What is he best known for?
The fields of study he is best known for:
The scientist’s investigation covers issues in Genetics, microRNA, Gene, RNA and Regulation of gene expression.
Gene silencing, Gene expression, Genome, RNA interference and Deep sequencing are the core of his Genetics study.
The Genome study combines topics in areas such as Solanum and Solanum pimpinellifolium.
His biological study spans a wide range of topics, including Muscle cell differentiation, Myogenesis, Molecular biology, Cell biology and SMAD.
His work in the fields of Gene, such as Gene family, overlaps with other areas such as Lineage.
The concepts of his RNA study are interwoven with issues in Computational biology and Bioinformatics.
His most cited work include:
- The tomato genome sequence provides insights into fleshy fruit evolution (1991 citations)
- An RNA-Dependent RNA Polymerase Gene in Arabidopsis Is Required for Posttranscriptional Gene Silencing Mediated by a Transgene but Not by a Virus (983 citations)
- Butterfly genome reveals promiscuous exchange of mimicry adaptations among species (875 citations)
What are the main themes of his work throughout his whole career to date?
Tamas Dalmay mostly deals with Genetics, microRNA, RNA, Gene and RNA silencing.
RNA interference, Gene expression, Small RNA, Gene silencing and Genome are subfields of Genetics in which his conducts study.
As part of one scientific family, Tamas Dalmay deals mainly with the area of Small RNA, narrowing it down to issues related to the Botany, and often Abiotic stress and Arabidopsis.
Tamas Dalmay has included themes like Downregulation and upregulation, Northern blot, Cell biology, Regulation of gene expression and Computational biology in his microRNA study.
His work carried out in the field of RNA brings together such families of science as Virus, Virology and Molecular biology.
His study on RNA silencing also encompasses disciplines like
- Argonaute which is related to area like Non-coding RNA,
- RNA-induced silencing complex which connect with RNA-induced transcriptional silencing.
He most often published in these fields:
- Genetics (43.35%)
- microRNA (38.73%)
- RNA (32.95%)
What were the highlights of his more recent work (between 2015-2021)?
- microRNA (38.73%)
- Gene (29.48%)
- Genetics (43.35%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include microRNA, Gene, Genetics, Computational biology and Small RNA.
His microRNA research is multidisciplinary, incorporating perspectives in Internal medicine, Hypophosphatemia, Downregulation and upregulation and Cell biology.
His studies in Cell biology integrate themes in fields like Chondrocyte, Gene silencing and Gene expression.
His Gene research integrates issues from Polyphenism and Larva.
His work on Aphid expands to the thematically related Genetics.
His RNA study combines topics from a wide range of disciplines, such as Osteosarcoma, DNA sequencing and Virology.
Between 2015 and 2021, his most popular works were:
- Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species. (251 citations)
- Chromosomal-level assembly of the Asian seabass genome using long sequence reads and multi-layered scaffolding (143 citations)
- The microRNA-29 family in cartilage homeostasis and osteoarthritis (68 citations)
In his most recent research, the most cited papers focused on:
Tamas Dalmay mainly investigates Genetics, microRNA, Gene, Cell biology and Small RNA.
His study in Genetics is interdisciplinary in nature, drawing from both Sexual selection and Genetic diversity.
His Cell biology research is multidisciplinary, incorporating perspectives in Chondrocyte, Ankyrin, Epigenetics and Auxin.
He has researched Small RNA in several fields, including RNA silencing, Computational biology, Mutant and Deep sequencing.
He studied Computational biology and RNA interference that intersect with Locus and MRNA cleavage.
His studies in RNA integrate themes in fields like Virus and Rapid amplification of cDNA ends.
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