Nebula Genomics customers get access to the Nebula Library, a weekly updated collection of personalized reports based on the latest genetic discoveries. It empowers our users to stay up to date with the latest research in human genetics and learn how it applies to them. Today, the Nebula Library includes over 200 genome-wide association studies (GWAS) and new reports are added every week. To access your personalized Nebula Library, you need to purchase our Whole Genome Sequencing (or upload existing DNA data to get partial access). However, we also made the content of the Nebula Library publicly available here to help you discover reports that interest you.
Nebula Genomics DNA Report for HDL Cholesterol Is HDL cholesterol genetic? We created a DNA report based on a study that attempted to answer this question. Below you can see a SAMPLE DNA report. To get your personalized DNA report, …
HDL cholesterol (Richardson, 2020) – Is HDL Cholesterol Genetic? Read More »
STUDY TITLE: Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis SUMMARY: Identification of 255 genetic variants associated with the apolipoprotein B level in the blood and analysis of …
STUDY TITLE: Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis SUMMARY: Identification of 440 genetic variants associated with the apolipoprotein A-1 level in the blood and analysis of …
STUDY TITLE: Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics SUMMARY: Identification of 4 novel genetic variants correlated with handedness. DESCRIPTION: Are you a righty or a lefty? Nearly 90% of individuals are right-handed. While your …
STUDY TITLE: Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease SUMMARY: Identification of over 100 novel genetic variants correlated with fat build-up around the body’s internal organs. DESCRIPTION: Visceral adipose tissue is a particularly …
STUDY TITLE: Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration SUMMARY: Identification of a novel genetic variant that is associated with prolonged gestational duration (pregnancy). DESCRIPTION: Gestation, the period of time that a …
STUDY TITLE: Genome-wide association study of cerebral small vessel disease (CSVD) reveals established and novel loci SUMMARY: Identification of novel genetic variants linked to cerebral small vessel disease, which can cause a variety of cognitive symptoms. DESCRIPTION: Cerebral small vessel …
STUDY TITLE: A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy SUMMARY: A genetic variant on chromosome 6 may be linked to dilated cardiomyopathy. DESCRIPTION: Dilated cardiomyopathy accounts for one-third of all heart failure cases. It …
STUDY TITLE: The genetic architecture of the human cerebral cortex SUMMARY: Identification of 27 genetic regions associated with cortical thickness. OVERVIEW: The cerebral cortex is the outer layer of the brain that is responsible for cognitive tasks such as perception, thought, and …
Nebula Genomics DNA Report for Familial Short Stature Is short stature genetic? We created a DNA report based on a study that attempted to answer this question. Below you can see a SAMPLE DNA report. To get your personalized DNA …
Familial short stature (Lin, 2020) – Is Short Stature Genetic? Read More »
