National Human Genome Research Institute (NHGRI): all 203 studies

Page 2 of 3. Open to participants first (32), then studies with results posted, then the rest; newest registration first within each.

• Parents With Bipolar Disorder: Relationship of Adaptation to Own Illness With Risk Perception and Coping With Perceived Risk to a ChildCompletedNCT01012180
• The Experience of Uncertainty in Parents of Children With an Undiagnosed Medical ConditionCompletedNCT00955370
• The Roles of Trust and Respect in Patient Reactions to Race-based and Personalized Medicine Vignettes: An Experimental StudyCompletedNCT00911833
• Adaptation Among Adolescents and Adults With Klinefelter SyndromeCompletedNCT00896272
• The Role of Family Functioning in Adaptation to Being a Caregiver of an Individual With Rett SyndromeCompletedNCT00891956
• The Nosology and Etiology of Leukodystrophies of Unknown CausesCompletedNCT00889174
• Genetics of Type 2 Diabetes Among Han ChineseCompletedNCT00837408
• Genetics of Type 2 Diabetes in West AfricansCompletedNCT00837122
• Clinical, Cellular, and Molecular Investigation Into Oculocutaneous AlbinismCompletedNCT00808106
• Reactions to Disease Risk InformationCompletedNCT00774254Not applicable
• Cultural Congruence in International Genetics ResearchTerminatedNCT00767858
• Use of Population Descriptors in Human Genetic ResearchCompletedNCT00767702
• Clinical and Genetic Studies of VACTERL AssociationCompletedNCT00766571
• The Experience of Caregivers of Children With Down SyndromeCompletedNCT00695695
• Screening Behavior in Adults With Hereditary Hemorrhagic TelangiectasiaCompletedNCT00684879
• Adaptation and Quality of Life Among Adults With Neurofibromatosis Type ICompletedNCT00684398
• Patient Provider Communication and Interaction in a Virtual Clinical SettingCompletedNCT00669188Not applicable
• A Study of the Genetic Analysis of Brain DisordersCompletedNCT00645645
• Risk Evaluation and Education for Alzheimer's DiseaseCompletedNCT00571025Not applicable
• Making Sense of a Positive Genetic Test Result for Huntington DiseaseCompletedNCT00539747
• Informed Choice Regarding Invasive Prenatal TestingCompletedNCT00514553
• Treatment Strategies for Children With Smith-Magenis SyndromeCompletedNCT00506259Phase 1
• Predictors of Caregiver Adaptation to Pervasive Developmental DisordersCompletedNCT00496210
• Individuals Patterns of Disclosure About Huntington s Disease (HD) and the Association With Adaptation to HDCompletedNCT00491842
• African American Families and Lung Cancer StudyCompletedNCT00487760
• Disclosing a Cystic Fibrosis Diagnosis to a Dating PartnerCompletedNCT00485082
• Risk Communication Within Mexican-American FamiliesCompletedNCT00469339
• Interventions to Educate An Underserved Population About Inherited Disease RisksCompletedNCT00441077Not applicable
• ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot StudyActive, not recruitingNCT00410241
• Genetic Analysis of Craniosynostosis, Philadelphia TypeCompletedNCT00367796
• Genetic Counselors' Experiences of Moral Value Conflicts With ClientsCompletedNCT00360711
• Patients' Perspectives on Identity, Ancestry and GeneticsCompletedNCT00359710
• Genetic Studies in the Amish and MennonitesCompletedNCT00359580
• Genetic Analysis of Oculocerebrorenal Syndrome of LoweCompletedNCT00359515
• Immunogenetics of Visceral LeishmaniasisCompletedNCT00342823
• Identification of Prostate Cancer GenesCompletedNCT00342784
• Family Studies of Eye TraitsCompletedNCT00342342
• Prevalence of Ambivalence Regarding Prenatal TestingCompletedNCT00342069
• Genetic Epidemiology of Lung CancerCompletedNCT00341835
• Invasive Prenatal Testing Decisions in Pregnancy After InfertilityCompletedNCT00341822
• Experiences of Genetics Patients With Visible Abnormalities Who Facilitate Teaching in Genetics ClinicsCompletedNCT00341718
• Psychosocial Aspects of Genetic Testing for Hereditary Nonpolyposis Colon CancerCompletedNCT00341575
• Family Myopia StudyCompletedNCT00341549
• Impact of Lung Cancer Diagnosis on Relatives' Understanding of Genetic Risk and Receptivity to Quit SmokingCompletedNCT00341341
• Analysis of Data From the Women's Contraceptive and Reproductive Experiences (CARE) StudyCompletedNCT00341159
• Genetic Analysis of Left-Right Axis FormationsCompletedNCT00341133
• Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish PopulationTerminatedNCT00341068
• Positive Exposure: A Photography and Video Intervention for Individuals With Craniofacial DifferencesCompletedNCT00340964
• Genetic Analysis of Hereditary Non-Syndromic Oral CleftsCompletedNCT00340626
