Auflistung 4 Medizinische Fakultät nach Titel

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Auflistung 4 Medizinische Fakultät nach Titel

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  • Genetic variants of interferon regulatory factor 5 associated with chronic hepatitis B infection
    Bui Tien Sy; Nghiem Xuan Hoan; Hoang Van Tong; Meyer, Christian G.; Nguyen Linh Toan; Le Huu Song; Bock, Claus-Thomas; Velavan, Thirumalaisamy P. (2018)
  • Genetic variants of programmed cell death 1 are associated with HBV infection and liver disease progression
    Hoan, Nghiem Xuan; Huyen, Pham Thi Minh; Binh, Mai Thanh; Trung, Ngo Tat; Giang, Dao Phuong; Linh, Bui Thuy; Dung, Dang Thi Ngoc; Pallerla, Srinivas Reddy; Kremsner, Peter G.; Velavan, Thirumalaisamy P.; Bang, Mai Hong; Song, Le Huu (2021)
  • Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
    Bonham, Luke W.; Steele, Natasha Z. R.; Karch, Celeste M.; Broce, Iris; Geier, Ethan G.; Wen, Natalie L.; Momeni, Parastoo; Hardy, John; Miller, Zachary A.; Gorno-Tempini, Maria Luisa; Hess, Christopher P.; Lewis, Patrick; Miller, Bruce L.; Seeley, William W.; Manzoni, Claudia; Desikan, Rahul S.; Baranzini, Sergio E.; Ferraris, Raffaele; Yokoyama, Jennifer S.; Hernandez, D. G.; Nalls, M. A.; Rohrer, J. D.; Ramasamy, A.; Kwok, J. B. J.; Dobson-Stone, C.; Schofield, P. R.; Halliday, G. M.; Hodges, J. R.; Piguet, O.; Bartley, L.; Thompson, E.; Haan, E.; Hernandez, I; Ruiz, A.; Boada, M.; Borroni, B.; Padovani, A.; Cruchaga, C.; Cairns, N. J.; Benussi, L.; Binetti, G.; Ghidoni, R.; Forloni, G.; Albani, D.; Galimberti, D.; Fenoglio, C.; Serpente, M.; Scarpini, E.; Clarimon, J.; Lleo, A.; Blesa, R.; Waldo, M. Landqvist; Nilsson, K.; Nilsson, C.; Mackenzie, I. R. A.; Hsiung, G-Y R.; Mann, D. M. A.; Grafman, J.; Morris, C. M.; Attems, J.; Griffiths, T. D.; McKeith, I. G.; Thomas, A. J.; Pietrini, P.; Huey, E. D.; Wassermann, E. M.; Baborie, A.; Jaros, E.; Tierney, M. C.; Pastor, P.; Razquin, C.; Ortega-Cubero, S.; Alonso, E.; Perneczky, R.; Diehl-Schmid, J.; Alexopoulos, P.; Kurz, A.; Rainero, I; Rubino, E.; Pinessi, L.; Rogaeva, E.; St George-Hyslop, P.; Rossi, G.; Tagliavini, F.; Giaccone, G.; Rowe, J. B.; Schlachetzki, J. C. M.; Uphill, J.; Collinge, J.; Mead, S.; Danek, A.; Van Deerlin, V. M.; Grossman, M.; Trojanowski, J. Q.; van der Zee, J.; Cruts, M.; Van Broeckhoven, C.; Cappa, S. F.; Leber, I; Hannequin, D.; Golfier, V (2019)
  • Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
    Johnson, Nichola; Dudbridge, Frank; Orr, Nick; Gibson, Lorna; Jones, Michael E.; Schoemaker, Minouk J.; Folkerd, Elizabeth J.; Haynes, Ben P.; Hopper, John L.; Southey, Melissa C.; Dite, Gillian S.; Apicella, Carmel; Schmidt, Marjanka K.; Broeks, Annegien; Van't Veer, Laura J.; Atsma, Femke; Muir, Kenneth; Lophatananon, Artitaya; Fasching, Peter A.; Beckmann, Matthias W.; Ekici, Arif B.; Renner, Stefan P.; Sawyer, Elinor; Tomlinson, Ian; Kerin, Michael; Miller, Nicola; Burwinkel, Barbara; Marme, Frederik; Schneeweiss, Andreas; Sohn, Christof; Guenel, Pascal; Truong, Therese; Cordina, Emilie; Menegaux, Florence; Bojesen, Stig E.; Nordestgaard, Borge G.; Flyger, Henrik; Milne, Roger; Zamora, M. Pilar; Arias Perez, Jose Ignacio; Benitez, Javier; Bernstein, Leslie; Anton-Culver, Hoda; Ziogas, Argyrios; Dur, Christina Clarke; Brenner, Hermann; Mueller, Heiko; Arndt, Volker; Dieffenbach, Aida Karina; Meindl, Alfons; Heil, Joerg; Bartram, Claus R.; Schmutzler, Rita K.; Brauch, Hiltrud; Justenhoven, Christina; Ko, Yon-Dschun; Nevanlinna, Heli; Muranen, Taru A.; Aittomaeki, Kristiina; Blomqvist, Carl; Matsuo, Keitaro; Doerk, Thilo; Bogdanova, Natalia V.; Antonenkova, Natalia N.; Lindblom, Annika; Mannermaa, Arto; Kataja, Vesa; Kosma, Veli-Matti; Hartikainen, Jaana M.; Chenevix-Trench, Georgia; Beesley, Jonathan; Wu, Anna H.; Van den Berg, David; Tseng, Chiu-Chen; Lambrechts, Diether; Smeets, Dominiek; Neven, Patrick; Wildiers, Hans; Chang-Claude, Jenny; Rudolph, Anja; Nickels, Stefan; Flesch-Janys, Dieter; Radice, Paolo; Peterlongo, Paolo; Bonanni, Bernardo; Pensotti, Valeria; Couch, Fergus J.; Olson, Janet E.; Wang, Xianshu; Fredericksen, Zachary; Pankratz, Vernon S.; Giles, Graham G.; Severi, Gianluca; Baglietto, Laura; Haiman, Chris; Simard, Jacques; Goldberg, Mark S.; Labreche, France; Dumont, Martine; Soucy, Penny; Teo, Soo (2014)
  • Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients
    McCormack, Mark; Gui, Hongsheng; Ingason, Andres; Speed, Doug; Wright, Galen E. B.; Zhang, Eunice J.; Secolin, Rodrigo; Yasuda, Clarissa; Kwok, Maxwell; Wolking, Stefan; Becker, Felicitas; Rau, Sarah; Avbersek, Andreja; Heggeli, Kristin; Leu, Costin; Depondt, Chantal; Sills, Graeme J.; Marson, Anthony G.; Auce, Pauls; Brodie, Martin J.; Francis, Ben; Johnson, Michael R.; Koeleman, Bobby P. C.; Striano, Pasquale; Coppola, Antonietta; Zara, Federico; Kunz, Wolfram S.; Sander, Josemir W.; Lerche, Holger; Klein, Karl Martin; Weckhuysen, Sarah; Krenn, Martin; Gudmundsson, Larus J.; Stefansson, Kari; Krause, Roland; Shear, Neil; Ross, Colin J. D.; Delanty, Norman; Pirmohamed, Munir; Carleton, Bruce C.; Cendes, Fernando; Lopes-Cendes, Iscia; Liao, Wei-ping; O'Brien, Terence J.; Sisodiya, Sanjay M.; Cherny, Stacey; Kwan, Patrick; Baum, Larry; Cavalleri, Gianpiero L. (2018)
  • Genetic variation in human drug-related genes
    Tremmel, R.; Schwab, M.; Kohlbacher, O.; Marks, D.S.; Schärfe, C.P.I. (2017)
  • Genetic Variation in MAOA Modulates Prefrontal Cortical Regulation of Approach-Avoidance Reactions
    Ernst, Lena H.; Lutz, Elisabeth; Ehlis, Ann-Christine; Fallgatter, Andreas J.; Reif, Andreas; Plichta, Michael M. (2013)
  • Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
    Purrington, Kristen S.; Slettedahl, Seth; Bolla, Manjeet K.; Michailidou, Kyriaki; Czene, Kamila; Nevanlinna, Heli; Bojesen, Stig E.; Andrulis, Irene L.; Cox, Angela; Hall, Per; Carpenter, Jane; Yannoukakos, Drakoulis; Haiman, Christopher A.; Fasching, Peter A.; Mannermaa, Arto; Winqvist, Robert; Brenner, Hermann; Lindblom, Annika; Chenevix-Trench, Georgia; Benitez, Javier; Swerdlow, Anthony; Kristensen, Vessela; Guenel, Pascal; Meindl, Alfons; Darabi, Hatef; Eriksson, Mikael; Fagerholm, Rainer; Aittomaki, Kristiina; Blomqvist, Carl; Nordestgaard, Borge G.; Nielsen, Sune F.; Flyger, Henrik; Wang, Xianshu; Olswold, Curtis; Olson, Janet E.; Mulligan, Anna Marie; Knight, Julia A.; Tchatchou, Sandrine; Reed, Malcolm W. R.; Cross, Simon S.; Liu, Jianjun; Li, Jingmei; Humphreys, Keith; Clarke, Christine; Scott, Rodney; Fostira, Florentia; Fountzilas, George; Konstantopoulou, Irene; Henderson, Brian E.; Schumacher, Fredrick; Le Marchand, Loic; Ekici, Arif B.; Hartmann, Arndt; Beckmann, Matthias W.; Hartikainen, Jaana M.; Kosma, Veli-Matti; Kataja, Vesa; Jukkola-Vuorinen, Arja; Pylkas, Katri; Kauppila, Saila; Dieffenbach, Aida Karina; Stegmaier, Christa; Arndt, Volker; Margolin, Sara; Balleine, Rosemary; Arias Perez, Jose Ignacio; Pilar Zamora, M.; Menendez, Primitiva; Ashworth, Alan; Jones, Michael; Orr, Nick; Arveux, Patrick; Kerbrat, Pierre; Therese Truong; Bugert, Peter; Toland, Amanda E.; Ambrosone, Christine B.; Labreche, France; Goldberg, Mark S.; Dumont, Martine; Ziogas, Argyrios; Lee, Eunjung; Dite, Gillian S.; Apicella, Carmel; Southey, Melissa C.; Long, Jirong; Shrubsole, Martha; Deming-Halverson, Sandra; Ficarazzi, Filomena; Barile, Monica; Peterlongo, Paolo; Durda, Katarzyna; Jaworska-Bieniek, Katarzyna; Tollenaar, Robert A. E. M.; Seynaeve, Caroline; Bruening, Thomas; Ko, Yon-Dschun; Van Deurzen, Carolien H. M.; Martens, John W. M.; Kriege, Mieke; Figueroa, Jonine D. (2014)
  • Genetic Variation in NR1H4 Encoding the Bile Acid Receptor FXR Determines Fasting Glucose and Free Fatty Acid Levels in Humans
    Heni, Martin; Wagner, Robert; Ketterer, Caroline; Boehm, Anja; Linder, Katarzyna; Machicao, Fausto; Machann, Juergen; Schick, Fritz; Hennige, Anita M.; Stefan, Norbert; Haering, Hans-Ulrich; Fritsche, Andreas; Staiger, Harald (2013)
  • Genetic variation in TCF7L2 rs7903146 and history of GDM negatively and independently impact on diabetes-associated metabolic traits
    Fritsche, Louise; Sarief, Mirjam; Wagner, Robert; Stefan, Norbert; Lehmann, Rainer; Haering, Hans-Ulrich; Grallert, Harald; Fritsche, Andreas; Lechner, Andreas (2018)
  • Genetic Variation in the 11 beta-hydroxysteroid-dehydrogenase 1 Gene Determines NAFLD and Visceral Obesity
