Works by Försti, Asta

Results: 225
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    Functional germline variants in driver genes of breast cancer.

    Published in:
    2017
    By:
    • Göhler, Stella;
    • Silva Filho, Miguel;
    • Johansson, Robert;
    • Enquist-Olsson, Kerstin;
    • Henriksson, Roger;
    • Hemminki, Kari;
    • Lenner, Per;
    • Försti, Asta;
    • Göhler, Stella;
    • Da Silva Filho, Miguel Inacio;
    • Försti, Asta
    Publication type:
    journal article
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    Association of NLRP1 Coding Polymorphism with Lung Function and Serum IL-1β Concentration in Patients Diagnosed with Chronic Obstructive Pulmonary Disease (COPD).

    Published in:
    Genes, 2019, v. 10, n. 10, p. 783, doi. 10.3390/genes10100783
    By:
    • Ozretić, Petar;
    • da Silva Filho, Miguel Inacio;
    • Catalano, Calogerina;
    • Sokolović, Irena;
    • Vukić-Dugac, Andrea;
    • Šutić, Maja;
    • Kurtović, Matea;
    • Bubanović, Gordana;
    • Popović-Grle, Sanja;
    • Skrinjarić-Cincar, Sanda;
    • Vugrek, Oliver;
    • Jukić, Irena;
    • Rumora, Lada;
    • Bosnar, Martina;
    • Samaržija, Miroslav;
    • Bals, Robert;
    • Jakopović, Marko;
    • Försti, Asta;
    • Knežević, Jelena
    Publication type:
    Article
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    Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.

    Published in:
    Nature Genetics, 2013, v. 45, n. 10, p. 1221, doi. 10.1038/ng.2733
    By:
    • Chubb, Daniel;
    • Weinhold, Niels;
    • Broderick, Peter;
    • Chen, Bowang;
    • Johnson, David C;
    • Försti, Asta;
    • Vijayakrishnan, Jayaram;
    • Migliorini, Gabriele;
    • Dobbins, Sara E;
    • Holroyd, Amy;
    • Hose, Dirk;
    • Walker, Brian A;
    • Davies, Faith E;
    • Gregory, Walter A;
    • Jackson, Graham H;
    • Irving, Julie A;
    • Pratt, Guy;
    • Fegan, Chris;
    • Fenton, James A L;
    • Neben, Kai
    Publication type:
    Article
    17

    The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.

    Published in:
    Nature Genetics, 2013, v. 45, n. 5, p. 522, doi. 10.1038/ng.2583
    By:
    • Weinhold, Niels;
    • Johnson, David C;
    • Chubb, Daniel;
    • Chen, Bowang;
    • Försti, Asta;
    • Hosking, Fay J;
    • Broderick, Peter;
    • Ma, Yussanne P;
    • Dobbins, Sara E;
    • Hose, Dirk;
    • Walker, Brian A;
    • Davies, Faith E;
    • Kaiser, Martin F;
    • Li, Ni L;
    • Gregory, Walter A;
    • Jackson, Graham H;
    • Witzens-Harig, Mathias;
    • Neben, Kai;
    • Hoffmann, Per;
    • Nöthen, Markus M
    Publication type:
    Article
    18

    Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.

    Published in:
    Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
    By:
    • Broderick, Peter;
    • Chubb, Daniel;
    • Johnson, David C;
    • Weinhold, Niels;
    • Försti, Asta;
    • Lloyd, Amy;
    • Olver, Bianca;
    • Ma, Yussanne P;
    • Dobbins, Sara E;
    • Walker, Brian A;
    • Davies, Faith E;
    • Gregory, Walter A;
    • Child, J Anthony;
    • Ross, Fiona M;
    • Jackson, Graham H;
    • Neben, Kai;
    • Jauch, Anna;
    • Hoffmann, Per;
    • Mühleisen, Thomas W;
    • Nöthen, Markus M
    Publication type:
    Article
    19

    A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).

