Results 131 to 140 of about 4,466,598 (375)
Leveraging Fuzzy Match: Building an Automated Record Linkage Template in SAS Dataflux
International Journal of Population Data ScienceBackground ICES has conducted Probabilistic Record Linkage (PRL) for heath and non-health data for over 15 years. The PRL process has made data linkable to many ICES data holdings.
Charlotte Ma +4 more
doaj +1 more source
Linkage disequilibrium connects genetic records of relatives typed with disjoint genomic marker sets [PDF]
, 2018 Jaehee Kim +4 more
openalex +1 more source
Characteristics of Cerebral Palsy in the Midwestern US
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Cerebral palsy (CP) is the most common lifelong motor disability worldwide. Yet, data is limited on how CP manifests in the US. Our objective was to characterize and determine factors affecting functional outcomes in a large population of young people with CP in the Midwestern US.
Susie Kim +6 more
wiley +1 more source
How Are Linkage Results Using Privacy-Preserving Record Linkage Different?
International Journal of Population Data Science, 2020 Introduction Privacy-Preserving Record Linkage (PPRL) presents opportunities to improve privacy protection when performing record linkage on the most sensitive data.
Michael Jarrett +7 more
doaj
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source
What predicts linkage to the 1900 and 1910 Censuses, given that a recruit entered the pension system? [PDF]
record linkage; selection bias; census ...
Tayatat Kanjanapipatkul
core
The Diverse Neuromuscular Spectrum of VPS13A Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger +16 more
wiley +1 more source
Algorithmic Accountability for Record Linkage
International Journal of Population Data ScienceThis session will examine record linkage approaches through the lens of principles for algorithmic accountability: responsibility, explainability, accuracy, auditability, and fairness.[1] It is easy to hypothesize cases where linkage algorithms could ...
Emily Wiegand, Aya Liu, Sabrina Sedovic
doaj +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini +13 more
wiley +1 more source