Výsledky vyhledávání - FinnGen

Cost-effective non-additive GWAS across 2329 diseases in 500,349 individuals Autor Ivan Molotkov, Mitja Kurki, FinnGen, Aarno Palotie, Mark J. Daly, Mykyta Artomov

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Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants Autor Heidi Hautakangas, Joonas Kartau, FinnGen, Aarno Palotie, Matti Pirinen, International Headache Genetics Consortium

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

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Large language models improve transferability of electronic health record-based predictions across countries and coding systems Autor Matthias Kirchler, Matteo Ferro, Veronica Lorenzini, Robin P. van de Water, FinnGen, Christoph Lippert, Andrea Ganna

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

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The genetic basis of dermatophytosis skin infection susceptibility Autor Hele Haapaniemi, Reyhane Eghtedarian, Anniina Tervi, Jesse Valliere, Estonian Biobank Research Team, FinnGen, Erik Abner, Hanna M. Ollila

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Genetic validation of ABI3 p.Ser209Phe variant and its effects on early brain pathology in asymptomatic elderly individuals Autor Mikko Koivumäki, Henna Martiskainen, Mari Takalo, Jenni Lehtisalo, Tiia Ngandu, FinnGen, Anniina Snellman, Mikko Hiltunen, Juha O. Rinne

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

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Mechanisms of thyrotropin receptor–mediated phenotype variability deciphered by gene mutations and M453T-knockin model Autor 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

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131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma Autor Elmo C. Saarentaus, Kasper Fischer-Rasmussen, Eeva Sliz, Argyro Bizaki-Vallaskangas, FinnGen, Tarja Laitinen, Sanna Toppila-Salmi, Hannu Kankaanranta, Johannes Kettunen, Klaus Bønnelykke, Aarno Palotie, Antti Mäkitie

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Chromatin state origins of uterine leiomyoma Autor 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

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Protective PLCG2 variants associate with a delayed onset of Alzheimer’s disease among heterozygous APOE ε4 carriers Autor Heli Jeskanen, Sami Heikkinen, Inka Kervinen, Jenni Lehtisalo, Tiia Ngandu, Roosa-Maria Willman, Jessica Rosa, Dorit Hoffmann, FinnGen, Ville Leinonen, Annakaisa Haapasalo, Mari Takalo, Henna Martiskainen, Mikko Hiltunen

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Cross‐sectional study of plasma phosphorylated tau 217 in persons without dementia Autor 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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Leveraging large-scale multi-omics evidences to identify therapeutic targets from genome-wide association studies Autor 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

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Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations Autor 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

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Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Autor 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

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Socio-demographic and genetic risk factors for drug adherence and persistence across 5 common medication classes Autor 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

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Blood donor biobank pipeline to collect genome-based samples for research Autor Jarno Honkanen, Veera A. Timonen, Jessica R. Koski, Julianna Juvila, Mikko Arvas, Blood Service Biobank, FinnGen, Linnea Hartwall, Outi Kilpivaara, Rodosthenis S. Rodosthenous, Ulla Wartiovaara-Kautto, Arja Vuorela, Mark Daly, Aarno Palotie, Esa Pitkänen, Jukka Partanen

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Genetic architecture of lumbar spinal stenosis Autor Ville Salo, Juhani Määttä, Jasmin Takala, Anni Heikkilä, FinnGen, Ene Reimann, Reedik Mägi, Estonian Biobank Research Team, Kadri Reis, Abdelrahman G. Elhanas, Anu Reigo, Priit Palta, Tõnu Esko, Ville Leinonen, Jaro Karppinen, Eeva Sliz, Johannes Kettunen

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Complex genetic effects linked to plasma protein abundance in the UK Biobank Autor Arnor I. Sigurdsson, Justus F. Gräf, Zhiyu Yang, Kirstine Ravn, Jonas Meisner, Roman Thielemann, Henry Webel, Roelof A. J. Smit, Lili Niu, Matthias Mann, FinnGen, Bjarni Vilhjalmsson, Benjamin M. Neale, Jens-Christian Holm, Andrea Ganna, Torben Hansen, Ruth J. F. Loos, Simon Rasmussen

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