    Published in:
    Nature Genetics, 2010, v. 42, n. 12, p. 1126, doi. 10.1038/ng.696
    By:
    • Enciso-Mora, Victor;
    • Broderick, Peter;
    • Ma, Yussanne;
    • Jarrett, Ruth F.;
    • Hjalgrim, Henrik;
    • Hemminki, Kari;
    • Van den Berg, Anke;
    • Olver, Bianca;
    • Lloyd, Amy;
    • Dobbins, Sara E.;
    • Lightfoot, Tracy;
    • Van Leeuwen, Flora E.;
    • Försti, Asta;
    • Diepstra, Arjan;
    • Broeks, Annegien;
    • Vijayakrishnan, Jayaram;
    • Shield, Lesley;
    • Lake, Annette;
    • Montgomery, Dorothy;
    • Roman, Eve
    Publication type:
    Article
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    Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.

    Published in:
    Carcinogenesis, 2015, v. 36, n. 11, p. 1299, doi. 10.1093/carcin/bgv127
    By:
    • Vodicka, Pavel;
    • Musak, Ludovit;
    • Frank, Christoph;
    • Kazimirova, Alena;
    • Vymetalkova, Veronika;
    • Barancokova, Magdalena;
    • Smolkova, Bozena;
    • Dzupinkova, Zuzana;
    • Jiraskova, Katerina;
    • Vodenkova, Sona;
    • Kroupa, Michal;
    • Osina, Oto;
    • Naccarati, Alessio;
    • Palitti, Fabrizio;
    • Försti, Asta;
    • Dusinska, Maria;
    • Vodickova, Ludmila;
    • Hemminki, Kari
    Publication type:
    Article
    29

    Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

    Published in:
    Carcinogenesis, 2014, v. 35, n. 2, p. 315, doi. 10.1093/carcin/bgt344
    By:
    • Yang, Rongxi;
    • Chen, Bowang;
    • Pfütze, Katrin;
    • Buch, Stephan;
    • Steinke, Verena;
    • Holinski-Feder, Elke;
    • Stöcker, Sarah;
    • von Schönfels, Witigo;
    • Becker, Thomas;
    • Schackert, Hans K.;
    • Royer-Pokora, Brigitte;
    • Kloor, Matthias;
    • Schmiegel, Wolff H.;
    • Büttner, Reinhard;
    • Engel, Christoph;
    • Lascorz Puertolas, Jesus;
    • Försti, Asta;
    • Kunkel, Nelli;
    • Bugert, Peter;
    • Schreiber, Stefan
    Publication type:
    Article
    30

    Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

    Published in:
    Carcinogenesis, 2010, v. 31, n. 9, p. 1612, doi. 10.1093/carcin/bgq146
    By:
    • Lascorz, Jesús;
    • Försti, Asta;
    • Bowang Chen;
    • Buch, Stephan;
    • Steinke, Verena;
    • Rahner, Nils;
    • Holinski-Feder, Elke;
    • Morak, Monika;
    • Schackert, Hans K.;
    • Görgens, Heike;
    • Schulmann, Karsten;
    • Goecke, Timm;
    • Kloor, Matthias;
    • Engel, Cristoph;
    • Büttner, Reinhard;
    • Kunkel, Nelli;
    • Weires, Marianne;
    • Hoffmeister, Michael;
    • Pardini, Barbara;
    • Naccarati, Alessio
    Publication type:
    Article
    31

    Functional dissection of inherited non-coding variation influencing multiple myeloma risk.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27666-x
    By:
    • Ajore, Ram;
    • Niroula, Abhishek;
    • Pertesi, Maroulio;
    • Cafaro, Caterina;
    • Thodberg, Malte;
    • Went, Molly;
    • Bao, Erik L.;
    • Duran-Lozano, Laura;
    • Lopez de Lapuente Portilla, Aitzkoa;
    • Olafsdottir, Thorunn;
    • Ugidos-Damboriena, Nerea;
    • Magnusson, Olafur;
    • Samur, Mehmet;
    • Lareau, Caleb A.;
    • Halldorsson, Gisli H.;
    • Thorleifsson, Gudmar;
    • Norddahl, Gudmundur L.;
    • Gunnarsdottir, Kristbjorg;
    • Försti, Asta;
    • Goldschmidt, Hartmut
    Publication type:
    Article
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    Systematic Pathway Enrichment Analysis of a Genome-Wide Association Study on Breast Cancer Survival Reveals an Influence of Genes Involved in Cell Adhesion and Calcium Signaling on the Patients’ Clinical Outcome.

