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 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.
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.
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The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus.
Fong-Ming Chang;Judith R. Kidd;Kenneth J. Livak;Andrew J. Pakstis.
Human Genetics (1996)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree.
James L. Kennedy;Luis A. Giuffra;Hans W. Moises;L. L. Cavalli-Sforza.
Bitter Receptor Gene (TAS2R38), 6‐n‐Propylthiouracil (PROP) Bitterness and Alcohol Intake
Valerie B. Duffy;Andrew C. Davidson;Judith R. Kidd;Kenneth K. Kidd.
Alcoholism: Clinical and Experimental Research (2004)
A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity.
Michael V. Osier;Andrew J. Pakstis;Himla Soodyall;David Comas.
American Journal of Human Genetics (2002)
Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism.
Michael Osier;Andrew J. Pakstis;Judith R. Kidd;Jia Fu Lee.
American Journal of Human Genetics (1999)
Developing a SNP panel for forensic identification of individuals.
Kenneth K. Kidd;Andrew J. Pakstis;William C. Speed;Elena L. Grigorenko.
Forensic Science International (2006)
Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Lea K. Davis;Dongmei Yu;Clare L. Keenan;Eric R. Gamazon.
PLOS Genetics (2013)
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus
Kenneth K. Kidd;Bharti Morar;Carmela M. Castiglione;Hongyu Zhao.
Human Genetics (1998)
Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples
Judith R Kidd;Françoise R Friedlaender;William C Speed;Andrew J Pakstis.
Investigative Genetics (2011)
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