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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 6

Zeitschriftenartikel

Slater, Emily P.; Wilke, Lisa M.; Boehm, Lutz Benedikt; Strauch, Konstantin; Lutz, Manuel; Gercke, Norman; Matthai, Elvira; Hemminki, Kari; Forsti, Asta; Schlesner, Matthias; Paramasivam, Nagarajan und Bartsch, Detlef K. (2021): Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer. In: Journal of Personalized Medicine, Bd. 11, Nr. 7, 631

Schmidt, Amand F.; Holmes, Michael V.; Preiss, David; Swerdlow, Daniel I.; Denaxas, Spiros; Fatemifar, Ghazaleh; Faraway, Rupert; Finan, Chris; Valentine, Dennis; Fairhurst-Hunter, Zammy; Hartwig, Fernando Pires; Horta, Bernardo Lessa; Hypponen, Elina; Power, Christine; Moldovan, Max; van Iperen, Erik; Hovingh, Kees; Demuth, Ilja; Norman, Kristina; Steinhagen-Thiessen, Elisabeth; Demuth, Juri; Bertram, Lars; Lill, Christina M.; Coassin, Stefan; Willeit, Johann; Kiechl, Stefan; Willeit, Karin; Mason, Dan; Wright, John; Morris, Richard; Wanamethee, Goya; Whincup, Peter; Ben-Shlomo, Yoav; McLachlan, Stela; Price, Jackie F.; Kivimaki, Mika; Welch, Catherine; Sanchez-Galvez, Adelaida; Marques-Vidal, Pedro; Nicolaides, Andrew; Panayiotou, Andrie G.; Onland-Moret, N. Charlotte; van der Schouw, Yvonne T.; Matullo, Giuseppe; Fiorito, Giovanni; Guarrera, Simonetta; Sacerdote, Carlotta; Wareham, Nicholas J.; Langenberg, Claudia; Scott, Robert A.; Luan, Jian'an; Bobak, Martin; Malyutina, Sofia; Pajak, Andrzej; Kubinova, Ruzena; Tamosiunas, Abdonas; Pikhart, Hynek; Grarup, Niels; Pedersen, Oluf; Hansen, Torben; Linneberg, Allan; Jess, Tine; Cooper, Jackie; Humphries, Steve E.; Brilliant, Murray; Kitchner, Terrie; Hakonarson, Hakon; Carrell, David S.; McCarty, Catherine A.; Lester, Kirchner H.; Larson, Eric B.; Crosslin, David R.; de Andrade, Mariza; Roden, Dan M.; Denny, Joshua C.; Carty, Cara; Hancock, Stephen; Attia, John; Holliday, Elizabeth; Scott, Rodney; Schofield, Peter; O'Donnell, Martin; Yusuf, Salim; Chong, Michael; Pare, Guillaume; van der Harst, Pim; Said, M. Abdullah; Eppinga, Ruben N.; Verweij, Niek; Snieder, Harold; Christen, Tim; Mook-Kanamori, D. O.; Gustafsson, Stefan; Lind, Lars; Ingelsson, Erik; Pazoki, Raha; Franco, Oscar; Hofman, Albert; Uitterlinden, Andre; Dehghan, Abbas; Teumer, Alexander; Baumeister, Sebastian; Doerr, Marcus; Lerch, Markus M.; Voelker, Uwe; Voelzke, Henry; Ward, Joey; Pell, Jill P.; Meade, Tom; Christophersen, Ingrid E.; Maitland-van der Zee, Anke H.; Baranova, Ekaterina V.; Young, Robin; Ford, Ian; Campbell, Archie; Padmanabhan, Sandosh; Bots, Michiel L.; Grobbee, Diederick E.; Froguel, Philippe; Thuillier, Dorothee; Roussel, Ronan; Bonnefond, Amelie; Cariou, Bertrand; Smart, Melissa; Bao, Yanchun; Kumari, Meena; Mahajan, Anubha; Hopewell, Jemma C.; Seshadri, Sudha; Dale, Caroline; Costa, Rui Providencia E.; Ridker, Paul M.; Chasman, Daniel I.; Reiner, Alex P.; Ritchie, Marylyn D.; Lange, Leslie A.; Cornish, Alex J.; Dobbins, Sara E.; Hemminki, Kari; Kinnersley, Ben; Sanson, Marc; Labreche, Karim; Simon, Matthias; Bondy, Melissa; Law, Philip; Speedy, Helen; Allan, James; Li, Ni; Went, Molly; Weinhold, Niels; Morgan, Gareth; Sonneveld, Pieter; Nilsson, Bjorn; Goldschmidt, Hartmut; Sud, Amit; Engert, Andreas; Hansson, Markus; Hemingway, Harry; Asselbergs, Folkert W.; Patel, Riyaz S.; Keating, Brendan J.; Sattar, Naveed; Houlston, Richard; Casas, Juan P. und Hingorani, Aroon D. (2019): Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. In: BMC Cardiovascular Disorders, Bd. 19, Nr. 1, 240

