Augustine Kong focuses on Genetics, Genome-wide association study, Single-nucleotide polymorphism, Allele and Internal medicine. Genetic association, Quantitative trait locus, Allele frequency, Genetic architecture and Gene are among the areas of Genetics where the researcher is concentrating her efforts. Augustine Kong focuses mostly in the field of Genetic architecture, narrowing it down to topics relating to Evolutionary biology and, in certain cases, Missing heritability problem and Common disease-common variant.
Her study in Genome-wide association study is interdisciplinary in nature, drawing from both CDKAL1, Locus, Heritability, Type 2 diabetes and SLC30A8. Her studies in Single-nucleotide polymorphism integrate themes in fields like Autism, Osteoporosis and Copy-number variation. Augustine Kong has researched Allele in several fields, including Genome and Immunology.
Augustine Kong spends much of her time researching Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Allele. Her work in Gene, Allele frequency, Locus, Genetic linkage and Genome are all subfields of Genetics research. Her Locus research is multidisciplinary, incorporating elements of Genetic determinism and Gene mapping.
Her Genome-wide association study study integrates concerns from other disciplines, such as SNP, Bioinformatics, Genetic association, Type 2 diabetes and Genetic architecture. Her Internal medicine study incorporates themes from Endocrinology, Oncology and Cardiology. Her Allele research integrates issues from Genetic variation, Genotype and Candidate gene.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Educational attainment, Genome and Allele. Her Genotype, Sequence, Single-nucleotide polymorphism, Gene and Mutation rate study are her primary interests in Genetics. Her research in Genome-wide association study intersects with topics in Evolutionary biology, SNP, Bioinformatics, Phenotype and Behavioural genetics.
Within one scientific family, she focuses on topics pertaining to Gastroenterology under Bioinformatics, and may sometimes address concerns connected to Internal medicine. Her Genome study combines topics in areas such as Computational biology, Genetic association and Genetic variation. Her studies deal with areas such as Sick sinus syndrome, Cardiac arrhythmia, Atrial fibrillation, Cardiology and Familial atrial fibrillation as well as Allele.
Her main research concerns Genetics, Genome-wide association study, Educational attainment, Genome and INDEL Mutation. Her Genetics study frequently draws connections between related disciplines such as Affect. Her research integrates issues of SNP, Quantitative trait locus, Genetic architecture, Behavioural genetics and Glucose homeostasis in her study of Genome-wide association study.
The Quantitative trait locus study combines topics in areas such as Imputation, Haplotype, Bioinformatics and 1000 Genomes Project. Her Genome research is multidisciplinary, incorporating perspectives in Annotation, Bonferroni correction and Single-nucleotide polymorphism, Genetic association. Augustine Kong has included themes like Whole genome sequencing, Mutation rate and Human genetics in her Single-nucleotide polymorphism study.
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.
Finding the missing heritability of complex diseases.
Teri A. Manolio;Francis S. Collins;Nancy J. Cox;David B. Goldstein.
Nature (2009)
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.
Struan F. A. Grant;Gudmar Thorleifsson;Inga Reynisdottir;Rafil Benediktsson.
Nature Genetics (2006)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini;L J Scott;R Saxena;B F Voight.
Nature Genetics (2008)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena.
Nature Genetics (2010)
Neuregulin 1 and Susceptibility to Schizophrenia
Hreinn Stefansson;Engilbert Sigurdsson;Valgerdur Steinthorsdottir;Soley Bjornsdottir.
American Journal of Human Genetics (2002)
A high-resolution recombination map of the human genome
Augustine Kong;Daniel F. Gudbjartsson;Jesus Sainz;Gudrun M. Jonsdottir.
Nature Genetics (2002)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight;Benjamin F. Voight;Laura J. Scott;Valgerdur Steinthorsdottir;Andrew P. Morris.
Nature Genetics (2010)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Nature (2008)
A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction
Anna Helgadottir;Gudmar Thorleifsson;Andrei Manolescu;Solveig Gretarsdottir.
Science (2007)
Rate of de novo mutations and the importance of father’s age to disease risk
Augustine Kong;Michael L. Frigge;Gisli Masson;Soren Besenbacher;Soren Besenbacher.
Nature (2012)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
University of Iceland
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
University of Hannover
IBM (United States)
Chongqing Jiaotong University
University of Bremen
Xi'an Jiaotong University
University of Minnesota
University of Oslo
University of New South Wales
University of Notre Dame
International Maize and Wheat Improvement Center
Manchester Royal Infirmary
Jeju National University
University of Exeter
University of Tennessee at Knoxville
London School of Economics and Political Science
University of Edinburgh