Leopold Curfs

Maastricht University Medical Centre — Netherlands

Biochemistry, Genetics and Molecular Biology · Life Sciences

49h-index7.9kcitations273works4.42yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(89), Genetic Syndromes and Imprinting(60), Autism Spectrum Disorder Research(46), Family and Disability Support Research(34), Prenatal Substance Exposure Effects(30)

Publications273 total

Integrative analysis of 115 transcriptomic studies decodes the molecular landscape of neurodevelopmental disorders
Communications Biology·2025· 1 citedOpen Access
Selective changes in vasopressin neurons and astrocytes in the suprachiasmatic nucleus of Prader–Willi syndrome subjects
Journal of Neuroendocrinology·2025· 1 citedOpen Access
Author response for "Selective changes in vasopressin neurons and astrocytes in the suprachiasmatic nucleus of Prader–Willi syndrome subjects"
2025
Author response for "Selective changes in vasopressin neurons and astrocytes in the suprachiasmatic nucleus of Prader–Willi syndrome subjects"
2025
Involvement of extracellular vesicle microRNA clusters in developing healthy and Rett syndrome brain organoids
Cellular and Molecular Life Sciences·2024· 6 citedOpen Access
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey
Orphanet Journal of Rare Diseases·2024· 8 citedOpen Access
A novel insight into neurological disorders through HDAC6 protein–protein interactions
Scientific Reports·2024· 10 citedOpen Access
Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion
Acta Neuropathologica·2024· 8 citedOpen Access
Sleep and the Social Profiles of Individuals With Rett Syndrome
Pediatric Neurology·2024· 6 citedOpen Access
Euthanasia and physician-assisted suicide in people with intellectual disabilities and/or autism spectrum disorders: investigation of 39 Dutch case reports (2012–2021)
BJPsych Open·2023· 9 citedOpen Access
Burden of Illness in Rett Syndrome: Initial Evaluation of a Disorder-Specific Caregiver Survey
2023· 1 citedOpen Access
An investigation of the sleep macrostructure of girls with Rett syndrome
Sleep Medicine·2022· 7 citedOpen Access
Sleep Respiratory Disturbances in Girls with Rett Syndrome
International Journal of Environmental Research and Public Health·2022· 10 citedOpen Access
Incontinence and sleep disturbances in young children: A population‐based study
Neurourology and Urodynamics·2022· 8 citedOpen Access
Food-Related Brain Activation Measured by fMRI in Adults with Prader–Willi Syndrome
Journal of Clinical Medicine·2021· 12 citedOpen Access
The Rett Syndrome Gross Motor Scale – Dutch Version (RSGMS-NL) Can Reliably Assess Gross Motor Skills in Dutch Individuals with Rett Syndrome
Developmental Neurorehabilitation·2021· 3 citedOpen Access
The role of Extracellular Vesicles during CNS development
Progress in Neurobiology·2021· 59 citedOpen Access
Sleep problems among children with Fetal Alcohol Spectrum Disorders (FASD)- an explorative study
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics·2021· 20 citedOpen Access
A resource to explore the discovery of rare diseases and their causative genes
Scientific Data·2021· 34 citedOpen Access
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration
Scientific Data·2021· 34 citedOpen Access
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Frequent Co-authors

Robert Didden(9), Gerjo Kok(8), Marcel G. Smits(8), C. T. R. M. Schrander‐Stumpel(7), Wiebe Braam(7), Irene Tuffrey‐Wijne(6), Hubert Korzilius(5), J. P. Fryns(4), Joke Stoffelen(4), Sheila Hollins(4), Marian A. Maaskant(4), Friederike Ehrhart(4), Eric Smeets(4), Sylvia Roozen(3), Henry Keijzer(3), Dilana Schaafsma(3), Margje Sinnema(3), Ute Moog(3), Gjalt-Jorn Peters(2), Jaap J.P. Schrander(2)