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Author: David Curtis

Rankings

  • All-time downloads: 30,437 (rank: 5,582 (tie) )
  • Categories:
    • addiction medicine: 212 (rank: 393 )
    • cardiovascular medicine: 190 (rank: 2,552 (tie) )
    • endocrinology: 259 (rank: 761 )
    • genetic and genomic medicine: 6,059 (rank: 126 )
    • genetics: 17,960 (rank: 785 )
    • genomics: 2,509 (rank: 9,892 (tie) )
    • microbiology: 323 (rank: 40,708 (tie) )
    • psychiatry and clinical psychology: 2,925 (rank: 275 )

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Preprints

Genomewide association study identifies 30 loci associated with bipolar disorder

genetics more details view paper
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Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

genetic and genomic medicine more details view paper
  • Downloaded 4,233 times
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    • In genetic and genomic medicine: 12
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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 2,746 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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    • In genetics: 427
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,469 times
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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: 994
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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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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
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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
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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
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    • In genetics: 1,857
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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 666 times
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    • In genetics: 1,870
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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 605 times
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Construction of an exome-wide risk score for schizophrenia based on a weighted burden test

genetics more details view paper
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    • In genetics: 2,269
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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 519 times
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    • Site-wide: 55,004
    • In genetics: 2,487
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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 370 times
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    • Site-wide: 77,896
    • In genetics: 3,475
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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 341 times
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    • In genetics: 3,716
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KCC1 Activation protects Mice from the Development of Experimental Cerebral Malaria.

microbiology more details view paper
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    • In microbiology: 6,095
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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 274 times
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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 269 times
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    • Site-wide: 99,056
    • In genetics: 4,325
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Association study of schizophrenia with variants in miR-137 binding sites

genetics more details view paper
  • Downloaded 269 times
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    • In genetics: 4,334
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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 260 times
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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
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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 251 times
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    • In genetic and genomic medicine: 469
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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 234 times
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    • In genetic and genomic medicine: 501
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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 212 times
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    • Site-wide: 112,391
    • In addiction medicine: 61
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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
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    • In cardiovascular medicine: 276
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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
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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 179 times
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