2022 - Research.com Best Female Scientist Award
Internal medicine, Genome-wide association study, Endocrinology, Genetics and Body mass index are her primary areas of study. Her Internal medicine research incorporates themes from Allele and Cardiology. Her work carried out in the field of Genome-wide association study brings together such families of science as Blood pressure, Quantitative trait locus, Genetic architecture, Genotyping and Kidney.
As part of the same scientific family, Meena Kumari usually focuses on Endocrinology, concentrating on Bedtime and intersecting with Cortisol secretion, Dyssomnia, Cortisol awakening response and Smoking cessation. Genetics is frequently linked to Type 2 diabetes in her study. In her research, Minor allele frequency, Childhood obesity and Alpha-Ketoglutarate-Dependent Dioxygenase FTO is intimately related to FTO gene, which falls under the overarching field of Body mass index.
Her main research concerns Internal medicine, Endocrinology, Genetics, Genome-wide association study and Gerontology. Meena Kumari has included themes like Diabetes mellitus and Type 2 diabetes in her Internal medicine study. Her Genome-wide association study study combines topics from a wide range of disciplines, such as Quantitative trait locus, Genetic association, Bioinformatics and Medical genetics.
Her research in Gerontology intersects with topics in Socioeconomic status, Demography and Risk factor. Her Single-nucleotide polymorphism research includes elements of Allele and Polymorphism. Her study in Body mass index is interdisciplinary in nature, drawing from both Obesity and C-reactive protein.
Her primary areas of study are Genetics, Genome-wide association study, Demography, Internal medicine and Genetic association. To a larger extent, she studies Single-nucleotide polymorphism with the aim of understanding Genome-wide association study. The various areas that Meena Kumari examines in her Demography study include Body mass index, Longitudinal study, Weight gain and Obesity.
Her studies in Body mass index integrate themes in fields like Gerontology and C-reactive protein. The Internal medicine study combines topics in areas such as Endocrinology, Mendelian randomization and Cardiology. Her Genetic association study integrates concerns from other disciplines, such as Genetic risk, Bioinformatics and Genomics.
The scientist’s investigation covers issues in Genome-wide association study, Genetic association, Genetics, Demography and Internal medicine. Her work deals with themes such as Genetic risk, European descent, Quantitative trait locus, Blood lipids and Locus, which intersect with Genome-wide association study. Her Genetic association research incorporates elements of DNA methylation, Data mining, Bioinformatics and Medical genetics.
The concepts of her Demography study are interwoven with issues in Body mass index, Loneliness, Life course approach and Gerontology. Meena Kumari combines subjects such as Endocrinology, Mendelian randomization and Cardiology with her study of Internal medicine. Her studies examine the connections between Cardiology and genetics, as well as such issues in Stroke, with regards to Type 2 Diabetes Mellitus and Risk factor.
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.
Inflammation, obesity, stress and coronary heart disease: is interleukin-6 the link?
John S Yudkin;Meena Kumari;Steve E Humphries;Vidya Mohamed-Ali.
Atherosclerosis (2000)
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)
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)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)
J Dupuis;C Langenberg;I Prokopenko;R Saxena.
Nature Genetics (2010)
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.
Nature (2011)
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
A genome-wide association search for type 2 diabetes genes in African Americans.
N D Palmer;C W McDonough;P J Hicks;B H Roh.
PLOS ONE (2012)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
James J. Lee;Robbee Wedow;Aysu Okbay;Edward Kong.
Nature Genetics (2018)
Job strain as a risk factor for coronary heart disease: a collaborative meta-analysis of individual participant data.
Mika Kivimäki;Mika Kivimäki;Mika Kivimäki;Solja T. Nyberg;G. David Batty;G. David Batty;Eleonor I. Fransson;Eleonor I. Fransson;Eleonor I. Fransson.
The Lancet (2012)
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