Editorial: Improving Early Detection and Risk Prediction in Heart Failure

por Tragante, Vinicius, Pilbrow, Anna, Poppe, Katrina
Publicado 2022

Integrative Bioinformatics Approaches for Identification of Drug Targets in Hypertension

por Hemerich, Daiane, van Setten, Jessica, Tragante, Vinicius, Asselbergs, Folkert W.
Publicado 2018

Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes

por Hemerich, Daiane, Smit, Roelof A. J., Preuss, Michael, Stalbow, Lauren, van der Laan, Sander W., Asselbergs, Folkert W., van Setten, Jessica, Tragante, Vinicius
Publicado 2023

Unravelling the Neospora caninum secretome through the secreted fraction (ESA) and quantification of the discharged tachyzoite using high-resolution mass spectrometry-based proteom...

por Pollo-Oliveira, Letícia, Post, Harm, Acencio, Marcio Luis, Lemke, Ney, van den Toorn, Henk, Tragante, Vinicius, Heck, Albert JR, Altelaar, AF Maarten, Yatsuda, Ana Patrícia
Publicado 2013

Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk

por Tragante, Vinicius, Asselbergs, Folkert W., Swerdlow, Daniel I., Palmer, Tom M., Moore, Jason H., de Bakker, Paul I. W., Keating, Brendan J., Holmes, Michael V.
Publicado 2016

Genetic Variants at Chromosome 9p21 and Risk of First Versus Subsequent Coronary Heart Disease Events: A Systematic Review and Meta-Analysis

por Patel, Riyaz S., Asselbergs, Folkert W., Quyyumi, Arshed A., Palmer, Tom M., Finan, Chris I., Tragante, Vinicius, Deanfield, John, Hemingway, Harry, Hingorani, Aroon D., Holmes, Michael V.
Publicado 2014

rs41291957 controls miR‐143 and miR‐145 expression and impacts coronary artery disease risk

por Hall, Ignacio Fernando, Climent, Montserrat, Viviani Anselmi, Chiara, Papa, Laura, Tragante, Vinicius, Lambroia, Luca, Farina, Floriana Maria, Kleber, Marcus E, März, Winfried, Biguori, Carlo, Condorelli, Gianluigi, Elia, Leonardo
Publicado 2021

Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype

por Tragante, Vinicius, Gho, Johannes M. I. H., Felix, Janine F., Vasan, Ramachandran S., Smith, Nicholas L., Voight, Benjamin F., Palmer, Colin, van der Harst, Pim, Moore, Jason H., Asselbergs, Folkert W.
Publicado 2017

Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk

por Brænne, Ingrid, Zeng, Lingyao, Willenborg, Christina, Tragante, Vinicius, Kessler, Thorsten, Willer, Cristen J., Laakso, Markku, Wallentin, Lars, Franks, Paul W., Salomaa, Veikko, Dehghan, Abbas, Meitinger, Thomas, Samani, Nilesh J., Asselbergs, Folkert W., Erdmann, Jeanette, Schunkert, Heribert
Publicado 2017

Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults

por Björnsson, Eythór, Thorleifsson, Guðmar, Helgadóttir, Anna, Guðnason, Thórarinn, Guðbjartsson, Tómas, Andersen, Karl, Grétarsdóttir, Sólveig, Ólafsson, Ísleifur, Tragante, Vinicius, Ólafsson, Ólafur Hreiðar, Jónsdóttir, Birna, Eyjólfsson, Guðmundur I., Sigurðardóttir, Ólöf, Thorgeirsson, Guðmundur, Guðbjartsson, Daníel F., Thorsteinsdóttir, Unnur, Hólm, Hilma, Stefánsson, Kári
Publicado 2019

