Author: Alicia R. Martin

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Preprints

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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Common risk variants identified in autism spectrum disorder

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Current clinical use of polygenic scores will risk exacerbating health disparities

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Human demographic history impacts genetic risk prediction across diverse populations

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Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies

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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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Population histories of the United States revealed through fine-scale migration and haplotype analysis

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Distance from Sub-Saharan Africa Predicts Mutational Load in Diverse Human Genomes

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Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

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Fine-scale human population structure in southern Africa reflects ecological boundaries

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An Unexpectedly Complex Architecture for Skin Pigmentation in Africans

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Population history and gene divergence in Native Mexicans inferred from 76 human exomes

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Haplotype sharing provides insights into fine-scale population history and disease in Finland

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Geographic variation and bias in polygenic scores of complex diseases and traits in Finland

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Imputation aware tag SNP selection to improve power for multi-ethnic association studies

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Tractor: A framework allowing for improved inclusion of admixed individuals in large-scale association studies.

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Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations

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Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx

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Fine-scale human population structure in southern Africa reflects ecogeographic boundaries

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