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  1. Study of Melanoma Risk in Australia and the United Kingdom dbGaP

    ID: phs000519.v1.p1

    Description: The results from a small number of melanoma GWAS have been published. Initial studies identified several pigmentation- and nevus-associated loci that ...

    Study Types: Case Set

  2. SLCO1B1 Variants and Methotrexate Clearance dbGaP

    ID: phs000426.v1.p1

    Description: Methotrexate plasma concentration is related to its clinical effects. To identify the genetic basis of interindividual variability in methotrexate...

    Study Types: Cohort

  3. Study of Irish Amyotrophic Lateral Sclerosis (SIALS) dbGaP

    ID: phs000127.v2.p1

    Description: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by loss of motor neurons. Epidemiological studies indicate...

    Study Types: Case-Control

  4. A Prognostic Role of APC in Colorectal Cancers dbGaP

    ID: phs001111.v1.p1

    Description: Colorectal cancer (CRC) is a highly heterogeneous disease, for which prognosis has been relegated to clinic-pathologic staging for decades. There is a...

    Study Types: Case Set

  5. Genetics Consortium for Late Onset of Alzheimer's Disease (LOAD CIDR Project) dbGaP

    ID: phs000160.v1.p1

    Description: Multiplex Family StudyThe purpose of the NIA Genetics Initiative: Multiplex Family Study is to identify families with multiple members diagnosed wit...

  6. Functionally Active Copy Number Variants Associated with Prostate Cancer Risk dbGaP

    ID: phs000487.v2.p1

    Description: Prostate cancer is a leading cause of cancer death in males throughout the world and has the largest estimated effect of heritability among the most c...

    Study Types: Case-Control

  7. Exome Sequencing of Pleuropulmonary Blastoma dbGaP

    ID: phs000543.v1.p1

    Description: Pleuropulmonary blastoma (PPB) is a rare, aggressive pediatric cancer arising from the lung or pleural cavity. In this study, we sequenced and analyze...

  8. NHLBI TOPMed: Genes-environments and Admixture in Latino Asthmatics (GALA II) Study dbGaP

    ID: phs000920.v1.p1

    Description: This is a case-only pharmacogenetic study of bronchodilator drug response among racially admixed Latino children with asthma. The overall goal is to i...

    Study Types: Case Set

  9. NHLBI and NIA The New England Centenarian Study (NECS) dbGaP

    ID: phs000451.v1.p1

    Description: Supercentenarians (age 110+ years old) generally delay or escape age-related diseases and disability well beyond the age one hundred and this exceptio...

    Study Types: Case Set

  10. A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD) dbGaP

    ID: phs000421.v1.p1

    Description: Fuchs' Endothelial Corneal Dystrophy (FECD) is a common disease that results in loss of vision associated with progressive corneal edema and loss ...

  11. Trisomy 21 Nondisjunction (T21NDJ) dbGaP

    ID: phs000718.v1.p1

    Description: The overall goal of the project is to identify genetic risk factors associated with chromosome 21 nondisjunction in the oocyte. The dataset derives fr...

  12. eMERGE Network Combined Dataset dbGaP

    ID: phs000360.v3.p1

    Description: The electronic Medical Records and Genomics (eMERGE) Network is a consortium of five participating sites (Group Health Seattle, Marshfield Clinic, May...

    Study Types: Case-Control

  13. Region-specific Transcriptome Analysis of the Human Retina and RPE/Choroid dbGaP

    ID: phs001151.v1.p1

    Description: Proper spatial differentiation of retinal cell types is necessary for normal human vision. Many retinal diseases, such as Best disease and male germ c...

    Study Types: Control Set

  14. Genetic Defects in Familial Renal Disorders dbGaP

    ID: phs000477.v1.p1

    Description: Several different genes cause, when mutated, increased urinary phosphate excretion and hypophosphatemia leading to rickets/osteomalacia; however, the ...

  15. Women's Health Initiative dbGaP

    ID: phs000200.v10.p3

    Description: The Women's Health Initiative (WHI) is a long-term national health study that has focused on strategies for preventing heart disease, breast and c...

  16. Glaucoma Exome Sequencing dbGaP

    ID: phs000558.v1.p1

    Description: This is a study of primary open angle glaucoma (POAG) conducted through exome sequencing of cases and comparison of variant frequencies with general p...

    Study Types: Case Set

  17. The Human Virome and Febrile Illness in Children dbGaP

    ID: phs000264.v2.p1

    Description: Definition of the human microbiome is an important scientific priority. This study will expand the scope of the investigation to include viruses, whic...

