Relationship of Genetic Differences to the Development of Chromosome Abnormalities
NCT00481793 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 361
Last updated 2019-12-17
Summary
This is a collaborative study by the National Cancer Institute, Columbia University, and the Southern Urals Biophysics Institute in Russia. It will examine the relationship of differences in certain genes to the development of chromosomal abnormalities in workers at the Mayak nuclear production plant in Ozyorsk, Russia. This population was exposed to higher radiation doses from external and internal sources than those received by their counterparts in other countries or considered permissible today. If a risk relationship is found between genetic differences and chromosome abnormalities, the information might be useful in studies designed to examine how high radiation exposures cause cancer.
Radiation-exposed Mayak workers employed from 1948 to 1972 in the three Ozyorsk plants directly related to nuclear weapons production may be eligible for this study. They must have remained local residents in the area and estimates of their external and internal radiation exposures must be available.
Participants provide a blood sample for genetic studies and answer a questionnaire that includes demographic information and information about their family health history, history of benign tumors, if any, and history of smoking and alcohol consumption. Additional information is collected from patients' medical records.
...
Conditions
- Radiation Exposure
Sponsors & Collaborators
-
National Cancer Institute (NCI)
lead NIH
Principal Investigators
-
Martha Linet, M.D. · National Cancer Institute (NCI)
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-06-09
- Completion
- 2014-09-17
Countries
- Russia
Study Locations
More Related Trials
-
Endocrine, Metabolic, Cardiovascular and Immunological Aspects of Sex Chromosome Abnormalities in Relation to Genotype
NCT05425953 ·Status: RECRUITING
-
Structural Chromosome Rearrangements and Brain Disorders
NCT06072079 ·Status: ENROLLING_BY_INVITATION
-
Genetic Study to Identify Gene Mutations in Participants Previously Enrolled in Clinical Trial NCI-99-C-0053 Who Have Von Hippel-Lindau Syndrome or Are at Risk for Von Hippel-Lindau Syndrome
NCT00075348 ·Status: COMPLETED
-
Linking Somatic Mutation Rate With Baseline Exposure in East Palestine
NCT06357845 ·Status: RECRUITING ·Phase: NA
-
Genetic Factors and Interrelationships for Cancer Risk-Related Behaviors and Complex Traits
NCT00001500 ·Status: COMPLETED
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Study of Inborn Errors of Cholesterol Synthesis and Related Disorders
NCT00046202 ·Status: COMPLETED
-
Genetic and Molecular Abnormalities in Congenital Cystic Adenomatoid Malformations
NCT01732185 ·Status: COMPLETED ·Phase: NA
-
The Genetic Characterization of Dementia
NCT01867359 ·Status: COMPLETED
-
Prospective Study to Assess Medical Performance of Optical Mapping and Long Read Sequencing in Detecting Numerical and Structural Chromosome Abnormalities
NCT05290051 ·Status: RECRUITING ·Phase: NA
-
Microarray Analysis in Syndromic Obesity
NCT01043198 ·Status: COMPLETED ·Phase: NA
-
The Role of Genetic Factors in the Development of Idiopathic Scoliosis in the Kazakh Population
NCT05095129 ·Status: COMPLETED
-
Study of Congenital Orofacial Clefts by Implementing Optical Genome Mapping
NCT06880094 ·Status: RECRUITING ·Phase: NA
-
The Clinical Study of Sex Chromosome Variants
NCT01661010 ·Status: COMPLETED
-
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
NCT01969370 ·Status: COMPLETED ·Phase: NA
-
Genetic Studies of Early-onset Dementia
NCT04906863 ·Status: RECRUITING
-
Psychosocial Impact of Disclosing Cancer Predisposition Genetic Testing Results During Childhood
NCT04848142 ·Status: COMPLETED
-
Somatic Mosaicism in Twins Discordant for Childhood Cancer
NCT06054295 ·Status: RECRUITING
-
Etude génétique Des Arméniens
NCT02027051 ·Status: COMPLETED
-
Genetics of Familial Testicular Cancer
NCT00342537 ·Status: COMPLETED
-
Risk of Recurrence of de Novo Mutations: Research and Quantification of Paternal Germinal Mosaicism by the Combined Use of Genomic Tools
NCT04564235 ·Status: COMPLETED ·Phase: NA
-
Genetics of Arteriovenous Malformations
NCT02445430 ·Status: UNKNOWN
-
Genetic Studies in Familial Dementia
NCT04680013 ·Status: COMPLETED
-
Genetic Factors and Interrelationships for Sexual Orientation, Susceptibility to HIV and Kaposi's Sarcoma, Alcoholism and Psychological Traits, and Histocompatibility Antigens
NCT00001294 ·Status: COMPLETED
-
Genetic Biomarkers of Executive Stress
NCT02933203 ·Status: COMPLETED