Search Results - FinnGen

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  1. 1

    Disentangling the link between maternal influences on birth weight and disease risk in 36,211 genotyped mother–child pairs by Jaakko T. Leinonen, FinnGen, Matti Pirinen, Taru Tukiainen

    Published in Communications Biology (2024-02-01)
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  2. 2

    Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes by Max Tamlander, Nina Mars, Matti Pirinen, FinnGen, Elisabeth Widén, Samuli Ripatti

    Published in Communications Biology (2022-02-01)
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  3. 3

    Narcolepsy as a potential risk factor for Schizophrenia by Reyhane Eghtedarian, Anniina M. Tervi, Samuel E. Jones, FinnGen, Markku Partinen, Essi Viippola, Hanna M. Ollila

    Published in Translational Psychiatry (2025-02-01)
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  4. 4

    Long‐term cardiovascular risk in women with hypertensive disorders of pregnancy: Insights from polygenic risk scores by Anna Kivioja, Jaakko Tyrmi, Elli Toivonen, Heini Huhtala, FinnGen, Tiina Jääskeläinen, Johannes Kettunen, Tanja Saarela, Hannele Laivuori

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  5. 5

    Causal relationship between gut microbiota and immune thrombocytopenia: a Mendelian randomization study of two samples by Dongmei Guo, Dongmei Guo, Qian Chen, Qian Chen, Guojun Wang, Guojun Wang, ChunPu Li, ChunPu Li, FinnGen consortium

    Published in Frontiers in Microbiology (2023-11-01)
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  6. 6

    Use of electronic health record data mining for heart failure subtyping by Matti A. Vuori, Tuomo Kiiskinen, Niina Pitkänen, Samu Kurki, Hannele Laivuori, Tarja Laitinen, Sampo Mäntylahti, Aarno Palotie, FinnGen, Teemu J. Niiranen

    Published in BMC Research Notes (2023-09-01)
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  7. 7

    Genome-wide association analysis of plasma lipidome identifies 495 genetic associations by Linda Ottensmann, Rubina Tabassum, Sanni E. Ruotsalainen, Mathias J. Gerl, Christian Klose, Elisabeth Widén, FinnGen, Kai Simons, Samuli Ripatti, Matti Pirinen

    Published in Nature Communications (2023-10-01)
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  8. 8

    ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. by Pyry Helkkula, Tuomo Kiiskinen, Aki S Havulinna, Juha Karjalainen, Seppo Koskinen, Veikko Salomaa, Mark J Daly, Aarno Palotie, Ida Surakka, Samuli Ripatti, FinnGen

    Published in PLoS Genetics (2021-04-01)
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  9. 9

    Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects by Martin Broberg, Minna Ampuja, Samuel Jones, Tiina Ojala, Otto Rahkonen, Riikka Kivelä, James Priest, FinnGen, Aarno Palotie, Hanna M. Ollila, Emmi Helle

    Published in BMC Genomics (2024-03-01)
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  10. 10

    Genome-Wide Association Study in the FinnGen Cohort for Risk Variants of Idiopathic Intracranial Hypertension by Mrs Katri Piilonen, PhD Anssi Lipponen, Docent Sami Heikkinen, PhD Paula Walle, Mr Joel Räsänen, Ville Leinonen, Docent Terhi Huuskonen, FinnGen

    Published in Brain and Spine (2025-01-01)
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  11. 11

    Mechanisms of thyrotropin receptor–mediated phenotype variability deciphered by gene mutations and M453T-knockin model by Kristiina Makkonen, Meeri Jännäri, Luís Crisóstomo, Matilda Kuusi, Konrad Patyra, Vladyslav Melnyk, Veli Linnossuo, Johanna Ojala, Rowmika Ravi, Christoffer Löf, Juho-Antti Mäkelä, Päivi Miettinen, Saila Laakso, Marja Ojaniemi, Jarmo Jääskeläinen, Markku Laakso, Filip Bossowski, Beata Sawicka, Karolina Stożek, Artur Bossowski, Gunnar Kleinau, Patrick Scheerer, FinnGen FinnGen, Mary Pat Reeve, Jukka Kero

