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151. Genome-wide association study identifies new locus associated with OCD

154. The 1st year of the COVID-19 epidemic in Estonia: an interrupted time series of population based nationwide cross-sectional studies.

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

156. Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine

157. Directional dominance on stature and cognition in diverse human populations

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

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

160. Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

161. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

162. Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection.

163. Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes.

164. DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases

166. Farmakogenoomika – teekond ravivastuse päriliku varieeruvuse baasteadusest kliinilisse meditsiini

167. Additional file 1 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

168. Additional file 5 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

169. Additional file 6 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

170. Additional file 4 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

171. Additional file 3 of Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

172. Genetic insights into biological mechanisms governing human ovarian ageing

173. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

174. Hybrid modelling for stroke care : Review and suggestions of new approaches for risk assessment and simulation of scenarios

175. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

176. Genome-wide association study identifies 48 common genetic variants associated with handedness.

177. Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.

178. Resource profile and user guide of the Polygenic Index Repository.

179. Meta-analyses identify DNA methylation associated with kidney function and damage

180. Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus

181. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

182. Mapping the human genetic architecture of COVID-19

183. Genetic regulation of spermine oxidase activity and cancer risk:a Mendelian randomization study

184. Genetic insights into biological mechanisms governing human ovarian ageing

187. Genetic predisposition to coronary artery disease in type 2 diabetes

188. Cerebral small vessel disease genomics and its implications across the lifespan

189. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

190. Biological insights from 108 schizophrenia-associated genetic loci

192. FinnGen provides genetic insights from a well-phenotyped isolated population

193. Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases

194. Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse.

195. Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci.

196. Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

197. Genome-wide association study identifies 48 common genetic variants associated with handedness

198. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

199. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

200. Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

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