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283 results on '"Manuel Mattheisen"'

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151. Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

152. Novel genetic loci underlying human intracranial volume identified through genome-wide association

153. Genetic architecture of subcortical brain structures in 38,851 individuals

154. Genetic Variants Associated With Anxiety and Stress-Related Disorders

155. Genome-wide association study identifies 30 loci associated with bipolar disorder

156. SA16A MAJOR ROLE FOR COMMON GENETIC VARIATION IN ANXIETY DISORDERS

157. META-ANALYSIS OF ALCOHOL DEPENDENCE GWAS DATA FROM EUROPEAN SAMPLES ASCERTAINED FROM CLINIC AND POPULATION BASED APPROACHES

158. IDENTIFYING SUSCEPTIBILITY LOCI FOR TOURETTE'S SYNDROME IN A DENSELY AFFECTED PEDIGREE

159. Emerging Evidence For Overlap of ADHD Genetic Risk Factors With Those of Other Psychiatric Illnesses

160. Genetic variation in thelymphotoxin-α(LTA)/tumour necrosis factor-α(TNFα) locus as a risk factor for idiopathic achalasia

161. Candidate gene association study implicatesp63in the etiology of nonsyndromic bladder-exstrophy-epispadias complex

162. Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder

163. Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

164. Cell-type specific open chromatin profiling in human postmortem brain infers functional roles for non-coding schizophrenia loci

165. Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1

166. Specific anxiety disorders and subsequent risk for bipolar disorder: a nationwide study

167. Dysregulation of miRNA-9 in a subset of schizophrenia patient-derived neural progenitor cells

168. Influence of Polygenic Risk Scores on the Association Between Infections and Schizophrenia

169. Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants

170. Mortality Among Persons With Obsessive-Compulsive Disorder in Denmark

171. A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

172. Genetic variants associated with response to lithium treatment in bipolar disorder:a genome-wide association study

173. Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3

174. Identification of the BRD1 interaction network and its impact on mental disorder risk

175. Role of common and rare APP DNA sequence variants in Alzheimer disease

176. Linkage-Disequilibrium-Based Binning Affects the Interpretation of GWASs

177. A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry

178. Hippocampal Function in Healthy Carriers of theCLUAlzheimer's Disease Risk Variant

179. Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

180. The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

181. Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients

182. Significance Levels in Genome-Wide Interaction Analysis (GWIA)

183. Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous iranian family

184. Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1

185. The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

186. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2

187. Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci

188. Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

189. High loading of polygenic risk in cases with chronic schizophrenia

190. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

191. Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia:A Danish Population-Based Study and Meta-analysis

192. A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31

193. Diagnosed Anxiety Disorders and the Risk of Subsequent Anorexia Nervosa: A Danish Population Register Study

194. The association between lower educational attainment and depression owing to shared genetic effects?: Results in ~25,000 subjects

195. Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function

196. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS

197. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

198. Contents Vol. 78, 2014

199. Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus

200. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

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