    Published in JCI Insight (2024-02-01)
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  12. 12

    Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events by Henrike O. Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, FinnGen, Estonian Biobank research team, Reetta Kälviainen, Mark J. Daly

    Published in Nature Communications (2024-07-01)
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  13. 13

    Chromatin state origins of uterine leiomyoma by Maritta Räisänen, Eevi Kaasinen, Maija Jäntti, Aurora Taira, Emma Siili, Ralf Bützow, Oskari Heikinheimo, Annukka Pasanen, Auli Karhu, FinnGen, Davide G. Berta, Niko Välimäki, Lauri A. Aaltonen

    Published in Nature Communications (2025-05-01)
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  14. 14

    Cross‐sectional study of plasma phosphorylated tau 217 in persons without dementia by Toni T. Saari, Teemu Palviainen, Mikko Hiltunen, Sanna‐Kaisa Herukka, Tarja Kokkola, Sari Kärkkäinen, Mia Urjansson, Aino Aaltonen, Aarno Palotie, Heiko Runz, Jaakko Kaprio, Valtteri Julkunen, Eero Vuoksimaa, for FinnGen

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  15. 15

    Leveraging large-scale multi-omics evidences to identify therapeutic targets from genome-wide association studies by Samuel Lessard, Michael Chao, Kadri Reis, FinnGen, Estonian Biobank Research Team, Mathieu Beauvais, Deepak K. Rajpal, Jennifer Sloane, Priit Palta, Katherine Klinger, Emanuele de Rinaldis, Khader Shameer, Clément Chatelain

    Published in BMC Genomics (2024-11-01)
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  16. 16

    Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations by Ville Salo, Juhani Määttä, Eeva Sliz, FinnGen, Ene Reimann, Reedik Mägi, Estonian Biobank Research Team, Kadri Reis, Abdelrahman G. Elhanas, Anu Reigo, Priit Palta, Tõnu Esko, Jaro Karppinen, Johannes Kettunen

    Published in Nature Communications (2024-11-01)
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  17. 17

    Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. by Anu Pasanen, Minna K Karjalainen, FinnGen, Ge Zhang, Heli Tiensuu, Antti M Haapalainen, Marja Ojaniemi, Bjarke Feenstra, Bo Jacobsson, Aarno Palotie, Hannele Laivuori, Louis J Muglia, Mika Rämet, Mikko Hallman

    Published in PLoS Genetics (2023-10-01)
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  18. 18

    Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma. by Yosuke Tanigawa, Michael Wainberg, Juha Karjalainen, Tuomo Kiiskinen, Guhan Venkataraman, Susanna Lemmelä, Joni A Turunen, Robert R Graham, Aki S Havulinna, Markus Perola, Aarno Palotie, FinnGen, Mark J Daly, Manuel A Rivas

    Published in PLoS Genetics (2020-05-01)
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  19. 19

    Socio-demographic and genetic risk factors for drug adherence and persistence across 5 common medication classes by Mattia Cordioli, Andrea Corbetta, Hanna Maria Kariis, Sakari Jukarainen, Pekka Vartiainen, Tuomo Kiiskinen, Matteo Ferro, FinnGen, Estonian Biobank Research Team, Markus Perola, Mikko Niemi, Samuli Ripatti, Kelli Lehto, Lili Milani, Andrea Ganna

    Published in Nature Communications (2024-10-01)
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  20. 20

    Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci by João Fadista, Line Skotte, Juha Karjalainen, Erik Abner, Erik Sørensen, Henrik Ullum, Thomas Werge, iPSYCH Group, Tõnu Esko, Lili Milani, Aarno Palotie, Mark Daly, FinnGen Consortium, Mads Melbye, Bjarke Feenstra, Frank Geller

    Published in Nature Communications (2022-06-01)
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