MIRAGE: Multi-Institutional Research in Alzheimer's Genetic Epidemiology

Genetic Studies in Familial Dementia

NCT04680013 ·Status: COMPLETED

A Genetic Study for Alzheimer Dementia: Case-control Study

NCT06330155 ·Status: NOT_YET_RECRUITING

Genetic Studies in Alzheimer's Disease

NCT00001235 ·Status: COMPLETED

Genetic Characterization of Movement Disorders and Dementias

NCT02014246 ·Status: RECRUITING

Genetic Studies of Early-onset Dementia

NCT04906863 ·Status: RECRUITING

Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network

NCT02450851 ·Status: RECRUITING

Biomarkers in Neurodegenerative Diseases

NCT04055532 ·Status: WITHDRAWN

Study of Clinical and Molecular Manifestations of Genetic Disorders

NCT00001466 ·Status: COMPLETED

Genetics of Inherited Eye Disease

NCT02471287 ·Status: RECRUITING

Delineation of Novel Monogenic Disorders in the United Arab Emirates Population

NCT03589079 ·Status: UNKNOWN

Genetics of Mendelian Forms of Young Onset Alzheimer Disease

NCT01622894 ·Status: COMPLETED ·Phase: NA

Clinical Integration of Genetic Risk Assessment in Family Medicine

NCT00339794 ·Status: COMPLETED

PROGENI (Parkinson's Research: The Organized Genetics Initiative) Family Study of LRRK2 (Leucine-rich Repeat Kinase 2)

NCT01536821 ·Status: COMPLETED

A Study of the Impact of Genetic Testing on Clinical Decision Making and Patient Care

NCT02487888 ·Status: UNKNOWN ·Phase: NA

Molecular Genetics of Retinal Degenerations

NCT00231010 ·Status: COMPLETED

Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

NCT05589714 ·Status: RECRUITING

Genetic Analysis of Chronic Central Serous Chorioretinopathy Masquerading as Neovascular AMD

NCT01880788 ·Status: COMPLETED

Adult Patients With Undiagnosed Conditions and Their Responses to Clinically Uncertain Results From Exome Sequencing

NCT03605004 ·Status: COMPLETED

Genetics of Familial and Sporadic ALS

NCT00821132 ·Status: COMPLETED

Genetic Analysis of Uncommon Disease Presentations in Non-US Populations

NCT06595940 ·Status: RECRUITING

A Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism Disorders

NCT06092346 ·Status: RECRUITING

A Study to Compare Genetic Variations of IGF-I and IGF-II

NCT01329523 ·Status: COMPLETED

Identification of Genomic Loci Determining Susceptibility to the Development of High Myopia

NCT02583620 ·Status: COMPLETED ·Phase: NA

Family Studies of Eye Traits

NCT00342342 ·Status: COMPLETED

Genetic Identification of Monogenic Disorders in Early-onset Stroke Using Targeted Next Generation Sequencing Panel

NCT04485598 ·Status: COMPLETED