S. Folstein
Nature · 2001–2014
A researcher in the Science corpus: 6 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Who trusts S. Folstein overall
Papers from S. Folstein's perspective
Ordered by how strongly the researchers S. Folstein trusts endorse each paper. Same corpus, a different order for every researcher.
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
- Diagnostic genome profiling in mental retardation. (American Journal of Human Genetics)
- The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism
- Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
- 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)
- 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)
Their papers
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders (2014) — 930 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
- Comorbid Psychiatric Disorders in Children with Autism: Interview Development and Rates of Disorders (2006) — 1,677 citations
- Genetics of autism: complex aetiology for a heterogeneous disorder. (2001) — 818 citations