F. Satterstrom
Management Science and Operations Research · 2006–2022
A researcher in the Science corpus: 9 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Management Science and Operations Research — 7 citations into it
Whom F. Satterstrom trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Valerie Belton
- Thomas L. Saaty
- R. Gregory
- T. Stewart
- Salvatore Greco
- John L. Rubenstein
- Robert J. Lempert
Who trusts F. Satterstrom overall
Papers from F. Satterstrom's perspective
Ordered by how strongly the researchers F. Satterstrom trusts endorse each paper. Same corpus, a different order for every researcher.
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
- Spatiotemporal gene expression trajectories reveal developmental hierarchies of the human cortex (Science)
- MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (Nature Genetics)
- regioneR: an R/Bioconductor package for the association analysis of genomic regions based on permutation tests (Bioinform.)
- ToppGene Suite for gene list enrichment analysis and candidate gene prioritization (Nucleic Acids Res.)
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (Nature)
- A Copy Number Variation Morbidity Map of Developmental Delay (Nature Genetics)
- ClinVar: public archive of relationships among sequence variation and human phenotype
- Refining analyses of copy number variation identifies specific genes associated with developmental delay (Nature Genetics)
Their papers
- Multi-criteria decision analysis and environmental risk assessment for nanomaterials (2007) — 185 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
- From comparative risk assessment to multi-criteria decision analysis and adaptive management: recent developments and applications. (2006) — 583 citations
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Transcript expression-aware annotation improves rare variant discovery and interpretation (2019) — 26 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- ASD and ADHD have a similar burden of rare protein-truncating variants (2018) — 29 citations
- Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations