Auflistung 4 Medizinische Fakultät nach Titel

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Auflistung 4 Medizinische Fakultät nach Titel

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  • Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist: Hip Ratio, Is Causal for Endometrial Cancer
    Painter, Jodie N.; O'Mara, Tracy A.; Marquart, Louise; Webb, Penelope M.; Attia, John; Medland, Sarah E.; Cheng, Timothy; Dennis, Joe; Holliday, Elizabeth G.; McEvoy, Mark; Scott, Rodney J.; Ahmed, Shahana; Healey, Catherine S.; Shah, Mitul; Gorman, Maggie; Martin, Lynn; Hodgson, Shirley V.; Beckmann, Matthias W.; Ekici, Arif B.; Fasching, Peter A.; Hein, Alexander; Ruebner, Matthias; Czene, Kamila; Darabi, Hatef; Hall, Per; Li, Jingmei; Doerk, Thilo; Duerst, Matthias; Hillemanns, Peter; Runnebaum, Ingo B.; Amant, Frederic; Annibali, Daniela; Depreeuw, Jeroen; Lambrechts, Diether; Neven, Patrick; Cunningham, Julie M.; Dowdy, Sean C.; Goode, Ellen L.; Fridley, Brooke L.; Winham, Stacey J.; Njolstad, Tormund S.; Salvesen, Helga B.; Trovik, Jone; Werner, Henrica M. J.; Ashton, Katie A.; Otton, Geoffrey; Proietto, Anthony; Mints, Miriam; Tham, Emma; Bolla, Manjeet K.; Michailidou, Kyriaki; Wang, Qin; Tyrer, Jonathan P.; Hopper, John L.; Peto, Julian; Swerdlow, Anthony J.; Burwinkel, Barbara; Brenner, Hermann; Meindl, Alfons; Brauch, Hiltrud; Lindblom, Annika; Chang-Claude, Jenny; Couch, Fergus J.; Giles, GrahamG.; Kristensen, Vessela N.; Cox, Angela; Pharoah, Paul D. P.; Tomlinson, Ian; Dunning, Alison M.; Easton, Douglas F.; Thompson, Deborah J.; Spurdle, Amanda B. (2016)
  • Genetic Risk, Lifestyle, and Age-Related Macular Degeneration in Europe The EYE-RISK Consortium
    Colijn, Johanna M.; Meester-Smoor, Magda; Verzijden, Timo; de Breuk, Anita; Silva, Rufino; Merle, Benedicte M. J.; Cougnard-Gregoire, Audrey; Hoyng, Carel B.; Fauser, Sascha; Coolen, Anthonius; Creuzot-Garcher, Catherine; Hense, Hans-Werner; Ueffing, Marius; Delcourt, Cecile; den Hollander, Anneke, I; Klaver, Caroline C. W. (2021)
  • Genetic Rodent Models of Huntington Disease
    Stricker-Shaver, J.; Novati, A.; Yu-Taeger, L.; Nguyen, H. P. (2018)
  • Genetic screening for NiemannPick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study
    Bauer, Peter; Balding, David J.; Kluenemann, Hans H.; Linden, David E. J.; Ory, Daniel S.; Pineda, Merce; Priller, Josef; Sedel, Frederic; Muller, Audrey; Chadha-Boreham, Harbajan; Welford, Richard W. D.; Strasser, Daniel S.; Patterson, Marc C. (2013)
  • Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
    Doll, Julia; Vona, Barbara; Schnapp, Linda; Rueschendorf, Franz; Khan, Imran; Khan, Saadullah; Muhammad, Noor; Alam Khan, Sher; Nawaz, Hamed; Khan, Ajmal; Ahmad, Naseer; Kolb, Susanne M.; Kuehlewein, Laura; Labonne, Jonathan D. J.; Layman, Lawrence C.; Hofrichter, Michaela A. H.; Roder, Tabea; Dittrich, Marcus; Mueller, Tobias; Graves, Tyler D.; Kong, Il-Keun; Nanda, Indrajit; Kim, Hyung-Goo; Haaf, Thomas (2020)
  • Genetic testing before epilepsy surgery-An exploratory survey and case collection from German epilepsy centers
    Bosselmann, Christian Malte; San Antonio-Arce, Victoria; Schulze-Bonhage, Andreas; Fauser, Susanne; Zacher, Pia; Mayer, Thomas; Aparicio, Javier; Albers, Kristina; Cloppenborg, Thomas; Kunz, Wolfram; Surges, Rainer; Syrbe, Steffen; Weber, Yvonne; Wolking, Stefan (2022)
  • Genetic Testing for Rare Diseases: A Systematic Review of Ethical Aspects
    Kruse, Judith; Mueller, Regina; Aghdassi, Ali A.; Lerch, Markus M.; Salloch, Sabine (2022)
