Genome Partitioning of Genetic Variation for Height from 11,214 Sibling Pairs

This publication has 39 references indexed in Scilit:

• Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
  Nature, 2007
• A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
  Nature Genetics, 2006
• Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings
  PLoS Genetics, 2006
• Estimating the additive genetic effect of the X chromosome
  Genetic Epidemiology, 2005
• A male-specific quantitative trait locus on 1p21 controlling human stature
  Journal of Medical Genetics, 2005
• Loci Contributing to Adult Height and Body Mass Index in African American Families Ascertained for Type 2 Diabetes
  Annals of Human Genetics, 2005
• Epistasis: too often neglected in complex trait studies?
  Nature Reviews Genetics, 2004
• A Genome Scan for Eye Color in 502 Twin Families: Most Variation is due to a QTL on Chromosome 15q
  Twin Research, 2004
• Understanding quantitative genetic variation
  Nature Reviews Genetics, 2002
• Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
  Nature Genetics, 1995