PUBLICATIONS
Frontiers | Combined Use of Serum Uromodulin and eGFR to Estimate Mortality Risk (frontiersin.org)
Yazdani B, Delgado GE, Scharnagl H, Krämer BK, Drexel H, März W, Scherberich JE, Leiherer A and Kleber ME (2021) Front. Med. 8:723546.
Gabin Drouard, et al. OMICS: A Journal of Integrative Biology. Mar 2022.130-141.
Gorski Mathias, et al. CLINICAL INVESTIGATION| volume 102, issue 3, p624-639, Sept (2022)
Saarinen A., et al. Brain and Behavior, 12, (2022) e2704.
Jutta Viinikainen, et al. Journal of Psychiatric Research, Volume 151, 2022, Pages 638-641
Beyene, S. D. et al. Annals of Noninvasive Electrocardiology, 27, (2022). e12968
-a general population study | Molecular Psychiatry (nature.com)
Saarinen, A., Lyytikäinen, LP., Hietala, J. et al. Mol Psychiatry 27, 3286–3293 (2022)
Interatrial block and P terminal force in the general population –
Longitudinal changes, risk factors and prognosis - ScienceDirect
Istolahti T, et al. J Electrocardiol. 2022 Jul-Aug; 73:12-20.
Lundgren, S, et al. J Intern Med. 2022; 292: 627– 640
Viitasalo A., et al. Frontiers in Endocrinology. VOL.13 (2022)
Mishra, B.H., et al. vol 361, P1-9, Nov 2022
Genetics of osteopontin in patients with chronic kidney disease:
The German Chronic Kidney Disease study | PLOS Genetics
Yurong Cheng, et al. Plos Gen. April 6, 2022
Pritha Dutta et al, arXiv, 23 Feb 2021 arXiv:2102.11690v1
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction
European Heart Journal | Oxford Academic (oup.com)
Jaana A Hartiala, et al. European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 919–933
Circulating cell-free DNA level predicts all-cause mortality independent of other predictors
in the Health 2000 survey | Scientific Reports (nature.com)
Kananen, L., et al. Sci Rep 10, 13809 (2020). https://doi.org/10.1038/s41598-020-70526-9
in the general population - ScienceDirect
Joonas Nurminen, et al., Journal of Electrocardiology, Volume 73, 2022.
Andreakos, E., Abel, L., Vinh, D.C. et al. Nat Immunol 23, 159–164 (2022).
Associations of long-term solar insolation with specific depressive symptoms:
Evidence from a prospective cohort study - ScienceDirect
Kaisla Komulainen, et al. Journal of Psychiatric Research,Volume 151,2022, Pages 606-610
Organized Youth Sports Trajectories and Adult Health Outcomes:
The Young Finns Study - American Journal of Preventive Medicine (ajpmonline.org)
Xiaolin Yang, et al. AJPM, volume 63, issue 6, p962-970, Dec 2022
Tölli, P, Keltikangas-Järvinen, L, Lehtimäki, T, et al. Genes, Brain and Behavior. 2022; 21(4): e12798.
