Lavinia Paternoster spends much of her time researching Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Disease. Her Genome-wide association study research incorporates themes from Odds ratio, Bioinformatics, Immunology, Quantitative trait locus and Heritability. The Quantitative trait locus study combines topics in areas such as Birth weight and Menarche.
Her Heritability research focuses on subjects like Phenotype, which are linked to Gene–environment interaction, Hay fever and Biobank. Her study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Bone mineral, Bone density, Anatomy and Locus. Her study looks at the relationship between Locus and fields such as Meta-analysis, as well as how they intersect with chemical problems.
The scientist’s investigation covers issues in Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Genetic association. Her research integrates issues of Phenotype, Meta-analysis, Quantitative trait locus, Locus and Computational biology in her study of Genome-wide association study. Genetics is a component of her Allele, Linkage disequilibrium, Offspring, Gene and Heritability studies.
Her Internal medicine research incorporates elements of Endocrinology and Mendelian randomization. Her research in Single-nucleotide polymorphism intersects with topics in Body mass index, Longitudinal study and Immunology, Atopic dermatitis. The various areas that she examines in her Body mass index study include Demography and Obesity.
Her main research concerns Genome-wide association study, Internal medicine, Mendelian randomization, Osteoarthritis and Longitudinal study. She combines subjects such as Expression quantitative trait loci, Linkage disequilibrium and Candidate gene with her study of Genome-wide association study. Her Linkage disequilibrium study introduces a deeper knowledge of Genetics.
Her work carried out in the field of Mendelian randomization brings together such families of science as Body mass index, Observational study, Mendelian Randomization Analysis, Blood pressure and Vitamin D and neurology. Her studies in Longitudinal study integrate themes in fields like Hip fracture, Proximal femur and Femoral neck. Her Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Filaggrin, Atopic dermatitis, Disease and Meta-analysis.
Her primary areas of investigation include Genome-wide association study, Single-nucleotide polymorphism, Disease, Genetics and Internal medicine. Her Genome-wide association study research integrates issues from Odds ratio, Evolutionary biology, Heritability, Mendelian randomization and Obesity. Her work in Evolutionary biology tackles topics such as Cranial neural crest which are related to areas like Genetic association.
Her biological study spans a wide range of topics, including Expression quantitative trait loci and Asthma, Immunology, Allergy. Her study in Linkage disequilibrium, Gene and Genetic correlation falls under the purview of Genetics. Her Meta-analysis, Osteoporosis and Bone remodeling study in the realm of Internal medicine connects with subjects such as BMP signaling pathway.
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-wide association study identifies 74 loci associated with educational attainment
Aysu Okbay;Jonathan P. Beauchamp;Mark Alan Fontana;James J. Lee.
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
Jie Zheng;Mesut A. Erzurumluoglu;Benjamin L. Elsworth;John P. Kemp.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Aysu Okbay;Bart M L Baselmans;Jan-Emmanuel De Neve;Patrick Turley.
Nature Genetics (2016)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Sonja I Berndt;Stefan Gustafsson;Stefan Gustafsson;Reedik Mägi;Reedik Mägi;Andrea Ganna.
Nature Genetics (2013)
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
Klaus Bønnelykke;Patrick Sleiman;Kasper Nielsen;Eskil Kreiner-Møller.
Nature Genetics (2014)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Thomas W. Winkler;Anne E. Justice;Mariaelisa Graff;Llilda Barata.
PLOS Genetics (2015)
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
John R.B. Perry;Felix Day;Cathy E. Elks;Patrick Sulem.
The UK10K project identifies rare variants in health and disease
Klaudia Walter;Josine L. Min;Jie Huang;Lucy Crooks.
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Lavinia Paternoster;Marie Standl;Johannes Waage;Hansjoerg Baurecht.
Nature Genetics (2015)
Genome-wide associations for birth weight and correlations with adult disease
Momoko Horikoshi;Robin N. Beaumont;Felix R. Day;Nicole M. Warrington;Nicole M. Warrington.
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