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