Works by Almgren, Peter

Results: 89
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    Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.

    Published in:
    European Heart Journal, 2012, v. 33, n. 18, p. 2331, doi. 10.1093/eurheartj/ehs058
    By:
    • Fedorowski, Artur;
    • Franceschini, Nora;
    • Brody, Jennifer;
    • Liu, Chunyu;
    • Verwoert, Germaine C.;
    • Boerwinkle, Eric;
    • Couper, David;
    • Rice, Kenneth M.;
    • Rotter, Jerome I.;
    • Mattace-Raso, Francesco;
    • Uitterlinden, Andre;
    • Hofman, Albert;
    • Almgren, Peter;
    • Sjögren, Marketa;
    • Hedblad, Bo;
    • Larson, Martin G.;
    • Newton-Cheh, Christopher;
    • Wang, Thomas J.;
    • Rose, Kathryn M.;
    • Psaty, Bruce M.
    Publication type:
    Article
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    Genetic Prediction of Future Type 2 Diabetes.

    Published in:
    PLoS Medicine, 2005, v. 2, n. 12, p. e345, doi. 10.1371/journal.pmed.0020345
    By:
    • Lyssenko, Valeriya;
    • Almgren, Peter;
    • Anevski, Dragi;
    • Orho-Melander, Marju;
    • Sjögren, Marketa;
    • Saloranta, Carola;
    • Tuomi, Tiinamaija;
    • Groop, Leif
    Publication type:
    Article
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    309 Tralokinumab demonstrated a consistent safety profile with up to 42 months of treatment in moderate-to-severe atopic dermatitis: including adverse events of special interest.

    Published in:
    British Journal of Dermatology, 2023, v. 188, p. ii6, doi. 10.1093/bjd/ljac140.009
    By:
    • Reich, Kristian;
    • Simpson, Eric;
    • Langley, Richard;
    • Warren, Richard B;
    • Costanzo, Antonio;
    • Hidehisa Saeki;
    • Almgren, Peter;
    • Gjerum, Le;
    • Carlsson, Anna;
    • Gooderham, Melinda;
    • Pinter, Andreas;
    • De Bruin Weller, Marjolein;
    • Blauvelt, Andrew
    Publication type:
    Article
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    A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia.

    Published in:
    Human Molecular Genetics, 2018, v. 27, n. 10, p. 1809, doi. 10.1093/hmg/ddy094
    By:
    • Xu Chen;
    • Gustafsson, Stefan;
    • Whitington, Thomas;
    • Borné, Yan;
    • Lorentzen, Erik;
    • Jitong Sun;
    • Almgren, Peter;
    • Jun Su;
    • Karlsson, Robert;
    • Jie Song;
    • Yi Lu;
    • Yiqiang Zhan;
    • Hägg, Sara;
    • Svensson, Per;
    • Smedby, Karin E.;
    • Slager, Susan L.;
    • Ingelsson, Erik;
    • Lindgren, Cecilia M.;
    • Morris, Andrew P.;
    • Melander, Olle
    Publication type:
    Article
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    Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality: a prospective study.

    Published in:
    Diabetologia, 2020, v. 63, n. 5, p. 1043, doi. 10.1007/s00125-020-05093-9
    By:
    • Jujić, Amra;
    • Atabaki-Pasdar, Naeimeh;
    • Nilsson, Peter M.;
    • Almgren, Peter;
    • Hakaste, Liisa;
    • Tuomi, Tiinamaija;
    • Berglund, Lisa M.;
    • Franks, Paul W.;
    • Holst, Jens J.;
    • Prasad, Rashmi B.;
    • Torekov, Signe S.;
    • Ravassa, Susana;
    • Díez, Javier;
    • Persson, Margaretha;
    • Melander, Olle;
    • Gomez, Maria F.;
    • Groop, Leif;
    • Ahlqvist, Emma;
    • Magnusson, Martin
    Publication type:
    Article
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    A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.

