Nina Mononen

8.0k total citations
88 papers, 2.4k citations indexed

About

Nina Mononen is a scholar working on Molecular Biology, Psychiatry and Mental health and Genetics. According to data from OpenAlex, Nina Mononen has authored 88 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 16 papers in Psychiatry and Mental health and 14 papers in Genetics. Recurrent topics in Nina Mononen's work include Epigenetics and DNA Methylation (11 papers), Bipolar Disorder and Treatment (11 papers) and Treatment of Major Depression (10 papers). Nina Mononen is often cited by papers focused on Epigenetics and DNA Methylation (11 papers), Bipolar Disorder and Treatment (11 papers) and Treatment of Major Depression (10 papers). Nina Mononen collaborates with scholars based in Finland, Germany and Sweden. Nina Mononen's co-authors include Terho Lehtimäki, Johanna Schleutker, Teuvo L.J. Tammela, Mika Kähönen, Mika Matikainen, Tarja Ikonen, Esa Leìnonen, Olli Kampman, Pasi A. Koivisto and Olli T. Raitakari and has published in prestigious journals such as Diabetes Care, Cancer Research and Scientific Reports.

In The Last Decade

Nina Mononen

83 papers receiving 2.4k citations

Peers

Countries citing papers authored by Nina Mononen

Since Specialization

Citations

This map shows the geographic impact of Nina Mononen's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Nina Mononen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nina Mononen more than expected).

Fields of papers citing papers by Nina Mononen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nina Mononen. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Nina Mononen. The network helps show where Nina Mononen may publish in the future.

