Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis
Scholz, Markus, Horn, Katrin, Pott, Janne, Gross, Arnd, Kleber, Marcus E., Delgado, Graciela E., Mishra, Pashupati Prasad, Kirsten, Holger, Gieger, Christian, Müller-Nurasyid, Martina, Tönjes, Anke, Kovacs, Peter, Lehtimäki, Terho, Raitakari, Olli, Kähönen, Mika, Gylling, Helena, Baber, Ronny, Isermann, Berend, Stumvoll, Michael, Loeffler, Markus, März, Winfried, Meitinger, Thomas, Peters, Annette, Thiery, Joachim, Teupser, Daniel, Ceglarek, Uta
Published in Nature communications (10.01.2022)
Published in Nature communications (10.01.2022)
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Comparison of genetic risk prediction models to improve prediction of coronary heart disease in two large cohorts of the MONICA/KORA study
Bauer, Alina, Zierer, Astrid, Gieger, Christian, Büyüközkan, Mustafa, Müller‐Nurasyid, Martina, Grallert, Harald, Meisinger, Christa, Strauch, Konstantin, Prokisch, Holger, Roden, Michael, Peters, Annette, Krumsiek, Jan, Herder, Christian, Koenig, Wolfgang, Thorand, Barbara, Huth, Cornelia
Published in Genetic epidemiology (01.09.2021)
Published in Genetic epidemiology (01.09.2021)
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Author Correction: Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis
Scholz, Markus, Horn, Katrin, Pott, Janne, Gross, Arnd, Kleber, Marcus E., Delgado, Graciela E., Mishra, Pashupati Prasad, Kirsten, Holger, Gieger, Christian, Müller-Nurasyid, Martina, Tönjes, Anke, Kovacs, Peter, Lehtimäki, Terho, Raitakari, Olli, Kähönen, Mika, Gylling, Helena, Baber, Ronny, Isermann, Berend, Stumvoll, Michael, Loeffler, Markus, März, Winfried, Meitinger, Thomas, Peters, Annette, Thiery, Joachim, Teupser, Daniel, Ceglarek, Uta
Published in Nature communications (25.02.2022)
Published in Nature communications (25.02.2022)
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Immunochip analysis identifies association of the RAD50/IL13 region with human longevity
Flachsbart, Friederike, Ellinghaus, David, Gentschew, Liljana, Heinsen, Femke‐Anouska, Caliebe, Amke, Christiansen, Lene, Nygaard, Marianne, Christensen, Kaare, Blanché, Hélène, Deleuze, Jean‐François, Derbois, Céline, Galan, Pilar, Büning, Carsten, Brand, Stephan, Peters, Anette, Strauch, Konstantin, Müller‐Nurasyid, Martina, Hoffmann, Per, Nöthen, Markus M., Lieb, Wolfgang, Franke, Andre, Schreiber, Stefan, Nebel, Almut
Published in Aging cell (01.06.2016)
Published in Aging cell (01.06.2016)
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pulver: an R package for parallel ultra-rapid p-value computation for linear regression interaction terms
Molnos, Sophie, Baumbach, Clemens, Wahl, Simone, Müller-Nurasyid, Martina, Strauch, Konstantin, Wang-Sattler, Rui, Waldenberger, Melanie, Meitinger, Thomas, Adamski, Jerzy, Kastenmüller, Gabi, Suhre, Karsten, Peters, Annette, Grallert, Harald, Theis, Fabian J, Gieger, Christian
Published in BMC bioinformatics (29.09.2017)
Published in BMC bioinformatics (29.09.2017)
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Empirical Hierarchical Bayes Approach to Gene-Environment Interactions: Development and Application to Genome-Wide Association Studies of Lung Cancer in TRICL
Sohns, Melanie, Viktorova, Elena, Amos, Christopher I., Brennan, Paul, Fehringer, Gord, Gaborieau, Valerie, Han, Younghun, Heinrich, Joachim, Chang-Claude, Jenny, Hung, Rayjean J., Müller-Nurasyid, Martina, Risch, Angela, Lewinger, Juan Pablo, Thomas, Duncan C., Bickeböller, Heike
Published in Genetic epidemiology (01.09.2013)
Published in Genetic epidemiology (01.09.2013)
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Harmonization of Study and Reference Data by PhaseLift: Saving Time When Imputing Study Data
Gorski, Mathias, Winkler, Thomas W., Stark, Klaus, Müller-Nurasyid, Martina, Ried, Janina S., Grallert, Harald, Weber, Bernhard H. F., Heid, Iris M.
