Sotabase

Career

· Senior Manager, ST Engineering2022–
· Cyber Security Specialist, GovTech Singapore2019–2022
· Senior R D Scientist, Principal Investigator, Singtel2015–2019
· Teaching Faculty, National University of Singapore2009–2015

Publications (32)

International electronic health record-derived COVID-19 clinical course profiles: the 4CE consortium
npj Digital Medicine · 2020
161
cited
Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision
Orphanet Journal of Rare Diseases · 2021
63
cited
Long-term kidney function recovery and mortality after COVID-19-associated acute kidney injury: An international multi-centre observational cohort study
EClinicalMedicine · 2023
60
cited
International Analysis of Electronic Health Records of Children and Youth Hospitalized With COVID-19 Infection in 6 Countries
JAMA Network Open · 2021
32
cited
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
American Journal of Human Genetics · 2023
27
cited
Validation of an Internationally Derived Patient Severity Phenotype to Support COVID-19 Analytics from Electronic Health Record Data
J. Am. Medical Informatics Assoc. · 2021
27
cited
Hospitalizations Associated With Mental Health Conditions Among Adolescents in the US and France During the COVID-19 Pandemic
JAMA Network Open · 2022
26
cited
Evolving phenotypes of non-hospitalized patients that indicate long COVID
BMC Medicine · 2021
25
cited
International electronic health record-derived post-acute sequelae profiles of COVID-19 patients
npj Digital Medicine · 2022
25
cited
Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases
Genetics in Medicine · 2021
23
cited
Clinical phenotypes and outcomes in children with multisystem inflammatory syndrome across SARS-CoV-2 variant eras: a multinational study from the 4CE consortium
EClinicalMedicine · 2023
22
cited
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain
Genetics in Medicine · 2020
22
cited
Informative Missingness: What can we learn from patterns in missing laboratory data in the electronic health record?
medRxiv · 2022
21
cited
Characterization of long COVID temporal sub-phenotypes by distributed representation learning from electronic health record data: a cohort study
EClinicalMedicine · 2023
19
cited
HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.
American Journal of Human Genetics · 2023
18
cited
International Changes in COVID-19 Clinical Trajectories Across 315 Hospitals and 6 Countries: Retrospective Cohort Study
Journal of Medical Internet Research · 2021
16
cited
International Comparisons of Harmonized Laboratory Value Trajectories to Predict Severe COVID-19: Leveraging the 4CE Collaborative Across 342 Hospitals and 6 Countries: A Retrospective Cohort Study
medRxiv · 2020
16
cited
International comparisons of laboratory values from the 4CE collaborative to predict COVID-19 mortality
npj Digital Medicine · 2022
15
cited
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment
npj Genomic Medicine · 2023
11
cited
Validation of a Derived International Patient Severity Phenotype to Support COVID-19 Analytics from Electronic Health Record Data
medRxiv · 2020
10
cited
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Amelia Tan | Researcher Profile | Sotabase | Sotabase