Your search returned 63 studies. (Get alerts for new studies):
- Genetic Studies of Lysosomal Storage Disorders
Conditions: Gaucher's Disease - Lysosomal Storage Disease
1 Location available
- Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics
Conditions: Periodic Disease
1 Location available
- Studies of Children With Metabolic and Other Genetic Disorders
Conditions: Genetic Disorder - Metabolic Disease
1 Location available
- Alzheimer's Disease Genetics Study
Conditions: Alzheimer Disease - Late Onset Alzheimer Disease - Dementia
1 Location available
- Detection and Characterization of Infections and Infection Susceptibility
Conditions: Immune Disorders - Chronic Granulomatous Disease - Genetic Immunological Deficiencies - Hyperimmunoglobulin-E Recurrent Infection Syndrome - Recurrent Infections
1 Location available
- Unrelated Hematopoietic Stem Cell Transplantation(HSCT) for Genetic Diseases of Blood Cells
Conditions: Sickle Cell Disease - Thalassemia - Anemia - Granuloma - Wiskott-Aldrich Syndrome - Chediak Higashi Syndrome - Osteopetrosis - Neutropenia - Thrombocytopenia - Hurler Disease - Niemann-Pick Disease - Fucosidosis
1 Location available
- Infusion of Genetically Modified T Cell for Post Transplant Patients With Relapsed Disease
Conditions: Leukemia - Lymphoma, Non-Hodgkin - Hodgkin Disease - Myelodysplastic Syndromes - Multiple Myeloma
1 Location available
- Multi-Analyte, Genetic, and Thrombogenic Markers of Atherosclerosis
Conditions: Coronary Artery Disease
1 Location available
- Personalized Genomic Research: Congenital Malformations
Conditions: Genetics - Genetic Disease - Genetic Linkage - Birth Defects - Genetic Variation
1 Location available
- Androgenetic Alopecia in Fabry Disease
Conditions: Fabry Disease
1 Location available
- Evaluating the Genetic Causes and Progression of Cholestatic Liver Diseases (LOGIC)
Conditions: Liver Diseases - Alagille Syndrome - Alpha 1-Antitrypsin Deficiency
11 Locations available
- Evaluating Genetic Factors That May Contribute to Elastin Function and the Development of Chronic Obstructive Pulmonary Disease
Conditions: Emphysema - Pulmonary Disease, Chronic Obstructive
1 Location available
- Genetic Modifiers of Cystic Fibrosis (CF) Liver Disease
Conditions: Cystic Fibrosis - Liver Disease
1 Location available
- Neural Oscillations as Genetic and Functional Biomarkers in Normal and Disease States
Conditions: Schizophrenia - Schizoaffective Disorder - Schizophreniform Disorder
1 Location available
- Role of Genetic Factors in the Development of Lung Disease
Conditions: Cystic Fibrosis - Sarcoidosis - Tuberous Sclerosis - Asthma
2 Locations available
- Tissue Specimen Collection for Study of Inherited Diseases Involving Non-muscle Gene Mutations
Conditions: Inborn Genetic Diseases - Pentalogy of Cantrell
5 Locations available
- Exploratory Data Analysis for Disease Pedigrees and Cancer Genetics
Conditions: Data Analysis - Cancer Genetics
1 Location available
- Genetic Disorders of Mucociliary Clearance in Nontuberculous Mycobacterial Lung Disease
Conditions: Mycobacteria, Atypical - Cystic Fibrosis - Ciliary Disorders - Pseudohypoaldosteronism - Bronchiectasis
1 Location available
- Hirschsprung Disease Genetic Study
Conditions: Hirschsprung Disease
1 Location available
- Genetic Markers as Predictors of Phenotypes in Pediatric Onset Crohn's Disease
Conditions: Crohn's Disease - Ulcerative Colitis - Inflammatory Bowel Disease
1 Location available
- Genetics of ALS: Identification of Genes With Roles in Familial and Sporadic Amyotrophic Lateral Sclerosis (ALS) and Amyotrophic Lateral Sclerosis (AL
