Search Results - "Freund, Malika"
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Probabilistic fine-mapping of transcriptome-wide association studies
Published in Nature genetics (01-04-2019)“…Transcriptome-wide association studies using predicted expression have identified thousands of genes whose locally regulated expression is associated with…”
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Leveraging Polygenic Functional Enrichment to Improve GWAS Power
Published in American journal of human genetics (03-01-2019)“…Functional genomics data has the potential to increase GWAS power by identifying SNPs that have a higher prior probability of association. Here, we introduce a…”
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Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data
Published in American journal of human genetics (04-06-2020)“…Despite strong transethnic genetic correlations reported in the literature for many complex traits, the non-transferability of polygenic risk scores across…”
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Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI
Published in Genetic epidemiology (01-09-2019)“…Dupuytren's disease is a common inherited tissue‐specific fibrotic disorder, characterized by progressive and irreversible fibroblastic proliferation affecting…”
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Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease
Published in Science translational medicine (01-05-2024)“…Human inborn errors of immunity include rare disorders entailing functional and quantitative antibody deficiencies due to impaired B cells called the common…”
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Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Published in Genome medicine (09-09-2022)“…Large medical centers in urban areas, like Los Angeles, care for a diverse patient population and offer the potential to study the interplay between genetic…”
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Phenotype-Specific Enrichment of Mendelian Disorder Genes near GWAS Regions across 62 Complex Traits
Published in American journal of human genetics (04-10-2018)“…Although recent studies provide evidence for a common genetic basis between complex traits and Mendelian disorders, a thorough quantification of their overlap…”
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BATMAN: Fast and Accurate Integration of Single-Cell RNA-Seq Datasets via Minimum-Weight Matching
Published in iScience (26-06-2020)“…Single-cell RNA-sequencing (scRNA-seq) is a set of technologies used to profile gene expression at the level of individual cells. Although the throughput of…”
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H3K27ac HiChIP in prostate cell lines identifies risk genes for prostate cancer susceptibility
Published in American journal of human genetics (02-12-2021)“…Genome-wide association studies (GWASs) have identified more than 200 prostate cancer (PrCa) risk regions, which provide potential insights into causal…”
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Exploring the Roles of Genetic Regulation in Human Phenotypes
Published 01-01-2020“…Human phenotypes are influenced to varying extents by inherited genetic variation, although specific mechanisms through which this variation affects the…”
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Dissertation -
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Increasing equity in science requires better ethics training: A course by trainees, for trainees
Published in Cell genomics (08-05-2024)“…Despite the profound impacts of scientific research, few scientists have received the necessary training to productively discuss the ethical and societal…”
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Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors
Published in iScience (19-03-2021)“…Coronavirus disease 2019 (COVID-19) has exposed health care disparities in minority groups including Hispanics/Latinxs (HL). Studies of COVID-19 risk factors…”
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