Search

Your search keyword '"Holm, Hilma"' showing total 731 results

Search Constraints

Start Over You searched for: Author "Holm, Hilma" Remove constraint Author: "Holm, Hilma"
731 results on '"Holm, Hilma"'

Search Results

101. Abstract 13222: Genetic Variants Close to NKX2-5 and MYH6 Are Associated With AV Nodal Reentry Tachycardia in First Genome-Wide Association Study

102. The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland

103. Rare mutations associating with serum creatinine and chronic kidney disease

104. Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies

105. The power of genetic diversity in genome-wide association studies of lipids

106. Mapping the human genetic architecture of COVID-19

107. The power of genetic diversity in genome-wide association studies of lipids

108. Cohort profile:Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

109. Genetic insight into sick sinus syndrome

110. Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants

111. Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis

112. Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLR

113. MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

114. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

115. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.

116. Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

117. Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

118. Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

119. Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

120. Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming

121. Seventy-five genetic loci influencing the human red blood cell

122. Sequence variants at CYP1A1–CYP1A2 and AHR associate with coffee consumption

123. Humoral Immune Response to SARS-CoV-2 in Iceland

124. Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

125. Spread of SARS-CoV-2 in the Icelandic Population

126. Early Spread of SARS-Cov-2 in the Icelandic Population

127. Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden

128. Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

129. Genomic risk scores, biomolecules, and clinical conditions to predict atrial fibrillation: time to integrate what we can measure.

131. Biological, clinical and population relevance of 95 loci for blood lipids

132. Long read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

134. Variants conferring risk of atrial fibrillation on chromosome 4q25

135. Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

136. Sequence variants with large effects on cardiac electrophysiology and disease

137. Sequence variants associating with urinary biomarkers

138. Quadricuspid Aortic Valve

139. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

140. Additional file 2: of Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

141. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

142. Genetic Variability in the Uptake of Dietary Sterols Affects the Risk of Coronary Artery Disease

143. Sequence variants associating with urinary biomarkers

144. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

145. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

146. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

147. Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

148. Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

149. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

150. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

Catalog

Books, media, physical & digital resources