1.
A Common Functional Regulatory Variant at a Type 2 Diabetes Locus Upregulates ARAP1 Expression in the Pancreatic Beta Cell
by Kulzer, Jennifer R
American journal of human genetics, 2014-02-06, Vol.94 (2), p.186-197
2.
The HapMap and genome-wide association studies in diagnosis and therapy
by Manolio, Teri A
Annual review of medicine, 2009, Vol.60 (1), p.443-456
3.
The case for a US prospective cohort study of genes and environment
by Collins, Francis S
Nature, 2004-05-27, Vol.429 (6990), p.475-477
4.
A vision for the future of genomics research
by Collins, Francis S
Nature (London), 2003-04-24, Vol.422 (6934), p.835-847
5.
NIH/Kennedy Center Workshop on Music and the Brain: Finding Harmony
by Cheever, Thomas
Neuron (Cambridge, Mass.), 2018-03-21, Vol.97 (6), p.1214-1218
6.
A targeted antisense therapeutic approach for Hutchinson-Gilford progeria syndrome
by Erdos, Michael R
Nature medicine, 2021-03, Vol.27 (3), p.536-545
7.
Genetic risk scores in the prediction of plasma glucose, impaired insulin secretion, insulin resistance and incident type 2 diabetes in the METSIM study
by Stančáková, Alena
Diabetologia, 2017-06-01, Vol.60 (9), p.1722-1730
8.
A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression
by Kycia, Ina
American journal of human genetics, 2018-04-05, Vol.102 (4), p.620-635
9.
Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol
by Roman, Tamara S
American journal of human genetics, 2015-12-03, Vol.97 (6), p.801-815
10.
Merging and emerging cohorts: Necessary but not sufficient
by Collins, Francis S
Nature (London), 2007-01-18, Vol.445 (7125), p.259-259
11.
PCORnet: turning a dream into reality
by Collins, Francis S
Journal of the American Medical Informatics Association : JAMIA, 2014-07, Vol.21 (4), p.576-577
12.
No Longer Just Looking under the Lamppost
by Collins, Francis S Francis S
American journal of human genetics, 2006-09-01, Vol.79 (3), p.421-426
13.
Genes, Environment, Health, and Disease: Facing up to Complexity
by Manolio, Teri A
Human heredity, 2007-01-01, Vol.63 (2), p.63-66
14.
Mutational analysis using oligonucleotide microarrays
by Hacia, Joseph G
Journal of Medical Genetics, 1999-10, Vol.36 (10), p.730-736
15.
Finding the missing heritability of complex diseases
by Haines, Jonathan L
Nature (London), 2009-10-08, Vol.461 (7265), p.747-753
16.
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits
by Civelek, Mete
American journal of human genetics, 2017-03-02, Vol.100 (3), p.428-443
17.
Replicating genotype–phenotype associations
by CHANOCK, Stephen J
Nature (London), 2007-06-07, Vol.447 (7145), p.655-660
18.
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome
by Collins, Francis S
Nature (London), 2003-05-15, Vol.423 (6937), p.293-298
19.
Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
by Guo, Xiuqing
American journal of human genetics, 2014-07-03, Vol.95 (1), p.49-65
20.
Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics
by Wheeler, Eleanor
American journal of human genetics, 2013-08-08, Vol.93 (2), p.236-248
