Within Amsterdam Public Health, researchers work extensively with both cohort studies and health registries. The cohorts, most of which are part of Amsterdam Cohort Hub (ACH), follow groups of people over time to investigate the causes and progression of health and disease. The registries, on the other hand, systematically collect data from clinical practice to monitor health outcomes and the quality of care. Together, these complementary data sources provide a crucial foundation for understanding, monitoring, and improving population health.
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ABCD cohort study
The Amsterdam Born Children and their Development cohort is a multi-ethnic birth study, which follows the health, growth and development of ±8,000 children.
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Academisch Netwerk Huisartsgeneeskunde Amsterdam UMC (ANHA) database
The Academic network of General Practice Amsterdam UMC (ANHA) database contains longitudinal routine care data extracted from the electronic medical records (EMRs) of patients in the participating general practices.
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ACS cohort study
The Amsterdam Cohort Studies (ACS) investigates the natural course, the development and development of HIV-1 infection in men who have sex with men and drug users.
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AGEhIV cohort study
The AGEhIV Cohort Study assesses aging and ageing-related diseases in people living with and without HIV.
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AGHLS cohort study
The Amsterdam Growth and Health Longitudinal Study is a multidisciplinary cohort which was set up to examine growth and health among teenagers.
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Amsterdam Cohort Of Gender dysphoria
In the ACOG study, clinical data is collected during diagnostic and therapeutic phases which people with gender dysphoria go through.
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Amsterdam MS study
The Amsterdam MS Cohort study is a longitudinal cohort affiliated with the MS Center Amsterdam focussed on multiple sclerosis diagnosis, progression and biomarkers.
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Dutch Famine Birth cohort study
The Dutch Famine Birth Cohort Study is investigating the effects of exposure to the 1944-1945 wartime famine (‘Hongerwinter’) in utero on health in adulthood.
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EPOSA registry
The European Project on OSteoArthritis focuses on the personal and societal burden and its determinants of osteoarthritis in the ageing European population.
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EQUAL cohort study
The EQUAL study, part of the ERA-EDTA registry, is an European prospective cohort study in elderly patients in chronic kidney disease stage 4.
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ERA-EDTA registry
The ERA-EDTA registry collects data on patients on dialysis and kidney transplant recipients from around 35 national and regional renal registries in Europe.
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Generations2 cohort study
The Generations2 cohort study is a big, ongoing, long-term cohort study, which aims to study the development of parenting and mental health.
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HELIUS cohort study
The Healthy Life in an Urban Setting study is a prospective cohort study on health and health care among an urban multi-ethnic population
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InterRAI registry
InterRAI consist of routine care cohorts of residents in long term care facilities, home care recipients and frail older adults with frail health.
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LASA cohort study
The Longitudinal Aging Study Amsterdam is a prospective cohort study of older adults in the Netherlands (55–84 years).
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Leren van Data - Peilstations
Within the program Leren van Data, a network of Peilstations is set up, consisting of nursing homes which will structurally register data.
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NESDA cohort study
The Netherlands Study of Depression and Anxiety investigates the course of these disorders, particular psychological, social, biological and genetic factors.
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NESDO cohort study
The Netherlands Study of Depression in Older persons examines the determinants, the course and the consequences of depressive disorders in older persons.
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Netherlands Autism Register
The Netherlands Autism Register (NAR) is a longitudinal register, including approximately 3,500 individuals with autism.
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Netherlands Twin Register
The Netherlands Twin Register (NTR) is a national register in which twins, multiples and their parents, siblings, spouses and other family members participate.
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NET‑QUBIC cohort study
NET-QUBIC is a multicentre longitudinal cohort study in the Netherlands in head and neck cancer patients and their informal caregivers, combining clinical, biomedical and quality of life data.
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NHR registry
The National Heart Registry collects data on all cardiac interventions performed in the Netherlands.
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NICE registry
NICE takes care of the continuous and complete registration of all available data of the participating intensive care units in the Netherlands.
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NL-SH cohort study
The Netherlands Longitudinal Study on Hearing is examining the relationship between hearing impairment and several life aspects in adults aged 18
to 70 years.
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NMCB cohort study
The NMCB cohort study is a large-scale national cohort and biobank initiative to uncover the biological and immunological drivers of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).
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NOCDA cohort study
The Netherlands Obsessive Compulsive Disorder Association investigates the biological, psychological and social determinants of chronicity in OCD patients.
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OMEGA cohort study
The OMEGA study investigates potential long-term health effects of fertility treatments.
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PACMAN cohort study
The Pharmacogenetics of Asthma medication in Children: Medication with Anti-inflammatory effects cohort study aims to examine asthma treatment response.
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RODAM cohort study
The Research on Obesity and Diabetes among African Migrants studies the high prevalence of cardiovascular diseases and risk factors among sub-Saharan Africans.
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Sarphati Amsterdam cohort
The Sarphati cohort collects data about the health and development of children up to 18 years to learn about certain non-communicable diseases.
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SECURE-AD registry
SECURE-AD is an online, de-identified international reporting registry for health care providers to report outcomes of COVID-19 in Atopic Dermatitis patients.
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The (New) Hoorn Studies
The (New) Hoorn studies were established to investigate the prevalence and risk factors of impaired glucose metabolism, diabetes and diabetes-related complications.
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The Hoorn DCS Cohort
The Hoorn DCS cohort is a prospective cohort representing a comprehensive dataset on the natural course of type 2 diabetes.
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TREAT NL registry
The TREAT NL registry is a national registry of children and adults with moderate-to-severe atopic eczema.
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WOMB cohort study
The WOMB project is the follow up of a preconception lifestyle intervention among women with obesity and an unfulfilled wish for a child.