Long-term tracking and population characteristics of lipoprotein (a) in the
Cardiovascular Risk in Young Finns Study - Atherosclerosis (atherosclerosis-journal.com)
Olli Raitakari, et al. Atherosclerosis volume 356, p18-27, Sept 2022
How location and cellular signaling combine to activate the NLRP3 inflammasome |
Cellular & Molecular Immunology (nature.com)
Akbal, A., Dernst, A., Lovotti, M. et al. Cell Mol Immunol 19, 1201–1214 (2022)
Red blood cell fatty acid patterns from 7 countries: Focus on the Omega-3 index - Prostaglandins,
Leukotrienes and Essential Fatty Acids (plefa.com)
179:102418 (2022)
Unfolding and disentangling coronary vascular disease through genome-wide association studies |
European Heart Journal | Oxford Academic (oup.com)
Erdmann, J., van der Laan, S. W., European Heart Journal Volume 42, Issue 9, 934–937 (2021)
Ma WF, Turner AW, Gancayco C, Wong D, Song Y, Mosquera JV, Auguste G, Hodonsky CJ, Prabhakar A, Ekiz HA, van der Laan SW and Miller CL Front. Cardiovasc. Med. 9:969421 (2022)
Schillemans T, Tragante V, Maitusong B, et al. Front. Physiol. 13:909870 (2022)
Lotte Slenders, Lennart P L Landsmeer, et al., European Heart Journal Open, Volume 2, Issue 1(2022)
Slenders L, Tessels DE, van der Laan SW, Pasterkamp G and Mokry M Front. Cardiovasc. Med. 9:826103 (2022)
PolarMorphism enables discovery of shared genetic variants across multiple traits from GWAS
summary statistics | Bioinformatics | Oxford Academic (oup.com)
von Berg J., ten Dam M., van der Laan S. W., de Ridder J., Bioinformatics, Volume 38, Issue Supplement_1, i212–i219 (2022)
A saturated map of common genetic variants associated with human height | Nature
Yengo, L., Vedantam, S., Marouli, E. et al. Nature 610, 704–712 (2022).
The gut microbiota and depressive symptoms across ethnic groups | Nature Communications
Bosch, J.A., Nieuwdorp, M., Zwinderman, A.H. et al. Nat Commun 13, 7129 (2022).
Gut microbiome-wide association study of depressive symptoms | Nature Communications
Radjabzadeh, D., Bosch, J.A., Uitterlinden, A.G. et al. Nat Commun 13, 7128 (2022).
Wielscher, M., Mandaviya, P.R., Kuehnel, B. et al. Nat Commun 13, 2408 (2022)
Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases.
Yong Li, Luca Rampoldi, Anna Köttgen. JCI Insight (2022)
Genome-wide meta-analysis of phytosterols reveals five novel loci and
a detrimental effect on coronary atherosclerosis.
Scholz, M., Horn, K., Pott, J. et al. Nat Commun 13, 143 (2022)
Reproductive history and blood cell DNA methylation later in life: the Young Finns Study.
Harville, E.W., Mishra, P.P., Kähönen, M. et al. Clin Epigenet 13, 227 (2021)
Assessment of plasma ceramides as predictor for subclinical atherosclerosis.
Pashupati P. Mishra, Binisha H. Mishra, Leo-Pekka Lyytikäinen, Mika Hilvo, Markus Juonala, Mika Kähönen, Nina Hutri-Kähönen, Dimitrios I. Fotiadis, Olli T. Raitakari, Reijo Laaksonen, Terho Lehtimäki, Atherosclerosis Plus, Volume 45, Pages 25-31 (2021)
Genomics-based identification of a potential causal role for acylcarnitine metabolism in depression.
Yuri Milaneschi, Matthias Arnold, Gabi Kastenmüller, Siamak Mahmoudian Dehkordi, Ranga R. Krishnan, Boadie W. Dunlop, A. John Rush, Brenda W. J. H. Penninx, Rima Kaddurah-Daouk, for the Mood Disorders Precision Medicine Consortium (MDPMC). medRxiv 2021.10.18.21265157 (2021)
Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci,
Jaakko Laaksonen, 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 Raitakari, Mika Kähönen, Jukka T Salonen, Terho Lehtimäki, Human Molecular Genetics (2021)
Uncovering the shared lipidomic markers of subclinical osteoporosis-atherosclerosis comorbidity: The Young Finns Study, Binisha H. Mishra, 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, Bone, Volume 151,116030 (2021)
Association between Oral Pathology, Carotid Stenosis, and Oral Bacterial DNA in Cerebral Thrombi of Patients with Stroke, Olli Patrakka, Helena Mehtonen, Sari Tuomisto, Juha-Pekka Pienimäki, Jyrki Ollikainen, Heini Huhtala, Tanja Pessi, Niku Oksala, Terho Lehtimäki,
Jorma Järnstedt, Mika Martiskainen, Pekka J. Karhunen, Stroke Research and Treatment, vol. 2021 (2021)
Genetic differential susceptibility to the parent–child relationship quality and the life span development of compassion. Henrik Dobewall, Liisa Keltikangas-Järvinen, Aino Saarinen, Leo-Pekka Lyytikäinen, Igor Zwir, Robert Cloninger, Olli T. Raitakari,
Terho Lehtimäki, Mirka Hintsanen, Developmental Psychobiology, 63, e22184 (2021)
C-reactive protein and temperament: An instrumental variable analysis,
Ari Clemens, Pashupati P. Mishra, Eirini Flouri, Terho Lehtimäki, Olli Raitakari, Liisa Keltikangas-Järvinen, Katriina Heikkilä,
Brain, Behavior, & Immunity - Health, Volume 14 (2021)
Methylation status of nc886 epiallele reflects periconceptional conditions and is associated
with glucose metabolism through nc886 RNAs.
