Genetics, Genome, Human genome, Gene duplication and Segmental duplication are his primary areas of study. His work in Genetics is not limited to one particular discipline; it also encompasses Epilepsy. His Genome research is multidisciplinary, incorporating elements of Quantitative trait locus, Genome-wide association study and Indel.
His Human genome study combines topics from a wide range of disciplines, such as Expression quantitative trait loci, Genetic variation and Genetic architecture. In his study, Chromosomal rearrangement is inextricably linked to Copy-number variation, which falls within the broad field of Gene duplication. His Microdeletion syndrome research is multidisciplinary, relying on both Microcephaly and Breakpoint.
Andrew J. Sharp mainly investigates Genetics, Genome, DNA methylation, Human genome and Gene. Copy-number variation, Gene duplication, Genomic imprinting, X chromosome and Tandem repeat are among the areas of Genetics where the researcher is concentrating his efforts. His studies in Gene duplication integrate themes in fields like Microdeletion syndrome, Gene rearrangement and Chromosomal rearrangement.
His Genome study combines topics from a wide range of disciplines, such as Expression quantitative trait loci, Single-nucleotide polymorphism and Computational biology. His DNA methylation research is multidisciplinary, incorporating elements of Epigenetics, Neuroscience and Comparative genomics. In his study, which falls under the umbrella issue of Human genome, Genotype is strongly linked to Genetic variation.
Andrew J. Sharp mainly focuses on DNA methylation, Genetics, Epigenetics, Human genome and Gene. His DNA methylation research includes elements of T lymphocyte and In vitro. As part of his studies on Genetics, Andrew J. Sharp often connects relevant subjects like Disease.
His research in Epigenetics intersects with topics in Cancer research, Methylation, Intellectual disability and Autism, Autism spectrum disorder. His Human genome study is focused on Genome in general. His Genome study also includes
His primary areas of investigation include DNA methylation, Epigenetics, Genetics, Epigenome and Haplotype. His DNA methylation research incorporates elements of Cytotoxic T cell and Glatiramer acetate. His Epigenetics research integrates issues from Epigenomics, Methylation, Immunology and CpG site.
In general Genetics, his work in Gene and Human genome is often linked to Dopamine receptor binding linking many areas of study. His Epigenome study incorporates themes from Differential Methylation, Transcriptome, Meta-analysis, Disease and Genetic association. His studies deal with areas such as Structural variation, Genome, Genomics, Sequence assembly and Computational biology as well as Haplotype.
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Fine-scale structural variation of the human genome.
Eray Tuzun;Andrew J Sharp;Jeffrey A Bailey;Rajinder Kaul.
Nature Genetics (2005)
Segmental Duplications and Copy-Number Variation in the Human Genome
Andrew J. Sharp;Devin P. Locke;Sean D. McGrath;Ze Cheng.
American Journal of Human Genetics (2005)
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
Heather C Mefford;Andrew J Sharp;Carl Baker;Andy Itsara.
The New England Journal of Medicine (2008)
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
Andrew J Sharp;Sierra Hansen;Rebecca R Selzer;Ze Cheng.
Nature Genetics (2006)
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
Ingo Helbig;Heather C. Mefford;Andrew J. Sharp;Michel Guipponi.
Nature Genetics (2009)
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Andrew J Sharp;Heather C Mefford;Kelly Li;Carl Baker.
Nature Genetics (2008)
Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome
Devin P. Locke;Andrew J. Sharp;Steven A. McCarroll;Steven A. McCarroll;Sean D. McGrath.
American Journal of Human Genetics (2006)
Age- and tissue-specific variation of X chromosome inactivation ratios in normal women.
Andrew Sharp;David Robinson;Patricia Jacobs.
Human Genetics (2000)
Structural Variation of the Human Genome
Andrew J. Sharp;Ze Cheng;Evan E. Eichler.
Annual Review of Genomics and Human Genetics (2006)
DNA methylation profiles of human active and inactive X chromosomes
Andrew J. Sharp;Elisavet Stathaki;Eugenia Migliavacca;Manisha Brahmachary.
Genome Research (2011)
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