Suchergebnisse - "Nolte, Ilja M"
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Validity of (Ultra-)Short Recordings for Heart Rate Variability Measurements
ISSN: 1932-6203, 1932-6203Veröffentlicht: United States Public Library of Science 28.09.2015Veröffentlicht in PloS one (28.09.2015)“… In order to investigate the applicability of routine 10s electrocardiogram (ECG) recordings for time-domain heart rate variability (HRV) calculation we …”
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Dominance genetic variation contributes little to the missing heritability for human complex traits
ISSN: 1537-6605, 1537-6605Veröffentlicht: United States 05.03.2015Veröffentlicht in American journal of human genetics (05.03.2015)“… For human complex traits, non-additive genetic variation has been invoked to explain "missing heritability," but its discovery is often neglected in …”
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DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring
ISSN: 1464-3685Veröffentlicht: England 01.08.2015Veröffentlicht in International journal of epidemiology (01.08.2015)“… We examined whether the effect of maternal smoking during pregnancy on birthweight of the offspring was mediated by smoking-induced changes to DNA methylation …”
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A genome-wide association study of 24-hour urinary excretion of endocrine disrupting chemicals
ISSN: 0160-4120, 1873-6750, 1873-6750Veröffentlicht: Netherlands Elsevier Ltd 01.01.2024Veröffentlicht in Environment international (01.01.2024)“… [Display omitted] •Unique genome-wide association study of multiple EDCs in 24-hour urine.•Four independent SNPs associated with EDCs through multi-trait GWAS …”
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Genotype–covariate interaction effects and the heritability of adult body mass index
ISSN: 1061-4036, 1546-1718, 1546-1718Veröffentlicht: New York Springer New York 01.08.2017Veröffentlicht in Nature genetics (01.08.2017)“… Matthew Robinson, Peter Visscher and colleagues use phenotypic data on 172,000 sibling pairs and phenotypic and SNP data on 150,832 unrelated individuals to …”
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Interleukin 6 and Development of Heart Failure With Preserved Ejection Fraction in the General Population
ISSN: 2047-9980, 2047-9980Veröffentlicht: England John Wiley and Sons Inc 01.06.2021Veröffentlicht in Journal of the American Heart Association (01.06.2021)“… Background The cause of heart failure with preserved ejection fraction (HFpEF) is poorly understood, and specific therapies are lacking. Previous studies …”
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Familial co-aggregation and shared genetics of cardiometabolic disorders and traits: data from the multi-generational Lifelines Cohort Study
ISSN: 1475-2840, 1475-2840Veröffentlicht: London BioMed Central 21.10.2023Veröffentlicht in Cardiovascular diabetology (21.10.2023)“… Background It is unclear to what extent genetics explain the familial clustering and the co-occurrence of distinct cardiometabolic disorders in the general …”
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C-Terminal Fibroblast Growth Factor 23, Iron Deficiency, and Mortality in Renal Transplant Recipients
ISSN: 1533-3450, 1533-3450Veröffentlicht: United States 01.12.2017Veröffentlicht in Journal of the American Society of Nephrology (01.12.2017)“… Iron deficiency (ID) is independently associated with an increased risk of death in renal transplant recipients (RTRs). ID promotes production and cleavage of …”
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A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease
ISSN: 2041-1723, 2041-1723Veröffentlicht: London Nature Publishing Group UK 03.01.2024Veröffentlicht in Nature communications (03.01.2024)“… Dupuytren’s disease (DD) is a highly heritable fibrotic disorder of the hand with incompletely understood etiology. A number of genetic loci, including Wnt …”
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Lipid and lipoprotein reference values from 133,450 Dutch Lifelines participants: Age- and gender-specific baseline lipid values and percentiles
ISSN: 1933-2874, 1876-4789Veröffentlicht: United States Elsevier Inc 01.07.2017Veröffentlicht in Journal of clinical lipidology (01.07.2017)“… Lipids and lipoproteins are recognized as the most important modifiable risk factors for cardiovascular disease. Although reference values for the major …”
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Iron Deficiency and Nephrotoxic Heavy Metals: A Dangerous Interplay?