    Lutz, Stefan Z.; Peter, Andreas; Machicao, Fausto; Lamprinou, Apostolia; Machann, Juergen; Schick, Fritz; Koenigsrainer, Ingmar; Koenigsrainer, Alfred; Fritsche, Andreas; Staiger, Harald; Haering, Hans-Ulrich; Stefan, Norbert; Kantartzis, Konstantinos (2016)
  • Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium
    Lei, Jieping; Rudolph, Anja; Moysich, Kirsten B.; Behrens, Sabine; Goode, Ellen L.; Bolla, Manjeet K.; Dennis, Joe; Dunning, Alison M.; Easton, Douglas F.; Wang, Qin; Benitez, Javier; Hopper, John L.; Southey, Melissa C.; Schmidt, Marjanka K.; Broeks, Annegien; Fasching, Peter A.; Haeberle, Lothar; Peto, Julian; dos-Santos-Silva, Isabel; Sawyer, Elinor J.; Tomlinson, Ian; Burwinkel, Barbara; Marme, Frederik; Guenel, Pascal; Truong, Therese; Bojesen, Stig E.; Flyger, Henrik; Nielsen, Sune F.; Nordestgaard, Borge G.; Gonzalez-Neira, Anna; Menendez, Primitiva; Anton-Culver, Hoda; Neuhausen, Susan L.; Brenner, Hermann; Arndt, Volker; Meindl, Alfons; Schmutzler, Rita K.; Brauch, Hiltrud; Hamann, Ute; Nevanlinna, Heli; Fagerholm, Rainer; Doerk, Thilo; Bogdanova, Natalia V.; Mannermaa, Arto; Hartikainen, Jaana M.; Van Dijck, Laurien; Smeets, Ann; Flesch-Janys, Dieter; Eilber, Ursula; Radice, Paolo; Peterlongo, Paolo; Couch, Fergus J.; Hallberg, Emily; Giles, Graham G.; Milne, Roger L.; Haiman, Christopher A.; Schumacher, Fredrick; Simard, Jacques; Goldberg, Mark S.; Kristensen, Vessela; Borresen-Dale, Anne-Lise; Zheng, Wei; Beeghly-Fadiel, Alicia; Winqvist, Robert; Grip, Mervi; Andrulis, Irene L.; Glendon, Gord; Garcia-Closas, Montserrat; Figueroa, Jonine; Czene, Kamila; Brand, Judith S.; Darabi, Hatef; Eriksson, Mikael; Hall, Per; Li, Jingmei; Cox, Angela; Cross, Simon S.; Pharoah, Paul D. P.; Shah, Mitul; Kabisch, Maria; Torres, Diana; Jakubowska, Anna; Lubinski, Jan; Ademuyiwa, Foluso; Ambrosone, Christine B.; Swerdlow, Anthony; Jones, Michael; Chang-Claude, Jenny (2016)
  • Genetic variation of platelet function and pharmacology: An update of current knowledge
    Geisler, Tobias; Schaeffeler, Elke; Gawaz, Meinrad; Schwab, Matthias (2013)
  • Genetically engineered CAR NK cells display selective cytotoxicity against FLT3-positive B-ALL and inhibit in vivo leukemia growth
    Oelsner, Sarah; Waldmann, Anja; Billmeier, Arne; Roeder, Jasmin; Lindner, Aline; Ullrich, Evelyn; Marschalek, Rolf; Dotti, Gianpietro; Jung, Gundram; Grosse-Hovest, Ludger; Oberoi, Pranav; Bader, Peter; Wels, Winfried S. (2019)
  • Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
