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Molecular Psychiatry|July 20, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptomsN Amin, O Jovanova, H H H Adams, et al.
Plos One|March 22, 2016
Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation: The AFGen ConsortiumFaye L Norby, Samuel Adamsson Eryd, Maartje N Niemeijer, et al.
European Heart Journal|April 28, 2017
CardioScape mapping the cardiovascular funding landscape in EuropeAxel Radlach Pries, Anastasia Naoum, Helmut Habazettl, et al.
Diabetes Care|February 9, 2020
Epigenetic Link Between Statin Therapy and Type 2 DiabetesCarolina Ochoa-Rosales, Eliana Portilla-Fernandez, Jana Nano, et al.
JAMA Internal Medicine|April 21, 2015
Thyroid function within the normal range and risk of coronary heart disease: an individual participant data analysis of 14 cohortsBjørn O Åsvold, Lars J Vatten, Trine Bjøro, et al.
European Journal of Epidemiology|September 9, 2019
Validated inference of smoking habits from blood with a finite DNA methylation marker setSilvana C E Maas, Athina Vidaki, Rory Wilson, et al.
Atherosclerosis|October 30, 2016
The relationship between the metabolic syndrome and arterial wall thickness: A mosaic still to be interpretedAngelo Scuteri, Oscar H Franco, AlGhatrif Majiid, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Hypertension (Dallas, Tex. : 1979)|March 12, 2014
Common carotid intima-media thickness measurements do not improve cardiovascular risk prediction in individuals with elevated blood pressure: the USE-IMT collaborationMichiel L Bots, Karlijn A Groenewegen, Todd J Anderson, et al.
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