Search Results - FinnGen

FinnGen

The FinnGen project was launched in 2017 with the aim of collecting biological samples from 500,000 participants in Finland over six years with the aim of improving health through genetic research. This is about 10% of the population. It is hoped that it will be a springboard for better diagnostics and new therapies. It is the key to Finland's Health Sector Growth Strategy for Research and Innovation Activities. __TOC__ Provided by Wikipedia
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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

    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 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

    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 2022-02-01
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  3. 3
    Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

    Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata by Eeva Sliz, Jaakko S. Tyrmi, Nilufer Rahmioglu, Krina T. Zondervan, Christian M. Becker, FinnGen, Outi Uimari, Johannes Kettunen

    Published 2023-02-01
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  4. 4
    Causal relationship between gut microbiota and immune thrombocytopenia: a Mendelian randomization study of two samples

    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 2023-11-01
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  5. 5
    Use of electronic health record data mining for heart failure subtyping

    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 2023-09-01
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  6. 6
    Genome-wide association analysis of plasma lipidome identifies 495 genetic associations

    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 2023-10-01
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  7. 7
    ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease.

    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 2021-04-01
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  8. 8
    Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

    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 2024-03-01
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  9. 9
    Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population

    Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population by Pyry Helkkula, Shabbeer Hassan, Elmo Saarentaus, Emilia Vartiainen, Sanni Ruotsalainen, Jaakko T. Leinonen, FinnGen, Aarno Palotie, Juha Karjalainen, Mitja Kurki, Samuli Ripatti, Taru Tukiainen

    Published 2023-01-01
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  10. 10
    Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

    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 2024-07-01
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  11. 11
    Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

    Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks by Rounak Dey, Wei Zhou, Tuomo Kiiskinen, Aki Havulinna, Amanda Elliott, Juha Karjalainen, Mitja Kurki, Ashley Qin, FinnGen, Seunggeun Lee, Aarno Palotie, Benjamin Neale, Mark Daly, Xihong Lin

    Published 2022-09-01
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  12. 12
    The role of polygenic risk and susceptibility genes in breast cancer over the course of life

    The role of polygenic risk and susceptibility genes in breast cancer over the course of life by Nina Mars, Elisabeth Widén, Sini Kerminen, Tuomo Meretoja, Matti Pirinen, Pietro della Briotta Parolo, Priit Palta, FinnGen, Aarno Palotie, Jaakko Kaprio, Heikki Joensuu, Mark Daly, Samuli Ripatti

    Published 2020-12-01
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  13. 13
    Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci.

    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 2023-10-01
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  14. 14
    Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma.

    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 2020-05-01
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  15. 15
    Genetic analyses implicate complex links between adult testosterone levels and health and disease

    Genetic analyses implicate complex links between adult testosterone levels and health and disease by Jaakko T. Leinonen, Nina Mars, Leevi E. Lehtonen, Ari Ahola-Olli, Sanni Ruotsalainen, Terho Lehtimäki, Mika Kähönen, Olli Raitakari, FinnGen Consortium, Terhi Piltonen, Mark Daly, Tiinamaija Tuomi, Samuli Ripatti, Matti Pirinen, Taru Tukiainen

    Published 2023-01-01
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  16. 16
    Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

    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 2022-06-01
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  17. 17
    NTHL1 is a recessive cancer susceptibility gene

    NTHL1 is a recessive cancer susceptibility gene by Anna K. Nurmi, Liisa M. Pelttari, Johanna I. Kiiski, Sofia Khan, Mika Nurmikolu, Maija Suvanto, Niina Aho, Tiina Tasmuth, Eija Kalso, Johanna Schleutker, Anne Kallioniemi, Päivi Heikkilä, FinnGen, Kristiina Aittomäki, Carl Blomqvist, Heli Nevanlinna

    Published 2023-11-01
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  18. 18
    APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study

    APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study by Samu N. Kurki, Jonas Kantonen, Karri Kaivola, Laura Hokkanen, Mikko I. Mäyränpää, Henri Puttonen, FinnGen, Juha Martola, Minna Pöyhönen, Mia Kero, Jarno Tuimala, Olli Carpén, Anu Kantele, Olli Vapalahti, Marjaana Tiainen, Pentti J. Tienari, Kai Kaila, Johanna Hästbacka, Liisa Myllykangas

    Published 2021-12-01
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  19. 19
    Deep learning of left atrial structure and function provides link to atrial fibrillation risk

    Deep learning of left atrial structure and function provides link to atrial fibrillation risk by James P. Pirruccello, Paolo Di Achille, Seung Hoan Choi, Joel T. Rämö, Shaan Khurshid, Mahan Nekoui, Sean J. Jurgens, Victor Nauffal, Shinwan Kany, FinnGen, Kenney Ng, Samuel F. Friedman, Puneet Batra, Kathryn L. Lunetta, Aarno Palotie, Anthony A. Philippakis, Jennifer E. Ho, Steven A. Lubitz, Patrick T. Ellinor

    Published 2024-05-01
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  20. 20
    A FinnGen pilot clinical recall study for Alzheimer’s disease

    A FinnGen pilot clinical recall study for Alzheimer’s disease by Valtteri Julkunen, Claudia Schwarz, Juho Kalapudas, Merja Hallikainen, Aino-Kaisa Piironen, Arto Mannermaa, Hanna Kujala, Timo Laitinen, Veli-Matti Kosma, Teemu I. Paajanen, Reetta Kälviäinen, Mikko Hiltunen, Sanna-Kaisa Herukka, Sari Kärkkäinen, Tarja Kokkola, Mia Urjansson, FinnGen, Markus Perola, Aarno Palotie, Eero Vuoksimaa, Heiko Runz

    Published 2023-08-01
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