Cordelia Langford mostly deals with Genetics, Genome-wide association study, Genetic association, Single-nucleotide polymorphism and Genetic predisposition. Many of her studies on Genetics apply to Computational biology as well. Her research in Genome-wide association study intersects with topics in Multiple sclerosis, Allele, Allele frequency and Bioinformatics.
Her Genetic association research integrates issues from Candidate gene, Psoriasis and Genetic architecture. The GENCODE study combines topics in areas such as Functional genomics, Annotation and Systems biology. Her studies in ENCODE integrate themes in fields like International HapMap Project and DNA.
Cordelia Langford focuses on Genetics, Genome-wide association study, Molecular biology, Genome and Gene expression profiling. Genetics is closely attributed to Cancer research in her study. Her Genome-wide association study research incorporates elements of SNP, Genetic association, Genetic architecture and Genetic predisposition.
Her research integrates issues of Tumor suppressor gene, Platelet, Transcriptome and Gene silencing in her study of Molecular biology. Cordelia Langford works mostly in the field of Genome, limiting it down to concerns involving Computational biology and, occasionally, Human genome. The Human genome study which covers ENCODE that intersects with GENCODE.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Genetic association, Allele frequency and Single-nucleotide polymorphism. Cordelia Langford performs multidisciplinary study in the fields of Genetics and Glucose homeostasis via her papers. Her studies deal with areas such as Odds ratio, Disease, Locus and Case-control study as well as Genome-wide association study.
Her study on Case-control study also encompasses disciplines like
Genetics, Genome-wide association study, Genetic association, Allele and Genetic architecture are her primary areas of study. The study of Genetics is intertwined with the study of Evolutionary biology in a number of ways. Her biological study spans a wide range of topics, including Case-control study, Gene, Type 2 diabetes and Linkage disequilibrium.
Her Genome-wide association study research entails a greater understanding of Single-nucleotide polymorphism. In her research, Regulation of gene expression is intimately related to Molecular biology, which falls under the overarching field of Gene expression profiling. Her Major histocompatibility complex research incorporates themes from Multiple sclerosis and Genotype, Allele frequency.
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.
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Ewan Birney;John A. Stamatoyannopoulos;Anindya Dutta;Roderic Guigó.
The ENCODE (ENCyclopedia of DNA elements) Project
E. A. Feingold;P. J. Good;M. S. Guyer;S. Kamholz.
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira.
Nature Genetics (2012)
The DNA sequence of human chromosome 22
I. Dunham;N. Shimizu;B. A. Roe;S. Chissoe.
Large-scale association analysis identifies new risk loci for coronary artery disease
Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall.
Nature Genetics (2013)
The DNA sequence of the human X chromosome
Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer.
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Ashley H. Beecham;Nikolaos A. Patsopoulos;Nikolaos A. Patsopoulos;Dionysia K. Xifara;Mary F. Davis.
Nature Genetics (2013)
A Genome-Wide Association Study Identifies New Psoriasis Susceptibility Loci and an Interaction Between HLA-C and ERAP1
Amy Strange;Francesca Capon;Chris C A Spencer.
Nature Genetics (2010)
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nick Craddock;Matthew E. Hurles;Niall Cardin;Richard D. Pearson.
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: