Works matching AU Palotie, Aarno

Results: 145
    1

    Cross‐sectional study of plasma phosphorylated tau 217 in persons without dementia.

    Published in:
    Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2025, v. 17, n. 2, p. 1, doi. 10.1002/dad2.70107
    By:
    • Saari, Toni T.;
    • Palviainen, Teemu;
    • Hiltunen, Mikko;
    • Herukka, Sanna‐Kaisa;
    • Kokkola, Tarja;
    • Kärkkäinen, Sari;
    • Urjansson, Mia;
    • Aaltonen, Aino;
    • Palotie, Aarno;
    • Runz, Heiko;
    • Kaprio, Jaakko;
    • Julkunen, Valtteri;
    • Vuoksimaa, Eero
    Publication type:
    Article
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    Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes.

    Published in:
    Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-021-02996-0
    By:
    • Tamlander, Max;
    • Mars, Nina;
    • Pirinen, Matti;
    • FinnGen;
    • Steering Committee;
    • Palotie, Aarno;
    • Daly, Mark;
    • Pharmaceutical companies;
    • Riley-Gills, Bridget;
    • Jacob, Howard;
    • Paul, Dirk;
    • Runz, Heiko;
    • John, Sally;
    • Plenge, Robert;
    • Maranville, Joseph;
    • Okafo, George;
    • Lawless, Nathan;
    • Salminen-Mankonen, Heli;
    • McCarthy, Mark;
    • Hunkapiller, Julie
    Publication type:
    Article
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    NordicDB: a Nordic pool and portal for genome-wide control data.

    Published in:
    European Journal of Human Genetics, 2010, v. 18, n. 12, p. 1322, doi. 10.1038/ejhg.2010.112
    By:
    • Leu, Monica;
    • Humphreys, Keith;
    • Surakka, Ida;
    • Rehnberg, Emil;
    • Juha Muilu;
    • Rosenström, Päivi;
    • Almgren, Peter;
    • Jääskeläinen, Juha;
    • Lifton, Richard P.;
    • Kyvik, Kirsten Ohm;
    • Kaprio, Jaakko;
    • Pedersen, Nancy L.;
    • Palotie, Aarno;
    • Hall, Per;
    • Grönberg, Henrik;
    • Groop, Leif;
    • Peltonen, Leena;
    • Palmgren, Juni;
    • Ripatti, Samuli
    Publication type:
    Article
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    MYO9B polymorphisms in multiple sclerosis.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 6, p. 840, doi. 10.1038/ejhg.2008.251
    By:
    • Kemppinen, Anu;
    • Suvela, Minna;
    • Tienari, Pentti J.;
    • Elovaara, Irina;
    • Koivisto, Keijo;
    • Pirttilä, Tuula;
    • Reunanen, Mauri;
    • Rautakorpi, Ilkka;
    • Hillert, Jan;
    • Lundmark, Frida;
    • Oturai, Annette;
    • Ryder, Lars;
    • Harbo, Hanne F.;
    • Celius, Elisabeth G.;
    • Palotie, Aarno;
    • Daly, Mark;
    • Peltonen, Leena;
    • Saarela, Janna
    Publication type:
    Article
    7

    Evaluation of HapMap data in six populations of European descent.

    Published in:
    European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1142, doi. 10.1038/ejhg.2008.77
    By:
    • Lundmark, Per E.;
    • Liljedahl, Ulrika;
    • Boomsma, Dorret I.;
    • Mannila, Heikki;
    • Martin, Nicholas G.;
    • Palotie, Aarno;
    • Peltonen, Leena;
    • Perola, Markus;
    • Spector, Tim D.;
    • Syvänen, Ann-Christine
    Publication type:
    Article
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    Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth.

    Published in:
    BMC Medical Genomics, 2010, v. 3, p. 62, doi. 10.1186/1755-8794-3-62
    By:
    • Plunkett, Jevon;
    • Doniger, Scott;
    • Morgan, Thomas;
    • Haataja, Ritva;
    • Hallman, Mikko;
    • Puttonen, Hilkka;
    • Menon, Ramkumar;
    • Kuczynski, Edward;
    • Norwitz, Errol;
    • Snegovskikh, Victoria;
    • Palotie, Aarno;
    • Peltonen, Leena;
    • Fellman, Vineta;
    • DeFranco, Emily A.;
    • Chaudhari, Bimal P.;
    • Oates, John;
    • Boutaud, Olivier;
    • McGregor, Tracy L.;
    • McElroy, Jude J.;
    • Teramo, Kari
    Publication type:
    Article
    13

    A framework for the interpretation of de novo mutation in human disease.

    Published in:
    Nature Genetics, 2014, v. 46, n. 9, p. 944, doi. 10.1038/ng.3050
    By:
    • Samocha, Kaitlin E;
    • Robinson, Elise B;
    • Sanders, Stephan J;
    • Stevens, Christine;
    • Sabo, Aniko;
    • McGrath, Lauren M;
    • Kosmicki, Jack A;
    • Rehnström, Karola;
    • Mallick, Swapan;
    • Kirby, Andrew;
    • Wall, Dennis P;
    • MacArthur, Daniel G;
    • Gabriel, Stacey B;
    • DePristo, Mark;
    • Purcell, Shaun M;
    • Palotie, Aarno;
    • Boerwinkle, Eric;
    • Buxbaum, Joseph D;
    • Cook, Edwin H;
    • Gibbs, Richard A
    Publication type:
    Article
    14

    Genome-wide association study reveals three susceptibility loci for common migraine in the general population.

    Published in:
    Nature Genetics, 2011, v. 43, n. 7, p. 695, doi. 10.1038/ng.856
    By:
    • Chasman, Daniel I.;
    • Schürks, Markus;
    • Anttila, Verneri;
    • de Vries, Boukje;
    • Schminke, Ulf;
    • Launer, Lenore J.;
    • Terwindt, Gisela M.;
    • van den Maagdenberg, Arn M. J. M.;
    • Fendrich, Konstanze;
    • Völzke, Henry;
    • Ernst, Florian;
    • Griffiths, Lyn R.;
    • Buring, Julie E.;
    • Kallela, Mikko;
    • Freilinger, Tobias;
    • Kubisch, Christian;
    • Ridker, Paul M.;
    • Palotie, Aarno;
    • Ferrari, Michel D.;
    • Hoffmann, Wolfgang
    Publication type:
    Article
    15

    Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.

    Published in:
    Nature Genetics, 2009, v. 41, n. 12, p. 1341, doi. 10.1038/ng.490
    By:
    • McCarroll, Steven A.;
    • Bradner, James E.;
    • Turpeinen, Hannu;
    • Volin, Liisa;
    • Martin, Paul J.;
    • Chilewski, Shannon D.;
    • Antin, Joseph H.;
    • Lee, Stephanie J.;
    • Ruutu, Tapani;
    • Storer, Barry;
    • Warren, Edus H.;
    • Bo Zhang;
    • Lue Ping Zhao;
    • Ginsburg, David;
    • Soiffer, Robert J.;
    • Partanen, Jukka;
    • Hansen, John A.;
    • Ritz, Jerome;
    • Palotie, Aarno;
    • Altshuler, David
    Publication type:
    Article
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    Substance Use and Sleep Problems in Patients With Psychotic Disorders.

    Published in:
    Schizophrenia Bulletin Open, 2023, v. 4, n. 1, p. 1, doi. 10.1093/schizbullopen/sgac073
    By:
    • Cederlöf, Erik;
    • Holm, Minna;
    • Ahti, Johan;
    • Lähteenvuo, Markku;
    • Hietala, Jarmo;
    • Häkkinen, Katja;
    • Isometsä, Erkki;
    • Kampman, Olli;
    • Lahdensuo, Kaisla;
    • Lönnqvist, Jouko;
    • Suvisaari, Jaana;
    • Tiihonen, Jari;
    • Wegelius, Asko;
    • Veijola, Juha;
    • Palotie, Aarno;
    • Kieseppä, Tuula;
    • Niemelä, Solja;
    • Paunio, Tiina
    Publication type:
    Article
    21

    A Genome-Wide Association Study of Monozygotic Twin-Pairs Suggests a Locus Related to Variability of Serum High-Density Lipoprotein Cholesterol.

    Published in:
    Twin Research & Human Genetics, 2012, v. 15, n. 6, p. 691, doi. 10.1017/thg.2012.63
    By:
    • Surakka, Ida;
    • Whitfield, John B.;
    • Perola, Markus;
    • Visscher, Peter M.;
    • Montgomery, Grant W.;
    • Falchi, Mario;
    • Willemsen, Gonneke;
    • de Geus, Eco J. C.;
    • Magnusson, Patrik K. E.;
    • Christensen, Kaare;
    • Sørensen, Thorkild I. A.;
    • Pietiläinen, Kirsi H.;
    • Rantanen, Taina;
    • Silander, Kaisa;
    • Widén, Elisabeth;
    • Muilu, Juha;
    • Rahman, Iffat;
    • Liljedahl, Ulrika;
    • Syvänen, Ann-Christine;
    • Palotie, Aarno
    Publication type:
    Article
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    Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30921-4
    By:
    • Fadista, João;
    • Skotte, Line;
    • Karjalainen, Juha;
    • Abner, Erik;
    • Sørensen, Erik;
    • Ullum, Henrik;
    • Werge, Thomas;
    • iPSYCH Group;
    • Hougaard, David M.;
    • Børglum, Anders D.;
    • Nordentoft, Merete;
    • Mortensen, Preben B.;
    • Esko, Tõnu;
    • Milani, Lili;
    • Palotie, Aarno;
    • Daly, Mark;
    • Melbye, Mads;
    • Feenstra, Bjarke;
    • Geller, Frank
    Publication type:
    Article
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    High prevalence of four long QT syndrome founder mutations in the Finnish population.

    Published in:
    Annals of Medicine, 2009, v. 41, n. 3, p. 234, doi. 10.1080/07853890802668530
    By:
    • Marjamaa, Annukka;
    • Salomaa, Veikko;
    • Newton-Cheh, Christopher;
    • Porthan, Kimmo;
    • Reunanen, Antti;
    • Karanko, Hannu;
    • Jula, Antti;
    • Lahermo, Päivi;
    • Väänänen, Heikki;
    • Toivonen, Lauri;
    • Swan, Heikki;
    • Viitasalo, Matti;
    • Nieminen, Markku S.;
    • Peltonen, Leena;
    • Oikarinen, Lasse;
    • Palotie, Aarno;
    • Kontula, Kimmo
    Publication type:
    Article
    26

    The molecular genetics of migraine.

    Published in:
    Annals of Medicine, 2004, v. 36, n. 6, p. 462, doi. 10.1080/07853890410018060
    By:
    • Wessman, Maija;
    • Kaunisto, Mari;
    • Kallela, Mikko;
    • Palotie, Aarno
    Publication type:
    Article
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    Metabonomic, transcriptomic, and genomic variation of a population cohort.

    Published in:
    Molecular Systems Biology, 2010, v. 6, n. 1, p. 441, doi. 10.1038/msb.2010.93
    By:
    • Inouye, Michael;
    • Kettunen, Johannes;
    • Soininen, Pasi;
    • Silander, Kaisa;
    • Ripatti, Samuli;
    • Kumpula, Linda S;
    • Hämäläinen, Eija;
    • Jousilahti, Pekka;
    • Kangas, Antti J;
    • Männistö, Satu;
    • Savolainen, Markku J;
    • Jula, Antti;
    • Leiviskä, Jaana;
    • Palotie, Aarno;
    • Salomaa, Veikko;
    • Perola, Markus;
    • Ala‐Korpela, Mika;
    • Peltonen, Leena
    Publication type:
    Article
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    Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons.