Co-authorship network of co-authors of Nina Mononen

This figure shows the co-authorship network connecting the top 25 collaborators of Nina Mononen. A scholar is included among the top collaborators of Nina Mononen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nina Mononen. Nina Mononen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Sleep disturbances, shift work, and epigenetic ageing in working-age adults: findings from the Young Finns study 2025 ·Clinical Epigenetics ·(unknown), Aino Saarinen, Saara Marttila, Emma Raitoharju, Pashupati P. Mishra, Nina Mononen, Mika Kähönen, Liisa Keltikangas–Järvinen, Olli T. Raitakari, Terho Lehtimäki	2
2	Identification and functional characterisation of DNA methylation differences between East- and West-originating Finns 2024 ·Epigenetics ·(unknown), Saara Marttila, (unknown), (unknown), Pashupati P. Mishra, Leo-Pekka Lyytikäinen, Nina Mononen, Marcus E. Kleber, Winfried März, Mika Kähönen, Olli Raitakari, Terho Lehtimäki, Emma Raitoharju	1
3	Leptin and leptin receptor gene polymorphisms and depression treatment response 2024 ·Acta Neuropsychiatrica ·(unknown), Anssi Solismaa, Leo-Pekka Lyytikäinen, Nina Mononen, Eeva Moilanen, Mari Hämäläinen, Terho Lehtimäki, Olli Kampman	0
4	Gene Set Based Integrated Methylome and Transcriptome Analysis Reveals Potential Molecular Mechanisms Linking Cigarette Smoking and Related Diseases 2023 ·OMICS A Journal of Integrative Biology ·Pashupati P. Mishra, (unknown), Emma Raitoharju, Nina Mononen, Jorma Viikari, Markus Juonala, Nina Hutri‐Kähönen, Mika Kähönen, Olli T. Raitakari, Terho Lehtimäki	3
5	Polygenic risk for schizophrenia, social dispositions, and pace of epigenetic aging: Results from the Young Finns Study 2023 ·Aging Cell ·Aino Saarinen, Saara Marttila, Pashupati P. Mishra, Leo‐Pekka Lyytikäinen, Emma Raitoharju, Nina Mononen, (unknown), Mika Kähönen, Olli T. Raitakari, Jarmo Hietala, Liisa Keltikangas‐Järvinen, Terho Lehtimäki	2
6	Gene set analysis of transcriptomics data identifies new biological processes associated with early markers of atherosclerosis but not with those of osteoporosis: Atherosclerosis-osteoporosis co/multimorbidity study in the Young Finns Study 2022 ·Atherosclerosis ·(unknown), Harri Sievänen, Emma Raitoharju, Nina Mononen, Jorma Viikari, Markus Juonala, Marika Laaksonen, (unknown), Mika Kähönen, Olli Raitakari, Terho Lehtimäki, Pashupati P. Mishra	0
7	Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci 2021 ·Human Molecular Genetics ·(unknown), Pashupati P. Mishra, Ilkka Seppälä, Emma Raitoharju, Saara Marttila, Nina Mononen, Leo‐Pekka Lyytikäinen, Marcus E. Kleber, Graciela E. Delgado, Maija Lepistö, Henrikki Almusa, Pekka Ellonen, Stefan Lorkowski, Winfried März, Nina Hutri‐Kähönen, Olli T. Raitakari, Mika Kähönen, Jukka T. Salonen, Terho Lehtimäki	4
8	Methylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs 2021 ·Clinical Epigenetics ·Saara Marttila, Leena E. Viiri, Pashupati P. Mishra, Brigitte Kühnel, Pamela R. Matías‐García, Leo‐Pekka Lyytikäinen, (unknown), Nina Mononen, Wolfgang Rathmann, Juliane Winkelmann, Annette Peters, Mika Kähönen, Nina Hutri‐Kähönen, Markus Juonala, Katriina Aalto‐Setälä, Olli T. Raitakari, Terho Lehtimäki, Mélanie Waldenberger, Emma Raitoharju	18
9	Uncovering the shared lipidomic markers of subclinical osteoporosis-atherosclerosis comorbidity: The Young Finns Study 2021 ·Bone ·(unknown), Pashupati P. Mishra, Nina Mononen, Mika Hilvo, Harri Sievänen, Markus Juonala, Marika Laaksonen, Nina Hutri‐Kähönen, Jorma Viikari, Mika Kähönen, Olli T. Raitakari, Reijo Laaksonen, Terho Lehtimäki	15
10	The SGLT2 Inhibitor Dapagliflozin Reduces Liver Fat but Does Not Affect Tissue Insulin Sensitivity: A Randomized, Double-Blind, Placebo-Controlled Study With 8-Week Treatment in Type 2 Diabetes Patients 2019 ·Diabetes Care ·Aino Latva‐Rasku, Miikka‐Juhani Honka, Joel Kullberg, Nina Mononen, Terho Lehtimäki, Juha Saltevo, Anna K. Kirjavainen, Virva Saunavaara, Patricia Iozzo, L. E. B. Johansson, Jan Oscarsson, Jarna C. Hannukainen, Pirjo Nuutila	183
11	The effect of apolipoprotein E polymorphism on serum metabolome – a population-based 10-year follow-up study 2019 ·Scientific Reports ·(unknown), Nina Mononen, Nina Hutri‐Kähönen, (unknown), Markus Juonala, Mika Ala‐Korpela, Mika Kähönen, Olli T. Raitakari, Terho Lehtimäki	30
12	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 2015 ·Human Genetics ·Hannu Turpeinen, Ilkka Seppälä, Leo‐Pekka Lyytikäinen, Emma Raitoharju, Nina Hutri‐Kähönen, Mari Levula, Niku Oksala, Mélanie Waldenberger, Norman Klopp, Thomas Illig, Nina Mononen, Reijo Laaksonen, Olli T. Raitakari, Mika Kähönen, Terho Lehtimäki, Marko Pesu	30
13	Polymorphism in alpha 2A adrenergic receptor gene is associated with sialorrhea in schizophrenia patients on clozapine treatment 2014 ·Human Psychopharmacology Clinical and Experimental ·Anssi Solismaa, Olli Kampman, Niko Seppälä, Merja Viikki, Kari-Matti Mäkelä, Nina Mononen, Terho Lehtimäki, Esa Leìnonen	16
14	Association Study of the HTR2C, Leptin and Adiponectin Genes and Serum Marker Analyses in Clozapine Treated Long-Term Patients with Schizophrenia 2014 ·European Psychiatry ·(unknown), Olli Kampman, Niko Seppälä, Merja Viikki, Mari Hämäläinen, Eeva Moilanen, Nina Mononen, Terho Lehtimäki, Esa Leìnonen	29
15	CYP1A2polymorphism −1545C > T (rs2470890) is associated with increased side effects to clozapine 2014 ·BMC Psychiatry ·Merja Viikki, Olli Kampman, Niko Seppälä, Nina Mononen, Terho Lehtimäki, Esa Leìnonen	10
16	No support for a role for BDNF gene polymorphisms rs11030101 and rs61888800 in major depressive disorder or antidepressant response in patients of Finnish origin 2012 ·Psychiatric Genetics ·Ari Illi, Merja Viikki, Outi Poutanen, Eija Setälä-Soikkeli, (unknown), Olli Kampman, Esa Leìnonen, Heini Huhtala, Nina Mononen, Terho Lehtimäki	14
17	Vascular endothelial growth factor (VEGF) polymorphism is associated with treatment resistant depression 2010 ·Neuroscience Letters ·Merja Viikki, Sami Anttila, Olli Kampman, Ari Illi, Martti Huuhka, Eija Setälä-Soikkeli, Nina Mononen, Terho Lehtimäki, Esa Leìnonen	62
18	The APOE −219G/T and +113G/C polymorphisms affect insulin resistance among Turks 2010 ·Metabolism ·Evrim Kömürcü-Bayrak, Altan Onat, (unknown), Nina Mononen, Reijo Laaksonen, Mika Kähönen, Gülay Hergenç, Terho Lehtimäki, Nihan Erginel‐Ünaltuna	9
19	5-HTR1A, 5-HTR2A, 5-HTR6, TPH1 and TPH2 polymorphisms and major depression 2009 ·Neuroreport ·Ari Illi, Eija Setälä-Soikkeli, Merja Viikki, Outi Poutanen, Heini Huhtala, Nina Mononen, Terho Lehtimäki, Esa Leìnonen, Olli Kampman	98
20	Polymorphism in the IL6 promoter region is associated with the risk factors and markers of subclinical atherosclerosis in men: The Cardiovascular Risk in Young Finns Study 2008 ·Atherosclerosis ·Janne Hulkkonen, Terho Lehtimäki, Nina Mononen, Markus Juonala, Nina Hutri‐Kähönen, Leena Taittonen, Jukka Marniemi, Tuomo Nieminen, Jorma Viikari, Olli T. Raitakari, Mika Kähönen	31

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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