What is he best known for?
The fields of study he is best known for:
Stephen T. Warren mainly focuses on Fragile X syndrome, Genetics, FMR1, Molecular biology and Messenger RNA.
His Fragile X syndrome research integrates issues from Synaptic plasticity, DNA methylation, Polysome, Translation and Neuroscience.
Stephen T. Warren studies Fragile X-associated tremor/ataxia syndrome which is a part of FMR1.
He has researched Fragile X-associated tremor/ataxia syndrome in several fields, including Sherman paradox and Fragile X Tremor/Ataxia Syndrome.
His work deals with themes such as Gene expression, HDAC4, Exon, RNA-binding protein and CpG site, which intersect with Molecular biology.
The various areas that Stephen T. Warren examines in his Messenger RNA study include RNA and microRNA.
His most cited work include:
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome (2825 citations)
- Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. (1762 citations)
- Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. (1762 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Genetics, Fragile X syndrome, Molecular biology, FMR1 and Gene.
His study in Allele, X chromosome, Trinucleotide repeat expansion, Chromosomal fragile site and Locus falls within the category of Genetics.
His biological study spans a wide range of topics, including Neuroscience, Metabotropic glutamate receptor, Phenotype and Messenger RNA, RNA-binding protein.
His work carried out in the field of Messenger RNA brings together such families of science as RNA and Polysome.
As a part of the same scientific study, he usually deals with the Molecular biology, concentrating on Methylation and frequently concerns with CpG site.
His study in FMR1 focuses on Fragile X-associated tremor/ataxia syndrome in particular.
He most often published in these fields:
- Genetics (65.90%)
- Fragile X syndrome (46.74%)
- Molecular biology (27.20%)
What were the highlights of his more recent work (between 2011-2021)?
- Genetics (65.90%)
- Fragile X syndrome (46.74%)
- Gene (18.01%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Genetics, Fragile X syndrome, Gene, FMR1 and DNA methylation.
His Genetics study frequently involves adjacent topics like Schizophrenia.
The study incorporates disciplines such as DNA damage, Trinucleotide repeat expansion, Mutation, RNA and Intellectual disability in addition to Fragile X syndrome.
The Gene study combines topics in areas such as Disease and Bioinformatics.
His research in FMR1 intersects with topics in Missense mutation, Metabotropic glutamate receptor, Molecular biology, Untranslated region and Neuroscience.
His research in DNA methylation tackles topics such as X chromosome which are related to areas like X-linked intellectual disability, Intellectual development, Gene expression profiling, Chromosomal fragile site and Cas9.
Between 2011 and 2021, his most popular works were:
- Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective (382 citations)
- Age-associated DNA methylation in pediatric populations (255 citations)
- Reversal of Disease-Related Pathologies in the Fragile X Mouse Model by Selective Activation of GABAB Receptors with Arbaclofen (179 citations)
In his most recent research, the most cited papers focused on:
His main research concerns Genetics, Fragile X syndrome, FMR1, Gene and DNA methylation.
His Genetics research incorporates themes from Odds ratio and Disease.
His Fragile X syndrome research incorporates elements of Trinucleotide repeat expansion, Mutation, Chromatin, Gene silencing and Gene product.
His FMR1 research is multidisciplinary, incorporating elements of Missense mutation, Metabotropic glutamate receptor, Psychiatry, Molecular biology and Neuroscience.
His Molecular biology research includes themes of Autism spectrum disorder, Intellectual disability and Chromosome abnormality.
Stephen T. Warren usually deals with DNA methylation and limits it to topics linked to Epigenetics and CpG site, Human genome, X chromosome, Reprogramming and 5-Hydroxymethylcytosine.
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