    Published in:
    PLoS Medicine, 2014, v. 11, n. 2, p. 1, doi. 10.1371/journal.pmed.1001606
    By:
    • Fischer, Krista;
    • Kettunen, Johannes;
    • Würtz, Peter;
    • Haller, Toomas;
    • Havulinna, Aki S.;
    • Kangas, Antti J.;
    • Soininen, Pasi;
    • Esko, Tõnu;
    • Tammesoo, Mari-Liis;
    • Mägi, Reedik;
    • Smit, Steven;
    • Palotie, Aarno;
    • Ripatti, Samuli;
    • Salomaa, Veikko;
    • Ala-Korpela, Mika;
    • Perola, Markus;
    • Metspalu, Andres
    Publication type:
    Article
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    NTHL1 is a recessive cancer susceptibility gene.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-47441-w
    By:
    • Nurmi, Anna K.;
    • Pelttari, Liisa M.;
    • Kiiski, Johanna I.;
    • Khan, Sofia;
    • Nurmikolu, Mika;
    • Suvanto, Maija;
    • Aho, Niina;
    • Tasmuth, Tiina;
    • Kalso, Eija;
    • Schleutker, Johanna;
    • Kallioniemi, Anne;
    • Heikkilä, Päivi;
    • FinnGen;
    • Palotie, Aarno;
    • Daly, Mark;
    • Riley-Gillis, Bridget;
    • Jacob, Howard;
    • Paul, Dirk;
    • Petrovski, Slavé;
    • Runz, Heiko
    Publication type:
    Article
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    Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 11, p. 2349, doi. 10.1093/hmg/ddw087
    By:
    • Orlando, Giulia;
    • Law, Philip J.;
    • Palin, Kimmo;
    • Tuupanen, Sari;
    • Gylfe, Alexandra;
    • Hänninen, Ulrika;
    • Cajuso, Tatiana;
    • Tanskanen, Tomas;
    • Kondelin, Johanna;
    • Kaasinen, Eevi;
    • Sarin, Antti-Pekka;
    • Kaprio, Jaakko;
    • Eriksson, Johan G.;
    • Rissanen, Harri;
    • Knekt, Paul;
    • Pukkala, Eero;
    • Jousilahti, Pekka;
    • Salomaa, Veikko;
    • Ripatti, Samuli;
    • Palotie, Aarno
    Publication type:
    Article
    41

    Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-35974-7
    By:
    • Sliz, Eeva;
    • Tyrmi, Jaakko S.;
    • Rahmioglu, Nilufer;
    • Zondervan, Krina T.;
    • Becker, Christian M.;
    • FinnGen;
    • Palotie, Aarno;
    • Daly, Mark;
    • Riley-Gills, Bridget;
    • Jacob, Howard;
    • Paul, Dirk;
    • Matakidou, Athena;
    • Platt, Adam;
    • Runz, Heiko;
    • John, Sally;
    • Okafo, George;
    • Lawless, Nathan;
    • Salminen-Mankonen, Heli;
    • Plenge, Robert;
    • Maranville, Joseph
    Publication type:
    Article
    42

    Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata.

    Published in:
    Nature Communications, 2023, v. 14, p. 1, doi. 10.1038/s41467-023-35974-7
    By:
    • Sliz, Eeva;
    • Tyrmi, Jaakko S.;
    • Rahmioglu, Nilufer;
    • Zondervan, Krina T.;
    • Becker, Christian M.;
    • FinnGen;
    • Palotie, Aarno;
    • Daly, Mark;
    • Riley-Gills, Bridget;
    • Jacob, Howard;
    • Paul, Dirk;
    • Matakidou, Athena;
    • Platt, Adam;
    • Runz, Heiko;
    • John, Sally;
    • Okafo, George;
    • Lawless, Nathan;
    • Salminen-Mankonen, Heli;
    • Plenge, Robert;
    • Maranville, Joseph
    Publication type:
    Article
    43

    Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-33626-w
    By:
    • Saarentaus, Elmo C.;
    • Karjalainen, Juha;
    • Rämö, Joel T.;
    • Kiiskinen, Tuomo;
    • Havulinna, Aki S.;
    • Mehtonen, Juha;
    • Hautakangas, Heidi;
    • Ruotsalainen, Sanni;
    • Tamlander, Max;
    • Mars, Nina;
    • Toppila-Salmi, Sanna;
    • Pirinen, Matti;
    • Kurki, Mitja;
    • Ripatti, Samuli;
    • Daly, Mark;
    • Palotie, Tuula;
    • Mäkitie, Antti;
    • Palotie, Aarno
    Publication type:
    Article
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    Polygenic burden in focal and generalized epilepsies.

    Published in:
    2019
    By:
    • Leu, Costin;
    • Stevelink, Remi;
    • Smith, Alexander W;
    • Goleva, Slavina B;
    • Kanai, Masahiro;
    • Ferguson, Lisa;
    • Campbell, Ciaran;
    • Kamatani, Yoichiro;
    • Okada, Yukinori;
    • Sisodiya, Sanjay M;
    • Cavalleri, Gianpiero L;
    • Koeleman, Bobby P C;
    • Lerche, Holger;
    • Jehi, Lara;
    • Davis, Lea K;
    • Najm, Imad M;
    • Palotie, Aarno;
    • Daly, Mark J;
    • Busch, Robyn M;
    • Consortium, Epi25
    Publication type:
    journal article
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