Aging-associated DNA methylation changes in middle-aged individuals: the Young Finns study
Kananen, L, Marttila, S, Nevalainen, T, Jylhävä, J, Mononen, N, Kähönen, M, Raitakari, O T, Lehtimäki, T, Hurme, M
Published in BMC genomics (09.02.2016)
Published in BMC genomics (09.02.2016)
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The trajectory of the blood DNA methylome ageing rate is largely set before adulthood: evidence from two longitudinal studies
Kananen, L., Marttila, S., Nevalainen, T., Kummola, L., Junttila, I., Mononen, N., Kähönen, M., Raitakari, O. T., Hervonen, A., Jylhä, M., Lehtimäki, T., Hurme, M., Jylhävä, J.
Published in AGE (01.06.2016)
Published in AGE (01.06.2016)
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Effect of Genetic Polymorphisms in CA6 Gene on the Expression and Catalytic Activity of Human Salivary Carbonic Anhydrase VI
Aidar, M., Marques, Rocha, Valjakka, J., Mononen, N., Lehtimäki, T., Parkkila, S., de Souza, A.P., Line, Peres
Published in Caries research (01.01.2013)
Published in Caries research (01.01.2013)
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Association study of the HTR2C, leptin and adiponectin genes and serum marker analyses in clozapine treated long-term patients with schizophrenia
Klemettilä, J.-P, Kampman, O, Seppälä, N, Viikki, M, Hämäläinen, M, Moilanen, E, Mononen, N, Lehtimäki, T, Leinonen, E
Published in European psychiatry (01.02.2015)
Published in European psychiatry (01.02.2015)
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The rs2516839 variation of USF1 gene is associated with 4‐year mortality of nonagenarian women: The Vitality 90+ study
Ozsait‐Selcuk, B., Komurcu‐Bayrak, E., Jylhä, M., Luukkaala, T., Perola, M., Kristiansson, K., Mononen, N., Hurme, M., Kähönen, M., Goebeler, S., Laaksonen, R., Hervonen, A., Erginel‐Unaltuna, N., Karhunen, P.J., Lehtimäki, T.
Published in Annals of human genetics (01.01.2019)
Published in Annals of human genetics (01.01.2019)
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Association study of arcuate nucleus neuropeptide Y neuron receptor gene variation and serum NPY levels in clozapine treated patients with schizophrenia
Klemettilä, J.-P, Kampman, O, Solismaa, A, Lyytikäinen, L.-P, Seppälä, N, Viikki, M, Hämäläinen, M, Moilanen, E, Mononen, N, Lehtimäki, T, Leinonen, E
Published in European psychiatry (01.02.2017)
Published in European psychiatry (01.02.2017)
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CHEK2 variants associate with hereditary prostate cancer
SEPPÄLÄ, E. H, IKONEN, T, MONONEN, N, AUTIO, V, RÖKMAN, A, MATIKAINEN, M. P, TAMMELA, T. L. J, SCHLEUTKER, J
Published in British journal of cancer (17.11.2003)
Published in British journal of cancer (17.11.2003)
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Neuropeptide Y polymorphism increases the risk for asthma in overweight subjects; protection from atherosclerosis in asthmatic subjects – The cardiovascular risk in young Finns study
Jaakkola, U, Kakko, T, Juonala, M, Lehtimäki, T, Viikari, J, Jääskeläinen, A.E, Mononen, N, Kähönen, M, Koskinen, T, Keltikangas-Järvinen, L, Raitakari, O, Kallio, J
Published in Neuropeptides (Edinburgh) (01.12.2012)
Published in Neuropeptides (Edinburgh) (01.12.2012)
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Association of C-reactive protein (CRP) gene allelic variants with serum CRP levels and hypertension in Turkish adults
Komurcu-Bayrak, E, Erginel-Unaltuna, N, Onat, A, Ozsait, B, Eklund, C, Hurme, M, Mononen, N, Laaksonen, R, Hergenc, G, Lehtimäki, T
Published in Atherosclerosis (01.10.2009)
Published in Atherosclerosis (01.10.2009)
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A missense substitution A49T in the steroid 5-alpha-reductase gene ( ) is not associated with prostate cancer in Finland
MONONEN, N, IKONEN, T, SYRJÄKOSKI, K, MATIKAINEN, M, SCHLEUTKER, J, TAMMELA, T. L. J, KOIVISTO, P. A, KALLIONIEMI, O. P
Published in British journal of cancer (18.05.2001)
Published in British journal of cancer (18.05.2001)
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BRCA1 and BRCA2 mutations have no major role in predisposition to prostate cancer in Finland
Ikonen, T, Matikainen, M P, Syrjäkoski, K, Mononen, N, Koivisto, P A, Rökman, A, Seppälä, E H, Kallioniemi, O-P, Tammela, T L J, Schleutker, J
Published in Journal of medical genetics (01.08.2003)
Published in Journal of medical genetics (01.08.2003)
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Identification of blood modular genome-wide gene expression biomarkers of cardiovascular health and depression in the young finns study
Mishra, B., Raitoharju, E., Mononen, N., Viikari, J., Juonala, M., Hutri-Kähönen, N., Kähönen, M., Raitakari, O., Lehtimäki, T., Mishra, P.
