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102. Rare and low-frequency coding variants alter human adult height

104. Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome

105. Stroke genetics informs drug discovery and risk prediction across ancestries

108. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment

109. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

110. Abstract 10469: Cardiometabolic Risk Factors as Causal Mediators of the Relationship Between High Body Mass Index and Chronic Kidney Disease: A Two-Step Mendelian Randomization Study and Mediation Analyses

112. Strengthening the Reporting of Observational Studies in Epidemiology Using Mendelian Randomization

113. Lipoprotein(a) Levels at Birth and in Early Childhood: The COMPARE Study

116. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

120. HEART DISEASE: Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

122. Obesity increases heart failure incidence and mortality: observational and Mendelian randomization studies totalling over 1 million individuals.

124. The UK10K project identifies rare variants in health and disease

126. Genetic and Functional Characterization of ANGPTL7 as a Therapeutic Target for Glaucoma

127. Triglyceride-rich lipoproteins and their remnants: metabolic insights, role in atherosclerotic cardiovascular disease, and emerging therapeutic strategies—a consensus statement from the European Atherosclerosis Society

131. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

135. rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis

143. Total and cause-specific mortality by elevated transferrin saturation and hemochromatosis genotype in individuals with diabetes: two general population studies

145. Assessing Risk Prediction Models Using Individual Participant Data From Multiple Studies

146. Variants in the GPR146Gene Are Associated With a Favorable Cardiometabolic Risk Profile

147. Equalization of four cardiovascular risk algorithms after systematic recalibration: individual-participant meta-analysis of 86 prospective studies

149. European Heart Journal: fulfilling the mission.

150. Plasma high-density lipoprotein cholesterol and risk of dementia: observational and genetic studies.

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