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Author: Valentina Escott-Price

  • ORCiD: http://orcid.org/0000-0003-1784-5483
  • Most recently observed institution: Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, GB

Rankings

  • All-time downloads: 39,504 (rank: 3,701 )
  • Categories:
    • bioinformatics: 404 (rank: 28,213 (tie) )
    • genetic and genomic medicine: 158 (rank: 8,399 (tie) )
    • genetics: 24,983 (rank: 282 )
    • genomics: 5,382 (rank: 4,171 (tie) )
    • neurology: 152 (rank: 5,008 (tie) )
    • neuroscience: 6,305 (rank: 2,633 (tie) )
    • psychiatry and clinical psychology: 2,120 (rank: 301 (tie) )

Downloads per author, site-wide

Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

genetics more details view paper
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Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

genomics more details view paper
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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

psychiatry and clinical psychology more details view paper
  • Downloaded 2,120 times
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A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

neuroscience more details view paper
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Genetic variability in response to Aβ deposition influences Alzheimer's risk

neuroscience more details view paper
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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

genomics more details view paper
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Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia.

neuroscience more details view paper
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Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank

genomics more details view paper
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Genome-wide analysis of risk-taking behaviour and cross-disorder genetic correlations in 116,255 individuals from the UK Biobank cohort

genetics more details view paper
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Genetic association study of psychotic experiences in UK Biobank

genetics more details view paper
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    • In genetics: 1,390
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The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function

genetics more details view paper
  • Downloaded 783 times
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Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia

genetics more details view paper
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Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

genetics more details view paper
  • Downloaded 749 times
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Heritability and genetic variance of dementia with Lewy bodies

neuroscience more details view paper
  • Downloaded 725 times
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A Transcriptome Wide Association Study implicates specific pre- and post-synaptic abnormalities in Schizophrenia

genetics more details view paper
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Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

genetics more details view paper
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Gene based Analysis in HRC Imputed Genome Wide Association Data Identifies Three Novel Genes for Alzheimer's Disease

genetics more details view paper
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Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

genetics more details view paper
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Positioning Personal Polygenic Risk score against the population background.

bioinformatics more details view paper
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Differences in Genetic Liability for Insomnia and Hypersomnia in Bipolar Disorder Subtypes

genomics more details view paper
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Monocyte-specific changes in gene expression implicate LACTB2 and PLIN2 in Alzheimer's disease.

neuroscience more details view paper
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Genetic variability associated with OAS1 expression in myeloid cells increases the risk of Alzheimer's disease and severe COVID-19 outcomes

genetics more details view paper
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Identifying genetic variants associated with cerebellar volume in 33,265 individuals from the UK-Biobank

neuroscience more details view paper
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    • In neuroscience: 17,981
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ASSESSING THE RELATIONSHIP BETWEEN MONOALLELIC PARK2 MUTATIONS AND PARKINSONS RISK

genetic and genomic medicine more details view paper
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DEFINING CANDIDATE PARKINSONS DISEASE GENES THROUGH THE ANALYSIS OF GENOME-WIDE HOMOZYGOSITY

neurology more details view paper
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Abi3 regulates microglial ramification and dynamic tissue surveillance in vivo.

neuroscience more details view paper
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