Christine M. Freitag
Cognitive Neuroscience · 2007–2021
A researcher in the Science corpus: 9 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Cognitive Neuroscience — 97 citations into it; #7,163 of 10,852 by trust here, #1,811 by citations
- Clinical Psychology — 41 citations into it
- Education — 8 citations into it
Whom Christine M. Freitag trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Christine M. Freitag overall
Papers from Christine M. Freitag's perspective
Ordered by how strongly the researchers Christine M. Freitag trusts endorse each paper. Same corpus, a different order for every researcher.
- Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism (Nature Genetics)
- Genome-wide association study of alcohol dependence (Archives of General Psychiatry)
- A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (American Journal of Human Genetics)
- Advances in autism genetics: on the threshold of a new neurobiology (Nature reviews genetics)
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
- The Broad Autism Phenotype Questionnaire (Journal of Autism and Developmental Disorders)
- A genome-wide scan for common alleles affecting risk for autism (Human Molecular Genetics)
- FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism (Cell)
- Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (Nature Genetics)
- Refining analyses of copy number variation identifies specific genes associated with developmental delay (Nature Genetics)
Their papers
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- The genetics of autistic disorders and its clinical relevance: a review of the literature (2007) — 679 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
- The Lancet Commission on the future of care and clinical research in autism. (2021) — 616 citations
- Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
- Hostile attribution bias and aggression in children and adolescents: A systematic literature review on the influence of aggression subtype and gender (2018) — 128 citations
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 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