative analysis highlighted how data type, integration and localization shape platform contributions to public-health decision making.

26 December 2025 in Vaccines
Verified
Journal Article
Open access
PDF file
WTWei Chuen Tan-Koi
Wei Chuen Tan-Koi
YKYoong Khean Khoo
Yoong Khean Khoo
JLJohn CW Lim
John CW Lim
The COVID-19 pandemic coupled with recent upheavals in global trade and development assistance funding has disrupted routine immunization programmes and diverted health systems from the targets set in the Immunization Agenda 2030. Regulatory systems are often underappreciated or misunderstood but in fact play a critical role in enabling innovation and facilitating timely access to vaccines for sustained immunization, thereby building vaccine confidence and health system resilience. Regulation is the constant denominator throughout the vaccine life cycle, shaping the pathway from early research and development to approval and market entry and ultimately to equitable distribution and sustained safe use. This paper examines the role of regulation and proposes that regulation be reframed as a function of health system resilience and a structural determinant of immunization sustainability. We synthesize evidence across the vaccine regulatory life cycle, examining innovation facilitation, regional cooperation, public health strengthening and describe the roles of regulation in building health system resilience, namely driving sustainable vaccine access, enabling innovation, supporting regional collaboration and strengthening social acceptance. Without this shift in perspective, regulatory systems strengthening risks being underfunded, reactive, and fragmented; this will perpetuate inequities in vaccine access and undermine the sustainability of immunization programmes.