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Author Details

Alicia R Martin
2014
51
29
PMIDPaper TitleJournal TitlePublished Year
36747613A harmonized public resource of deeply sequenced diverse human genomes.bioRxiv2024
38057664A genomic mutational constraint map using variation in 76,156 human genomes.Nature2024
36865265Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases.medRxiv2023
37961173Decoding Genetics, Ancestry, and Geospatial Context for Precision Health.medRxiv2023
37868036Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology.Cell Genom2023
37148359The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.Diabetologia2023
37078667Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility.Hastings Cent Rep2023
36873096Low and differential polygenic score generalizability among African populations due largely to genetic diversity.2023
37066248Prediction and stratification of longitudinal risk for chronic obstructive pulmonary disease across smoking behaviors.medRxiv2023
35145307A roadmap to increase diversity in genomic studies.Nature Medicine2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35591975Genome-wide risk prediction of common diseases across ancestries in one million people.Cell Genom2022
35513724Improving polygenic prediction in ancestrally diverse populations.Nat Genet2022
35576555Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores.2022
35668301Increasing diversity in genomics requires investment in equitable partnerships and capacity building.Nat Genet2022
35354965Polygenic scores in biomedical research.Nat Rev Genet2022
36778051Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity.Cell Genom2022
34192436Problems with Using Polygenic Scores to Select Embryos.N Engl J Med2021
36017067Neuropsychiatric Genetics of Psychosis in the Mexican Population: A Genome-Wide Association Study Protocol for Schizophrenia, Schizoaffective, and Bipolar Disorder Patients and Controls.Complex Psychiatry2021
33462486Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power.Nat Genet2021
33770507Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations.Am J Hum Genet2021
33007199Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.Am J Hum Genet2020
31848607Population History and Gene Divergence in Native Mexicans Inferred from 76 Human Exomes.Mol Biol Evol2020
30782936Neuropsychiatric Genetics of African Populations-Psychosis (NeuroGAP-Psychosis): a case-control study protocol and GWAS in Ethiopia, Kenya, South Africa and Uganda.BMJ Open2019
31594949International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.Nat Commun2019
31740837Comparative genetic architectures of schizophrenia in East Asian and European populations.Nat Genet2019
31607513Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.Cell2019
30408154Shades of complexity: New perspectives on the evolution and genetic architecture of human skin.American Journal of Physical Anthropology2019
30478444Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.Nat Genet2019
30926966Clinical use of current polygenic risk scores may exacerbate health disparities.Nat Genet2019
30813945Potential use of clinical polygenic risk scores in psychiatry - ethical implications and communicating high polygenic risk.Philosophy, Ethics, and Humanities in Medicine2019
30737014Predicting Polygenic Risk of Psychiatric Disorders.Biol Psychiatry2019
30895926Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies.Elife2019
31155286Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland.Am J Hum Genet2019
29706349Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.Am J Hum Genet2018
28439101Largest GWAS of PTSD (N=20â¿¿070) yields genetic overlap with schizophrenia and sex differences in heritability.Mol Psychiatry2018
30240950The critical needs and challenges for genetic architecture studies in Africa.Curr Opin Genet Dev2018
30530665Rapid evolution of a skin-lightening allele in southern African KhoeSan.Proc Natl Acad Sci U S A2018
29861106Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.Am J Hum Genet2018
30131328Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies.G3 (Bethesda)2018
29195075An Unexpectedly Complex Architecture for Skin Pigmentation in Africans.Cell2017
28983069Fine-Scale Genetic Structure in Finland.G3 (Bethesda)2017
28366442Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.Am J Hum Genet2017
27973554Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array.PLoS One2016
27474727Fine-Scale Human Population Structure in Southern Africa Reflects Ecogeographic Boundaries.Genetics2016
26712023Distance from sub-Saharan Africa predicts mutational load in diverse human genomes.Proc Natl Acad Sci U S A2016
26300125Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions.Cell2015
25121757Transcriptome sequencing from diverse human populations reveals differentiated regulatory architecture.PLoS Genet2014
24708091Exome capture from saliva produces high quality genomic and metagenomic data.BMC Genomics2014
24297551Imputation-based assessment of next generation rare exome variant arrays.Pac Symp Biocomput2014
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