3.8 Article

Extremes of Unexplained Variation as a Phenotype An Efficient Approach for Genome-Wide Association Studies of Cardiovascular Disease

Journal

CIRCULATION-CARDIOVASCULAR GENETICS
Volume 3, Issue 2, Pages 215-221

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGENETICS.109.934505

Keywords

cardiovascular disease; atherosclerosis; risk factors; stroke; genome-wide association studies; ultrasound

Funding

  1. CIHR [CTP-79853, MOP-79523, MOP-13430] Funding Source: Medline
  2. NCRR NIH HHS [UL1 RR025774-03, UL1 RR025774, U54 RR0252204-01] Funding Source: Medline
  3. NHLBI NIH HHS [U01 HL064777, U01 HL064777-01] Funding Source: Medline
  4. NIA NIH HHS [U19 AG023122, U19 AG023122-01, U19 AG023122-01A1] Funding Source: Medline
  5. NIDA NIH HHS [U01 DA024417-01, U01 DA024417] Funding Source: Medline
  6. NIMH NIH HHS [R01 MH078151, MH078151-01A1, N01 MH022005, P50 MH081755-01, P50 MH081755, R01 MH094483, R01 MH078151-03] Funding Source: Medline

Ask authors/readers for more resources

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available