Conditions: Amyotrophic Lateral Sclerosis - Familial Amyotrophic Lateral Sclerosis - Amyotrophic Lateral Sclerosis With Frontotemporal Dementia - Lou Gehrig's Disease - Motor Neuron Disease - Primary Lateral Sclerosis
1 Location available
- Immunogenetic Mechanisms in Behcet's Disease
Conditions: Behcet's Disease - Uveitis
1 Location available
- Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2
Conditions: Charcot-Marie-Tooth Disease, Type Ia (Disorder) - HMSN
6 Locations available
- Study of Fludarabine Drug Exposure in Pediatric Bone Marrow Transplantation
Conditions: Hematologic Malignancies - Nonmalignant Diseases - Immunodeficiencies - Hemoglobinopathies - Genetic Inborn Errors of Metabolism - Fanconi's Anemia, - Thalassemia - Sickle Cell Disease
1 Location available
- Genetics of Obesity, Diabetes, and Heart Disease in African Diaspora Populations
Conditions: Diabetes - Cardiovascular Disease
1 Location available
- Genetics and Pain Severity in Sickle Cell Disease
Conditions: Genotype - Pain - Sickle Cell Anemia - Vaso-Occlusive Pain Crisis
1 Location available
- Genetic Analysis of Hereditary Disorders of Hearing and Balance
Conditions: Sensorineural Hearing Loss - Hearing Disorder - Vestibular Disease
1 Location available
- Genetics of Peripheral Artery Genomics
Conditions: Peripheral Artery Disease
1 Location available
- Biomarkers and Genetic Factors Related to Emphysema
Conditions: Emphysema - Pulmonary Disease, Chronic Obstructive
1 Location available
- Determining Genetic Role in Treatment Response to Anti-Platelet Interventions (The PAPI Study)
Conditions: Platelet Aggregation Inhibitors - Coronary Heart Disease
1 Location available
- Prenatal Cytogenetic Diagnosis by Array-Based Copy Number Analysis
Conditions: Genetic Diseases
1 Location available
- Web-based Genetic Research on Parkinson's Disease
Conditions: Parkinson's Disease
1 Location available
- Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
Conditions: Genetic Diseases
1 Location available
- The Role of Family Functioning in Promoting Adaptation in Siblings of Individuals With Duchenne Muscular Dystrophy (DMD)
Conditions: Genetic Disease - Communication
1 Location available
- Inherited Reproductive Disorders
Conditions: Endocrine Diseases - Genetic Disorder - Infertility - Hypogonadism - Amenorrhea
1 Location available
- Molecular and Genetic Studies of Congenital Myopathies
Conditions: Central Core Disease - Centronuclear Myopathy - Congenital Fiber Type Disproportion - Multiminicore Disease - Myotubular Myopathy - Nemaline Myopathy - Rigid Spine Muscular Dystrophy - Undefined Congenital Myopathy
1 Location available
- Genetic Studies in the Amish and Mennonites
Conditions: Genetic Disease
2 Locations available
- Blood Collection From Individuals With Lung Disease for Genetic Studies
Conditions: Asthma - COPD - Interstitial Lung Disease - Cystic Fibrosis - Lung Cancer
1 Location available
- Genetic Variations in Toll-like Receptors and Susceptibility to Chronic Lung Disease in Very Low Birth Weight Babies
Conditions: Chronic Lung Disease
4 Locations available
- Genetic Study of Familial and Sporadic ALS/Motor Neuron Disease, Miyoshi Myopathy and Other Neuromuscular Disorders
Conditions: Amyotrophic Lateral Sclerosis - Frontotemporal Dementia - PLS - Motor Neuron Disease - Lou Gehrigs Disease - Familial Disease - Amyotrophic Lateral Sclerosis, Sporadic
1 Location available
- Family Genetics Health Education and Healthy Behaviors
Conditions: Diabetes - Cancer - Heart Disease
1 Location available
- Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex
