2022 - Research.com Best Female Scientist Award
Internal medicine, Genome-wide association study, Genetics, Dementia and Genetic association are her primary areas of study. Her Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and Cardiology. Her biological study spans a wide range of topics, including Bioinformatics, Meta-analysis, Disease, Allele and Locus.
Lenore J. Launer works mostly in the field of Genetics, limiting it down to concerns involving Body mass index and, occasionally, Obesity, FTO gene and SH2B1. Her Dementia research includes themes of Alzheimer's disease, Prospective cohort study and Gerontology. Her work carried out in the field of Genetic association brings together such families of science as SNP and Atrial fibrillation.
Her scientific interests lie mostly in Internal medicine, Dementia, Genome-wide association study, Genetics and Gerontology. Her work deals with themes such as Endocrinology and Cardiology, which intersect with Internal medicine. Her studies deal with areas such as Alzheimer's disease, Cognition and Risk factor as well as Dementia.
Her Genome-wide association study research is within the category of Single-nucleotide polymorphism. Lenore J. Launer interconnects Epidemiology and Disease in the investigation of issues within Gerontology. Her studies in Cohort study integrate themes in fields like Odds ratio and Prospective cohort study.
Lenore J. Launer spends much of her time researching Internal medicine, Dementia, Cardiology, Genome-wide association study and Genetics. Lenore J. Launer has researched Internal medicine in several fields, including Diabetes mellitus and Type 2 diabetes. The study incorporates disciplines such as Cognition, Effects of sleep deprivation on cognitive performance, Gerontology and Cohort in addition to Dementia.
Her Cardiology research integrates issues from Young adult, Hyperintensity and Risk factor. Her Genome-wide association study research includes elements of SNP, Cholesterol and Genetic association. Her Genetics research incorporates elements of Mean arterial pressure and Pulse pressure.
Lenore J. Launer mostly deals with Internal medicine, Dementia, Genome-wide association study, Genetics and Cardiology. Her Internal medicine research is multidisciplinary, relying on both Diabetes mellitus and Type 2 diabetes. Her work deals with themes such as Hyperintensity, Cognition and Gerontology, which intersect with Dementia.
Her research integrates issues of Coagulation, Polymorphism, Genetic association and Genetic architecture in her study of Genome-wide association study. She has included themes like Blood lipids, Cholesterol and Lipid metabolism in her Genetics study. The concepts of her Cardiology study are interwoven with issues in Magnetic resonance imaging and Risk factor.
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Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)
Vascular Contributions to Cognitive Impairment and Dementia A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Philip B. Gorelick;Angelo Scuteri;Sandra E. Black;Charles Decarli.
Stroke (2011)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Nature (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)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)
Prevalence of dementia and major subtypes in Europe : A collaborative study of population-based cohorts
A. Lobo;L. J. Launer;L. Fratiglioni;K. Andersen.
Neurology (2000)
Cerebral microbleeds: a guide to detection and interpretation
Steven M. Greenberg;Meike W. Vernooij;Charlotte Cordonnier;Anand Viswanathan.
Lancet Neurology (2009)
Genome-wide association study of blood pressure and hypertension
Daniel Levy;Georg B. Ehret;Georg B. Ehret;Kenneth Rice;Germaine C. Verwoert.
Nature Genetics (2009)
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