Marttila, S., Viiri, L.E., Mishra, P.P. et al. Clin Epigenet 13, 143 (2021)
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
McCartney, D.L., Min, J.L., Richmond, R.C. et al. Genome Biol 22, 194 (2021)
Meta-analysis of epigenome-wide association studies of carotid intima-media thickness.
Portilla-Fernández, E., Hwang, SJ., Wilson, R. et al. Eur J Epidemiol 36, 1143–1155 (2021)
Prehospital Adenosine Diphosphate Receptor Blocker Use, Culprit Artery Flow, and Mortality in STEMI: The MADDEC Study. Hautamäki M, Lyytikäinen LP, Eskola M, et al. Clin Drug Investig. 41(7):605-613 (2021)
Marttila, S., Rovio, S., Mishra, P.P. et al. Sci Rep 11, 9203 (2021)
Modular genome-wide gene expression architecture shared by early traits
of osteoporosis and atherosclerosis in the Young Finns
Study. Mishra, B.H., Mishra, P.P., Raitoharju, E. et al. Sci Rep 11, 7111 (2021)
Kalaoja, M., Corbin, L.J., Tan, V.Y., Ahola-Olli, A.V., Havulinna, A.S., Santalahti, K., Pitkänen, N., Lehtimäki, T., Lyytikäinen, L.-P., Raitoharju, E., Seppälä, I., Kähönen, M., Ripatti, S., Palotie, A., Perola, M., Viikari, J.S., Jalkanen, S., Maksimow, M., Salomaa, V., Salmi, M., Raitakari,
O.T., Kettunen, J. and Timpson, N.J. Obesity, 29: 428-437 (2021)
Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts.
Laaksonen, J., Mishra, P.P., Seppälä, I. et al. Sci Rep 11, 611 (2021)
The prognostic significance of T-wave inversion according to ECG lead group
during long-term follow-up in the general population.
Istolahti, T, Lyytikäinen, L-P, Huhtala, H, et al. Ann Noninvasive Electrocardiol. 26:e12799 (2021)
DNA methylation signatures of aggression and closely related constructs:
A meta-analysis of epigenome-wide studies across the lifespan.
van Dongen, J., Hagenbeek, F.A., Suderman, M. et al. Mol Psychiatry 26, 2148–2162 (2021)
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Gorski, MathiasAlizadeh, Behrooz Z.Abecasis, Goncalo et al., Kidney International, Volume 99, Issue 4, 926 - 939 (2020)
Epigenome-450K-wide methylation signatures of active cigarette smoking: The Young Finns Study.
Pashupati P. Mishra, Ismo Hänninen, Emma Raitoharju, Saara Marttila, Binisha H. Mishra, Nina Mononen, Mika Kähönen, Mikko Hurme, Olli Raitakari, Petri Törönen, Liisa Holm, Terho Lehtimäki; Biosci Rep; 40 (7): BSR20200596 (2020)
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