ISSN: 1422-0067, 1661-6596, 1422-0067Veröffentlicht: Switzerland MDPI AG 10.03.2023Veröffentlicht in International journal of molecular sciences (10.03.2023)“… Heavy metals are common in our environment, and all individuals are exposed to them to some extent. These toxic metals have several harmful effects on the …”
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Functional and internalizing disorders co-aggregate with cardiometabolic and immune-related diseases within families: a population-based cohort study
ISSN: 1741-7015, 1741-7015Veröffentlicht: London BioMed Central 11.08.2025Veröffentlicht in BMC medicine (11.08.2025)“… Background Functional disorders share familial risk with internalizing disorders such as generalized anxiety disorder and depression, and are comorbid with …”
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Metasubtract: an R‐package to analytically produce leave‐one‐out meta‐analysis GWAS summary statistics
ISSN: 1367-4803, 1367-4811, 1460-2059, 1367-4811Veröffentlicht: England Oxford University Press 15.08.2020Veröffentlicht in Bioinformatics (15.08.2020)“… Abstract Summary Summary statistics from a meta‐analysis of genome‐wide association studies (meta-GWAS) can be used for many follow-up analyses. One valuable …”
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Mitochondrial Genome Study Identifies Association Between Primary Open-Angle Glaucoma and Variants in MT-CYB, MT-ND4 Genes and Haplogroups
ISSN: 1664-8021, 1664-8021Veröffentlicht: Switzerland Frontiers Media S.A 16.12.2021Veröffentlicht in Frontiers in genetics (16.12.2021)“… Background and purpose: Primary open-angle glaucoma (POAG) is an optic neuropathy characterized by death of retinal ganglion cells and atrophy of the optic …”
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Corrigendum to “A genome-wide association study of 24-hour urinary excretion of endocrine disrupting chemicals” [Environ. Int., A Genome-Wide Association Study of 24-Hour Urinary Excretion of Endocrine Disrupting Chemicals 183 (2024) 108396]
ISSN: 0160-4120, 1873-6750Veröffentlicht: Netherlands Elsevier Ltd 01.04.2024Veröffentlicht in Environment international (01.04.2024)Volltext
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Killer Cell Immunoglobulin-Like Receptor Haplotype B Modulates Susceptibility to EBV-Associated Classic Hodgkin Lymphoma
ISSN: 1664-3224, 1664-3224Veröffentlicht: Switzerland Frontiers Media S.A 27.01.2022Veröffentlicht in Frontiers in immunology (27.01.2022)“… Tumor cells of classic Hodgkin lymphoma (cHL) are derived from antigen presenting B cells that are infected by Epstein Barr virus (EBV) in ~30% of patients …”
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Correction: Role of inflammation in depressive and anxiety disorders, affect, and cognition: genetic and non-genetic findings in the lifelines cohort study
ISSN: 2158-3188, 2158-3188Veröffentlicht: London Nature Publishing Group UK 29.10.2025Veröffentlicht in Translational psychiatry (29.10.2025)Volltext
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Role of inflammation in depressive and anxiety disorders, affect, and cognition: genetic and non-genetic findings in the lifelines cohort study
ISSN: 2158-3188, 2158-3188Veröffentlicht: London Nature Publishing Group UK 10.05.2025Veröffentlicht in Translational psychiatry (10.05.2025)“… Inflammation is associated with a range of neuropsychiatric symptoms, but the issue of causality remains unclear. We used complementary non-genetic, genetic …”
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Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study
ISSN: 1018-4813, 1476-5438, 1476-5438Veröffentlicht: England Nature Publishing Group 01.06.2017Veröffentlicht in European journal of human genetics : EJHG (01.06.2017)“… Despite the recent explosive rise in number of genetic markers for complex disease traits identified in genome-wide association studies, there is still a large …”
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MicroRNA High Throughput Loss-of-Function Screening Reveals an Oncogenic Role for miR-21-5p in Hodgkin Lymphoma
ISSN: 1015-8987, 1421-9778, 1421-9778Veröffentlicht: Basel, Switzerland S. Karger AG 01.09.2018Veröffentlicht in Cellular physiology and biochemistry (01.09.2018)“… Background/Aims: Classical Hodgkin lymphoma (cHL) is among the most frequent lymphoma subtypes. The tumor cells originate from crippled germinal center (GC)-B …”
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