A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors

por Brænne, Ingrid, Willenborg, Christina, Tragante, Vinicius, Kessler, Thorsten, Zeng, Lingyao, Reiz, Benedikt, Kleinecke, Mariana, von Ameln, Simon, Willer, Cristen J., Laakso, Markku, Wild, Philipp S., Zeller, Tanja, Wallentin, Lars, Franks, Paul W., Salomaa, Veikko, Dehghan, Abbas, Meitinger, Thomas, Samani, Nilesh J., Asselbergs, Folkert W., Erdmann, Jeanette, Schunkert, Heribert
Publicado 2017

Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland

por Sveinbjornsson, Gardar, Benediktsdottir, Bara D., Sigfusson, Gunnlaugur, Norland, Kristjan, Davidsson, Olafur B., Thorolfsdottir, Rosa B., Tragante, Vinicius, Arnadottir, Gudny A., Jensson, Brynjar O., Katrinardottir, Hildigunnur, Fridriksdottir, Run, Gudmundsdottir, Hallbera, Aegisdottir, Hildur M., Fridriksson, Brynjar, Thorgeirsson, Gudmundur, Magnusson, Vidar, Oddsson, Asmundur, Sulem, Patrick, Gudbjartsson, Daniel F., Holm, Hilma, Arnar, David O., Stefansson, Kari
Publicado 2023

Sequence variants with large effects on cardiac electrophysiology and disease

por Norland, Kristjan, Sveinbjornsson, Gardar, Thorolfsdottir, Rosa B., Davidsson, Olafur B., Tragante, Vinicius, Rajamani, Sridharan, Helgadottir, Anna, Gretarsdottir, Solveig, van Setten, Jessica, Asselbergs, Folkert W., Sverrisson, Jon Th., Stephensen, Sigurdur S., Oskarsson, Gylfi, Sigurdsson, Emil L., Andersen, Karl, Danielsen, Ragnar, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Arnar, David O., Sulem, Patrick, Holm, Hilma, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado 2019

Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets

por Lempiäinen, Harri, Brænne, Ingrid, Michoel, Tom, Tragante, Vinicius, Vilne, Baiba, Webb, Tom R., Kyriakou, Theodosios, Eichner, Johannes, Zeng, Lingyao, Willenborg, Christina, Franzen, Oscar, Ruusalepp, Arno, Goel, Anuj, van der Laan, Sander W., Biegert, Claudia, Hamby, Stephen, Talukdar, Husain A., Foroughi Asl, Hassan, Pasterkamp, Gerard, Watkins, Hugh, Samani, Nilesh J., Wittenberger, Timo, Erdmann, Jeanette, Schunkert, Heribert, Asselbergs, Folkert W., Björkegren, Johan L. M.
Publicado 2018

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

por Ivarsdottir, Erna V., Holm, Hilma, Benonisdottir, Stefania, Olafsdottir, Thorhildur, Sveinbjornsson, Gardar, Thorleifsson, Gudmar, Eggertsson, Hannes P., Halldorsson, Gisli H., Hjorleifsson, Kristjan E., Melsted, Pall, Gylfason, Arnaldur, Arnadottir, Gudny A., Oddsson, Asmundur, Jensson, Brynjar O., Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Juliusdottir, Thorhildur, Stefansdottir, Lilja, Tragante, Vinicius, Halldorsson, Bjarni V., Petersen, Hannes, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Sulem, Patrick, Hinriksdottir, Ingibjorg, Jonsdottir, Ingileif, Gudbjartsson, Daniel F., Stefansson, Kari
Publicado 2021

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

por Gudmundsson, Julius, Sigurdsson, Jon K., Stefansdottir, Lilja, Agnarsson, Bjarni A., Isaksson, Helgi J., Stefansson, Olafur A., Gudjonsson, Sigurjon A., Gudbjartsson, Daniel F., Masson, Gisli, Frigge, Michael L., Stacey, Simon N., Sulem, Patrick, Halldorsson, Gisli H., Tragante, Vinicius, Holm, Hilma, Eyjolfsson, Gudmundur I., Sigurdardottir, Olof, Olafsson, Isleifur, Jonsson, Thorvaldur, Jonsson, Eirikur, Barkardottir, Rosa B., Hilmarsson, Rafn, Asselbergs, Folkert W., Geirsson, Gudmundur, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Thorleifsson, Gudmar, Stefansson, Kari
Publicado 2018

Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor

por Dowsett, Joseph, Ferkingstad, Egil, Rasmussen, Line Jee Hartmann, Thørner, Lise Wegner, Magnússon, Magnús K., Sugden, Karen, Thorleifsson, Gudmar, Frigge, Mike, Burgdorf, Kristoffer Sølvsten, Ostrowski, Sisse Rye, Sørensen, Erik, Erikstrup, Christian, Pedersen, Ole Birger, Hansen, Thomas Folkmann, Banasik, Karina, Brunak, Søren, Tragante, Vinicius, Lund, Sigrun Helga, Stefansdottir, Lilja, Gunnarson, Bjarni, Poulton, Richie, Arseneault, Louise, Caspi, Avshalom, Moffitt, Terrie E., Gudbjartsson, Daníel, Eugen-Olsen, Jesper, Stefánsson, Hreinn, Stefánsson, Kári, Ullum, Henrik
Publicado 2021

Sequence variants affecting voice pitch in humans

por Gisladottir, Rosa S., Helgason, Agnar, Halldorsson, Bjarni V., Helgason, Hannes, Borsky, Michal, Chien, Yu-Ren, Gudnason, Jon, Gudjonsson, Sigurjon A., Moisik, Scott, Dediu, Dan, Thorleifsson, Gudmar, Tragante, Vinicius, Bustamante, Mariana, Jonsdottir, Gudrun A., Stefansdottir, Lilja, Rutsdottir, Gudrun, Magnusson, Sigurdur H., Hardarson, Marteinn, Ferkingstad, Egil, Halldorsson, Gisli H., Rognvaldsson, Solvi, Skuladottir, Astros, Ivarsdottir, Erna V., Norddahl, Gudmundur, Thorgeirsson, Gudmundur, Jonsdottir, Ingileif, Ulfarsson, Magnus O., Holm, Hilma, Stefansson, Hreinn, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Kari
Publicado 2023

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

por Olafsdottir, Thorhildur, Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Olafur A., Medek, Helga, Olafsson, Karl, Ingthorsson, Orri, Gudmundsson, Valur, Jonsdottir, Ingileif, Halldorsson, Gisli H., Kristjansson, Ragnar P., Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Oddsson, Asmundur, Sigurdsson, Asgeir, Eggertsson, Hannes P., Melsted, Pall, Halldorsson, Bjarni V., Lund, Sigrun H., Styrkarsdottir, Unnur, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Holm, Hilma, Tragante, Vinicius, Asselbergs, Folkert W., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Jonsdottir, Kristin, Rafnar, Thorunn, Stefansson, Kari
Publicado 2020

Genetic variants associated with platelet count are predictive of human disease and physiological markers

por Mikaelsdottir, Evgenia, Thorleifsson, Gudmar, Stefansdottir, Lilja, Halldorsson, Gisli, Sigurdsson, Jon K., Lund, Sigrun H., Tragante, Vinicius, Melsted, Pall, Rognvaldsson, Solvi, Norland, Kristjan, Helgadottir, Anna, Magnusson, Magnus K., Ragnarsson, Gunnar B., Kristinsson, Sigurdur Y., Reykdal, Sigrun, Vidarsson, Brynjar, Gudmundsdottir, Ingibjorg J., Olafsson, Isleifur, Onundarson, Pall T., Sigurdardottir, Olof, Sigurdsson, Emil L., Grondal, Gerdur, Geirsson, Arni J., Geirsson, Gudmundur, Gudmundsson, Julius, Holm, Hilma, Saevarsdottir, Saedis, Jonsdottir, Ingileif, Thorgeirsson, Gudmundur, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Publicado 2021