His primary areas of investigation include Genetics, Human genome, Childhood Acute Lymphoblastic Leukemia, Allele and Genome. The concepts of his Genetics study are interwoven with issues in Evolutionary biology and Population genetics. In Human genome, Damian Labuda works on issues like Sequence, which are connected to RNA splicing, Coding region, Genome evolution and Genetic variability.
His biological study spans a wide range of topics, including Pediatric cancer, Case-control study and Acute lymphocytic leukemia. His Allele research includes themes of Epigenetics, Fixation, Pleistocene and Dystrophin gene. He interconnects Lineage, Mendelian inheritance, DNA profiling, Sequence repeat and Polymerase chain reaction in the investigation of issues within Genome.
Damian Labuda mainly investigates Genetics, Haplotype, Gene, Molecular biology and Genome. Genetics and Evolutionary biology are commonly linked in his work. His research in Evolutionary biology focuses on subjects like Population genetics, which are connected to Genetic diversity.
His Haplotype research is multidisciplinary, incorporating elements of Microsatellite, Y chromosome, Coalescent theory and Gene flow, Genetic variation. In his study, Polymerase chain reaction is strongly linked to DNA, which falls under the umbrella field of Molecular biology. His research integrates issues of Odds ratio, Case-control study, Childhood Acute Lymphoblastic Leukemia, Locus and Genotype in his study of Allele.
Genetics, Genome, Genealogy, Evolutionary biology and Haplotype are his primary areas of study. His research is interdisciplinary, bridging the disciplines of Population genetics and Genetics. His Human genome study, which is part of a larger body of work in Genome, is frequently linked to Indo-European languages and Diversity, bridging the gap between disciplines.
His Genealogy research incorporates elements of Beringia, Ancient DNA, Gene flow and Native american population. The Evolutionary biology study combines topics in areas such as Genetic predisposition, Genetic admixture, Genomics, Genetic heterogeneity and Genetic variation. His study in Haplotype is interdisciplinary in nature, drawing from both Osteology, Operating time, Identification, Genetic marker and Genotyping.
His main research concerns Genetics, Genome, Exome, Compound heterozygosity and Joubert syndrome. His Genetics study incorporates themes from Pathological and Biological dispersal. His Biological dispersal study combines topics from a wide range of disciplines, such as Evolutionary biology, Panama and Native american population.
His Genome study integrates concerns from other disciplines, such as Population stratification, Lineage and Population genetics. His Exome research incorporates themes from Hypotonia, Missense mutation, Exon skipping and Oculomotor apraxia. His Human genome research incorporates themes from Reference genome and Genomics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genome Fingerprinting by Simple Sequence Repeat (SSR)-Anchored Polymerase Chain Reaction Amplification
Ewa Zietkiewicz;Antoni Rafalski;Damian Labuda.
Genomics (1994)
Genetic Variation and Population Structure in Native Americans
Sijia Wang;Cecil M. Lewis;Mattias Jakobsson;Sohini Ramachandran.
PLOS Genetics (2007)
Reconstructing Native American population history
David Emil Reich;David Emil Reich;Nick Patterson;Desmond Campbell;Desmond Campbell;Arti Tandon;Arti Tandon.
Nature (2012)
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)
Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases and forensic implications
Kaye N. Ballantyne;Miriam Goedbloed;Rixun Fang;Onno Schaap.
American Journal of Human Genetics (2010)
Susceptibility to Childhood Acute Lymphoblastic Leukemia: Influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 Genetic Polymorphisms
Maja Krajinovic;Damian Labuda;Chantal Richer;Sepideh Karimi.
Blood (1999)
Alu sequences in the coding regions of mRNA: a source of protein variability
Wojciech Makałowski;Grant A. Mitchell;Damian Labuda.
Trends in Genetics (1994)
Standardized nomenclature for Alu repeats
Mark A. Batzer;Prescott L. Deininger;Utha Hellmann-Blumberg;Jerzy Jurka.
Journal of Molecular Evolution (1996)
A survey of genetic and epigenetic variation affecting human gene expression.
Tomi Pastinen;Robert Sladek;Scott Gurd;Alya’a Sammak.
Physiological Genomics (2004)
Risk of childhood leukemia associated with exposure to pesticides and with gene polymorphisms.
Claire Infante-Rivard;Damian Labuda;Maja Krajinovic;Daniel Sinnett.
Epidemiology (1999)
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