The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports

LA Cupples, HT Arruda, EJ Benjamin… - BMC medical …, 2007 - Springer
Abstract Background The Framingham Heart Study (FHS), founded in 1948 to examine the
epidemiology of cardiovascular disease, is among the most comprehensively characterized …

Applications of linkage disequilibrium and association mapping in crop plants

ES Ersoz, J Yu, ES Buckler - Genomics-Assisted Crop Improvement: Vol. 1 …, 2007 - Springer
The investigations of patterns of linkage disequilibrium for designing associationmapping
studies are fast becoming a method of interest for complex trait dissection and improvement …

The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts

HN Lyon, V Emilsson, A Hinney, IM Heid… - PLoS …, 2007 - journals.plos.org
A SNP upstream of the INSIG2 gene, rs7566605, was recently found to be associated with
obesity as measured by body mass index (BMI) by Herbert and colleagues. The association …

[HTML][HTML] Candidate gene and locus analysis of myopia

DO Mutti, ME Cooper, S O'Brien, LA Jones… - Molecular …, 2007 - ncbi.nlm.nih.gov
Purpose A previous study has reported evidence of a strong linkage, but no association,
between paired box gene 6 (PAX6) and myopia. We attempted to replicate these findings …

Altered brain‐derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia

JM Mercader, M Ribasés, M Gratacòs… - Genes, brain and …, 2007 - Wiley Online Library
Murine models and association studies in eating disorder (ED) patients have shown a role
for the brain‐derived neurotrophic factor (BDNF) in eating behavior. Some studies have …

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

M Luciano, PA Lind, DL Duffy, A Castles, MJ Wright… - Biological …, 2007 - Elsevier
BACKGROUND: KIAA0319 (6p22. 2) has recently been implicated as a susceptibility gene
for dyslexia. We aimed to find further support for this gene by examining its association with …

Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth

NL Ehn, ME Cooper, K Orr, MIN Shi, MK Johnson… - Pediatric …, 2007 - nature.com
Progesterone plays a critical role in the maintenance of pregnancy and has been effectively
used to prevent recurrences of preterm labor. We investigated the role of genetic variation in …

Association of short‐term memory with a variant within DYX1C1 in developmental dyslexia

C Marino, A Citterio, R Giorda, A Facoetti… - Genes, Brain and …, 2007 - Wiley Online Library
A substantial genetic contribution in the etiology of developmental dyslexia (DD) has been
well documented with independent groups reporting a susceptibility locus on chromosome …

Statistics for biology and health

M Gail, K Krickeberg, J Samet, A Tsiatis, W Wong - 2007 - Springer
Survival and event history analysis have developed into one of the major areas of
biostatistics, with important applications in other fields as well, including reliability theory …

A polymorphism in SOD2 is associated with development of Alzheimer's disease

HW Wiener, RT Perry, Z Chen… - Genes, brain and …, 2007 - Wiley Online Library
Genes involved in cellular mechanisms to repair oxidative damage are strong candidates as
etiologic factors for Alzheimer's disease (AD). One important enzyme involved in this …