Items where Author is "Snieder, H."

Article

(2022) Bioinformatic Prioritization and Functional Annotation of GWAS-Based Candidate Genes for Primary Open-Angle Glaucoma. GENES. ISSN 2073-4425 J9 - GENES-BASEL

(2022) DNA methylation: a potential mediator between air pollution and metabolic syndrome. CLINICAL EPIGENETICS. ISSN 1868-7075 1868-7083 J9 - CLIN EPIGENETICS

(2022) Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population. FRONTIERS IN CARDIOVASCULAR MEDICINE. ISSN 2297-055X J9 - FRONT CARDIOVASC MED

(2022) Large-Scale Multi-Omics Studies Provide New Insights into Blood Pressure Regulation. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. ISSN 1422-0067 J9 - INT J MOL SCI

(2022) A Mendelian randomization cytokine screen reveals IL-13 as causal factor in risk of severe COVID-19. J Infect. pp. 334-363. ISSN 0163-4453 (Print) 0163-4453

(2022) Multidisciplinary approach to functional somatic syndromes: study protocol for a population-based prospective cohort study. BMJ OPEN. ISSN 2044-6055 J9 - BMJ OPEN

(2021) GWASinspector: comprehensive quality control of genome-wide association study results. Bioinformatics. pp. 129-130. ISSN 1367-4803

(2021) Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population. Front Cardiovasc Med. p. 809717. ISSN 2297-055X (Print) 2297-055x

(2021) Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Nat Hum Behav. ISSN 2397-3374

(2020) Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Molecular Psychiatry. pp. 1420-1429. ISSN 1359-4184

(2019) Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Mol Psychiatry. ISSN 1476-5578 (Electronic) 1359-4184 (Linking)

(2019) Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci. American Journal of Nephrology. pp. 193-202. ISSN 0250-8095

(2017) Genetic and environmental influences on stability and change in baseline levels of C-reactive protein: A longitudinal twin study. Atherosclerosis. pp. 172-178. ISSN 0021-9150

(2017) Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nature Genetics. pp. 403-415. ISSN 1061-4036

(2016) DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis. American Journal of Human Genetics. pp. 680-696. ISSN 0002-9297

(2016) Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study. Plos Medicine. ISSN 1549-1676

(2016) lodGWAS: a software package for genome-wide association analysis of biomarkers with a limit of detection. Bioinformatics. pp. 1552-1554. ISSN 1367-4803

(2015) In Silico Post Genome-Wide Association Studies Analysis of C-Reactive Protein Loci Suggests an Important Role for Interferons. Circulation-Cardiovascular Genetics. pp. 487-497. ISSN 1942-325X