Roel A. Ophoff
Genetics · 2008–2022
A researcher in the Science corpus: 18 papers; trusts 3 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 307 citations into it
- Molecular Biology — 240 citations into it; #16,179 of 17,773 by trust here, #3,938 by citations
Whom Roel A. Ophoff trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Steve Horvath (in Molecular Biology)
- M. Whitlock (in Genetics)
- Peter Langfelder (in Molecular Biology)
Who trusts Roel A. Ophoff
- Steve Horvath (in Molecular Biology)
Papers from Roel A. Ophoff's perspective
Ordered by how strongly the researchers Roel A. Ophoff trusts endorse each paper. Same corpus, a different order for every researcher.
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- Geometric Interpretation of Gene Coexpression Network Analysis (PLoS Comput. Biol.)
- Identifying biological themes within lists of genes with EASE (Genome Biology)
- Hierarchical Organization of Modularity in Metabolic Networks (Science)
- Eigengene networks for studying the relationships between co-expression modules (BMC Systems Biology)
- Polycomb complexes repress developmental regulators in murine embryonic stem cells (Nature)
- Structuring and extracting knowledge for the support of hypothesis generation in molecular biology (BMC Bioinformatics)
- Intra-individual change over time in DNA methylation with familial clustering. (Journal of the American Medical Association (JAMA))
- Gene network interconnectedness and the generalized topological overlap measure (BMC Bioinformatics)
Their papers
- Large recurrent microdeletions associated with schizophrenia (2008) — 1,814 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
- Common genetic variants influence human subcortical brain structures (2015) — 868 citations
- Aging effects on DNA methylation modules in human brain and blood tissue (2012) — 625 citations
- The genetic architecture of the human cerebral cortex (2020) — 777 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
- 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
- Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group (2017) — 708 citations
- Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium (2015) — 1,151 citations
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) — 790 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
- Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) — 740 citations
- Common variants conferring risk of schizophrenia (2009) — 1,753 citations