Thomas Bourgeron

Genetics · 2003–2015

A researcher in the Science corpus: 10 papers; trusts 14 researchers and is trusted by 4 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 123 citations into it; #3,766 of 6,854 by trust here, #347 by citations
• Cognitive Neuroscience — 93 citations into it; #10,410 of 10,852 by trust here, #538 by citations
• Molecular Biology — 75 citations into it; #10,855 of 17,773 by trust here, #2,983 by citations
• Cellular and Molecular Neuroscience — 19 citations into it
• Developmental Neuroscience — 18 citations into it
• Clinical Psychology — 11 citations into it
• Psychiatry and Mental health — 10 citations into it
• Neurology — 9 citations into it

Whom Thomas Bourgeron trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Takao K. Hensch
2. H. Zoghbi
3. Eric Courchesne
4. Gina G. Turrigiano
5. Wickliffe C. Abraham
6. C. Betancur
7. R. J. Kelleher
8. Mark F. Bear
9. T. Sūdhof
10. C. Gillberg

Who trusts Thomas Bourgeron overall

1. George A. Mashour
2. Paula M. Niedenthal
3. P. Penzes
4. D. Rossignol

Papers from Thomas Bourgeron's perspective

Ordered by how strongly the researchers Thomas Bourgeron trusts endorse each paper. Same corpus, a different order for every researcher.

1. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism (Nature Genetics)
2. Advances in autism genetics: on the threshold of a new neurobiology (Nature reviews genetics)
3. Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? (Science)
4. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. (Brain Research)
5. Correction of fragile X syndrome in mice. (Neuron)
6. Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
7. Epidemiology of Pervasive Developmental Disorders (Pediatric Research)
8. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism (Cell)
9. Neuroligins determine synapse maturation and function. (Neuron)
10. A genome-wide scan for common alleles affecting risk for autism (Human Molecular Genetics)

Their papers

• Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
• Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism (2003) — 1,840 citations
• Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (2007) — 1,531 citations
• Searching for ways out of the autism maze: genetic, epigenetic and environmental clues. (2006) — 600 citations
• A synaptic trek to autism. (2009) — 659 citations
• From the genetic architecture to synaptic plasticity in autism spectrum disorder (2015) — 892 citations
• Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders (2014) — 930 citations
• Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2 (2012) — 614 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