Works matching AU Mononen, Nina


Results: 41
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    Genetic Profiling Using Genome-Wide Significant Coronary Artery Disease Risk Variants Does Not Improve the Prediction of Subclinical Atherosclerosis: The Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey - A Meta-Analysis of Three Independent Studies

    Published in:
    PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0028931
    By:
    • Hernesniemi, Jussi A.;
    • Seppälä, Ilkka;
    • Lyytikäinen, Leo-Pekka;
    • Mononen, Nina;
    • Oksala, Niku;
    • Hutri-Kähönen, Nina;
    • Juonala, Markus;
    • Taittonen, Leena;
    • Smith, Erin N.;
    • Schork, Nicholas J.;
    • Wei Chen;
    • Srinivasan, Sathanur R.;
    • Berenson, Gerald S.;
    • Murray, Sarah S.;
    • Laitinen, Tomi;
    • Jula, Antti;
    • Kettunen, Johannes;
    • Ripatti, Samuli;
    • Laaksonen, Reijo;
    • Viikari, Jorma
    Publication type:
    Article
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    Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 10, p. 1720, doi. 10.1093/hmg/ddab339
    By:
    • Laaksonen, Jaakko;
    • Mishra, Pashupati P;
    • Seppälä, Ilkka;
    • Raitoharju, Emma;
    • Marttila, Saara;
    • Mononen, Nina;
    • Lyytikäinen, Leo-Pekka;
    • Kleber, Marcus E;
    • Delgado, Graciela E;
    • Lepistö, Maija;
    • Almusa, Henrikki;
    • Ellonen, Pekka;
    • Lorkowski, Stefan;
    • März, Winfried;
    • Hutri-Kähönen, Nina;
    • Raitakari, Olli;
    • Kähönen, Mika;
    • Salonen, Jukka T;
    • Lehtimäki, Terho
    Publication type:
    Article
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    Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: a population-based mtDNA sequencing study.

    Published in:
    Human Molecular Genetics, 2019, v. 28, n. 8, p. 1381, doi. 10.1093/hmg/ddz011
    By:
    • Laaksonen, Jaakko;
    • Seppälä, Ilkka;
    • Raitoharju, Emma;
    • Mononen, Nina;
    • Lyytikäinen, Leo-Pekka;
    • Waldenberger, Melanie;
    • Illig, Thomas;
    • Lepistö, Maija;
    • Almusa, Henrikki;
    • Ellonen, Pekka;
    • Hutri-Kähönen, Nina;
    • Juonala, Markus;
    • Kähönen, Mika;
    • Raitakari, Olli;
    • Salonen, Jukka T;
    • Lehtimäki, Terho
    Publication type:
    Article
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    Androgen receptor CAG polymorphism and prostate cancer risk.

    Published in:
    Human Genetics, 2002, v. 111, n. 2, p. 166, doi. 10.1007/s00439-002-0776-5
    By:
    • Mononen, Nina;
    • Ikonen, Tarja;
    • Autio, Ville;
    • Rökman, Annika;
    • Matikainen, Mika P.;
    • Tammela, Teuvo L.;
    • Kallioniemi, Olli-P.;
    • Koivisto, Pasi A.;
    • Schleutker, Johanna
    Publication type:
    Article
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    Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke.

    Published in:
    Scientific Reports, 2016, p. 23207, doi. 10.1038/srep23207
    By:
    • Seppälä, Ilkka;
    • Kleber, Marcus E.;
    • Bevan, Steve;
    • Lyytikäinen, Leo-Pekka;
    • Oksala, Niku;
    • Hernesniemi, Jussi A.;
    • Mäkelä, Kari-Matti;
    • Rothwell, Peter M.;
    • Sudlow, Cathie;
    • Dichgans, Martin;
    • Mononen, Nina;
    • Vlachopoulou, Efthymia;
    • Sinisalo, Juha;
    • Delgado, Graciela E.;
    • Laaksonen, Reijo;
    • Koskinen, Tuomas;
    • Scharnagl, Hubert;
    • Kähönen, Mika;
    • Markus, Hugh S.;
    • März, Winfried
    Publication type:
    Article
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    Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-79931-6
    By:
    • Laaksonen, Jaakko;
    • Mishra, Pashupati P.;
    • Seppälä, Ilkka;
    • Lyytikäinen, Leo-Pekka;
    • Raitoharju, Emma;
    • Mononen, Nina;
    • Lepistö, Maija;
    • Almusa, Henrikki;
    • Ellonen, Pekka;
    • Hutri-Kähönen, Nina;
    • Juonala, Markus;
    • Raitakari, Olli;
    • Kähönen, Mika;
    • Salonen, Jukka T.;
    • Lehtimäki, Terho
    Publication type:
    Article
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    Predicting sudden cardiac death using common genetic risk variants for coronary artery disease.

