D. Curtis

Genetics · Nature · 2008–2022

A researcher in the Science corpus: 13 papers; trusts 8 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 249 citations into it
• Computational Biology & Bioinformatics — 25 citations into it

Whom D. Curtis trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Shaun Purcell
2. Christopher C. Chang
3. Benjamin M. Neale
4. Carson C. Chow
5. Evan A. Boyle
6. Laurent Tellier
7. Alicia R. Martin

Who trusts D. Curtis overall

1. Alicia R. Martin
2. L. Duncan

Papers from D. Curtis's perspective

Ordered by how strongly the researchers D. Curtis trusts endorse each paper. Same corpus, a different order for every researcher.

1. MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
2. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
3. FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
4. Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
5. 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
6. The support of human genetic evidence for approved drug indications (Nature Genetics)
7. Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study (The Lancet)
8. Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease
9. Rare chromosomal deletions and duplications increase risk of schizophrenia (Nature)
10. Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)

Their papers

• The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
• 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
• Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
• Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) — 994 citations
• Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia (2018) — 125 citations
• Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes (2018) — 667 citations
• The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability (2017) — 228 citations
• Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 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
• Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder (2008) — 1,273 citations