Published in Genetic epidemiology (01.07.2014)
Published in Genetic epidemiology (01.07.2014)
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Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests
Schweiger, Regev, Fisher, Eyal, Weissbrod, Omer, Rahmani, Elior, Müller-Nurasyid, Martina, Kunze, Sonja, Gieger, Christian, Waldenberger, Melanie, Rosset, Saharon, Halperin, Eran
Published in Nature communications (21.11.2018)
Published in Nature communications (21.11.2018)
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Network reconstruction for trans acting genetic loci using multi-omics data and prior information
Hawe, Johann S, Saha, Ashis, Waldenberger, Melanie, Kunze, Sonja, Wahl, Simone, Müller-Nurasyid, Martina, Prokisch, Holger, Grallert, Harald, Herder, Christian, Peters, Annette, Strauch, Konstantin, Theis, Fabian J, Gieger, Christian, Chambers, John, Battle, Alexis, Heinig, Matthias
Published in Genome medicine (07.11.2022)
Published in Genome medicine (07.11.2022)
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Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes
Jäger, Susanne, Wahl, Simone, Kröger, Janine, Sharma, Sapna, Hoffmann, Per, Floegel, Anna, Pischon, Tobias, Prehn, Cornelia, Adamski, Jerzy, Müller-Nurasyid, Martina, Waldenberger, Melanie, Strauch, Konstantin, Peters, Annette, Gieger, Christian, Suhre, Karsten, Grallert, Harald, Boeing, Heiner, Schulze, Matthias B., Meidtner, Karina
Published in Scientific reports (20.07.2017)
Published in Scientific reports (20.07.2017)
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META-GSA: Combining Findings from Gene-Set Analyses across Several Genome-Wide Association Studies
Rosenberger, Albert, Friedrichs, Stefanie, Amos, Christopher I, Brennan, Paul, Fehringer, Gordon, Heinrich, Joachim, Hung, Rayjean J, Muley, Thomas, Müller-Nurasyid, Martina, Risch, Angela, Bickeböller, Heike
Published in PloS one (26.10.2015)
Published in PloS one (26.10.2015)
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Implications of the Codominance Model for Hardy-Weinberg Testing in Genetic Association Studies
Wellek, Stefan, Müller-Nurasyid, Martina, Strauch, Konstantin
Published in Human heredity (02.03.2024)
Published in Human heredity (02.03.2024)
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Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
Xue, Angli, Wu, Yang, Zhu, Zhihong, Zhang, Futao, Kemper, Kathryn E., Zheng, Zhili, Yengo, Loic, Lloyd-Jones, Luke R., Sidorenko, Julia, Wu, Yeda, McRae, Allan F., Visscher, Peter M., Zeng, Jian, Yang, Jian
Published in Nature communications (27.07.2018)
Published in Nature communications (27.07.2018)
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y., Kravic, Jasmina, Ahlqvist, Emma, Rosengren, Anders, Groop, Leif, V Varga, Tibor, Franks, Paul, Almgren, Peter, Melander, Olle, Orho-Melander, Marju, McCarthy, Mark I.
Published in Nature genetics (01.04.2018)
Published in Nature genetics (01.04.2018)
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RL-SKAT: An Exact and Efficient Score Test for Heritability and Set Tests
Schweiger, Regev, Weissbrod, Omer, Rahmani, Elior, Müller-Nurasyid, Martina, Kunze, Sonja, Gieger, Christian, Waldenberger, Melanie, Rosset, Saharon, Halperin, Eran
Published in Genetics (Austin) (01.12.2017)
Published in Genetics (Austin) (01.12.2017)
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Joint Linkage and Association Analysis Using GENEHUNTER-MODSCORE with an Application to Familial Pancreatic Cancer
Brugger, Markus, Lutz, Manuel, Müller-Nurasyid, Martina, Lichtner, Peter, Slater, Emily P., Matthäi, Elvira, Bartsch, Detlef K., Strauch, Konstantin
Published in Human heredity (01.01.2024)
Published in Human heredity (01.01.2024)
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OTTERS: a powerful TWAS framework leveraging summary-level reference data
Dai, Qile, Zhou, Geyu, Zhao, Hongyu, Võsa, Urmo, Franke, Lude, Battle, Alexis, Teumer, Alexander, Lehtimäki, Terho, Raitakari, Olli T., Esko, Tõnu, Epstein, Michael P., Yang, Jingjing
Published in Nature communications (07.03.2023)
Published in Nature communications (07.03.2023)
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Common electrocardiogram measures are not associated with telomere length
von Falkenhausen, Aenne S., Freudling, Rebecca, Waldenberger, Melanie, Gieger, Christian, Peters, Annette, Müller-Nurasyid, Martina, Kääb, Stefan, Sinner, Moritz F.
