Suchergebnisse - "Nolte, Ilja M"

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    Validity of (Ultra-)Short Recordings for Heart Rate Variability Measurements von Munoz, M. Loretto, van Roon, Arie, Riese, Harriëtte, Thio, Chris, Oostenbroek, Emma, Westrik, Iris, de Geus, Eco J. C., Gansevoort, Ron, Lefrandt, Joop, Nolte, Ilja M., Snieder, Harold

    ISSN: 1932-6203, 1932-6203
    Veröffentlicht: United States Public Library of Science 28.09.2015
    Veröffentlicht 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 von Zhu, Zhihong, Bakshi, Andrew, Vinkhuyzen, Anna A E, Hemani, Gibran, Lee, Sang Hong, Nolte, Ilja M, van Vliet-Ostaptchouk, Jana V, Snieder, Harold, Esko, Tonu, Milani, Lili, Mägi, Reedik, Metspalu, Andres, Hill, William G, Weir, Bruce S, Goddard, Michael E, Visscher, Peter M, Yang, Jian

    ISSN: 1537-6605, 1537-6605
    Veröffentlicht: United States 05.03.2015
    Veröffentlicht 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 von Küpers, Leanne K, Xu, Xiaojing, Jankipersadsing, Soesma A, Vaez, Ahmad, la Bastide-van Gemert, Sacha, Scholtens, Salome, Nolte, Ilja M, Richmond, Rebecca C, Relton, Caroline L, Felix, Janine F, Duijts, Liesbeth, van Meurs, Joyce B, Tiemeier, Henning, Jaddoe, Vincent W, Wang, Xiaoling, Corpeleijn, Eva, Snieder, Harold

    ISSN: 1464-3685
    Veröffentlicht: England 01.08.2015
    Veröffentlicht 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 von Lu, Xueling, van der Meer, Thomas P., Kamali, Zoha, van Faassen, Martijn, Kema, Ido P., van Beek, André P., Xu, Xijin, Huo, Xia, Ani, Alireza, Nolte, Ilja M., Wolffenbuttel, Bruce H.R., van Vliet-Ostaptchouk, Jana V., Snieder, Harold

    ISSN: 0160-4120, 1873-6750, 1873-6750
    Veröffentlicht: Netherlands Elsevier Ltd 01.01.2024
    Veröffentlicht 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 von Robinson, Matthew R, English, Geoffrey, Moser, Gerhard, Lloyd-Jones, Luke R, Triplett, Marcus A, Zhu, Zhihong, Nolte, Ilja M, van Vliet-Ostaptchouk, Jana V, Snieder, Harold, Esko, Tonu, Milani, Lili, Mägi, Reedik, Metspalu, Andres, Magnusson, Patrik K E, Pedersen, Nancy L, Ingelsson, Erik, Johannesson, Magnus, Yang, Jian, Cesarini, David, Visscher, Peter M

    ISSN: 1061-4036, 1546-1718, 1546-1718
    Veröffentlicht: New York Springer New York 01.08.2017
    Veröffentlicht 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 von Chia, Yook Chin, Kieneker, Lyanne M., van Hassel, Gaston, Binnenmars, S. Heleen, Nolte, Ilja M., van Zanden, Jelmer J., van der Meer, Peter, Navis, Gerjan, Voors, Adriaan A., Bakker, Stephan J. L., De Borst, Martin H., Eisenga, Michele F.

    ISSN: 2047-9980, 2047-9980
    Veröffentlicht: England John Wiley and Sons Inc 01.06.2021
    Veröffentlicht 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 von Triatin, Rima D., Chen, Zekai, Ani, Alireza, Wang, Rujia, Hartman, Catharina A., Nolte, Ilja M., Thio, Chris H. L., Snieder, Harold

    ISSN: 1475-2840, 1475-2840
    Veröffentlicht: London BioMed Central 21.10.2023
    Veröffentlicht 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 von Eisenga, Michele F, van Londen, Marco, Leaf, David E, Nolte, Ilja M, Navis, Gerjan, Bakker, Stephan J L, de Borst, Martin H, Gaillard, Carlo A J M

    ISSN: 1533-3450, 1533-3450
    Veröffentlicht: United States 01.12.2017
    Veröffentlicht 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 von Riesmeijer, Sophie A., Kamali, Zoha, Ng, Michael, Drichel, Dmitriy, Piersma, Bram, Becker, Kerstin, Layton, Thomas B., Nanchahal, Jagdeep, Nothnagel, Michael, Vaez, Ahmad, Hennies, Hans Christian, Werker, Paul M. N., Furniss, Dominic, Nolte, Ilja M.

