What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Genetics, Allele frequency, Single-nucleotide polymorphism, Haplotype and Linkage disequilibrium.
His research on Genetics frequently links to adjacent areas such as Population genetics.
His Allele frequency research incorporates themes from Genetic variation and Selection.
His research investigates the connection between Single-nucleotide polymorphism and topics such as Evolutionary biology that intersect with issues in Chromosome, DNA sequencing and Genetic marker.
His research investigates the link between Haplotype and topics such as Genetic drift that cross with problems in SNP genotyping.
Linkage disequilibrium connects with themes related to Genetic association in his study.
His most cited work include:
- Analysis of shared heritability in common disorders of the brain (726 citations)
- The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus. (365 citations)
- Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree. (341 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Genetics, Single-nucleotide polymorphism, Haplotype, Allele frequency and Allele.
His work in Locus, Linkage disequilibrium, Gene, Genetic linkage and Genetic association is related to Genetics.
His study explores the link between Single-nucleotide polymorphism and topics such as Massive parallel sequencing that cross with problems in Computational biology.
His research in Haplotype intersects with topics in Population genetics, Conduct disorder, Genetic drift, Genetic variation and Candidate gene.
His study looks at the relationship between Allele frequency and topics such as Database, which overlap with Dna polymorphism.
His work in the fields of Polymorphism overlaps with other areas such as ADH1B.
He most often published in these fields:
- Genetics (69.37%)
- Single-nucleotide polymorphism (41.44%)
- Haplotype (40.54%)
What were the highlights of his more recent work (between 2016-2021)?
- Single-nucleotide polymorphism (41.44%)
- Evolutionary biology (16.22%)
- Allele (27.03%)
In recent papers he was focusing on the following fields of study:
His main research concerns Single-nucleotide polymorphism, Evolutionary biology, Allele, Massive parallel sequencing and Haplotype.
His work deals with themes such as Genetic diversity, Genotyping and Allele frequency, which intersect with Single-nucleotide polymorphism.
Andrew J. Pakstis usually deals with Allele frequency and limits it to topics linked to Reference population and Data mining.
The Evolutionary biology study combines topics in areas such as Locus, Population genetics and Genotype.
His Massive parallel sequencing research is within the category of Genetics.
His study focuses on the intersection of Haplotype and fields such as 1000 Genomes Project with connections in the field of Multiplex.
Between 2016 and 2021, his most popular works were:
- Analysis of shared heritability in common disorders of the brain (726 citations)
- Evaluating 130 microhaplotypes across a global set of 83 populations (62 citations)
- Increasing the reference populations for the 55 AISNP panel: the need and benefits. (28 citations)
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