    Guo, Yan; Andersen, Shaneda Warren; Shu, Xiao-Ou; Michailidou, Kyriaki; Bolla, Manjeet K.; Wang, Qin; Garcia-Closas, Montserrat; Milne, Roger L.; Schmidt, Marjanka K.; Chang-Claude, Jenny; Dunning, Allison; Bojesen, Stig E.; Ahsan, Habibul; Aittomaki, Kristiina; Andrulis, Irene L.; Anton-Culver, Hoda; Arndt, Volker; Beckmann, Matthias W.; Beeghly-Fadiel, Alicia; Benitez, Javier; Bogdanova, Natalia V.; Bonanni, Bernardo; Borresen-Dale, Anne-Lise; Brand, Judith; Brauch, Hiltrud; Brenner, Hermann; Bruening, Thomas; Burwinkel, Barbara; Casey, Graham; Chenevix-Trench, Georgia; Couch, Fergus J.; Cox, Angela; Cross, Simon S.; Czene, Kamila; Devilee, Peter; Doerk, Thilo; Dumont, Martine; Fasching, Peter A.; Figueroa, Jonine; Flesch-Janys, Dieter; Fletcher, Olivia; Flyger, Henrik; Fostira, Florentia; Gammon, Marilie; Giles, Graham G.; Guenel, Pascal; Haiman, Christopher A.; Hamann, Ute; Hooning, Maartje J.; Hopper, John L.; Jakubowska, Anna; Jasmine, Farzana; Jenkins, Mark; John, Esther M.; Johnson, Nichola; Jones, Michael E.; Kabisch, Maria; Kibriya, Muhammad; Knight, Julia A.; Koppert, Linetta B.; Kosma, Veli-Matti; Kristensen, Vessela; Le Marchand, Loic; Lee, Eunjung; Li, Jingmei; Lindblom, Annika; Luben, Robert; Lubinski, Jan; Malone, Kathi E.; Mannermaa, Arto; Margolin, Sara; Marme, Frederik; McLean, Catriona; Meijers-Heijboer, Hanne; Meindl, Alfons; Neuhausen, Susan L.; Nevanlinna, Heli; Neven, Patrick; Olson, Janet E.; Perez, Jose I. A.; Perkins, Barbara; Peterlongo, Paolo; Phillips, Kelly-Anne; Pylkas, Katri; Rudolph, Anja; Santella, Regina; Sawyer, Elinor J.; Schmutzler, Rita K.; Seynaeve, Caroline; Shah, Mitul; Shrubsole, Martha J.; Southey, Melissa C.; Swerdlow, Anthony J.; Toland, Amanda E.; Tomlinson, Ian; Torres, Diana; Truong, Therese; Ursin, Giske; Van Der Luijt, Rob B.; Verhoef, Senno; Whittemore, Alice S. (2016)
  • Genetics and Disease Expression in the CNGA3 Form of Achromatopsia Steps on the Path to Gene Therapy
    Zelinger, Lina; Cideciyan, Artur V.; Kohl, Susanne; Schwartz, Sharon B.; Rosenmann, Ada; Eli, Dalia; Sumaroka, Alexander; Roman, Alejandro J.; Luo, Xunda; Brown, Cassondra; Rosin, Boris; Blumenfeld, Anat; Wissinger, Bernd; Jacobson, Samuel G.; Banin, Eyal; Sharon, Dror (2015)
  • Genetics and iron in the systems biology of Parkinson's disease and some related disorders
    Funke, Claudia; Schneider, Susanne A.; Berg, Daniela; Kell, Douglas B. (2013)
  • Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1
    Nies, Anne T.; Niemi, Mikko; Burk, Oliver; Winter, Stefan; Zanger, Ulrich M.; Stieger, Bruno; Schwab, Matthias; Schaeffeler, Elke (2013)
  • Genetics of longevity. Data from the studies on Sicilian centenarians
    Balistreri, Carmela R.; Candore, Giuseppina; Accardi, Giulia; Bova, Manuela; Buffa, Silvio; Bulati, Matteo; Forte, Giusi I.; Listi, Florinda; Martorana, Adriana; Palmeri, Marisa; Pellicano, MariaValeria; Vaccarino, Loredana; Scola, Letizia; Lio, Domenico; Colonna-Romano, Giuseppina (2012)
  • Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related Disorders
    Kegele, Josua; Krueger, Johanna; Koko, Mahmoud; Lange, Lara; Marco Hernandez, Ana Victoria; Martinez, Francisco; Muenchau, Alexander; Lerche, Holger; Lauxmann, Stephan (2021)