Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic and phenotypic characterization of Parkinson’s disease at the clinic-wide level

3 May 2024

Abstract excerpt

Observational studies in Parkinson's disease (PD) deeply characterize relatively small numbers of participants. The Molecular Integration in Neurological Diagnosis Initiative seeks to characterize molecular and clinical features of every PD patient at the University of Pennsylvania (UPenn). The objectives of this study are to determine the feasibility of genetic characterization in PD and assess clinical features...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Autism Spectrum Disorder Research
Share to Nuclear Receptors and Signaling
Share to Parkinson's Disease Mechanisms and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 38702337
DOI: 10.1038/s41531-024-00690-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic and phenotypic characterization of Parkinson’s disease at the clinic-wide levelPMID 38702337Read ↗

Whole Clinic Research Enrollment in Parkinson's Disease: The Molecular Integration in Neurological Diagnosis (MIND) Study.Semantic proximity Read ↗

Genetics of Parkinson's Disease: From Causes to Treatment.Semantic proximity Read ↗

Understanding Parkinson disease in Spain: Genetic and clinical insights.Semantic proximity Read ↗

Genetics of Parkinson's disease: An introspection of its journey towards precision medicine.Semantic proximity Read ↗

Parkinson's disease variant detection and disclosure: PD GENEration, a North American study.Semantic proximity Read ↗

Genome sequencing in the Parkinson’s disease clinicSemantic proximity Read ↗

Dystonia-Parkinsonism Gene Variants in Individuals with Parkinsonism and Brain Scans without Evidence for Dopaminergic Deficit (SWEDD)Semantic proximity Read ↗

<p class="MDPI13authornamesori1" style="margin-bottom: 12.0pt; mso-line-height-alt: 14.0pt;">Genetic Associations of Parkinson’s Disease Clinical, Pathological, and Data-driven SubtypesSemantic proximity Read ↗

Global Parkinson’s Genetics Program (GP2) Monogenic Network Protocol: Elucidating causative gene variants in hereditary Parkinson’s diseaseSemantic proximity Read ↗

An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.Semantic proximity Read ↗

Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing.Semantic proximity Read ↗

Beyond Parkinson’s disease: expanding the neurodegenerative spectrum of GBA1- associated disordersSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.