    Published in:
    Diabetologia, 2019, v. 62, n. 2, p. 292, doi. 10.1007/s00125-018-4783-z
    By:
    • Ahluwalia, Tarunveer S.;
    • Schulz, Christina-Alexandra;
    • Waage, Johannes;
    • Skaaby, Tea;
    • Sandholm, Niina;
    • van Zuydam, Natalie;
    • Charmet, Romain;
    • Bork-Jensen, Jette;
    • Almgren, Peter;
    • Thuesen, Betina H.;
    • Bedin, Mathilda;
    • Brandslund, Ivan;
    • Christensen, Cramer K.;
    • Linneberg, Allan;
    • Ahlqvist, Emma;
    • Groop, Per-Henrik;
    • Hadjadj, Samy;
    • Tregouet, David-Alexandre;
    • Jørgensen, Marit E.;
    • Grarup, Niels
    Publication type:
    Article
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    Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes.

    Published in:
    Diabetologia, 2016, v. 59, n. 8, p. 1702, doi. 10.1007/s00125-016-3973-9
    By:
    • Prasad, Rashmi;
    • Lessmark, Anna;
    • Almgren, Peter;
    • Kovacs, Györgyi;
    • Hansson, Ola;
    • Oskolkov, Nikolay;
    • Vitai, Marta;
    • Ladenvall, Claes;
    • Kovacs, Peter;
    • Fadista, Joao;
    • Lachmann, Michael;
    • Zhou, Yuedan;
    • Sonestedt, Emily;
    • Poon, Wenny;
    • Wollheim, Claes;
    • Orho-Melander, Marju;
    • Stumvoll, Michael;
    • Tuomi, Tiinamaija;
    • Pääbo, Svante;
    • Koranyi, Laszlo
    Publication type:
    Article
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    Dietary and genetic risk scores and incidence of type 2 diabetes.

    Published in:
    Genes & Nutrition, 2018, v. 13, n. 1, p. N.PAG, doi. 10.1186/s12263-018-0599-1
    By:
    • Ericson, Ulrika;
    • Hindy, George;
    • Drake, Isabel;
    • Schulz, Christina-Alexandra;
    • Brunkwall, Louise;
    • Hellstrand, Sophie;
    • Almgren, Peter;
    • Orho-Melander, Marju
    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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    The genomics of heart failure: design and rationale of the HERMES consortium.

    Published in:
    ESC Heart Failure, 2021, v. 8, n. 6, p. 5531, doi. 10.1002/ehf2.13517
    By:
    • Lumbers, R. Thomas;
    • Shah, Sonia;
    • Lin, Honghuang;
    • Czuba, Tomasz;
    • Henry, Albert;
    • Swerdlow, Daniel I.;
    • Mälarstig, Anders;
    • Andersson, Charlotte;
    • Verweij, Niek;
    • Holmes, Michael V.;
    • Ärnlöv, Johan;
    • Svensson, Per;
    • Hemingway, Harry;
    • Sallah, Neneh;
    • Almgren, Peter;
    • Aragam, Krishna G.;
    • Asselin, Geraldine;
    • Backman, Joshua D.;
    • Biggs, Mary L.;
    • Bloom, Heather L.
    Publication type:
    Article
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    Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 23, p. 4662, doi. 10.1093/hmg/ddp423
    By:
    • Tönjes, Anke;
    • Koriath, Moritz;
    • Schleinitz, Dorit;
    • Dietrich, Kerstin;
    • Böttcher, Yvonne;
    • Rayner, Nigel W.;
    • Almgren, Peter;
    • Enigk, Beate;
    • Richter, Olaf;
    • Rohm, Silvio;
    • Fischer-Rosinsky, Antje;
    • Pfeiffer, Andreas;
    • Hoffmann, Katrin;
    • Krohn, Knut;
    • Aust, Gabriela;
    • Spranger, Joachim;
    • Groop, Leif;
    • Blüher, Matthias;
    • Kovacs, Peter;
    • Stumvoll, Michael
    Publication type:
    Article
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    Apolipoproteins, lipids and risk of cancer.

