Michael L. Cuccaro mainly investigates Genetics, Autism, Genome-wide association study, Heritability of autism and Copy-number variation. Single-nucleotide polymorphism, Genetic architecture, Locus, Genetic linkage and Genotyping are subfields of Genetics in which his conducts study. He works in the field of Autism, focusing on Developmental disorder in particular.
His Developmental disorder research is multidisciplinary, relying on both Genetic determinism and Chromosome 15. His work carried out in the field of Genome-wide association study brings together such families of science as Bipolar disorder, Psychiatry, Schizophrenia and Genetic association. His Heritability of autism research is multidisciplinary, incorporating elements of Neurodevelopmental disorder, Epigenetics of autism, Genetic testing and Candidate gene.
The scientist’s investigation covers issues in Genetics, Autism, Developmental disorder, Alzheimer's disease and Disease. His Genetics and Gene, Single-nucleotide polymorphism, Candidate gene, Heritability of autism and Genome-wide association study investigations all form part of his Genetics research activities. His Single-nucleotide polymorphism research integrates issues from Haplotype and Genetic architecture.
His study in Genome-wide association study is interdisciplinary in nature, drawing from both Apolipoprotein E, Genetic linkage and Allele. His work on Autism spectrum disorder and Neurodevelopmental disorder as part of his general Autism study is frequently connected to Copy-number variation, thereby bridging the divide between different branches of science. His Developmental disorder study incorporates themes from Genetic determinism, Genetic heterogeneity, Linkage and Linkage disequilibrium.
Michael L. Cuccaro mainly focuses on Genetics, Alzheimer's disease, Disease, Gerontology and Apolipoprotein E. His research in Alzheimer's disease intersects with topics in Expression quantitative trait loci, Computational biology and SORL1. His Disease research includes elements of RNA editing and Gene regulatory network.
His studies in Apolipoprotein E integrate themes in fields like Genome-wide association study, Phenotype, Function, Cell biology and Allele. His research integrates issues of Genetic association, Population genetics and Allele frequency in his study of Genome-wide association study. His work is dedicated to discovering how Gene expression profiling, Neuroscience are connected with Autism and other disciplines.
Michael L. Cuccaro mostly deals with Genetics, Allele, Apolipoprotein E, Genetic genealogy and Alzheimer's disease. His research in Gene, Locus, Phenotype, Human genetics and Chromosome are components of Genetics. As part of his studies on Apolipoprotein E, Michael L. Cuccaro often connects relevant subjects like Genome-wide association study.
His Genome-wide association study research incorporates themes from Genetic association, Population genetics and Allele frequency. His Genetic genealogy research includes themes of Genotyping, Dementia, Haplotype and White. Michael L. Cuccaro has included themes like Age of onset, Cohort and Cognitive decline in his Alzheimer's disease study.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
Nature (2010)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
Nature (2009)
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto;Elsa Delaby;Elsa Delaby;Elsa Delaby;Daniele Merico;Mafalda Barbosa.
American Journal of Human Genetics (2014)
A genome-wide linkage and association scan reveals novel loci for autism
Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti.
Nature (2009)
A genome-wide scan for common alleles affecting risk for autism
Richard Anney;Lambertus Klei;Dalila Pinto;Regina Regan.
Human Molecular Genetics (2010)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan.
Nature Neuroscience (2015)
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.
Simon G Gregory;Jessica J Connelly;Aaron J Towers;Jessica Johnson.
BMC Medicine (2009)
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
Richard J.L. Anney;Richard J.L. Anney;Stephan Ripke;Stephan Ripke;Stephan Ripke;Verneri Anttila;Jakob Grove;Jakob Grove.
Molecular Autism (2017)
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