American Journal of Human Genetics Journal

Overview

publication venue for

• Declining autozygosity over time: An exploration in over 1 million individuals from three diverse cohorts 2023
• RAREsim: A simulation method for very rare genetic variants 2022
• Genomic partitioning of inbreeding depression in humans 2021
• Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways 2019
• Estimation of SNP Heritability from Dense Genotype Data 2013
Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent 2013
Frank Ruddle (1929-2013) OBITUARY 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism 2013
Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors 2013
On the replication of genetic associations:: Timing can be everything! 2008
Optimal two-stage testing for family-based genome-wide association studies - Response to Macgregor 2008
Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan 2007
A Genomewide Admixture Mapping Panel for Hispanic/Latino Populations 2007
Variance Calculations for Identity-by-Descent Estimation 2006
Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q 2005
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States 2004
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family 2004
Investigation of the CHRNA4 gene for a possible role in tobacco use and addiction. 2003
Linkage and association analysis of COPD-related phenotypes on chromosome 19. 2003
Refinement of the 6p21.3 QTL influencing dyslexia through linkage and association analysis 2003
Fine mapping linkage analysis of COPD-related phenotypes on chromosome 19. 2002
Profiling SMAD4-mediated transcriptional regulation by TGF-beta on a global scale using high density microarrays. 2002
Evidence for linkage and association with reading disability, on 6p21.3-22 2002
Mutation screening of the SynGAP gene in patients with dyslexia. 2001
Linkage disequilibrium studies of reading disability on 6p22. 2000
Linkage of an ADHD phenotype to 6p21.3 in a population with reading disability. 2000
Progress toward gene identification for alcohol-related phenotypes. 2000
Resolution of marker order and distance to refine linkage in specific reading disability. 2000
Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data 2000
High-throughout sequencing of candidate genes for alcohol-related QTLs. 1999
The ABCR gene recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration. 1999
A new locus for autosomal dominant Stargardt-like disease maps to chromosome 4 1999
Combined linkage and association sib-pair analysis for quantitative traits 1999
Quantitative-trait locus for specific language and reading deficits on chromosome 6p 1999
ANALYZING THE RELATIONSHIP BETWEEN AGE AT ONSET AND RISK TO RELATIVES 1989
GENE-PRODUCTS OF SPECIFIC CHROMOSOMES - NEW APPROACH 1979
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Research

keywords

• 06 Biological Sciences, 11 Medical and Health Sciences