Published in Aging (Albany, NY.) (31.07.2022)
Published in Aging (Albany, NY.) (31.07.2022)
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Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies
Hammerschlag, Anke R., Byrne, Enda M., Agbessi, Mawussé, Ahsan, Habibul, Alves, Isabel, Andiappan, Anand, Awadalla, Philip, Battle, Alexis, Beutner, Frank, Bonder, Marc Jan, Claringbould, Annique, Deelen, Patrick, Esko, Tõnu, Favé, Marie-Julie, Franke, Lude, Frayling, Timothy, Gibson, Gregory, Heijmans, Bastiaan T., Hemani, Gibran, Jansen, Rick, Kähönen, Mika, Kasela, Silva, Kim, Yungil, Kirsten, Holger, Kovacs, Peter, Krohn, Knut, Kronberg-Guzman, Jaanika, Kukushkina, Viktorija, Kutalik, Zoltan, Lee, Bernett, Lehtimäki, Terho, Loeffler, Markus, Marigorta, Urko M., Mei, Hailang, Milani, Lili, Montgomery, Grant W., Müller-Nurasyid, Martina, Nauck, Matthias, Nivard, Michel, Penninx, Brenda, Pervjakova, Natalia, Pierce, Brandon L., Powell, Joseph, Psaty, Bruce M., Raitakari, Olli T., Ripatti, Samuli, Rüeger, Sina, Saha, Ashis, Scholz, Markus, Seppälä, Ilkka, Slagboom, Eline P., Stehouwer, Coen D.A., Sullivan, Patrick, Teumer, Alexander, Thiery, Joachim, Tong, Lin, Tönjes, Anke, van Dongen, Jenny, van Iterson, Maarten, van Meurs, Joyce, Veldink, Jan H., Verlouw, Joost, Visscher, Peter M., Võsa, Urmo, Westra, Harm-Jan, Yang, Jian, Zeng, Biao, Zhang, Futao, Isaacs, Aaron, Pool, René, Hottenga, Jouke J., van Greevenbroek, Marleen MJ, van der Kallen, Carla J.H., Schalkwijk, Casper G., Tigchelaar, Ettje F., Slagboom, P. Eline, Beekman, Marian, Deelen, Joris, van den Berg, Leonard H., van Duijn, Cornelia M., Hofman, Bert A., Uitterlinden, André G., Jhamai, P. Mila, Suchiman, H.Eka D., van der Breggen, Ruud, Lakenberg, Nico, van Galen, Michiel, Bot, Jan, Zhernakova, Daria V., Hof, Peter van ‘t, Nooren, Irene, Moed, Matthijs, Vermaat, Martijn, van Dijk, Freerk, Kielbasa, Szymon M., Swertz, Morris A., van Zwet, Erik. W., Hoen, Peter-Bram ‘t, Wray, Naomi R., Middeldorp, Christel M.
Published in Biological psychiatry (1969) (15.09.2020)
Published in Biological psychiatry (1969) (15.09.2020)
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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Chiang, David Y, Jouni, Mariam, Simonet, Floriane, Jurgens, Sean J, Baudic, Manon, Nicastro, Michele, Potet, Franck, Offerhaus, Joost A, Walsh, Roddy, Choi, Seung Hoan, Verkerk, Arie O, Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Wijeyeratne, Yanushi D, Muir, Alison, Papadakis, Michael, Castelletti, Silvia, Torchio, Margherita, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F, Cerrato, Natascia, Martins, Raphaël P, Campuzano, Oscar, van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Clémenty, Nicolas, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Noël, Antoine, Honarbakhsh, Shohreh, Rudic, Boris, Marzak, Halim, Rowe, Matthew K, Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Krapels, Ingrid P, Steinfurt, Johannes, Winkel, Bo Gregers, Jabbari, Reza, Shoemaker, Moore B, Boukens, Bas J, Škorić-Milosavljević, Doris, Bikker, Hennie, Manevy, Federico, Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Müller-Nurasyid, Martina, Strauch, Konstantin, Peters, Annette, Schulz, Holger, Schwettmann, Lars, Leidl, Reiner, Heier, Margit, Veldink, Jan H, van den Berg, Leonard H, van Damme, Philip, Cusi, Daniele, Lanzani, Chiara, Rigade, Sidwell, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Le Marec, Hervé, Chatel, Stéphanie, Karakachoff, Matilde, Bézieau, Stéphane, London, Barry, Tfelt-Hansen, Jacob, Roden, Dan, Odening, Katja E, Cerrone, Marina, Chinitz, Larry A, Volders, Paul G, van de Berg, Maarten P, Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Kääb, Stefan, Arnaout, Alain Al, Dupuis, Jean-Marc, Pasquie, Jean-Luc
Published in Nature genetics (01.09.2022)
Published in Nature genetics (01.09.2022)
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