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
Showing 1 - 10 results of 10 for search 'FinnGen', query time: 0.03s Refine Results
  1. 1
    Chromatin state origins of uterine leiomyoma

    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 2025-05-01
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  2. 2
    Cross‐sectional study of plasma phosphorylated tau 217 in persons without dementia

    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

    Published 2025-04-01
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  3. 3
    Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations

    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 2024-11-01
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  4. 4
    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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  5. 5
    Loss of CFHR5 function reduces the risk for age-related macular degeneration

    Loss of CFHR5 function reduces the risk for age-related macular degeneration by Mary Pat Reeve, Stephanie Loomis, Eija Nissilä, Thomas W. Soare, Tobias Rausch, Zhili Zheng, Pietro DELLA BRIOTTA PAROLO, Daniel Ben-Isvy, Elias Aho, Emilia Cesetti, Yoko Okunuki, Helen McLaughlin, Johanna Mäkelä, FinnGen, Mitja Kurki, Michael E. Talkowski, Jan O. Korbel, Kip Connor, Seppo Meri, Mark J. Daly, Heiko Runz

    Published 2025-07-01
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  6. 6
    Genome-wide association study of pulpal and apical diseases

    Genome-wide association study of pulpal and apical diseases by Aino Salminen, Kati Hyvärinen, Jarmo Ritari, Jussi M. Leppilahti, Ulla Palotie, Ville Vuollo, Oleg Kambur, FinnGen, Estonian Biobank Research Team, Kadri Reis, Anu Reigo, Priit Palta, Markus Perola, Juha Sinisalo, Aki S. Havulinna, Päivi Mäntylä, Ulvi Kahraman Gürsoy, A. Liisa Suominen, David P. Rice, Vuokko Anttonen, Pekka Nieminen, Pirkko J. Pussinen

    Published 2025-07-01
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  7. 7
    Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study

    Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study by Joel Räsänen, Seppo Helisalmi, Sami Heikkinen, Joose Raivo, Ville E. Korhonen, Henna Martiskainen, Antti Junkkari, Benjamin Grenier-Boley, Céline Bellenguez, Minna Oinas, Cecilia Avellan, Janek Frantzen, Anna Kotkansalo, Jaakko Rinne, Antti Ronkainen, Mikko Kauppinen, Mikael von und zu Fraunberg, Kimmo Lönnrot, Jarno Satopää, Markus Perola, Anne M. Koivisto, Valtteri Julkunen, Anne M. Portaankorva, Arto Mannermaa, Hilkka Soininen, Juha E. Jääskeläinen, Jean-Charles Lambert, Per K. Eide, FinnGen, Aarno Palotie, Mitja I. Kurki, Mikko Hiltunen, Ville Leinonen, Anssi Lipponen

    Published 2025-02-01
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  8. 8
    Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease

    Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease by Henna Martiskainen, Roosa-Maria Willman, Päivi Harju, Sami Heikkinen, Mette Heiskanen, Stephan A. Müller, Rosa Sinisalo, Mari Takalo, Petra Mäkinen, Teemu Kuulasmaa, Viivi Pekkala, Ana Galván del Rey, Sini-Pauliina Juopperi, Heli Jeskanen, Inka Kervinen, Kirsi Saastamoinen, FinnGen, Marja Niiranen, Sami V. Heikkinen, Mitja I. Kurki, Jarkko Marttila, Petri I. Mäkinen, Hannah Rostalski, Tomi Hietanen, Tiia Ngandu, Jenni Lehtisalo, Céline Bellenguez, Jean-Charles Lambert, Christian Haass, Juha Rinne, Juhana Hakumäki, Tuomas Rauramaa, Johanna Krüger, Hilkka Soininen, Annakaisa Haapasalo, Stefan F. Lichtenthaler, Ville Leinonen, Eino Solje, Mikko Hiltunen

    Published 2025-04-01
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  9. 9
    Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma

    Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma by Joel T. Rämö, Bryan R. Gorman, Lu-Chen Weng, Sean J. Jurgens, Panisa Singhanetr, Marisa G. Tieger, Elon HC van Dijk, Christopher W. Halladay, Xin Wang, Blake M. Hauser, Soo Hyun Kim, Joost Brinks, Seung Hoan Choi, Yuyang Luo, FinnGen, VA Million Veteran Program, Saiju Pyarajan, Cari L. Nealon, Michael B. Gorin, Wen-Chih Wu, Scott A. Anthony, David P. Roncone, Lucia Sobrin, Kai Kaarniranta, Suzanne Yzer, Aarno Palotie, Neal S. Peachey, Joni A. Turunen, Camiel JF Boon, Patrick T. Ellinor, Sudha K. Iyengar, Mark J. Daly, Elizabeth J. Rossin

    Published 2025-05-01
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  10. 10
    Novel loci and biomedical consequences of iron homoeostasis variation

    Novel loci and biomedical consequences of iron homoeostasis variation by Elias Allara, Steven Bell, Rebecca Smith, Spencer J. Keene, Dipender Gill, Liam Gaziano, Deisy Morselli Gysi, Feiyi Wang, Vinicius Tragante, Amy Mason, Savita Karthikeyan, R. Thomas Lumbers, Emmanuela Bonglack, Willem Ouwehand, David J. Roberts, Joseph Dowsett, Sisse Rye Ostrowski, Margit Hørup Larsen, Henrik Ullum, Ole Birger Pedersen, Søren Brunak, Karina Banasik, Christian Erikstrup, DBDS Genomic Consortium, Jonathan Mitchell, Christian Fuchsberger, Cristian Pattaro, Peter P. Pramstaller, Domenico Girelli, Mikko Arvas, Jarkko Toivonen, Sophie Molnos, Annette Peters, Ozren Polasek, Igor Rudan, Caroline Hayward, Ciara McDonnell, Nicola Pirastu, James F. Wilson, Katja van den Hurk, Franke Quee, Luigi Ferrucci, Stefania Bandinelli, Toshiko Tanaka, Giorgia Girotto, Maria Pina Concas, Alessandro Pecori, Niek Verweij, Pim van der Harst, Yordi J. van de Vegte, Lambertus A. Kiemeney, Fred C. Sweep, Tessel E. Galesloot, Patrick Sulem, Daniel Gudbjartsson, Egil Ferkingstad, FinnGen Consortium, Luc Djousse, Kelly Cho, Michael Inouye, Stephen Burgess, Beben Benyamin, Konrad Oexle, Dorine Swinkels, Kari Stefansson, Magnus Magnusson, Andrea Ganna, Michael Gaziano, Kerry Ivey, John Danesh, Alexandre Pereira, Angela M. Wood, Adam S. Butterworth, Emanuele Di Angelantonio

    Published 2024-12-01
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