What is he best known for?
The fields of study he is best known for:
Gary H. Thorgaard mostly deals with Genetics, Rainbow trout, Ploidy, Trout and Salmo.
His study in Locus, Chromosome, Sperm, Doubled haploidy and Gene is carried out as part of his Genetics studies.
His Rainbow trout research includes elements of Amplified fragment length polymorphism, Genome, Genetic marker, Quantitative trait locus and Microsatellite.
In his study, which falls under the umbrella issue of Ploidy, Interference and Centromere is strongly linked to Inbred strain.
His Trout research includes themes of Y chromosome, Diploid cells and Hatchery.
His Salmo study incorporates themes from Zoology, Sexual maturity and Human fertilization.
His most cited work include:
- Tetraploidy and the Evolution of Salmonid Fishes (773 citations)
- The rainbow trout genome provides novel insights into evolution after whole-genome duplication in vertebrates (587 citations)
- A Detailed Linkage Map of Rainbow Trout Produced Using Doubled Haploids (288 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Rainbow trout, Genetics, Trout, Zoology and Gene.
His Rainbow trout study also includes fields such as
- Ecology which connect with Phylogeography,
- Salmo which intersects with area such as Sexual maturity.
All of his Genetics and Quantitative trait locus, Chromosome, Locus, Genome and Ploidy investigations are sub-components of the entire Genetics study.
Gary H. Thorgaard studied Ploidy and Sperm that intersect with Cryopreservation.
His Trout study combines topics in areas such as Infectious hematopoietic necrosis virus, Genetic variation, Major histocompatibility complex and Hatchery.
As part of the same scientific family, Gary H. Thorgaard usually focuses on Zoology, concentrating on Hybrid and intersecting with Fishery and Introgression.
He most often published in these fields:
- Rainbow trout (67.84%)
- Genetics (62.57%)
- Trout (24.56%)
What were the highlights of his more recent work (between 2011-2021)?
- Rainbow trout (67.84%)
- Genetics (62.57%)
- Gene (19.88%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Rainbow trout, Genetics, Gene, Zoology and Genome.
The study incorporates disciplines such as Evolutionary biology, Ecology, Domestication, Phenotype and Quantitative trait locus in addition to Rainbow trout.
Gary H. Thorgaard interconnects Trout and Dominance in the investigation of issues within Zoology.
His research integrates issues of Virology, Allele frequency, Predation, Hatchery and Genetic variation in his study of Trout.
His Genome study combines topics from a wide range of disciplines, such as Vertebrate and Single-nucleotide polymorphism.
His work carried out in the field of Contig brings together such families of science as Chromosome, Karyotype, Ploidy and Sequence assembly.
Between 2011 and 2021, his most popular works were:
- The rainbow trout genome provides novel insights into evolution after whole-genome duplication in vertebrates (587 citations)
- A conserved haplotype controls parallel adaptation in geographically distant salmonid populations. (193 citations)
- Migration‐related phenotypic divergence is associated with epigenetic modifications in rainbow trout (92 citations)
In his most recent research, the most cited papers focused on:
Gary H. Thorgaard spends much of his time researching Rainbow trout, Genetics, Genome, Gene and Reference genome.
His Rainbow trout research incorporates elements of Vertebrate genome, Phenotype, Transcriptome, Adaptation and Single-nucleotide polymorphism.
His work deals with themes such as Phylogeography, Genetic variation and Genomics, which intersect with Adaptation.
Bisulfite sequencing, DNA methylation, Phenotypic plasticity, Epigenetics and Differentially methylated regions are the primary areas of interest in his Genetics study.
His studies in Gene integrate themes in fields like Evolutionary biology, Receptor and Immune system.
The concepts of his Reference genome study are interwoven with issues in dbSNP, SNP array and Locus.
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