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1.
Metformin induces FOXO3-dependent fetal hemoglobin production in human primary erythroid cells.
Blood
; 132(3): 321-333, 2018 07 19.
Article
in English
| MEDLINE | ID: mdl-29884740
2.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
Am J Hum Genet
; 94(2): 223-32, 2014 Feb 06.
Article
in English
| MEDLINE | ID: mdl-24507774
3.
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
Am J Hum Genet
; 94(2): 233-45, 2014 Feb 06.
Article
in English
| MEDLINE | ID: mdl-24507775
4.
Inactivating mutations in NPC1L1 and protection from coronary heart disease.
N Engl J Med
; 371(22): 2072-82, 2014 Nov 27.
Article
in English
| MEDLINE | ID: mdl-25390462
5.
Loss-of-function mutations in APOC3, triglycerides, and coronary disease.
N Engl J Med
; 371(1): 22-31, 2014 Jul 03.
Article
in English
| MEDLINE | ID: mdl-24941081
6.
Small dense low-density lipoprotein-cholesterol concentrations predict risk for coronary heart disease: the Atherosclerosis Risk In Communities (ARIC) study.
Arterioscler Thromb Vasc Biol
; 34(5): 1069-77, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24558110
7.
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders.
Hum Mol Genet
; 20(17): 3366-75, 2011 Sep 01.
Article
in English
| MEDLINE | ID: mdl-21624971
8.
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.
PLoS One
; 9(10): e110740, 2014.
Article
in English
| MEDLINE | ID: mdl-25360671
9.
Deep resequencing reveals excess rare recent variants consistent with explosive population growth.
Nat Commun
; 1: 131, 2010 Nov 30.
Article
in English
| MEDLINE | ID: mdl-21119644
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