Conditions: Cushing's Syndrome - Hereditary Neoplastic Syndrome - Lentigo - Neoplasm - Testicular Neoplasm
1 Location available
- Genetic and Environmental Characteristics of Primary Pulmonary Hypertension
Conditions: Lung Diseases - Hypertension, Pulmonary
1 Location available
- Screening Protocol for Genetic Diseases of Lymphocyte Homeostasis and Programmed Cell Death
Conditions: Lymphocyte Homeostasis - Genetic Diseases
2 Locations available
- Clinical and Genetic Studies in Families With Myopia and Related Diseases
Conditions: Myopia
1 Location available
- Genetic Epidemiology Risk Assessment Program or Usual Care in Colorectal Cancer Screening for Healthy Participants
Conditions: Colorectal Cancer - Healthy, no Evidence of Disease
1 Location available
- Genetics and Markers of Degenerative and Inflammatory Eye Diseases
Conditions: Diabetic Retinopathy - Age-Related Macular Degeneration (AMD) - Uveitis
1 Location available
- Screening Protocol for Genetic Diseases of Mast Cell Homeostasis and Activation
Conditions: Piebaldism - Idiopathic Anaphylaxis - Allergy - Chronic Urticara - Angioedema
1 Location available
- Evaluation of Radiculitis Following Use of Bone Morphogenetic Protein-2 for Interbody Arthrodesis in Spinal Surgery
Conditions: Lumbar Degenerative Disease
1 Location available
- Identification of Genetic Mechanisms of Bicuspid Aortic Valve Disease
Conditions: Bicuspid Aortic Valve
1 Location available
- Role of Donor Genetics and Recipient Genetics in Kidney Transplant Outcomes
Conditions: Kidney Disease - Kidney Transplantation - Kidney Failure, Chronic
1 Location available
- Identification of Genetic Markers for Cardiopulmonary Diseases (Genotype)
Conditions: Cardiovascular Diseases
1 Location available
- Natural History of Diseases Associated With Allergic Inflammation: Atopic Dermatitis and Genetic and Congenital Diseases Associated With Atopic Pathwa
Conditions: Atopic Dermatitis - Netheron's Syndrome - Piebaldism - Hyper IgE Syndrome - Ichthyosis - Anaphylaxis - Severe Allergy
1 Location available
- 4R for Guideline Indicated BRCA Testing of Newly Diagnosed Breast Cancer Patients
Conditions: Newly Diagnosed Carcinoma of Breast - Genetic Predisposition to Disease
1 Location available
- Genetic Effect on Omega 3 Fatty Acids for the Treatment of Fatty Liver Disease
Conditions: Non Alcoholic Fatty Liver Disease - Steatohepatitis - Hypertriglyceridemia - Alanine Aminotransferase, Plasma Level of, Quantitative Trait Locus 1
1 Location available
- Understanding the Impact of Genetics on the Risk for Respiratory Distress Syndrome in Infants
Conditions: Lung Diseases - Respiratory Distress Syndrome, Newborn
1 Location available
- Genetic Studies of Chronic Active Epstein-Barr Disease
Conditions: Epstein-Barr Virus Infections
1 Location available
- The Role of Bacteria and Genetic Variations in Cystic Fibrosis
Conditions: Lung Diseases
4 Locations available
- The Effects of Genetic Differences Among AIDS Patients on Cytomegalovirus Retinitis
Conditions: CMV Disease
1 Location available
- Genetics of Congenital Heart Disease
Conditions: Congenital Heart Disease
1 Location available
- Congenital Heart Disease GEnetic NEtwork Study (CHD GENES)
Conditions: Congenital Heart Defects
9 Locations available
- STudy to Assess Rapid Disease Progression by Clinical and Genetic Factors In Glaucoma patientS That Are High Risk (STARFISH)
Conditions: Primary Open Angle Glaucoma
1 Location available
- The Parkinson's Genetic Research Study
Conditions: Parkinson's Disease
9 Locations available
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