2022 - Research.com Best Female Scientist Award
Genetics, Genome-wide association study, Single-nucleotide polymorphism, Gene and Locus are her primary areas of study. Her Genetics study typically links adjacent topics like Disease. Her Genome-wide association study research is multidisciplinary, incorporating perspectives in Odds ratio, Internal medicine, Meta-analysis, Body mass index and Genetic association.
Her work in the fields of Single-nucleotide polymorphism, such as SNP, intersects with other areas such as EIF2AK3. In Locus, Dena G. Hernandez works on issues like Molecular biology, which are connected to Liver function, Mutant, Ataxia and Spinocerebellar ataxia. Her studies deal with areas such as C9orf72 Protein, C9orf72, Trinucleotide repeat expansion and TARDBP as well as Haplotype.
Dena G. Hernandez spends much of her time researching Genetics, Genome-wide association study, Single-nucleotide polymorphism, Disease and Internal medicine. Her study in Genetics focuses on Locus, Gene, Genetic variation, Allele and Haplotype. Her Genome-wide association study research is multidisciplinary, relying on both Odds ratio, Meta-analysis, Quantitative trait locus, Genetic association and Heritability.
Her Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Genotyping and Case-control study. Her Disease study combines topics in areas such as Genetic correlation and Bioinformatics. The study incorporates disciplines such as Endocrinology, Methylation and Oncology in addition to Internal medicine.
Her primary areas of study are Disease, Genome-wide association study, Genetics, Internal medicine and Parkinson's disease. Dena G. Hernandez has researched Disease in several fields, including Gene and Genetic architecture. Her Genome-wide association study research includes elements of Mendelian randomization, Genetic variability, Genetic association, Heritability and Genetic variation.
Her research on Genetics often connects related topics like Alpha-synuclein. Her research in Internal medicine intersects with topics in Methylation and Oncology. Her Parkinson's disease research incorporates elements of Glucocerebrosidase, Heterozygote advantage, Genotyping and Clinical trial.
Dena G. Hernandez focuses on Genome-wide association study, Genetics, Disease, Internal medicine and Single-nucleotide polymorphism. The concepts of her Genome-wide association study study are interwoven with issues in Genetic variation, Locus and Medical genetics. Her Genetics study integrates concerns from other disciplines, such as Meta-analysis and Parkinson's disease.
Her study looks at the relationship between Disease and topics such as Allele, which overlap with Loss function, Haploinsufficiency, Case-control study and Immunology. The study incorporates disciplines such as Oncology and DNA methylation in addition to Internal medicine. Missense mutation, Genetic analysis, Phenotype, Hereditary spastic paraplegia and Genetic heterogeneity is closely connected to Amyotrophic lateral sclerosis in her research, which is encompassed under the umbrella topic of Single-nucleotide polymorphism.
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.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud.
Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simón-Sánchez;Claudia Schulte;Jose M Bras;Jose M Bras;Manu Sharma.
Nature Genetics (2009)
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra;Marjolein J Peters;Tõnu Esko;Hanieh Yaghootkar.
Nature Genetics (2013)
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
Janel O. Johnson;Jessica Mandrioli;Michael Benatar;Yevgeniya Abramzon.
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie;Alan E. Renton;Kin Mok;Elise G. P. Dopper;Elise G. P. Dopper.
Lancet Neurology (2012)
Genotype, haplotype and copy-number variation in worldwide human populations
Mattias Jakobsson;Sonja W. Scholz;Sonja W. Scholz;Paul A Scheet;J. Raphael Gibbs;J. Raphael Gibbs.
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Michael A. Nalls;Vincent Plagnol;Dena G. Hernandez;Dena G. Hernandez;Manu Sharma;Manu Sharma.
The Lancet (2011)
Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain
J. Raphael Gibbs;J. Raphael Gibbs;Marcel P. van der Brug;Marcel P. van der Brug;Dena G. Hernandez;Dena G. Hernandez;Bryan J. Traynor.
PLOS Genetics (2010)
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