S. Catts
Nature · 2001–2022
A researcher in the Science corpus: 9 papers; trusts 0 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Who trusts S. Catts
- Martin Brüne (in Clinical Psychology)
Papers from S. Catts's perspective
Ordered by how strongly the researchers S. Catts trusts endorse each paper. Same corpus, a different order for every researcher.
- Specific impairments of planning.
- Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. (The Lancet)
- Genetic effects on gene expression across human tissues
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- Systematic identification of trans-eQTLs as putative drivers of known disease associations (Nature Genetics)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (Nature)
- A systematic review of mortality in schizophrenia: is the differential mortality gap worsening over time? (Archives of General Psychiatry)
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
Their papers
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
- Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
- Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 controls via the ENIGMA consortium (2018) — 815 citations
- Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group (2017) — 636 citations
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) — 7,422 citations
- Mentalising, executive planning and disengagement in schizophrenia (2001) — 149 citations