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731 results on '"Holm, Hilma"'

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

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

153. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

154. Genome-wide analysis yields new loci associating with aortic valve stenosis

155. Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk

156. Variants inNKX2-5andFLNCCause Dilated Cardiomyopathy and Sudden Cardiac Death

157. Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease

158. A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta

159. Genome-wide analysis yields new loci associating with aortic valve stenosis

160. Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

161. Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

162. Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

163. Genome-wide analysis yields new loci associating with aortic valve stenosis

164. Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias

165. Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk

166. A Missense Variant in PLEC Increases Risk of Atrial Fibrillation

167. A rare missense mutation inMYH6confers high risk of coarctation of the aorta

168. Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability

169. Identification of sequence variants influencing immunoglobulin levels

170. Sequence variant at 4q25 near PITX2 associates with appendicitis

171. A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease

172. Diversity in non-repetitive human sequences not found in the reference genome

173. Epigenetic and genetic components of height regulation

174. Genetic studies of body mass index yield new insights for obesity biology

175. New genetic loci link adipose and insulin biology to body fat distribution

176. Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations

178. Weighting sequence variants based on their annotation increases power of whole-genome association studies

179. A frameshift deletion in the sarcomere geneMYL4causes early-onset familial atrial fibrillation

180. VariantASGR1Associated with a Reduced Risk of Coronary Artery Disease

181. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

182. Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

183. A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

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

185. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

186. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

187. A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

188. Common and rare variants associated with kidney stones and biochemical traits

189. Large-scale whole-genome sequencing of the Icelandic population

190. Identification of a large set of rare complete human knockouts

191. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

192. Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

194. A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.

195. Nationwide Study on Hypertrophic Cardiomyopathy in Iceland

197. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

198. Large-scale association analysis identifies new risk loci for coronary artery disease

199. Discovery and refinement of loci associated with lipid levels

200. The Role of Adiposity in Cardiometabolic Traits : A Mendelian Randomization Analysis

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