• Genetic Studies of Inflammatory Bowel DiseaseCompletedNCT00340444
• Influence of Genetics on Vitamin Metabolism in Pregnant WomenCompletedNCT00340366
• Physicians' Understanding of Human Genetic VariationCompletedNCT00339924
• Mapping Genes for Type 2 (Non-Insulin Dependent) Diabetes MellitusCompletedNCT00339885
• Genetic Analysis of Craniofrontonasal SyndromeCompletedNCT00339846
• Clinical Integration of Genetic Risk Assessment in Family MedicineCompletedNCT00339794
• Exploratory Data Analysis for Disease Pedigrees and Cancer GeneticsCompletedNCT00339508
• Genetic Analysis of Familial MelanomaCompletedNCT00339404
• Use of Virtual Reality to Communicate Concepts of Genomics to the General PublicCompletedNCT00316056
• Positron Emission Tomography (PET) Imaging in People With Gaucher MutationsCompletedNCT00302146
• Perspectives of Individuals With Bipolar Disorder and Siblings of Individuals With Bipolar Disorder; A Telephone Interview StudyCompletedNCT00300820
• Intravenous Immune Globulin to Treat Hereditary Inclusion Body MyopathyCompletedNCT00195637Phase 1
• Developing Newborn Screening for Infants With Primary ImmunodeficiencyCompletedNCT00113464
• Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis)CompletedNCT00106977
• Clinical Studies of ProgeriaCompletedNCT00094393
• Clinical and Genetic Studies on HoloprosencephalyCompletedNCT00088426
• Study of Megakaryocytes From Patients With Abnormal Platelet VesiclesCompletedNCT00086476
• Analysis of Specimens From Individuals With Pulmonary FibrosisActive, not recruitingNCT00084305
• Genetics and Clinical Characteristics of Bardet-Biedl SyndromeTerminatedNCT00078091
• Cell Studies of Parkinson's DiseaseCompletedNCT00076505
• Genetic Analysis of Gray Platelet SyndromeCompletedNCT00069680
• Clinical and Molecular Investigations Into CiliopathiesCompletedNCT00068224
• The Value of Genetic Information to Adult Adopted IndividualsCompletedNCT00057694
• Transitional Life Events in Patients With Friedreich's Ataxia: Implications for Genetic CounselingCompletedNCT00056186
• Pilot Study of the Process of Prenatal Genetic CounselingCompletedNCT00047905Not applicable
• Genetic Analysis of Attention Deficit Hyperactivity Disorder (ADHD)CompletedNCT00046059
• Genetic Analysis of Fraser Syndrome and Fryns SyndromeCompletedNCT00032877
• Analysis of Prostate Cancer Short-Term Cultures Using Molecular Cytogenetic MethodsCompletedNCT00022919
• Gene Transfer Therapy for Severe Combined Immunodeficieny Disease (SCID) Due to Adenosine Deaminase (ADA) DeficiencyCompletedNCT00018018Phase 1
• Natural History Study of Smith-Magenis SyndromeCompletedNCT00013559
• Genetic Analysis of Familial Brain AneurysmsCompletedNCT00011856
• Molecular Analysis of Microphthalmia/AnophthalmiaCompletedNCT00011843
• Influences on Female Adolescents' Decisions Regarding Testing for Carrier Status of XSCIDCompletedNCT00006335
• Molecular and Clinical Studies of Primary Immunodeficiency DiseasesActive, not recruitingNCT00006319
• Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion BodiesCompletedNCT00006176
• Gene Therapy and Ganciclovir in Treating Patients With Stage IV MelanomaCompletedNCT00005057Phase 1
• Study of the Experiences and Needs of Parents Continuing a Pregnancy Following a Prenatal Diagnosis of HolopresencephalyCompletedNCT00005016
• Study of the Results of Education and Counseling for Persons Undergoing Genetic Testing for Hereditary Nonpolyposis Colon CancerCompletedNCT00004210Not applicable
• Mind-Body Therapy for Pain in Ehlers-Danlos SyndromeCompletedNCT00001966Phase 2
• Microarray Analysis for Human Genetic DiseaseCompletedNCT00001898
• Lung Disease Associated With Rheumatoid ArthritisCompletedNCT00001876
• Study of Skeletal Disorders and Short StatureCompletedNCT00001754
• Gene Analysis of Parkinson's DiseaseCompletedNCT00001643
• Positional Cloning of the Gene(s) Responsible for Alagille SyndromeCompletedNCT00001642
• Study of Heritable Connective Tissue DisordersCompletedNCT00001641
• Genetic Analysis of Parkinson's DiseaseCompletedNCT00001640
• Evaluation of Patients With Unresolved Chromosome AbnormalitiesCompletedNCT00001639
• Issues Surrounding Prenatal Genetic Testing for AchondroplasiaCompletedNCT00001536
• Twins Study of Gene Therapy for HIV InfectionCompletedNCT00001535Phase 1
• Genetic Analysis of Hereditary Prostate CancerCompletedNCT00001469
• Outcomes of Education and Counseling for BRCA1 TestingCompletedNCT00001468

← National Human Genome Research Institute (NHGRI) overview and focus areas