    Published in:
    European Heart Journal, 2015, v. 36, n. 26, p. 1669, doi. 10.1093/eurheartj/ehv106
    By:
    • Hernesniemi, Jussi A.;
    • Lyytikäinen, Leo-Pekka;
    • Oksala, Niku;
    • Seppälä, Ilkka;
    • Kleber, Marcus E.;
    • Mononen, Nina;
    • März, Winfried;
    • Mikkelsson, Jussi;
    • Pessi, Tanja;
    • Louhelainen, Anne-Mari;
    • Martiskainen, Mika;
    • Nikus, Kjell;
    • Klopp, Norman;
    • Waldenberger, Melanie;
    • Illig, Thomas;
    • Kähönen, Mika;
    • Laaksonen, Reijo;
    • Karhunen, Pekka J.;
    • Lehtimäki, Terho
    Publication type:
    Article
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    Methylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs.

    Published in:
    Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01132-3
    By:
    • Marttila, Saara;
    • Viiri, Leena E.;
    • Mishra, Pashupati P.;
    • Kühnel, Brigitte;
    • Matias-Garcia, Pamela R.;
    • Lyytikäinen, Leo-Pekka;
    • Ceder, Tiina;
    • Mononen, Nina;
    • Rathmann, Wolfgang;
    • Winkelmann, Juliane;
    • Peters, Annette;
    • Kähönen, Mika;
    • Hutri-Kähönen, Nina;
    • Juonala, Markus;
    • Aalto-Setälä, Katriina;
    • Raitakari, Olli;
    • Lehtimäki, Terho;
    • Waldenberger, Melanie;
    • Raitoharju, Emma
    Publication type:
    Article
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    Regulation of nc886 (vtRNA2-1) RNAs is associated with cardiometabolic risk factors and diseases.

    Published in:
    Clinical Epigenetics, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13148-025-01871-7
    By:
    • Rajić, Sonja;
    • Delerue, Thomas;
    • Ronkainen, Justiina;
    • Zhang, Ruiyuan;
    • Ciantar, Joanna;
    • Kostiniuk, Daria;
    • Mishra, Pashupati P.;
    • Lyytikäinen, Leo-Pekka;
    • Mononen, Nina;
    • Kananen, Laura;
    • Peters, Annette;
    • Winkelmann, Juliane;
    • Kleber, Marcus E.;
    • Lorkowski, Stefan;
    • Kähönen, Mika;
    • Lehtimäki, Terho;
    • Raitakari, Olli;
    • Waldenberger, Melanie;
    • Gieger, Christian;
    • März, Winfried
    Publication type:
    Article
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    TPH1 A218C polymorphism and temperament in major depression.

    Published in:
    BMC Psychiatry, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-244X-13-118
    By:
    • Andre, Kadri;
    • Kampman, Olli;
    • Viikki, Merja;
    • Illi, Ari;
    • Setälä-Soikkeli, Eija;
    • Poutanen, Outi;
    • Mononen, Nina;
    • Leinonen, Esa;
    • Lehtimäki, Terho
    Publication type:
    Article
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    A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure.

    Published in:
    Human Genetics, 2015, v. 134, n. 6, p. 627, doi. 10.1007/s00439-015-1546-5
    By:
    • Turpeinen, Hannu;
    • Seppälä, Ilkka;
    • Lyytikäinen, Leo-Pekka;
    • Raitoharju, Emma;
    • Hutri-Kähönen, Nina;
    • Levula, Mari;
    • Oksala, Niku;
    • Waldenberger, Melanie;
    • Klopp, Norman;
    • Illig, Thomas;
    • Mononen, Nina;
    • Laaksonen, Reijo;
    • Raitakari, Olli;
    • Kähönen, Mika;
    • Lehtimäki, Terho;
    • Pesu, Marko
    Publication type:
    Article
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    SERT and NET polymorphisms, temperament and antidepressant response.

    Published in:
    Nordic Journal of Psychiatry, 2015, v. 69, n. 7, p. 531, doi. 10.3109/08039488.2015.1012554
    By:
    • Andre, Kadri;
    • Kampman, Olli;
    • Illi, Ari;
    • Viikki, Merja;
    • Setälä-Soikkeli, Eija;
    • Mononen, Nina;
    • Lehtimäki, Terho;
    • Haraldsson, Susann;
    • Koivisto, Pasi A.;
    • Leinonen, Esa
    Publication type:
    Article
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