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251. Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis

252. Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

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

254. The impact of low-frequency and rare variants on lipid levels

255. A functional brain-derived neurotrophic factor (BDNF) gene variant increases the risk of moderate-to-severe allergic rhinitis

256. Cell Specific eQTL Analysis without Sorting Cells

257. The Gut Microbiome Contributes to a Substantial Proportion of the Variation in Blood Lipids

258. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

259. Genome-wide analysis identifies 12 loci influencing human reproductive behavior

260. No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population

261. A microarray screen for novel candidate genes in coeliac disease pathogenesis

262. Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population

263. P831 Habitual dietary intake of Dutch IBD patients differs from population controls: A case–control study

264. Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels

265. Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesity

266. Genetic variants of inducible costimulator are associated with allergic asthma susceptibility

267. Correction for Rietveld et al., Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

268. Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

269. The transcriptional landscape of age in human peripheral blood

270. Genetic and epigenetic regulation of gene expression in fetal and adult human livers

271. Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis

272. An introduction to LifeLines DEEP: study design and baseline characteristics

273. Copper Metabolism Domain-containing 1 Represses Genes that Promote Inflammation and Protects Mice From Colitis and Colitis-associated Cancer

274. Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

275. Cell specific eQTL analysis without sorting cells

276. Ciliary Genes Are Down-Regulated in Bronchial Tissue of Primary Ciliary Dyskinesia Patients

277. From genome to function by studying eQTLs

278. ATR inhibition preferentially targets homologous recombination-deficient tumor cells

279. Biological insights from 108 schizophrenia-associated genetic loci

280. Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

281. Genome-wide association analyses identify variants in developmental genes associated with hypospadias

282. Automated workflow-based exploitation of pathway databases provides new insights into genetic associations of metabolite profiles

283. Human Genetics in Rheumatoid Arthritis Guides a High-Throughput Drug Screen of the CD40 Signaling Pathway

284. Identification of heart rate-associated loci and genes

285. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

286. GWAS of 126559 Individuals Identifies Genetic Variants Associated with Educational Attainment

287. Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

288. Erratum: Corrigendum: Inter-individual variability and genetic influences on cytokine responses to bacteria and fungi

289. Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

290. Abstract 2683: The landscape of chromosomal aberrations in mouse models of breast cancer reveals driver-specific routes to tumor development

291. 87 Gene-Microbiome Interactions Underlying the Onset and the Clinical Phenotypes of Inflammatory Bowel Disease

292. A Genome-Wide Association Study of Circulating Galectin-3

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

294. Blood Pressure Loci Identified with a Gene-Centric Array

295. A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention

296. Wnt signaling and Dupuytren's disease

297. Celiac disease: moving from genetic associations to causal variants

298. Identification Of Novel Genes That Contribute To Both Asthma And COPD, With Replication In A Large Population-Based Cohort

299. Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci

300. Copy number variants on the X chromosome in women with primary ovarian insufficiency

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