A Comparison of Multivariate Genome-Wide Association Methods

por Galesloot, Tessel E., van Steen, Kristel, Kiemeney, Lambertus A. L. M., Janss, Luc L., Vermeulen, Sita H.
Publicado 2014

Whole Genome Sequencing Identifies Novel Common and Low-Frequency Variants Associated With Age-Related Macular Degeneration

por Acar, Ilhan E., Galesloot, Tessel E., Luhmann, Ulrich F. O., Fauser, Sascha, Gayán, Javier, den Hollander, Anneke I., Nogoceke, Everson
Publicado 2023

Known susceptibility SNPs for sporadic prostate cancer show a similar association with “hereditary” prostate cancer

por Cremers, Ruben G., Galesloot, Tessel E., Aben, Katja K., van Oort, Inge M., Vasen, Hans F., Vermeulen, Sita H., Kiemeney, Lambertus A.
Publicado 2015

Cohort Profile: The Nijmegen Biomedical Study (NBS)

por Galesloot, Tessel E, Vermeulen, Sita H, Swinkels, Dorine W, de Vegt, F, Franke, B, den Heijer, M, de Graaf, J, Verbeek, André LM, Kiemeney, Lambertus ALM
Publicado 2017

The Effects of Common Genetic Variation in 96 Genes Involved in Thyroid Hormone Regulation on TSH and FT4 Concentrations

por Sterenborg, Rosalie B T M, Galesloot, Tessel E, Teumer, Alexander, Netea-Maier, Romana T, Speed, Doug, Meima, Marcel E, Visser, W Edward, Smit, Johannes W A, Peeters, Robin P, Medici, Marco
Publicado 2022

Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?

por Galesloot, Tessel E., Janss, Luc L., Burgess, Stephen, Kiemeney, Lambertus A. L. M., den Heijer, Martin, de Graaf, Jacqueline, Holewijn, Suzanne, Benyamin, Beben, Whitfield, John B., Swinkels, Dorine W., Vermeulen, Sita H.
Publicado 2015

Candidate Gene Sequencing of SLC11A2 and TMPRSS6 in a Family with Severe Anaemia: Common SNPs, Rare Haplotypes, No Causative Mutation

por Kloss-Brandstätter, Anita, Erhart, Gertraud, Lamina, Claudia, Meister, Bernhard, Haun, Margot, Coassin, Stefan, Seifert, Markus, Klein-Franke, Andreas, Paulweber, Bernhard, Kedenko, Lyudmyla, Kollerits, Barbara, Swinkels, Dorine W., Vermeulen, Sita H., Galesloot, Tessel E., Kronenberg, Florian, Weiss, Günter
Publicado 2012

Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6-Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia

por van der Staaij, Hilde, Donker, Albertine E., Bakkeren, Dirk L., Salemans, Jan M. J. I., Mignot-Evers, Lisette A. A., Bongers, Marlies Y., Dieleman, Jeanne P., Galesloot, Tessel E., Laarakkers, Coby M., Klaver, Siem M., Swinkels, Dorine W.
Publicado 2022

Semi-Quantitative Multiplex Profiling of the Complement System Identifies Associations of Complement Proteins with Genetic Variants and Metabolites in Age-Related Macular Degenerat...

por Acar, I. Erkin, Willems, Esther, Kersten, Eveline, Keizer-Garritsen, Jenneke, Kragt, Else, Bakker, Bjorn, Galesloot, Tessel E., Hoyng, Carel B., Fauser, Sascha, van Gool, Alain J., Lechanteur, Yara T. E., Koertvely, Elod, Nogoceke, Everson, Gloerich, Jolein, de Jonge, Marien I., Lorés-Motta, Laura, den Hollander, Anneke I.
Publicado 2021

Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin

por Galesloot, Tessel E., Verweij, Niek, Traglia, Michela, Barbieri, Caterina, van Dijk, Freerk, Geurts-Moespot, Anneke J., Girelli, Domenico, Kiemeney, Lambertus A. L. M., Sweep, Fred C. G. J., Swertz, Morris A., van der Meer, Peter, Camaschella, Clara, Toniolo, Daniela, Vermeulen, Sita H., van der Harst, Pim, Swinkels, Dorine W.
Publicado 2016

Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting S...

por van Rooij, Iris ALM, Ludwig, Kerstin U, Welzenbach, Julia, Ishorst, Nina, Thonissen, Michelle, Galesloot, Tessel E, Ongkosuwito, Edwin, Bergé, Stefaan J, Aldhorae, Khalid, Rojas-Martinez, Augusto, Kiemeney, Lambertus ALM, Vermeesch, Joris Robert, Brunner, Han, Roeleveld, Nel, Devriendt, Koen, Dormaar, Titiaan, Hens, Greet, Knapp, Michael, Carels, Carine, Mangold, Elisabeth
Publicado 2019

