User profiles for Douwe J. Horsthuis

Douwe John Horsthuis

Data Scientist, Albert Einstein College of Medicine
Verified email at einsteinmed.org
Cited by 52

[HTML][HTML] Assessing auditory processing endophenotypes associated with Schizophrenia in individuals with 22q11. 2 deletion syndrome

AA Francisco, JJ Foxe, DJ Horsthuis, D DeMaio… - Translational …, 2020 - nature.com
22q11.2 Deletion Syndrome (22q11.2DS) is the strongest known molecular risk factor for
schizophrenia. Brain responses to auditory stimuli have been studied extensively in …

[HTML][HTML] Atypical response inhibition and error processing in 22q11. 2 Deletion Syndrome and schizophrenia: Towards neuromarkers of disease progression and risk

AA Francisco, DJ Horsthuis, M Popiel, JJ Foxe… - NeuroImage: Clinical, 2020 - Elsevier
22q11.2 deletion syndrome (also known as DiGeorge syndrome or velo-cardio-facial
syndrome) is characterized by increased vulnerability to neuropsychiatric symptoms, with …

[HTML][HTML] Early visual processing and adaptation as markers of disease, not vulnerability: EEG evidence from 22q11. 2 deletion syndrome, a population at high risk for …

AA Francisco, JJ Foxe, DJ Horsthuis, S Molholm - Schizophrenia, 2022 - nature.com
We investigated visual processing and adaptation in 22q11.2 deletion syndrome (22q11.2DS),
a condition characterized by an increased risk for schizophrenia. Visual processing …

[HTML][HTML] Impaired auditory sensory memory in Cystinosis despite typical sensory processing: A high-density electrical mapping study of the mismatch negativity (MMN)

AA Francisco, JJ Foxe, DJ Horsthuis, S Molholm - NeuroImage: Clinical, 2020 - Elsevier
Cystinosis, a genetic rare disease characterized by cystine accumulation and crystallization,
results in significant damage in a multitude of tissues and organs, such as the kidney, thyroid…

Neural signature of mobility-related everyday function in older adults at-risk of cognitive impairment

…, S Molholm, JJ Foxe, HM Blumen, DJ Horsthuis - Neurobiology of …, 2023 - Elsevier
Assessment of everyday activities is central to the diagnosis of dementia. Yet, little is known
about brain processes associated with everyday functional limitations, particularly during …

[HTML][HTML] Response inhibition and error-monitoring in cystinosis (CTNS gene mutations): Behavioral and electrophysiological evidence of a diverse set of difficulties

AA Francisco, JJ Foxe, A Berruti, DJ Horsthuis… - bioRxiv, 2023 - ncbi.nlm.nih.gov
Cystinosis, a rare lysosomal storage disease, is characterized by cystine crystallization and
accumulation within tissues and organs, including the kidneys and brain. Its impact on neural …

[HTML][HTML] Event-related potential (ERP) evidence for visual processing differences in children and adults with cystinosis (CTNS gene mutations)

DJ Horsthuis, S Molholm, JJ Foxe… - Orphanet Journal of Rare …, 2023 - Springer
Background Cystinosis, a rare lysosomal storage disease caused by mutations in the CTNS
gene, is characterized by cystine crystallization and accumulation within multiple tissues, …

[HTML][HTML] No evidence for differential saccadic adaptation in children and adults with an autism spectrum diagnosis

…, AA Francisco, DJ Horsthuis… - Frontiers in …, 2023 - ncbi.nlm.nih.gov
Background Altered patterns of eye-movements during scene exploration, and atypical gaze
preferences in social settings, have long been noted as features of the Autism phenotype. …

Early visual processing as a marker of disease, not vulnerability: Event-related potential (ERP) evidence from 22q11. 2 deletion syndrome, a population at high risk for …

AA Francisco, JJ Foxe, DJ Horsthuis, S Molholm - medRxiv, 2021 - medrxiv.org
We investigated visual processing in 22q11.2 deletion syndrome (22q11.2DS), a condition
characterized by an increased risk for schizophrenia. Visual processing differences have …

[HTML][HTML] Event-related potential (ERP) evidence of early visual processing differences in cystinosis

DJ Horsthuis, S Molholm, JJ Foxe, AA Francisco - bioRxiv, 2023 - ncbi.nlm.nih.gov
Cystinosis, a rare lysosomal storage disease, is characterized by cystine crystallization and
accumulation within tissues and organs, including the kidneys and brain. Its impact on neural …