Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population von Corredor, Zuray, Filho, Miguel Inácio da Silva, Rodríguez-Ribera, Lara, Velázquez, Antonia, Hernández, Alba, Catalano, Calogerina, Hemminki, Kari, Coll, Elisabeth, Silva, Irene, Diaz, Juan Manuel, Ballarin, José, Vallés Prats, Martí, Calabia Martínez, Jordi, Försti, Asta, Marcos, Ricard, Pastor, Susana

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Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients von Mahmoudpour, Seyed Hamidreza, Bandapalli, Obul Reddy, da Silva Filho, Miguel Inácio, Campo, Chiara, Hemminki, Kari, Goldschmidt, Hartmut, Merz, Maximilian, Försti, Asta

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Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population von Marouf, Chaymaa, Göhler, Stella, Filho, Miguel Inacio Da Silva, Hajji, Omar, Hemminki, Kari, Nadifi, Sellama, Försti, Asta

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Evidence of Inbreeding in Hodgkin Lymphoma von Thomsen, Hauke, Inacio da Silva Filho, Miguel, Fuchs, Michael, Ponader, Sabine, Pogge von Strandmann, Elke, Eisele, Lewin, Herms, Stefan, Hoffmann, Per, Engert, Andreas, Hemminki, Kari, Försti, Asta

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Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes von Went, Molly, Kinnersley, Ben, Sud, Amit, Johnson, David C, Weinhold, Niels, Försti, Asta, van Duin, Mark, Orlando, Giulia, Mitchell, Jonathan S, Kuiper, Rowan, Walker, Brian A, Gregory, Walter M, Hoffmann, Per, Jackson, Graham H, Nöthen, Markus M, da Silva Filho, Miguel Inacio, Thomsen, Hauke, Broyl, Annemiek, Davies, Faith E, Thorsteinsdottir, Unnur, Hansson, Markus, Kaiser, Martin, Sonneveld, Pieter, Goldschmidt, Hartmut, Stefansson, Kari, Hemminki, Kari, Nilsson, Björn, Morgan, Gareth J, Houlston, Richard S

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Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts von Meziane, Iman, Huhn, Stefanie, Filho, Miguel Inacio da Silva, Weinhold, Niels, Campo, Chiara, Nickel, Jolanta, Hoffmann, Per, Nöthen, Markus M, Jöckel, Karl-Heinz, Landi, Stefano, Mitchell, Jonathan S, Johnson, David, Jauch, Anna, Morgan, Gareth J, Houlston, Richard, Goldschmidt, Hartmut, Milani, Paolo, Merlini, Giampaolo, Rowcieno, Dorota, Hawkins, Philip, Hegenbart, Ute, Palladini, Giovanni, Wechalekar, Ashutosh, Försti, Asta, Schönland, Stefan O, Hemminki, Kari

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Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma von Chattopadhyay, Subhayan, Thomsen, Hauke, Yadav, Pankaj, da Silva Filho, Miguel Inacio, Weinhold, Niels, Nöthen, Markus M., Hoffman, Per, Bertsch, Uta, Huhn, Stefanie, Morgan, Gareth J., Goldschmidt, Hartmut, Houlston, Richard, Hemminki, Kari, Försti, Asta

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Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype von Migliorini, Gabriele, Fiege, Bettina, Hosking, Fay J., Ma, Yussanne, Kumar, Rajiv, Sherborne, Amy L., da Silva Filho, Miguel Inacio, Vijayakrishnan, Jayaram, Koehler, Rolf, Thomsen, Hauke, Irving, Julie A., Allan, James M., Lightfoot, Tracy, Roman, Eve, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela, Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Zimmermann, Martin, Bartram, Claus R., Schrappe, Martin, Greaves, Mel, Stanulla, Martin, Hemminki, Kari, Houlston, Richard S.

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Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy: Replication of the Reported Candidate Susceptibility Loci von Campo, Chiara, Da Silva Filho, Miguel Inacio, Weinhold, Niels, Goldschmidt, Hartmut, Hemminki, Kari, Merz, Maximilian, Försti, Asta

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Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer von Catalano, Calogerina, da Silva Filho, Miguel Inacio, Frank, Christoph, Jiraskova, Katerina, Vymetalkova, Veronika, Levy, Miroslav, Liska, Vaclav, Vycital, Ondrej, Naccarati, Alessio, Vodickova, Ludmila, Hemminki, Kari, Vodicka, Pavel, Weber, Alexander N R, Försti, Asta

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Bortezomib‐induced peripheral neuropathy: A genome‐wide association study on multiple myeloma patients von Campo, Chiara, Silva Filho, Miguel Inacio, Weinhold, Niels, Mahmoudpour, Seyed Hamidreza, Goldschmidt, Hartmut, Hemminki, Kari, Merz, Maximilian, Försti, Asta