    Published in:
    PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0098229
    By:
    • Woltmann, Andrea;
    • Chen, Bowang;
    • Lascorz, Jesús;
    • Johansson, Robert;
    • Eyfjörd, Jorunn E.;
    • Hamann, Ute;
    • Manjer, Jonas;
    • Enquist-Olsson, Kerstin;
    • Henriksson, Roger;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Hemminki, Kari;
    • Lenner, Per;
    • Försti, Asta
    Publication type:
    Article
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    Gender-Specific Effects of Genetic Variants within Th1 and Th17 Cell-Mediated Immune Response Genes on the Risk of Developing Rheumatoid Arthritis.

    Published in:
    PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072732
    By:
    • Cáliz, Rafael;
    • Canet, Luz María;
    • Lupiañez, Carmen Belén;
    • Canhão, Helena;
    • Escudero, Alejandro;
    • Filipescu, Ileana;
    • Segura-Catena, Juana;
    • Soto-Pino, María José;
    • Expósito-Ruiz, Manuela;
    • Ferrer, Miguel Ángel;
    • García, Antonio;
    • Romani, Lurdes;
    • González-Utrilla, Alfonso;
    • Vallejo, Teresa;
    • Pérez-Pampin, Eva;
    • Hemminki, Kari;
    • Försti, Asta;
    • Collantes, Eduardo;
    • Fonseca, João Eurico;
    • Sainz, Juan
    Publication type:
    Article
    38

    Genetic Variants in Hormone-Related Genes and Risk of Breast Cancer.

    Published in:
    PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069367
    By:
    • Clendenen, Tess;
    • Zeleniuch-Jacquotte, Anne;
    • Wirgin, Isaac;
    • Koenig, Karen L.;
    • Afanasyeva, Yelena;
    • Lundin, Eva;
    • Arslan, Alan A.;
    • Axelsson, Tomas;
    • Försti, Asta;
    • Hallmans, Göran;
    • Hemminki, Kari;
    • Lenner, Per;
    • Roy, Nirmal;
    • Shore, Roy E.;
    • Chen, Yu
    Publication type:
    Article
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    A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer.

    Published in:
    PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032784
    By:
    • Campa, Daniele;
    • Sainz, Juan;
    • Pardini, Barbara;
    • Vodickova, Ludmila;
    • Naccarati, Alessio;
    • Rudolph, Anja;
    • Novotny, Jan;
    • Försti, Asta;
    • Buch, Stephan;
    • von Schönfels, Witigo;
    • Schafmayer, Clemens;
    • Völzke, Henry;
    • Hoffmeister, Michael;
    • Frank, Bernd;
    • Barale, Roberto;
    • Hemminki, Kari;
    • Hampe, Jochen;
    • Chang-Claude, Jenny;
    • Brenner, Hermann;
    • Vodicka, Pavel
    Publication type:
    Article
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    Runs of homozygosity and inbreeding in thyroid cancer.

    Published in:
    2016
    By:
    • Thomsen, Hauke;
    • Chen, Bowang;
    • Figlioli, Gisella;
    • Elisei, Rossella;
    • Romei, Cristina;
    • Cipollini, Monica;
    • Cristaudo, Alfonso;
    • Bambi, Franco;
    • Hoffmann, Per;
    • Herms, Stefan;
    • Landi, Stefano;
    • Hemminki, Kari;
    • Gemignani, Federica;
    • Försti, Asta
    Publication type:
    journal article
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    Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.

    Published in:
    Mutagenesis, 2019, v. 34, n. 4, p. 323, doi. 10.1093/mutage/gez024
    By:
    • Niazi, Yasmeen;
    • Thomsen, Hauke;
    • Smolkova, Bozena;
    • Vodickova, Ludmila;
    • Vodenkova, Soňa;
    • Kroupa, Michal;
    • Vymetalkova, Veronika;
    • Kazimirova, Alena;
    • Barancokova, Magdalena;
    • Volkovova, Katarina;
    • Staruchova, Marta;
    • Hoffmann, Per;
    • Nöthen, Markus M;
    • Dusinska, Maria;
    • Musak, Ludovit;
    • Vodicka, Pavel;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
    48

    Ancestral susceptibility to colorectal cancer.

    Published in:
    Mutagenesis, 2012, v. 27, n. 2, p. 197, doi. 10.1093/mutage/ger061
    By:
    • Huhn, Stefanie;
    • Pardini, Barbara;
    • Naccarati, Alessio;
    • Vodička, Pavel;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
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