Catherine Lord
Cognitive Neuroscience · 2000–2021
A researcher in the Science corpus: 27 papers; trusts 16 researchers and is trusted by 24 researchers here, as inferred from the citation graph.
Subfields
- Cognitive Neuroscience — 283 citations into it; #1,642 of 10,852 by trust here, #238 by citations
- Genetics — 216 citations into it; #1,345 of 6,854 by trust here, #204 by citations
- Molecular Biology — 126 citations into it
- Clinical Psychology — 93 citations into it; #1,585 of 8,024 by trust here, #406 by citations
- Social Psychology — 39 citations into it
- Pediatrics, Perinatology and Child Health — 28 citations into it
- Behavioral Neuroscience — 26 citations into it
- Epidemiology — 19 citations into it
Whom Catherine Lord trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Susan Risi
- Bruce S. McEwen
- Edwin H. Cook Jr.
- R. Sapolsky
- Michael Joseph Meaney
- Dennis S. Charney
- A. Pickles
- Eric Fombonne
- K. Gotham
- Sally J. Rogers
Who trusts Catherine Lord overall
- K. Gotham
- Brooke Ingersoll
- Ben Alderson-Day
- Cheryl Smith Gabig
- Meng-Chuan Lai
- Daniel P. Kennedy
- G. Fischbach
- Naomi Davis
- Michael V. Lombardo
- Simon Baron-Cohen
Papers from Catherine Lord's perspective
Ordered by how strongly the researchers Catherine Lord trusts endorse each paper. Same corpus, a different order for every researcher.
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (Nature)
- 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)
- Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins. (Cell)
- The Broad Autism Phenotype Questionnaire (Journal of Autism and Developmental Disorders)
- Global variation in copy number in the human genome (Nature)
- Genome-wide association study of alcohol dependence (Archives of General Psychiatry)
- 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)
- Diagnostic genome profiling in mental retardation. (American Journal of Human Genetics)
- Epidemiology of Pervasive Developmental Disorders (Pediatric Research)
Their papers
- Detection of eye contact with deep neural networks is as accurate as human experts (2020) — 60 citations
- 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
- Self-esteem, locus of control, hippocampal volume, and cortisol regulation in young and old adulthood (2005) — 332 citations
- The Lancet Commission on the future of care and clinical research in autism. (2021) — 616 citations
- Autism spectrum disorder (2020) — 1,164 citations
- Autism Diagnostic Interview (2019) — 106 citations
- Enhancing studies of the connectome in autism using the autism brain imaging data exchange II (2017) — 670 citations
- Autism Diagnostic Observation Schedule--Generic (2016) — 221 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
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders (2014) — 930 citations
- Language and Communication in Autism (2014) — 959 citations
- Effects of a Brief Early Start Denver Model (ESDM)–Based Parent Intervention on Toddlers at Risk for Autism Spectrum Disorders: A Randomized Controlled Trial (2012) — 612 citations
- Chronic stress, cognitive functioning and mental health. (2011) — 638 citations
- The Simons Simplex Collection: a resource for identification of autism genetic risk factors. (2010) — 738 citations
- Behavioural phenotyping assays for mouse models of autism (2010) — 1,424 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Abnormalities of Intrinsic Functional Connectivity in Autism Spectrum Disorders (2009) — 598 citations
- Standardizing ADOS Scores for a Measure of Severity in Autism Spectrum Disorders (2008) — 1,603 citations