C. Betancur

Genetics · 2003–2019

A researcher in the Science corpus: 10 papers; trusts 1 researcher and is trusted by 5 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 136 citations into it; #2,367 of 6,854 by trust here, #256 by citations
• Molecular Biology — 87 citations into it
• Cognitive Neuroscience — 62 citations into it; #4,620 of 10,852 by trust here, #372 by citations

Whom C. Betancur trusts overall

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

1. G. Baird

Who trusts C. Betancur overall

1. M. Del Giudice
2. H. Zoghbi
3. Thomas Bourgeron
4. Daniele Merico
5. Silvia De Rubeis
6. Luis de la Torre-Ubieta
7. Mark F. Bear
8. Pauline Chaste

Papers from C. Betancur's perspective

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

1. Genome-wide association study of alcohol dependence (Archives of General Psychiatry)
2. Prevalence of autism-spectrum conditions: UK school-based population study (British Journal of Psychiatry)
3. The Broad Autism Phenotype Questionnaire (Journal of Autism and Developmental Disorders)
4. Epidemiology of Pervasive Developmental Disorders (Pediatric Research)
5. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (American Journal of Human Genetics)
6. Global variation in copy number in the human genome (Nature)
7. Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
8. Advances in autism genetics: on the threshold of a new neurobiology (Nature reviews genetics)
9. Pervasive developmental disorders in preschool children: confirmation of high prevalence. (American Journal of Psychiatry)
10. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. (Brain Research)

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
• Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
• Analysis of shared heritability in common disorders of the brain (2018) — 1,836 citations
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
• Patterns and rates of exonic de novo mutations in autism spectrum disorders (2012) — 1,772 citations
• Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. (2011) — 916 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