Collaborate

Below is a listing for all eMERGE studies currently submitted to and/or accessible in dbGaP.

Accession Number Study Description Molecular Data Type Release Date
phs000203 Case/control study aiming to identify the generic variants mediating susceptibility to peripheral arterial disease (PAD). N= 3,337. Whole Genome Genotyping 11/05/2010
phs000188 Case set of participants exploring QRS duration on the electrocardiogram. N= 3,021. Whole Genome Genotyping 10/08/2011
phs000408 Case set containing data from the Geisinger eMERGE Genome-wide Association Study of Obesity Project. N= 962. Whole Genome Genotyping 12/06/2011
phs000387 Case set exploring the genetic determinants of Abdominal Aortic Aneurysm. N= 910. Whole Genome Genotyping 12/19/2011
phs000381 Control set of data from participants enrolled from community-based primary care clinics of Geisinger Health System. N= 1,231. Whole Genome Genotyping 12/19/2011
phs000380 Case set containing data from the Geisinger eMERGE Genome Wide Association Studies of Obesity (Metabochip). N= 982. Whole Genome Genotyping 01/12/2012
phs000237 Case/control study of data exploring the genetic determinants and race differences in prevalence of Type 2 Diabetes. N= 3,563. Whole Genome Genotyping 04/22/2012
phs000494 Cohort studies of data from participants enrolled across seven cohorts at Cincinnati Children’s Hospital. N= 4,562. Whole Genome Genotyping 07/23/2012
phs000297 Case/control study exploring the genetic determinants of resistant hypertension. N= 5,281. Whole Genome Genotyping 09/26/2012
phs000495 Prospective longitudinal study of participants enrolled in the Gene Partnership at Boston Children’s Hospital. N= 1,024. Whole Genome Genotyping 08/30/2013
phs000490 Case/control study of data exploring the genetic causes of complex pediatric disorders. N= 7,431. Whole Genome Genotyping 10/02/2013
phs000170 Case/control study exploring the genetic determinants of cataract and lipid abnormalities. N= 3,989. Whole Genome Genotyping 03/09/2015
phs000948 Cohort study containing data from participants, aged 50-65, enrolled at GroupHealth Cooperative. N= 1,968. Whole Exome Genotyping 08/28/2015
phs000957 Case/control exome chip study for Abdominal Aortic Aneurysm and extreme obesity. N= 9,212. Whole Exome Genotyping 11/16/2015
phs000944 Cross-sectional study of data from a subset of participants enrolled in the Partners Healthcare Biobank. N= 4,929. Whole Genome Genotyping 03/07/2016
phs000961 Prospective case/control cohort study of participants enrolled in the Columbia University GENIE study. N= 3,065. Whole Genome Genotyping 06/07/2016
phs000360 Case/control study exploring the genetics determinants of five individual phenotypes. N= 18,663. Targeted Genomic Sequencing 08/11/2016
phs000888 A cohort study exploring the genetic determinants of more than 40 individual phenotypes (case/control sets included). N= 55,029. Imputation 08/11/2016
phs001011 Case/control cohort study of data from participants enrolled across six cohorts at Cincinnati Children’s Hospital. N= 1,568. Whole Genome Genotyping 09/27/2016
phs001191 Longitudinal cohort study from Northwestern University’s NUgene project containing whole genome sequencing data. N= 900. Whole Genome Sequencing 10/03/2017
phs000906 Cohort study exploring clinical implementation of pharmacogenomics sequence data. N= 9,010. Targeted Genomic Sequencing 12/06/2017
phs001165 Longitudinal cohort study from the Children’s Hospital of Philadelphia containing whole genome sequencing data. N= 900. Whole Genome Sequencing 05/25/2018
phs000234 Case/control study focusing on dementia participants. N= 3,756. Whole Genome Genotyping 05/30/2018
In the News

Here's what's happening with eMerge:

06
DEC

eMERGE Network is excited to share that Taryn Hall's project, Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling; was published in Genes...

20
JUL

eMERGE Network is excited to share that Dr. Douglas Pet's project, Physicians Raise Concerns on Receiving Unsolicited Genomic Results; was published in Genetics in Medicine. The publication...

14
MAY

CDC's new blog post: Precision Medicine in Action: How well does cascade screening for hereditary conditions work in the real world? Posted on May 8, 2018 by 

23
APR

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