Etude génétique Des Arméniens
NCT02027051 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500
Last updated 2021-08-30
Summary
This study aims at better understanding the genetic structure of the Armenians, an old population whose genetics has not been the subject of many studies. We will study 500 individuals whom grandparents originate from different regions of Armenia. Each individual will be genotyped using a large panel of genetic markers. Principal component analysis will be used to analyze the genetic structure of this population.
Conditions
- Healthy
Sponsors & Collaborators
-
Institut National de la Santé Et de la Recherche Médicale, France
lead OTHER_GOV
Principal Investigators
-
Emmanuelle Genin, Researcher · Institut National de la Santé Et de la Recherche Médicale, France
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-01-31
- Primary Completion
- 2014-06-30
- Completion
- 2017-01-31
Countries
- France
Study Locations
More Related Trials
-
Genetic Studies of Early-onset Dementia
NCT04906863 ·Status: RECRUITING
-
Cancer Risk Assessment in Patients With a Constitutional Alteration of the PTEN Gene
NCT05630105 ·Status: SUSPENDED
-
Reinterpretation of CNV With Unknown Significance: a 5-year Retrospective Analysis
NCT04575350 ·Status: COMPLETED
-
Integrative Sequencing In Germline and Hereditary Tumours
NCT03857594 ·Status: ACTIVE_NOT_RECRUITING
-
The Role of Genetic Factors in the Development of Idiopathic Scoliosis in the Kazakh Population
NCT05095129 ·Status: COMPLETED
-
The Informed Genetics Annotated Patient Registry
NCT04419896 ·Status: ENROLLING_BY_INVITATION
-
Primary Premature Ejaculation Genetics
NCT02109302 ·Status: COMPLETED ·Phase: NA
-
Patients' Perspectives on Identity, Ancestry and Genetics
NCT00359710 ·Status: COMPLETED
-
Genome-wide Analysis of Single Nucleotide Polymorphisms of Brain Arteriovenous Malformations and Cerebral Aneurysm
NCT01801488 ·Status: TERMINATED
-
Identification of Genomic Loci Determining Susceptibility to the Development of High Myopia
NCT02583620 ·Status: COMPLETED ·Phase: NA
-
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders
NCT04399694 ·Status: COMPLETED
-
Genetics of Middle Ear Disease
NCT00422136 ·Status: COMPLETED
-
The Role of Genetic Factors in the Development of Epilepsy in the Kazakh Population
NCT05088499 ·Status: COMPLETED
-
Hereditary Tubulointerstitial Nephritis
NCT01312727 ·Status: COMPLETED ·Phase: NA
-
Implications of Maternal 45,X Mosaicism as a Secondary Genomic Finding Following Cell-Free DNA Sequencing During Pregnancy: A Deep Phenotype Study
NCT05548881 ·Status: WITHDRAWN
-
Pharmacogenetics Study in Taiwan's Ethnic Groups
NCT00459251 ·Status: COMPLETED
-
Analyzing Genes That May Increase the Risk of Developing High Blood Pressure
NCT00549991 ·Status: COMPLETED
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Prospective Lung Transplant Database for Genetic Research
NCT00339209 ·Status: COMPLETED
-
Genetics of Arteriovenous Malformations
NCT02445430 ·Status: UNKNOWN
-
Autosomal Dominant Polycystic Kidney Disease Somatic Mutation Biorepository
NCT03901521 ·Status: ENROLLING_BY_INVITATION
-
Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN
NCT05499091 ·Status: RECRUITING ·Phase: NA
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Alzheimer's Disease Genetics Study
NCT00064870 ·Status: RECRUITING
-
Genetic Examination of Patients With Primary Multiple Hernia
NCT00979095 ·Status: UNKNOWN