  • Genetic testing in neurological diseases
    Biskup, Saskia; Gasser, Thomas (2012)
  • Genetic Testing in the Diagnosis and Biology of Myeloid Neoplasms (Excluding Acute Leukemias) : 2017 Society for Hematopathology/European Association for Haematopathology Workshop Report
    Hasserjian, Robert P.; Kelley, Todd W.; Weinberg, Olga K.; Morgan, Elizabeth A.; Fend, Falko (2019)
  • Genetic Testing is Superior Over Endogenous Pharmacometabolomic Markers to Predict Safety of Haloperidol in Patients with Alcohol-induced Psychotic Disorder
    Skryabin, Valentin; Zastrozhin, Mikhail; Parkhomenko, Alexandra; Lauschke, Volker M.; Smirnov, Valery; Petukhov, Aleksey; Pankratenko, Elena; Pozdnyakov, Sergei; Koporov, Sergei; Denisenko, Natalia; Akmalova, Kristina; Bryun, Evgeny; Sychev, Dmitry (2022)
  • Genetic underpinnings of left superior temporal gyrus thickness in patients with schizophrenia
    Wolthusen, Rick P. F.; Hass, Johanna; Walton, Esther; Turner, Jessica A.; Roessner, Veit; Sponheim, Scott R.; Ho, Beng-Choon; Holt, Daphne J.; Gollub, Randy L.; Calhoun, Vince; Ehrlich, Stefan (2015)
  • Genetic Variant ABCC1 rs45511401 Is Associated with Increased Response to Statins in Patients with Familial Hypercholesterolemia
    Dagli-Hernandez, Carolina; Borges, Jessica Bassani; Rodrigues Marcal, Elisangela da Silva; Costa de Freitas, Renata Caroline; Mori, Augusto Akira; Goncalves, Rodrigo Marques; Faludi, Andre Arpad; de Oliveira, Victor Fernandes; Ferreira, Glaucio Monteiro; Bastos, Gisele Medeiros; Zhou, Yitian; Lauschke, Volker M.; Cerda, Alvaro; Hirata, Mario Hiroyuki; Crespo Hirata, Rosario Dominguez (2022)
  • Genetic Variants Associated With Glycine Metabolism and Their Role in Insulin Sensitivity and Type 2 Diabetes
    Xie, Weijia; Wood, Andrew R.; Lyssenko, Valeriya; Weedon, Michael N.; Knowles, Joshua W.; Alkayyali, Sami; Assimes, Themistocles L.; Quertermous, Thomas; Abbasi, Fahim; Paananen, Jussi; Haering, Hans; Hansen, Torben; Pedersen, Oluf; Smith, Ulf; Laakso, Markku; Dekker, Jacqueline M.; Nolan, John J.; Groop, Leif; Ferrannini, Ele; Adam, Klaus-Peter; Gall, Walter E.; Frayling, Timothy M.; Walker, Mark (2013)
  • Genetic variants in genes involved in creatine biosynthesis in patients with severe obesity or anorexia nervosa
    Rajcsanyi, Luisa S.; Hoffmann, Anne; Ghosh, Adhideb; Matrisch-Dinkler, Birgit; Zheng, Yiran; Peters, Triinu; Sun, Wenfei; Dong, Hua; Noe, Falko; Wolfrum, Christian; Herpertz-Dahlmann, Beate; Seitz, Jochen; de Zwaan, Martina; Herzog, Wolfgang; Ehrlich, Stefan; Zipfel, Stephan; Giel, Katrin; Egberts, Karin; Burghardt, Roland; Foecker, Manuel; Tsai, Linus T.; Mueller, Timo D.; Blueher, Matthias; Hebebrand, Johannes; Hirtz, Raphael; Hinney, Anke (2023)
  • Genetic variants in VEGF pathway genes in neoadjuvant breast cancer patients receiving bevacizumab: Results from the randomized phase III GeparQuinto study
    Hein, Alexander; Lambrechts, Diether; von Minckwitz, Gunter; Haeberle, Lothar; Eidtmann, Holger; Tesch, Hans; Untch, Michael; Hilfrich, Joern; Schem, Christian; Rezai, Mahdi; Gerber, Bernd; Costa, Serban Dan; Blohmer, Jens-Uwe; Schwedler, Kathrin; Kittel, Kornelia; Fehm, Tanja; Kunz, Georg; Beckmann, Matthias W.; Ekici, Arif B.; Hanusch, Claus; Huober, Jens; Liedtke, Cornelia; Mau, Christine; Moisse, Matthieu; Mueller, Volkmar; Nekljudova, Valentina; Peuteman, Gilian; Rack, Brigitte; Rubner, Matthias; Van Brussel, Thomas; Wang, Liewei; Weinshilboum, Richard M.; Loibl, Sibylle; Fasching, Peter A. (2015)
  • 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)