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Author: Christina M Hultman

  • Most recently observed institution: Karolinska Institutet

Rankings

  • All-time downloads: 49,628 (rank: 778 out of 404,161)
  • Categories:
    • genetics: 25,042 (rank: 220 out of 36,792)
    • genomics: 24,586 (rank: 330 out of 42,763)

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Preprints

Analysis of protein-coding genetic variation in 60,706 humans

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

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Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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Regulatory variants explain much more heritability than coding variants across 11 common diseases

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

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The weighting is the hardest part: on the behavior of the likelihood ratio test and score test under weight misspecification in rare variant association studies

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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

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Large-scale analysis of DNA methylation identifies cellular alterations in blood from psychosis patients and molecular biomarkers of treatment-resistant schizophrenia.

genomics more details view paper
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