C. Corsello
Cognitive Neuroscience · 2005–2012
A researcher in the Science corpus: 5 papers; trusts 3 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Cognitive Neuroscience — 44 citations into it; #3,448 of 10,852 by trust here, #1,393 by citations
- Clinical Psychology — 10 citations into it; #2,013 of 8,024 by trust here, #4,314 by citations
- Pediatrics, Perinatology and Child Health — 6 citations into it
Whom C. Corsello trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts C. Corsello overall
- G. Mahoney
- A. Wetherby
- Jacqueline Roberts
- Glen O. Sallows
- F. Perales
- Gena P. Barnhill
- Rose Iovannone
- Helena McCabe
- Ognjen Rudovic
- Juliann J. Woods
Papers from C. Corsello's perspective
Ordered by how strongly the researchers C. Corsello trusts endorse each paper. Same corpus, a different order for every researcher.
- Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
- De Novo Gene Disruptions in Children on the Autistic Spectrum (Neuron)
- Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome (Nature Genetics)
- Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (Nature Genetics)
- Genome-wide association study of alcohol dependence (Archives of General Psychiatry)
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations (Nature)
- Global variation in copy number in the human genome (Nature)
- Principal components analysis corrects for stratification in genome-wide association studies
- A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (American Journal of Human Genetics)
- Diagnostic genome profiling in mental retardation. (American Journal of Human Genetics)
Their papers
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- Whole Genome Sequencing in Autism Identifies Hotspots for De Novo Germline Mutation (2012) — 547 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007) — 1,398 citations
- Early Intervention in Autism (2005) — 613 citations