Reifenberger, Guido; Sill, Martin; Hentschel, Bettina; Felsberg, Jörg; Jones, David T. W.; Gramatzki, Dorothee; Kaulich, Kerstin; Tonn, Joerg-Christian; Herrlinger, Ulrich; Schackert, Gabriele; Westphal, Manfred; Sabel, Michael; Capper, David; Kumar, Rajiv; Hemminki, Kari; Pietsch, Torsten; Loeffler, Markus; Pfister, Stefan M.; Deimling, Andreas von und Weller, Michael (2016): Long-term survival with glioblastoma in the elderly. In: Neuro-Oncology, Bd. 18: S. 110-111

Carrai, Maura; Steinke, Verena; Vodicka, Pavel; Pardini, Barbara; Rahner, Nils; Holinski-Feder, Elke; Morak, Monika; Schackert, Hans K.; Görgens, Heike; Stemmler, Susanne; Betz, Beate; Kloor, Matthias; Engel, Christoph; Büttner, Reinhard; Naccarati, Alessio; Vodickova, Ludmila; Novotny, Jan; Stein, Angelika; Hemminki, Kari; Propping, Peter; Försti, Asta; Canzian, Federico; Barale, Roberto und Campa, Daniele (2011): Association between TAS2R38 gene polymorphisms and colorectal cancer risk. A case-control study in two independent populations of Caucasian origin.
In: PLOS ONE 6(6), e20464 [PDF, 112kB]

Campa, Daniele; Pardini, Barbara; Naccarati, Alessio; Vodickova, Ludmila; Novotny, Jan; Steinke, Verena; Rahner, Nils; Holinski-Feder, Elke; Morak, Monika; Schackert, Hans K.; Goergens, Heike; Koetting, Judith; Betz, Beate; Kloor, Matthias; Engel, Christoph; Buettner, Reinhard; Propping, Peter; Foersti, Asta; Hemminki, Kari; Barale, Roberto; Vodicka, Pavel und Canzian, Federico (2010): Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study. In: BMC Gastroenterology 10:112 [PDF, 235kB]

Hartmaier, Ryan J.; Tchatchou, Sandrine; Richter, Alexandra S.; Wang, Jay; McGuire, Sean E.; Skaar, Todd C.; Rae, Jimmy M.; Hemminki, Kari; Sutter, Christian; Ditsch, Nina; Bugert, Peter; Weber, Bernhard H. F.; Niederacher, Dieter; Arnold, Norbert; Varon-Mateeva, Raymonda; Wappenschmidt, Barbara; Schmutzler, Rita K.; Meindl, Alfons; Bartram, Claus R.; Burwinkel, Barbara und Oesterreich, Steffi (2009): Nuclear receptor coregulator SNP discovery and impact on breast cancer risk. In: BMC Cancer 9:438 [PDF, 879kB]

Diese Liste wurde am Sat Apr 13 22:19:30 2024 CEST erstellt.