Hilary Coon mainly focuses on Genetics, Autism, Genome-wide association study, Copy-number variation and Genetic linkage. Her work on Meta-analysis expands to the thematically related Genetics. She interconnects Intellectual disability, Clinical psychology and Macrocephaly in the investigation of issues within Autism.
The study incorporates disciplines such as Autism spectrum disorder and Haplotype in addition to Genome-wide association study. Her work deals with themes such as Structural variation, Genetic variation, Allele frequency and Genetic architecture, which intersect with Copy-number variation. Her research in Genetic linkage intersects with topics in Genetic marker, Linkage and Pedigree chart.
Genetics, Genetic linkage, Autism, Gene and Autism spectrum disorder are her primary areas of study. Her study in Linkage, Pedigree chart, Locus, Gene mapping and Genotype is carried out as part of her Genetics studies. Her studies deal with areas such as Quantitative trait locus, Chromosome and Genome Scan as well as Linkage.
As a member of one scientific family, Hilary Coon mostly works in the field of Genetic linkage, focusing on Single-nucleotide polymorphism and, on occasion, Internal medicine. As part of the same scientific family, Hilary Coon usually focuses on Autism, concentrating on Copy-number variation and intersecting with Genome-wide association study. Hilary Coon has researched Genome-wide association study in several fields, including Genetic association and Genetic architecture.
Autism, Autism spectrum disorder, Genetics, Gene and Genome-wide association study are her primary areas of study. Hilary Coon combines subjects such as Exome sequencing, Clinical psychology, Cognition and Offspring with her study of Autism. Her Exome sequencing research includes themes of Chromatin, Genomic Segment, Computational biology and Copy-number variation.
Her Autism spectrum disorder research incorporates themes from genomic DNA and Neurodevelopmental disorder. In the subject of general Gene, her work in Genotype is often linked to Completed Suicide, Extended family and Medical examiner, thereby combining diverse domains of study. Her Genome-wide association study study combines topics in areas such as Pleiotropy, Psychiatry, Depression, Cause of death and Genetic association.
Hilary Coon mainly focuses on Autism spectrum disorder, Autism, Genetics, Gene and Genome-wide association study. Her Autism spectrum disorder study combines topics from a wide range of disciplines, such as Sample, Independent living and Clinical psychology. The Autism study combines topics in areas such as Odds ratio, Relative risk, Cognition and Cumulative incidence.
Her study involves Copy-number variation, Mutation and Genome, a branch of Genetics. In her study, which falls under the umbrella issue of Copy-number variation, False discovery rate is strongly linked to Regulation of gene expression. Her Genome-wide association study research is multidisciplinary, incorporating elements of Schizophrenia, Psychiatry, Psychiatric genetics, Pleiotropy and Bipolar disorder.
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Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
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)
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Joseph T. Glessner;Kai Wang;Guiqing Cai;Olena Korvatska.
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
Cathryn M. Lewis;Douglas F. Levinson;Lesley H. Wise;Lynn E. DeLisi.
American Journal of Human Genetics (2003)
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
Robert Freedman;Hilary Coon;Marina Myles-Worsley;Avi Orr-Urtreger.
Proceedings of the National Academy of Sciences of the United States of America (1997)
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
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.
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)
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