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Author: David Curtis

Rankings

  • All-time downloads: 43,117 (rank: 6,017 (tie) )
  • Categories:
    • addiction medicine: 573 (rank: 445 )
    • cardiovascular medicine: 1,404 (rank: 618 )
    • endocrinology: 499 (rank: 1,039 (tie) )
    • genetic and genomic medicine: 11,326 (rank: 129 )
    • genetics: 20,252 (rank: 842 )
    • genomics: 2,701 (rank: 11,787 (tie) )
    • microbiology: 371 (rank: 55,299 (tie) )
    • psychiatry and clinical psychology: 4,023 (rank: 339 )

Downloads per author, site-wide

Preprints

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

genetic and genomic medicine more details view paper
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    • Site-wide: 831

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics 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 3,654 times
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Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia

genetics 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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Analysis of 200,000 exome-sequenced UK Biobank subjects implicates genes involved in increased and decreased risk of hypertension

cardiovascular medicine more details view paper
  • Downloaded 1,624 times
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    • In cardiovascular medicine: 39
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,606 times
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    • In genomics: 1,618
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
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    • In genomics: 2,528
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A weighted burden test using logistic regression for integrated analysis of sequence variants, copy number variants and polygenic risk score

genetics more details view paper
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    • In genetics: 1,243
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Coding variants in ACE2 and TMPRSS2 are not major drivers of COVID-19 severity in UK Biobank subjects.

genetic and genomic medicine more details view paper
  • Downloaded 972 times
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Weighted burden analysis of exome-sequenced late onset Alzheimer’s cases and controls provides further evidence for a role for PSEN1 and suggests involvement of the PI3K/Akt/GSK-3β and WNT signalling pathways

genetics more details view paper
  • Downloaded 931 times
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    • Site-wide: 42,855
    • In genetics: 1,779
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Polygenic risk score for schizophrenia is not strongly associated with the expression of specific genes or gene sets

genetics more details view paper
  • Downloaded 830 times
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    • Site-wide: 51,083
    • In genetics: 2,041
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Common variants of NRXN1, LRP1B and RORA are associated with increased ventricular volumes in psychosis - GWAS findings from the B-SNIP deep phenotyping study

genetics more details view paper
  • Downloaded 827 times
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    • Site-wide: 51,333
    • In genetics: 2,007
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Construction of an exome-wide risk score for schizophrenia based on a weighted burden test

genetics more details view paper
  • Downloaded 736 times
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    • Site-wide: 60,945
    • In genetics: 2,381
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    • Site-wide: 146,805
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Analysis of exome-sequenced UK Biobank subjects implicates genes affecting risk of hyperlipidaemia

genetic and genomic medicine more details view paper
  • Downloaded 675 times
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    • Site-wide: 68,877
    • In genetic and genomic medicine: 479
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    • Site-wide: 32,833
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Investigation of association of rare, functional genetic variants with heavy drinking and problem drinking in exome sequenced UK Biobank participants

addiction medicine more details view paper
  • Downloaded 597 times
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    • Site-wide: 80,947
    • In addiction medicine: 60
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    • Site-wide: 52,213
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Weighted burden analysis of exome-sequenced case-control sample implicates synaptic genes in schizophrenia aetiology

genetics more details view paper
  • Downloaded 579 times
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    • In genetics: 3,161
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Analysis of 200,000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia

endocrinology more details view paper
  • Downloaded 530 times
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Weighted burden analysis in 200 000 exome-sequenced UK Biobank subjects characterises effects of rare genetic variants on BMI

genetic and genomic medicine more details view paper
  • Downloaded 493 times
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    • In genetic and genomic medicine: 637
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Analysis of 200,000 exome-sequenced UK Biobank subjects fails to identify genes influencing probability of developing a mood disorder resulting in psychiatric referral

psychiatry and clinical psychology more details view paper
  • Downloaded 491 times
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    • In psychiatry and clinical psychology: 530
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Weighted burden analysis in 200,000 exome-sequenced subjects characterises rare variant effects on risk of type 2 diabetes

genetic and genomic medicine more details view paper
  • Downloaded 488 times
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    • In genetic and genomic medicine: 645
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LD scores are associated with differences in allele frequencies between populations but LD score regression can still distinguish confounding from polygenicity

genetics more details view paper
  • Downloaded 487 times
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    • Site-wide: 103,268
    • In genetics: 3,913
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In silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia

genetics more details view paper
  • Downloaded 460 times
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    • Site-wide: 109,649
    • In genetics: 4,091
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Do damaging variants of SLC6A9, the gene for the glycine transporter 1 (GlyT-1), protect against schizophrenia?

genetics more details view paper
  • Downloaded 409 times
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    • In genetics: 4,637
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Analysis of 50,000 exome-sequenced UK Biobank subjects fails to identify genes influencing probability of psychiatric referral

genetic and genomic medicine more details view paper
  • Downloaded 406 times
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    • In genetic and genomic medicine: 791
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KCC1 Activation protects Mice from the Development of Experimental Cerebral Malaria.

microbiology more details view paper
  • Downloaded 389 times
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    • In microbiology: 8,524
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Association study of schizophrenia with variants in miR-137 binding sites

genetics more details view paper
  • Downloaded 361 times
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    • In genetics: 5,056
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Multiple linear regression allows weighted burden analysis of rare coding variants in an ethnically heterogeneous population

genetics more details view paper
  • Downloaded 328 times
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    • In genetics: 5,490
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Study of association of migraine susceptibility genes with common migraine in 200,000 exome-sequenced UK Biobank participants

genetic and genomic medicine more details view paper
  • Downloaded 195 times
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    • In genetic and genomic medicine: 1,313
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Clinical features of UK Biobank subjects carrying protein truncating variants in genes implicated in schizophrenia pathogenesis

genetic and genomic medicine more details view paper
  • Downloaded 145 times
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    • In genetic and genomic medicine: 1,429
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