Her primary areas of study are Genome-wide association study, Genetics, Autism, Autism spectrum disorder and Clinical psychology. The various areas that Elise B. Robinson examines in her Genome-wide association study study include Evolutionary biology, Genetic variation, Population genetics and Genetic architecture. Her Autism research is multidisciplinary, relying on both Twin study, Schizophrenia and Proband.
Her Autism spectrum disorder study integrates concerns from other disciplines, such as Exome sequencing, Copy-number variation, Transmission disequilibrium test, Multifactorial Inheritance and Behavioural genetics. Her Clinical psychology research incorporates themes from Concordance and Heritability. She combines subjects such as Quantitative trait locus and Genetic correlation with her study of Single-nucleotide polymorphism.
Her primary scientific interests are in Autism, Clinical psychology, Autism spectrum disorder, Genetics and Schizophrenia. Her studies in Autism integrate themes in fields like Twin study and Comorbidity. Her work carried out in the field of Clinical psychology brings together such families of science as Psychosis, Genetic risk, Cognition and Genetic architecture.
Her research integrates issues of Attention deficit hyperactivity disorder, Proband, Intellectual disability and Genetic variation in her study of Autism spectrum disorder. Her Genetics research focuses on Gene, Copy-number variation, Phenotype, Exome sequencing and Genome-wide association study. In her study, Single-nucleotide polymorphism is inextricably linked to Evolutionary biology, which falls within the broad field of Genome-wide association study.
Elise B. Robinson focuses on Autism spectrum disorder, Clinical psychology, Autism, Cognition and Genetic risk. Her Autism spectrum disorder research includes themes of Genetics, De novo mutations and Pediatrics. She has included themes like Schizophrenia and Gene Discovery in her Clinical psychology study.
Autism is frequently linked to Genome-wide association study in her study. Her Genome-wide association study study combines topics from a wide range of disciplines, such as Exome sequencing, Exome, Copy-number variation, Allele frequency and Spectrum disorder. As a part of the same scientific study, she usually deals with the Genetic risk, concentrating on Polygenic risk score and frequently concerns with Genetic variation and Phenotype.
The scientist’s investigation covers issues in Autism spectrum disorder, Autism, Heritability, Cohort and Genetic correlation. Her biological study spans a wide range of topics, including Exome sequencing, Genetics, Gene, Genome-wide association study and Copy-number variation. Elise B. Robinson carries out multidisciplinary research, doing studies in Genetics and Gene expression profiling.
Her work deals with themes such as Spectrum disorder, Exome and Allele frequency, which intersect with Autism. Her Heritability study incorporates themes from Neurocognitive, Cognition, Developmental psychology, Genetic variation and Etiology. Combining a variety of fields, including Cohort, Cognitive development, Clinical psychology, Genetic predisposition and Motor skill, are what the author presents in her essays.
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An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K Finucane;Verneri Anttila;Verneri Anttila;Alexander Gusev.
Nature Genetics (2015)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Ditte Demontis;Ditte Demontis;Raymond K Walters;Raymond K Walters;Joanna Martin;Joanna Martin;Joanna Martin;Manuel Mattheisen.
Nature Genetics (2019)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Science (2018)
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J. Sanders;Xin He;A. Jeremy Willsey;A. Gulhan Ercan-Sencicek.
Neuron (2015)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom;F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S. Breen.
Cell (2020)
A framework for the interpretation of de novo mutation in human disease
Kaitlin E Samocha;Elise B Robinson;Stephan J Sanders;Christine Stevens.
Nature Genetics (2014)
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S Breen;Michael S Breen.
Social Science Research Network (2019)
Examining and interpreting the female protective effect against autistic behavior
Elise B. Robinson;Paul Lichtenstein;Henrik Anckarsäter;Francesca Happé.
Proceedings of the National Academy of Sciences of the United States of America (2013)
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Daniel J Weiner;Daniel J Weiner;Emilie M Wigdor;Emilie M Wigdor;Stephan Ripke;Raymond K Walters;Raymond K Walters.
Nature Genetics (2017)
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Elise B Robinson;Elise B Robinson;Beate St Pourcain;Verneri Anttila;Verneri Anttila;Jack A Kosmicki.
Nature Genetics (2016)
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