A to Z
American Journal of Human Genetics
06 Biological Sciences, 11 Medical and Health Sciences
publication venue for
Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways
Estimation of SNP Heritability from Dense Genotype Data
Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent
Frank Ruddle (1929-2013) OBITUARY
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors
On the replication of genetic associations: Timing can be everything!
Optimal two-stage testing for family-based genome-wide association studies - Response to Macgregor
Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan
A Genomewide Admixture Mapping Panel for Hispanic/Latino Populations
Variance Calculations for Identity-by-Descent Estimation
Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
Investigation of the CHRNA4 gene for a possible role in tobacco use and addiction.
Linkage and association analysis of COPD-related phenotypes on chromosome 19.
Fine mapping linkage analysis of COPD-related phenotypes on chromosome 19.
Profiling SMAD4-mediated transcriptional regulation by TGF-beta on a global scale using high density microarrays.
Progress toward gene identification for alcohol-related phenotypes.
Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data
High-throughout sequencing of candidate genes for alcohol-related QTLs.
The ABCR gene recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration.
A new locus for autosomal dominant Stargardt-like disease maps to chromosome 4
Combined linkage and association sib-pair analysis for quantitative traits
ANALYZING THE RELATIONSHIP BETWEEN AGE AT ONSET AND RISK TO RELATIVES