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Loci associated with genomic damage levels in chronic kidney disease patients and controls von Corredor, Zuray, da Silva Filho, Miguel Inácio, Rodríguez-Ribera, Lara, Catalano, Calogerina, Hemminki, Kari, Coll, Elisabeth, Silva, Irene, Diaz, Juan Manuel, Ballarin, José Aurelio, Henández, Alba, Försti, Asta, Marcos, Ricard, Pastor, Susana

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Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance von Chattopadhyay, Subhayan, Thomsen, Hauke, Weinhold, Niels, Meziane, Iman, Huhn, Stefanie, da Silva Filho, Miguel Inacio, Vodicka, Pavel, Vodickova, Ludmila, Hoffmann, Per, Nöthen, Markus M., Jöckel, Karl-Heinz, Schmidt, Börge, Landi, Stefano, Hajek, Roman, Hallmans, Göran, Pettersson-Kymmer, Ulrika, Ohlsson, Claes, Milani, Paolo, Merlini, Giampaolo, Rowcieno, Dorota, Hawkins, Philip, Hegenbart, Ute, Palladini, Giovanni, Wechalekar, Ashutosh, Schönland, Stefan O., Houlston, Richard, Goldschmidt, Hartmut, Hemminki, Kari, Försti, Asta

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Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci von Law, Philip J., Sud, Amit, Mitchell, Jonathan S., Henrion, Marc, Orlando, Giulia, Lenive, Oleg, Broderick, Peter, Speedy, Helen E., Johnson, David C., Kaiser, Martin, Weinhold, Niels, Cooke, Rosie, Sunter, Nicola J., Jackson, Graham H., Summerfield, Geoffrey, Harris, Robert J., Pettitt, Andrew R., Allsup, David J., Carmichael, Jonathan, Bailey, James R., Pratt, Guy, Rahman, Thahira, Pepper, Chris, Fegan, Chris, von Strandmann, Elke Pogge, Engert, Andreas, Försti, Asta, Chen, Bowang, Filho, Miguel Inacio da Silva, Thomsen, Hauke, Hoffmann, Per, Noethen, Markus M., Eisele, Lewin, Jöckel, Karl-Heinz, Allan, James M., Swerdlow, Anthony J., Goldschmidt, Hartmut, Catovsky, Daniel, Morgan, Gareth J., Hemminki, Kari, Houlston, Richard S.

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Impact of functional germline variants and a deletion polymorphism in APOBEC3A and APOBEC3B on breast cancer risk and survival in a Swedish study population von Göhler, Stella, Da Silva Filho, Miguel Inacio, Johansson, Robert, Enquist-Olsson, Kerstin, Henriksson, Roger, Hemminki, Kari, Lenner, Per, Försti, Asta

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Epistatic effect of TLR3 and cGAS‐STING‐IKKε‐TBK1‐IFN signaling variants on colorectal cancer risk von Catalano, Calogerina, Silva Filho, Miguel Inacio, Frank, Christoph, Lu, Shun, Jiraskova, Katerina, Vymetalkova, Veronika, Levy, Miroslav, Liska, Vaclav, Vycital, Ondrej, Naccarati, Alessio, Vodickova, Ludmila, Hemminki, Kari, Vodicka, Pavel, Weber, Alexander N. R., Försti, Asta

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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) von 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

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Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study von Chattopadhyay, Subhayan, Thomsen, Hauke, da Silva Filho, Miguel Inacio, Weinhold, Niels, Hoffmann, Per, Nöthen, Markus M, Marina, Arendt, Jöckel, Karl-Heinz, Schmidt, Börge, Pechlivanis, Sonali, Langer, Christian, Goldschmidt, Hartmut, Hemminki, Kari, Försti, Asta

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The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A von Vijayakrishnan, Jayaram, Henrion, Marc, Moorman, Anthony V., Fiege, Bettina, Kumar, Rajiv, Inacio da Silva Filho, Miguel, Holroyd, Amy, Koehler, Rolf, Thomsen, Hauke, Irving, Julie A., Allan, James M., Lightfoot, Tracy, Roman, Eve, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Bartram, Claus R., Schrappe, Martin, Greaves, Mel, Hemminki, Kari, Harrison, Christine J., Stanulla, Martin, Houlston, Richard S.

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Inbreeding and homozygosity in breast cancer survival von Thomsen, Hauke, Filho, Miguel Inacio da Silva, Woltmann, Andrea, Johansson, Robert, Eyfjörd, Jorunn E., Hamann, Ute, Manjer, Jonas, Enquist-Olsson, Kerstin, Henriksson, Roger, Herms, Stefan, Hoffmann, Per, Chen, Bowang, Huhn, Stefanie, Hemminki, Kari, Lenner, Per, Försti, Asta

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