Antti Sajantila mostly deals with Genetics, Haplotype, Y chromosome, Allele frequency and Genetic variation. His research in Microsatellite, Allele, Locus, Haplogroup and Genetic marker are components of Genetics. His study in Haplotype is interdisciplinary in nature, drawing from both Natural selection, Melanocortin 1 receptor, Function and SLC24A5.
His Y chromosome research integrates issues from Germline mutation, Commission and Germline. The concepts of his Allele frequency study are interwoven with issues in Population structure and Population genetics. His Genetic variation study combines topics from a wide range of disciplines, such as mtDNA control region, Genetic variability, Genetic diversity and Ecology.
His main research concerns Genetics, Haplotype, Microsatellite, Allele and Evolutionary biology. His works in Allele frequency, Genetic variation, Locus, Y chromosome and Mitochondrial DNA are all subjects of inquiry into Genetics. His Mitochondrial DNA research also works with subjects such as
Antti Sajantila works in the field of Haplotype, namely Linkage disequilibrium. He interconnects Identification, Mutation rate and DNA profiling in the investigation of issues within Microsatellite. His work in Allele addresses issues such as Molecular biology, which are connected to fields such as DNA.
Pharmacogenetics, Ancient DNA, CYP2D6, Internal medicine and Genetics are his primary areas of study. The study incorporates disciplines such as Bronze Age, Genetic diversity, Genome, Mitochondrial DNA and Iron Age in addition to Ancient DNA. His Mitochondrial DNA study incorporates themes from Evolutionary biology, Typing, Computational biology and Haplogroup.
The Odds ratio research Antti Sajantila does as part of his general Internal medicine study is frequently linked to other disciplines of science, such as Citalopram, therefore creating a link between diverse domains of science. His research investigates the connection between Genetics and topics such as ADME that intersect with problems in Genome-wide association study. Antti Sajantila combines subjects such as Polymorphism, MEDLINE, Genotyping, Massive parallel sequencing and Haplotype with his study of 1000 Genomes Project.
The scientist’s investigation covers issues in Internal medicine, Pharmacogenetics, Odds ratio, Ancient DNA and Ethnology. Within one scientific family, Antti Sajantila focuses on topics pertaining to Population study under Internal medicine, and may sometimes address concerns connected to CYP2D6 and CYP2C19. Pharmacogenetics is a subfield of Genetics that Antti Sajantila studies.
Genetics is closely attributed to Drug development in his work. His Odds ratio research is multidisciplinary, incorporating elements of Disease progression and Disease. His Ancient DNA research is multidisciplinary, relying on both Genome and Mitochondrial DNA.
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A promoter-level mammalian expression atlas
Alistair R.R. Forrest;Hideya Kawaji;Michael Rehli;J. Kenneth Baillie.
Nature (2014)
Ancient human genomes suggest three ancestral populations for present-day Europeans
Iosif Lazaridis;Iosif Lazaridis;Nick Patterson;Alissa Mittnik;Gabriel Renaud.
Nature (2014)
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Swapan Mallick;Swapan Mallick;Swapan Mallick;Heng Li;Mark Lipson;Iain Mathieson.
Nature (2016)
Correlation between genetic and geographic structure in Europe.
Oscar Lao;Timothy T. Lu;Michael Nothnagel;Olaf Junge.
Current Biology (2008)
Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs.
Manfred Kayser;Lutz Roewer;Minttu Hedman;Lotte Henke.
American Journal of Human Genetics (2000)
Evidence for Variable Selective Pressures at MC1R
Rosalind M. Harding;Eugene Healy;Amanda J. Ray;Nichola S. Ellis.
American Journal of Human Genetics (2000)
CYP2D6 worldwide genetic variation shows high frequency of altered activity variants and no continental structure.
Johanna Sistonen;Antti Sajantila;Oscar Lao;Jukka Corander.
Pharmacogenetics and Genomics (2007)
DNA commission of the International Society of Forensic Genetics: Recommendations on forensic analysis using Y-chromosome STRs
P. Gill;C. Brenner;B. Brinkmann;Bruce Budowle.
International Journal of Legal Medicine (2001)
Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis.
T. Zerjal;B. Dashnyam;A. Pandya;Manfred Kayser.
American Journal of Human Genetics (1997)
Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing.
Ann-Christine Syvänen;A Sajantila;M Lukka.
American Journal of Human Genetics (1993)
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