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.
STUDY TITLE: HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype SUMMARY: Identification of 2 novel genetic variants associated with aortic calcification. OVERVIEW: The aorta is one of the main arteries in the heart that …
STUDY TITLE: Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease SUMMARY: Identification of 22 new genetic variants associated with venous thromboembolism. OVERVIEW: Venous thromboembolism is characterized by the formation of blood …
STUDY TITLE: GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways SUMMARY: Discovery of 13 novel genetic variants associated with the development of systemic sclerosis. OVERVIEW: Normally, the immune system works to protect the body …
STUDY TITLE: GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI SUMMARY: Identification of 4 novel genetic variants that correlate with childhood growth and BMI. DESCRIPTION: Obesity remains one of the biggest epidemics of …
STUDY TITLE: Genome-wide association study in essential tremor identifies three new loci SUMMARY: Identification of 3 genetic variants associated with essential tremor (ET). OVERVIEW: ET is a neurological disorder characterized by involuntary shaking, especially of the hands, legs, and head. …
STUDY TITLE: Genome-wide analysis identifies 12 loci influencing human reproductive behavior SUMMARY: Discovery of 10 genetic variants associated with age at first birth. OVERVIEW: Human reproductive behavior has been associated with infertility and neuropsychiatric disorders. While environmental factors (e.g. cultural …
STUDY TITLE: Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways SUMMARY: Identification of 2 novel genetic variants associated with an increased risk of developing diffuse large B-cell lymphoma. DESCRIPTION: …
STUDY TITLE: A genome-wide investigation of food addiction SUMMARY: Identification of 2 genetic loci correlated with the development of an addiction to food. DESCRIPTION: Foods, especially those that are high in sugar, fat, or salt, can trigger the release of …
STUDY TITLE: Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status SUMMARY: Discovery of four genetic variants associated with eosinophilic granulomatosis, a rare autoimmune disease that affects the blood vessels. OVERVIEW: Eosinophilic granulomatosis with …
Eosinophilic granulomatosis with polyangiitis (Lyons, 2019) Read More »
STUDY TITLE: Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis SUMMARY: Identification of 153 new genetic variants associated with bone mineral density. OVERVIEW: Bone mineral density is the amount of …