    Study Types: Prospective

  18. Genomic Analysis of Pediatric Low Grade Gliomas dbGaP

    ID: phs000614.v1.p1

    Description: Pediatric low-grade gliomas (PLGGs) are among the most common solid tumors in children but, apart from mutations or duplications in the BRAF kinase in...

    Study Types: Case Set

  19. NCI TARGET: Therapeutically Applicable Research to Generate Effective Treatments dbGaP

    ID: phs000218.v17.p6

    Description: The Therapeutically Applicable Research to Generate Effective Treatments (TARGET) Initiative seeks to accelerate research in novel marker and drug dev...

    Study Types: Cohort

  20. NCI TARGET: Therapeutically Applicable Research to Generate Effective Treatments dbGaP

    ID: phs000218.v16.p6

    Description: The Therapeutically Applicable Research to Generate Effective Treatments (TARGET) Initiative seeks to accelerate research in novel marker and drug dev...

    Study Types: Cohort

  21. NCI TARGET: Therapeutically Applicable Research to Generate Effective Treatments dbGaP

    ID: phs000218.v14.p4

    Description: The Therapeutically Applicable Research to Generate Effective Treatments (TARGET) Initiative seeks to accelerate research in novel marker and drug dev...

    Study Types: Cohort

  22. CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) dbGaP

    ID: phs000126.v2.p1

    Description: This proposal brings together the two largest NIH funded genetic studies focused on the identification of novel genes that influence the risk of PD. T...

    Study Types: Case-Control

  23. ADGC Genome Wide Association Study dbGaP

    ID: phs000372.v1.p1

    Description: The National Institute on Aging (NIA) Alzheimer's Disease Centers (ADCs) cohort includes subjects ascertained and evaluated by the clinical an...

    Study Types: Case-Control

  24. Prostate Cancer Genome-Wide Association Study for Uncommon Susceptibility Loci (PEGASUS) dbGaP

    ID: phs000882.v1.p1

    Description: This genome-wide association study was funded by the National Cancer Institute (NCI) to identify uncommon susceptibility loci for prostate cancer. A t...

    Study Types: Case-Control

  25. Health and Retirement Study (HRS) dbGaP

    ID: phs000428.v2.p2

    Description: Introduction to V2: This data release comprises data from the V1 release combined with approximately 3,000 additional samples, collected during the HR...

    Study Types: Longitudinal

  26. Autism Genome Project (AGP) Consortium - GWAS - Stage I and II dbGaP

    ID: phs000267.v2.p2

    Description: Autism spectrum disorders (ASDs) are highly heritable (~90%), yet the underlying genetic determinants are largely unknown. To understand the genetic a...

    Study Types: Parent-Offspring Trios

  27. COGA: African American Family GWAS dbGaP

    ID: phs000976.v1.p1

    Description: COGA is a family study of alcoholism, in which the subjects have been drawn from the Collaborative Study on the Genetics of Alcoholism (COGA), a large...

    Study Types: Family

  28. International Standards for Cytogenomic Arrays dbGaP

    ID: phs000205.v4.p2

    Description: The International Standards for Cytogenomic Arrays (ISCA) Consortium is a rapidly growing group of clinical cytogenetics and molecular genetics labora...

    Study Types: Array Comparative Genomic Hybridization

  29. Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families dbGaP

    ID: phs000415.v1.p1

    Description: This study consists of 771 individuals from 15 extended, multi-generational Tourette Syndrome (TS) pedigrees collected by the Tourette Syndrome Associ...

    Study Types: Extended Pedigrees

  30. Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study dbGaP

    ID: phs000636.v1.p1

    Description: The goal of this study is to identify the genes underlying the risk of intracranial aneurysm (IA). The FIA Study initially recruited families appropri...

    Study Types: Family

  31. International Standards for Cytogenomic Arrays dbGaP

    ID: phs000205.v6.p2

    Description: The International Standards for Cytogenomic Arrays (ISCA) Consortium is a rapidly growing group of clinical cytogenetics and molecular genetics labora...

    Study Types: Clinical Genetic Testing

  32. Genome-Wide Association Analysis of Serum Iron in the InCHIANTI and BLSA dbGaP

    ID: phs000215.v1.p1

    Description: The aim of this study was to identify gene(s) associated with serum iron concentrations. This dataset contains the results from a meta-analysis of 1...

  33. NHGRI Tumor Sequencing Project (Lung Adenocarcinoma) dbGaP

    ID: phs000144.v1.p1

    Description: The Tumor Sequencing Project (TSP) Consortium is a collaboration among participants at the Baylor College of Medicine Human Genome Sequencing Center...

    Study Types: Tumor vs. Matched-Normal

  34. Chromothripsis in Patient WHIM-09 dbGaP

    ID: phs000856.v1.p1

    Description: We are studying the natural history, pathogenesis and treatment of patients with WHIM syndrome, an immunodeficiency disorder characterized by warts, h...

