Author: Iuliana Ionita-Laza

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Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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Estimate of disease heritability using 7.4 million familial relationships inferred from electronic health records

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  • Site-wide: 3,632
  • In genetics: 146
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A statistical framework for mapping risk genes from de novo mutations in whole-genome sequencing studies

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  • In genetics: 406
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FUN-LDA: A latent Dirichlet allocation model for predicting tissue-specific functional effects of noncoding variation

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  • In bioinformatics: 1,544
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Multitrait genetic-phenotype associations to connect disease variants and biological mechanisms

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  • In genetics: 1,256
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A novel quantile regression approach for eQTL discovery

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  • In bioinformatics: 3,943
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GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

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Differences in Plasma Metabolites Related to Alzheimer's Disease, APOE-e4 Status and Ethnicity

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  • In neurology: 155
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Ancestry adjustment improves genome-wide estimates of regional intolerance

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A multi-dimensional integrative scoring framework for predicting functional variants in the human genome

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  • In genetics: 3,697
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  • Site-wide: 5,635
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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics

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  • In genetics: 4,463
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