Eric Fombonne
Genetics · 2001–2022
A researcher in the Science corpus: 17 papers; trusts 10 researchers and is trusted by 49 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 115 citations into it
- Cognitive Neuroscience — 93 citations into it; #558 of 10,852 by trust here, #363 by citations
- Clinical Psychology — 38 citations into it; #287 of 8,024 by trust here, #456 by citations
- Psychiatry and Mental health — 26 citations into it
- Pediatrics, Perinatology and Child Health — 8 citations into it; #66 of 722 by trust here, #60 by citations
Whom Eric Fombonne trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Eric Fombonne overall
- S. Robinson
- Mayada Elsabbagh
- Shafali S. Jeste
- Daniel H. Geschwind
- E. Hill
- Pauline Chaste
- G. Divan
- Yun-Joo Koh
- C. Corsello
- R. Karpinski
Papers from Eric Fombonne's perspective
Ordered by how strongly the researchers Eric Fombonne trusts endorse each paper. Same corpus, a different order for every researcher.
- The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism
- Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (Nature Genetics)
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
- 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)
- Global variation in copy number in the human genome (Nature)
- Principal components analysis corrects for stratification in genome-wide association studies
- Diagnostic genome profiling in mental retardation. (American Journal of Human Genetics)
- X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. (American Journal of Human Genetics)
- Neuroligins determine synapse maturation and function. (Neuron)
Their papers
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011) — 1,286 citations
- Global prevalence of autism: A systematic review update (2022) — 2,466 citations
- Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (2015) — 1,391 citations
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
- Global Prevalence of Autism and Other Pervasive Developmental Disorders (2012) — 2,543 citations
- Prevalence of autism spectrum disorders in a total population sample. (2011) — 1,532 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Epidemiology of Pervasive Developmental Disorders (2009) — 2,025 citations
- Breastfeeding and child cognitive development: new evidence from a large randomized trial. (2008) — 1,014 citations
- Behavioral and Emotional Problems Reported by Parents of Children Ages 6 to 16 in 31 Societies (2007) — 413 citations
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007) — 1,398 citations
- Epidemiology of autistic disorder and other pervasive developmental disorders. (2005) — 832 citations
- Pervasive developmental disorders in preschool children: confirmation of high prevalence. (2005) — 861 citations
- Epidemiological Surveys of Autism and Other Pervasive Developmental Disorders: An Update (2003) — 1,672 citations
- The prevalence of autism. (2003) — 811 citations
- Pervasive developmental disorders in preschool children. (2001) — 1,233 citations