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151. A susceptibility locus for migraine with aura, on chromosome 4q24

152. An integrated map of genetic variation from 1,092 human genomes

158. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development

159. Common variants at VRK2 and TCF4 conferring risk of schizophrenia

160. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

162. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

163. Phenotype mining in CNV carriers from a population cohort†

166. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

168. Dissection of the genetics of Parkinsonʼs disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21

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

174. A population-specific HTR2B stop codon predisposes to severe impulsivity

177. A map of human genome variation from population-scale sequencing

178. Hundreds of variants clustered in genomic loci and biological pathways affect human height

179. Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies

181. Integrating common and rare genetic variation in diverse human populations

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

184. A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

185. European lactase persistence genotype shows evidence of association with increase in body mass index

186. Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

187. Recurrence of Marfan syndrome as a result of parental germ-line mosaicism for an FBN1 mutation

190. A genome-wide linkage and association scan reveals novel loci for autism

191. Common variants conferring risk of schizophrenia

196. Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS

197. Common variants in the region around Osterix are associated with bone mineral density and growth in childhood

198. Disruption of the neurexin 1 gene is associated with schizophrenia

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