Sex-Specific Regulation of Inflammation and Metabolic Syndrome in Obesity

por ter Horst, Rob, van den Munckhof, Inge C.L., Schraa, Kiki, Aguirre-Gamboa, Raul, Jaeger, Martin, Smeekens, Sanne P., Brand, Tessa, Lemmers, Heidi, Dijkstra, Helga, Galesloot, Tessel E., de Graaf, Jacqueline, Xavier, Ramnik J., Li, Yang, Joosten, Leo A.B., Rutten, Joost H.W., Netea, Mihai G., Riksen, Niels P.
Publicado 2020

Intravesical BCG in patients with non-muscle invasive bladder cancer induces trained immunity and decreases respiratory infections

por van Puffelen, Jelmer H, Novakovic, Boris, van Emst, Liesbeth, Kooper, Denise, Zuiverloon, Tahlita C M, Oldenhof, Ursula T H, Witjes, J Alfred, Galesloot, Tessel E, Vrieling, Alina, Aben, Katja K H, Kiemeney, Lambertus A L M, Oosterwijk, Egbert, Netea, Mihai G, Boormans, Joost L, van der Heijden, Antoine G, Joosten, Leo A B, Vermeulen, Sita H
Publicado 2023

Sequence variant at 4q25 near PITX2 associates with appendicitis

por Kristjansson, Ragnar P., Benonisdottir, Stefania, Oddsson, Asmundur, Galesloot, Tessel E., Thorleifsson, Gudmar, Aben, Katja K., Davidsson, Olafur B., Jonsson, Stefan, Arnadottir, Gudny A., Jensson, Brynjar O., Walters, G. Bragi, Sigurdsson, Jon K., Sigurdsson, Snaevar, Holm, Hilma, Arnar, David O., Thorgeirsson, Gudmundur, Alexiusdottir, Kristin, Jonsdottir, Ingileif, Thorsteinsdottir, Unnur, Kiemeney, Lambertus A., Jonsson, Thorvaldur, Gudbjartsson, Daniel F., Rafnar, Thorunn, Sulem, Patrick, Stefansson, Kari
Publicado 2017

Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing

por Corominas, Jordi, Klein, Marieke, Zayats, Tetyana, Rivero, Olga, Ziegler, Georg C., Pauper, Marc, Neveling, Kornelia, Poelmans, Geert, Jansch, Charline, Svirin, Evgeniy, Geissler, Julia, Weber, Heike, Reif, Andreas, Arias Vasquez, Alejandro, Galesloot, Tessel E., Kiemeney, Lambertus A. L. M., Buitelaar, Jan K., Ramos-Quiroga, Josep-Antoni, Cormand, Bru, Ribasés, Marta, Hveem, Kristian, Gabrielsen, Maiken Elvestad, Hoffmann, Per, Cichon, Sven, Haavik, Jan, Johansson, Stefan, Jacob, Christian P., Romanos, Marcel, Franke, Barbara, Lesch, Klaus-Peter
Publicado 2018

Measurement and genetic architecture of lifetime depression in the Netherlands as assessed by LIDAS (Lifetime Depression Assessment Self-report)

por Fedko, Iryna O., Hottenga, Jouke-Jan, Helmer, Quinta, Mbarek, Hamdi, Huider, Floris, Amin, Najaf, Beulens, Joline W., Bremmer, Marijke A., Elders, Petra J., Galesloot, Tessel E., Kiemeney, Lambertus A., van Loo, Hanna M., Picavet, H. Susan J., Rutters, Femke, van der Spek, Ashley, van de Wiel, Anne M., van Duijn, Cornelia, de Geus, Eco J. C., Feskens, Edith J. M., Hartman, Catharina A., Oldehinkel, Albertine J., Smit, Jan H., Verschuren, W. M. Monique, Penninx, Brenda W. J. H., Boomsma, Dorret I., Bot, Mariska
Publicado 2021

Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis

por Yarmolinsky, James, Robinson, Jamie W, Mariosa, Daniela, Karhunen, Ville, Huang, Jian, Dimou, Niki, Murphy, Neil, Burrows, Kimberley, Bouras, Emmanouil, Smith-Byrne, Karl, Lewis, Sarah J, Galesloot, Tessel E, Kiemeney, Lambertus A, Vermeulen, Sita, Martin, Paul, Albanes, Demetrius, Hou, Lifang, Newcomb, Polly A, White, Emily, Wolk, Alicja, Wu, Anna H, Marchand, Loïc Le, Phipps, Amanda I, Buchanan, Daniel D, Zhao, Sizheng Steven, Gill, Dipender, Chanock, Stephen J, Purdue, Mark P, Smith, George Davey, Brennan, Paul, Herzig, Karl-Heinz, Jarvelin, Marjo-Riitta, Dehghan, Abbas, Johansson, Mattias, Gunter, Marc J, Tsilidis, Kostas K, Martin, Richard M
Publicado 2023

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

por Heilmann-Heimbach, Stefanie, Herold, Christine, Hochfeld, Lara M., Hillmer, Axel M., Nyholt, Dale R., Hecker, Julian, Javed, Asif, Chew, Elaine G. Y., Pechlivanis, Sonali, Drichel, Dmitriy, Heng, Xiu Ting, del Rosario, Ricardo C. -H., Fier, Heide L., Paus, Ralf, Rueedi, Rico, Galesloot, Tessel E., Moebus, Susanne, Anhalt, Thomas, Prabhakar, Shyam, Li, Rui, Kanoni, Stavroula, Papanikolaou, George, Kutalik, Zoltán, Deloukas, Panos, Philpott, Michael P., Waeber, Gérard, Spector, Tim D., Vollenweider, Peter, Kiemeney, Lambertus A. L. M., Dedoussis, George, Richards, J. Brent, Nothnagel, Michael, Martin, Nicholas G., Becker, Tim, Hinds, David A., Nöthen, Markus M.
Publicado 2017

Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations

por van de Putte, Romy, Wijers, Charlotte H. W., Reutter, Heiko, Vermeulen, Sita H., Marcelis, Carlo L. M., Brosens, Erwin, Broens, Paul M. A., Homberg, Markus, Ludwig, Michael, Jenetzky, Ekkehart, Zwink, Nadine, Sloots, Cornelius E. J., de Klein, Annelies, Brooks, Alice S., Hofstra, Robert M. W., Holsink, Sophie A. C., van der Zanden, Loes F. M., Galesloot, Tessel E., Tam, Paul Kwong-Hang, Steehouwer, Marloes, Acuna-Hidalgo, Rocio, van de Vorst, Maartje, Kiemeney, Lambertus A., Garcia-Barceló, Maria-Mercè, de Blaauw, Ivo, Brunner, Han G., Roeleveld, Nel, van Rooij, Iris A. L. M.
Publicado 2019

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

por van der Laan, Sander W., Fall, Tove, Soumaré, Aicha, Teumer, Alexander, Sedaghat, Sanaz, Baumert, Jens, Zabaneh, Delilah, van Setten, Jessica, Isgum, Ivana, Galesloot, Tessel E., Arpegård, Johannes, Amouyel, Philippe, Trompet, Stella, Waldenberger, Melanie, Dörr, Marcus, Magnusson, Patrik K., Giedraitis, Vilmantas, Larsson, Anders, Morris, Andrew P., Felix, Janine F., Morrison, Alanna C., Franceschini, Nora, Bis, Joshua C., Kavousi, Maryam, O’Donnell, Christopher, Drenos, Fotios, Tragante, Vinicius, Munroe, Patricia B., Malik, Rainer, Dichgans, Martin, Worrall, Bradford B., Erdmann, Jeanette, Nelson, Christopher P., Samani, Nilesh J., Schunkert, Heribert, Marchini, Jonathan, Patel, Riyaz S., Hingorani, Aroon D., Lind, Lars, Pedersen, Nancy L., de Graaf, Jacqueline, Kiemeney, Lambertus A.L.M., Baumeister, Sebastian E., Franco, Oscar H., Hofman, Albert, Uitterlinden, André G., Koenig, Wolfgang, Meisinger, Christa, Peters, Annette, Thorand, Barbara, Jukema, J. Wouter, Eriksen, Bjørn Odvar, Toft, Ingrid, Wilsgaard, Tom, Onland-Moret, N. Charlotte, van der Schouw, Yvonne T., Debette, Stéphanie, Kumari, Meena, Svensson, Per, van der Harst, Pim, Kivimaki, Mika, Keating, Brendan J., Sattar, Naveed, Dehghan, Abbas, Reiner, Alex P., Ingelsson, Erik, den Ruijter, Hester M., de Bakker, Paul I.W., Pasterkamp, Gerard, Ärnlöv, Johan, Holmes, Michael V., Asselbergs, Folkert W.
Publicado 2016