    Published in:
    International Journal of Cancer, 2016, v. 138, n. 11, p. 2648, doi. 10.1002/ijc.30013
    By:
    • Borgquist, Signe;
    • Butt, Talha;
    • Almgren, Peter;
    • Shiffman, Dov;
    • Stocks, Tanja;
    • Orho‐Melander, Marju;
    • Manjer, Jonas;
    • Melander, Olle
    Publication type:
    Article
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    Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-13690-5
    By:
    • Shah, Sonia;
    • Henry, Albert;
    • Roselli, Carolina;
    • Lin, Honghuang;
    • Sveinbjörnsson, Garðar;
    • Fatemifar, Ghazaleh;
    • Hedman, Åsa K.;
    • Wilk, Jemma B.;
    • Morley, Michael P.;
    • Chaffin, Mark D.;
    • Helgadottir, Anna;
    • Verweij, Niek;
    • Dehghan, Abbas;
    • Almgren, Peter;
    • Andersson, Charlotte;
    • Aragam, Krishna G.;
    • Ärnlöv, Johan;
    • Backman, Joshua D.;
    • Biggs, Mary L.;
    • Bloom, Heather L.
    Publication type:
    Article
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    Common Genetic Determinants of Lung Function, Subclinical Atherosclerosis and Risk of Coronary Artery Disease.

    Published in:
    PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104082
    By:
    • Sabater-Lleal, Maria;
    • Mälarstig, Anders;
    • Folkersen, Lasse;
    • Soler Artigas, María;
    • Baldassarre, Damiano;
    • Kavousi, Maryam;
    • Almgren, Peter;
    • Veglia, Fabrizio;
    • Brusselle, Guy;
    • Hofman, Albert;
    • Engström, Gunnar;
    • Franco, Oscar H.;
    • Melander, Olle;
    • Paulsson-Berne, Gabrielle;
    • Watkins, Hugh;
    • Eriksson, Per;
    • Humphries, Steve E.;
    • Tremoli, Elena;
    • de Faire, Ulf;
    • Tobin, Martin D.
    Publication type:
    Article
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    Plasma Lipid Composition and Risk of Developing Cardiovascular Disease.

    Published in:
    PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071846
    By:
    • Fernandez, Celine;
    • Sandin, Marianne;
    • Sampaio, Julio L.;
    • Almgren, Peter;
    • Narkiewicz, Krzysztof;
    • Hoffmann, Michal;
    • Hedner, Thomas;
    • Wahlstrand, Björn;
    • Simons, Kai;
    • Shevchenko, Andrej;
    • James, Peter;
    • Melander, Olle
    Publication type:
    Article
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    A Central Role for <i>GRB10</i> in Regulation of Islet Function in Man.

    Published in:
    PLoS Genetics, 2014, v. 10, n. 4, p. 1, doi. 10.1371/journal.pgen.1004235
    By:
    • Prokopenko, Inga;
    • Poon, Wenny;
    • Mägi, Reedik;
    • Prasad B, Rashmi;
    • Salehi, S. Albert;
    • Almgren, Peter;
    • Osmark, Peter;
    • Bouatia-Naji, Nabila;
    • Wierup, Nils;
    • Fall, Tove;
    • Stančáková, Alena;
    • Barker, Adam;
    • Lagou, Vasiliki;
    • Osmond, Clive;
    • Xie, Weijia;
    • Lahti, Jari;
    • Jackson, Anne U.;
    • Cheng, Yu-Ching;
    • Liu, Jie;
    • O'Connell, Jeffrey R.
    Publication type:
    Article
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    Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases.

    Published in:
    PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002741
    By:
    • Perry, John R. B.;
    • Voight, Benjamin F.;
    • Yengo, Loïc;
    • Amin, Najaf;
    • Dupuis, Josée;
    • Ganser, Martha;
    • Grallert, Harald;
    • Navarro, Pau;
    • Man Li;
    • Lu Qi;
    • Steinthorsdottir, Valgerdur;
    • Scott, Robert A.;
    • Almgren, Peter;
    • Arking, Dan E.;
    • Aulchenko, Yurii;
    • Balkau, Beverley;
    • Benediktsson, Rafn;
    • Bergman, Richard N.;
    • Boerwinkle, Eric;
    • Bonnycastle, Lori
    Publication type:
    Article
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