    Study Types: Single Patient

  35. Alzheimer's Disease Sequencing Project (ADSP) dbGaP

    ID: phs000572.v3.p2

    Description: The overarching goals of the ADSP are to: (1) identify new genomic variants contributing to increased risk of developing AD, (2) identify new genomic ...

  36. Genetics of Human Developmental Brain Disorders dbGaP

    ID: phs000492.v1.p1

    Description: Developmental brain malformations are at the core of significant neurological diseases affecting many families in the United States and around the wor...

  37. Genomic Characterization of Pediatric Low-Grade Gliomas dbGaP

    ID: phs001054.v1.p1

    Description: Pediatric low-grade gliomas (PLGGs) are the most common pediatric brain-tumor, with more than ten histologic subtypes recognized by the World Health O...

    Study Types: Case Set

  38. NextGen/GENESiPS dbGaP

    ID: phs001139.v1.p1

    Description: Variability in induced pluripotent stem cell (iPSC) lines remains a roadblock for disease modeling and regenerative medicine. Through linear mixed mod...

    Study Types: Case-Control

  39. Genome-Wide Association Study of Anorexia Nervosa dbGaP

    ID: phs000679.v1.p1

    Description: Twin studies are consistent with substantial heritability in anorexia nervosa (AN), although detecting and confirming individual risk alleles has been...

    Study Types: Case-Control

  40. T1DGC: Genome-Wide Association Study in Type 1 Diabetes, 2008 dbGaP

    ID: phs000180.v2.p2

    Description: Cases with Type 1 Diabetes (T1D) in the UK, were part of the Wellcome Trust Case Control Consortium (WTCCC) - http://www.wtccc.org.uk - that first rep...

    Study Types: Case Set

  41. Family Genomics of Bipolar Disorder dbGaP

    ID: phs000866.v1.p1

    Description: This study examined the segregation of variants with phenotype in pedigrees harboring bipolar disorder.

    Study Types: Family

  42. Genome-wide Analysis of Lymphoma dbGaP

    ID: phs000328.v1.p1

    Description: Diffuse Large B-cell Lymphoma (DLBCL) represents the most common form of B-cell non-Hodgkin Lymphoma (B-NHL), accounting for ~30% of the de-novo diag...

    Study Types: Tumor vs. Matched-Normal

  43. NINDS Parkinson's Disease dbGaP

    ID: phs000089.v3.p2

    Description: Epidemiological studies have estimated a cumulative prevalence of PD of greater than 1 per thousand. When prevalence is limited to senior population...

    Study Types: Case-Control

  44. Brain Metastases in Squamous Cell Lung Cancers dbGaP

    ID: phs000907.v1.p1

    Description: Putative oncogenic pathways in squamous cell lung cancer have been recently characterized, although their biologic repercussions in patients is largel...

    Study Types: Case Set

  45. CSER-MedSeq dbGaP

    ID: phs000958.v1.p1

    Description: Whole genome sequencing (WGS) and whole exome sequencing (WES) services are currently available to and being utilized by physicians and their patients...

    Study Types: Case-Control

  46. Cutaneous Microbiome in Psoriasis (HMP Demonstration Study) dbGaP

    ID: phs000251.v2.p2

    Description: Psoriasis, a highly prevalent disease of humans of unknown cause, is a chronic inflammatory disorder primarily involving skin, with distinctive clinic...

    Study Types: Case-Control

  47. Natural Variation in Fish Transcriptomes: Comparative Analysis of the Fathead Minnow (Pimephales promelas) and Zebrafish (Danio rerio) OmicsDI

    ID: E-GEOD-60202

    Date Released: 08-19-2015

    Description: This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

  48. Dazl is required for TET-mediated reprogramming to a naïve pluripotent state (I) OmicsDI

    ID: E-GEOD-69055

    Date Released: 08-19-2015

    Description: Embryonic stem cell (ESC) cultures display a heterogeneous gene expression profile, ranging from a pristine naïve pluripotent state to a primed epibl...

  49. Gata6 potently initiates reprogramming of pluripotent and differentiated cells to extraembryonic endoderm stem cells [time-course microarray] OmicsDI

    ID: E-GEOD-69321

    Date Released: 08-19-2015

    Description: Transcription factor-mediated reprogramming is a powerful method to study cell fate changes. In this work, we demonstrate that the transcription facto...

  50. E. histolytica and E. invadens OmicsDI

    ID: E-GEOD-67232

    Date Released: 08-19-2015

    Description: This SuperSeries is composed of the SubSeries listed below. Refer to individual Series


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