    ISSN: 2041-1723, 2041-1723
    Veröffentlicht: London Nature Publishing Group UK 03.01.2024
    Veröffentlicht 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 von Balder, Jan W., de Vries, Jeroen K., Nolte, Ilja M., Lansberg, Peter J., Kuivenhoven, Jan A., Kamphuisen, Pieter W.

    ISSN: 1933-2874, 1876-4789
    Veröffentlicht: United States Elsevier Inc 01.07.2017
    Veröffentlicht 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? von Rawee, Pien, Kremer, Daan, Nolte, Ilja M., Leuvenink, Henri G. D., Touw, Daan J., De Borst, Martin H., Bakker, Stephan J. L., Hanudel, Mark R., Eisenga, Michele F.

    ISSN: 1422-0067, 1661-6596, 1422-0067
    Veröffentlicht: Switzerland MDPI AG 10.03.2023
    Veröffentlicht 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 von Steen, Olivier D., Bos, Martje, van Ockenburg, Sonja L., Zhou, Yiling, Nolte, Ilja M., Snieder, Harold, Kendler, Kenneth, Rosmalen, Judith G. M., van Loo, Hanna M.

    ISSN: 1741-7015, 1741-7015
    Veröffentlicht: London BioMed Central 11.08.2025
    Veröffentlicht 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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  13. 13

    Metasubtract: an R‐package to analytically produce leave‐one‐out meta‐analysis GWAS summary statistics von Nolte, Ilja M

    ISSN: 1367-4803, 1367-4811, 1460-2059, 1367-4811
    Veröffentlicht: England Oxford University Press 15.08.2020
    Veröffentlicht 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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  14. 14

    Mitochondrial Genome Study Identifies Association Between Primary Open-Angle Glaucoma and Variants in MT-CYB, MT-ND4 Genes and Haplogroups von Lo Faro, Valeria, Nolte, Ilja M., Ten Brink, Jacoline B., Snieder, Harold, Jansonius, Nomdo M., Bergen, Arthur A., Lifelines Cohort Study

    ISSN: 1664-8021, 1664-8021
    Veröffentlicht: Switzerland Frontiers Media S.A 16.12.2021
    Veröffentlicht 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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    Killer Cell Immunoglobulin-Like Receptor Haplotype B Modulates Susceptibility to EBV-Associated Classic Hodgkin Lymphoma von Jiang, Peijia, Nolte, Ilja M., Hepkema, Bouke G., Stulp, Marijke, van den Berg, Anke, Diepstra, Arjan

    ISSN: 1664-3224, 1664-3224
    Veröffentlicht: Switzerland Frontiers Media S.A 27.01.2022
    Veröffentlicht 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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    Role of inflammation in depressive and anxiety disorders, affect, and cognition: genetic and non-genetic findings in the lifelines cohort study von Mac Giollabhui, Naoise, Slaney, Chloe, Hemani, Gibran, Foley, Éimear M., van der Most, Peter J., Nolte, Ilja M., Snieder, Harold, Davey Smith, George, Khandaker, Golam M., Hartman, Catharina A.

    ISSN: 2158-3188, 2158-3188
    Veröffentlicht: London Nature Publishing Group UK 10.05.2025
    Veröffentlicht 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 von Nolte, Ilja M, van der Most, Peter J, Alizadeh, Behrooz Z, de Bakker, Paul IW, Boezen, H Marike, Bruinenberg, Marcel, Franke, Lude, van der Harst, Pim, Navis, Gerjan, Postma, Dirkje S, Rots, Marianne G, Stolk, Ronald P, Swertz, Morris A, Wolffenbuttel, Bruce HR, Wijmenga, Cisca, Snieder, Harold

    ISSN: 1018-4813, 1476-5438, 1476-5438
    Veröffentlicht: England Nature Publishing Group 01.06.2017
    Veröffentlicht 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 von Yuan, Ye, Niu, Fubiao, Nolte, Ilja M., Koerts, Jasper, de Jong, Debora, Rutgers, Bea, Osinga, Jan, Azkanaz, Maria, Terpstra, Martijn, Bystrykh, Leonid, Diepstra, Arjan, Visser, Lydia, Dzikiewicz-Krawczyk, Agnieszka, Kok, Klaas, Kluiver, Joost , van den Berg, Anke

    ISSN: 1015-8987, 1421-9778, 1421-9778
    Veröffentlicht: Basel, Switzerland S. Karger AG 01.09.2018
    Veröffentlicht 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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