Published in Atherosclerosis (01.08.2023)
Published in Atherosclerosis (01.08.2023)
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Journal Article
Genetic and epigenetic regulation of nc886 RNA levels and their association to cardiometabolic phenotypes
Rajic, S., Marttila, S., Mishra, P., Mononen, N., Raitakari, O., Lyytikäinen, L.-P., Kähönen, M., Hutri-Kähönen, N., Waldenberger, M., Lehtimäki, T., Raitoharju, E.
Published in Atherosclerosis (01.08.2022)
Published in Atherosclerosis (01.08.2022)
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Regulation of NC886 RNAs is associated with cardiometabolic risk factors, death and stroke
Rajić, S., Marttila, S., Hutri-Kähönen, N., Kähönen, M., Lehtimäki, T., Lyytikäinen, L.-P., Mishra, P., Mononen, N., Raitakari, O., Waldenberger, M., Delerue, T., März, W., Kleber, M., Harville, E., Zhang, R., Raitoharju, E.
Published in Atherosclerosis (01.08.2023)
Published in Atherosclerosis (01.08.2023)
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Journal Article
Obesity accelerates epigenetic aging in middle-aged but not in elderly individuals
Nevalainen, Tapio, Kananen, Laura, Marttila, Saara, Jylhävä, Juulia, Mononen, Nina, Kähönen, Mika, Raitakari, Olli T, Hervonen, Antti, Jylhä, Marja, Lehtimäki, Terho, Hurme, Mikko
Published in Clinical epigenetics (14.02.2017)
Published in Clinical epigenetics (14.02.2017)
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5-HTR1A, 5-HTR2A, 5-HTR6, TPH1 and TPH2 polymorphisms and major depression
Illi, Ari, Setälä-Soikkeli, Eija, Viikki, Merja, Poutanen, Outi, Huhtala, Heini, Mononen, Nina, Lehtimäki, Terho, Leinonen, Esa, Kampman, Olli
Published in Neuroreport (05.08.2009)
Published in Neuroreport (05.08.2009)
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Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer
Rökman, Annika, Ikonen, Tarja, Seppälä, Eija H., Nupponen, Nina, Autio, Ville, Mononen, Nina, Bailey-Wilson, Joan, Trent, Jeffrey, Carpten, John, Matikainen, Mika P., Koivisto, Pasi A., Tammela, Teuvo L.J., Kallioniemi, Olli-P., Schleutker, Johanna
Published in American journal of human genetics (01.05.2002)
Published in American journal of human genetics (01.05.2002)
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Journal Article
No support for a role for BDNF gene polymorphisms rs11030101 and rs61888800 in major depressive disorder or antidepressant response in patients of Finnish origin
Illi, Ari, Viikki, Merja, Poutanen, Outi, Setälä-Soikkeli, Eija, Nuolivirta, Timo, Kampman, Olli, Leinonen, Esa, Huhtala, Heini, Mononen, Nina, Lehtimäki, Terho
Published in Psychiatric genetics (01.02.2013)
Published in Psychiatric genetics (01.02.2013)
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Profiling genetic variation along the androgen biosynthesis and metabolism pathways implicates several single nucleotide polymorphisms and their combinations as prostate cancer risk factors
MONONEN, Nina, SEPPÄLÄ, Eija H, KALLIONIEMI, Olli, BAILEY-WILSON, Joan E, SCHLEUTKER, Johanna, DUGGAL, Priya, AUTIO, Ville, IKONEN, Tarja, ELLONEN, Pekka, SAHARINEN, Juha, SAARELA, Janna, VIHINEN, Mauno, TAMMELA, Teuvo L. J
Published in Cancer research (Chicago, Ill.) (15.01.2006)
Published in Cancer research (Chicago, Ill.) (15.01.2006)
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