Auflistung 4 Medizinische Fakultät nach Titel

DSpace Repositorium (Manakin basiert)

Auflistung 4 Medizinische Fakultät nach Titel

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  • Genetic and epigenetic characterization of posterior pituitary tumors
    Schmid, Simone; Solomon, David A.; Perez, Eilis; Thieme, Anne; Kleinschmidt-DeMasters, Bette K.; Giannini, Caterina; Reinhardt, Annekathrin; Asa, Sylvia L.; Mete, Ozgur; Stichel, Damian; Siewert, Christin; Dittmayer, Carsten; Hasselblatt, Martin; Paulus, Werner; Nagel, Christoph; Harter, Patrick N.; Schittenhelm, Jens; Honegger, Juergen; Rushing, Elisabeth; Coras, Roland; Pfister, Stefan M.; Buslei, Rolf; Koch, Arend; Perry, Arie; Jones, David T. W.; von Deimling, Andreas; Capper, David; Lopes, M. Beatriz (2021)
  • Genetic and functional analysis of chymotrypsin-like protease (CTRL) in chronic pancreatitis
    Eiseler, Katharina; Neppl, Lea; Schmidt, Andreas W.; Rauscher, Beate; Ewers, Maren; Masson, Emmanuelle; Chen, Jian-Min; Ferec, Claude; Rebours, Vinciane; Grammatikopoulos, Tassos; Foskett, Pierre; Greenhalf, William; Halloran, Christopher; Neoptolemos, John; Haack, Tobias B.; Ossowski, Stephan; Sturm, Marc; Rosendahl, Jonas; Laumen, Helmut; Witt, Heiko (2023)
  • Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
    Mignot, Cyril; Nava, Caroline; Ville, Dorothee; Sanlaville, Damien; Lesca, Gaetan; Rastetter, Agnes; Gachet, Benoit; Marie, Yannick; Korenke, G. Christoph; Borggraefe, Ingo; Hoffmann-Zacharska, Dorota; Szczepanik, Elzbieta; Rudzka-Dybala, Mariola; Yis, Uluc; Caglayan, Hande; Isapof, Arnaud; Marey, Isabelle; Panagiotakaki, Eleni; Korff, Christian; Rossier, Eva; Riess, Angelika; Beck-Woedl, Stefanie; Rauch, Anita; Zweier, Christiane; Hoyer, Juliane; Reis, Andre; Mironov, Mikhail; Bobylova, Maria; Mukhin, Konstantin; Hernandez-Hernandez, Laura; Maher, Bridget; Sisodiya, Sanjay; Kuhn, Marius; Glaeser, Dieter; Wechuysen, Sarah; Myers, Candace T.; Mefford, Heather C.; Biskup, Saskia; Lemke, Johannes R.; Heron, Delphine; Kluger, Gerhard; Depienne, Christel; von Stülpnagel, Celina; Hörtnagel, Konstanze (2016)
  • Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort
    Lesage, Suzanne; Houot, Marion; Mangone, Graziella; Tesson, Christelle; Bertrand, Helene; Forlani, Sylvie; Anheim, Mathieu; Brefel-Courbon, Christine; Broussolle, Emmanuel; Thobois, Stephane; Damier, Philippe; Durif, Franck; Roze, Emmanuel; Tison, Francois; Grabli, David; Ory-Magne, Fabienne; Degos, Bertrand; Viallet, Francois; Cormier-Dequaire, Florence; Ouvrard-Hernandez, Anne-Marie; Vidailhet, Marie; Lohmann, Ebba; Singleton, Andrew; Corvol, Jean-Christophe; Brice, Alexis (2020)
  • Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
    Wolff, Markus; Johannesen, Katrine M.; Hedrich, Ulrike B. S.; Masnada, Silvia; Rubboli, Guido; Gardella, Elena; Lesca, Gaetan; Ville, Dorothee; Milh, Mathieu; Villard, Laurent; Afenjar, Alexandra; Chantot-Bastaraud, Sandra; Mignot, Cyril; Lardennois, Caroline; Nava, Caroline; Schwarz, Niklas; Gerard, Marion; Perrin, Laurence; Doummar, Diane; Auvin, Stephane; Miranda, Maria J.; Hempel, Maja; Brilstra, Eva; Knoers, Nine; Verbeek, Nienke; van Kempen, Marjan; Braun, Kees P.; Mancini, Grazia; Biskup, Saskia; Hoertnagel, Konstanze; Doecker, Miriam; Bast, Thomas; Loddenkemper, Tobias; Wong-Kisiel, Lily; Baumeister, Friedrich M.; Fazeli, Walid; Striano, Pasquale; Dilena, Robertino; Fontana, Elena; Zara, Federico; Kurlemann, Gerhard; Klepper, Joerg; Thoene, Jess G.; Arndt, Daniel H.; Deconinck, Nicolas; Schmitt-Mechelke, Thomas; Maier, Oliver; Muhle, Hiltrud; Wical, Beverly; Finetti, Claudio; Brueckner, Reinhard; Pietz, Joachim; Golla, Guenther; Jillella, Dinesh; Linnet, Karen M.; Charles, Perrine; Moog, Ute; Oiglane-Shlik, Eve; Mantovani, John F.; Park, Kristen; Deprez, Marie; Lederer, Damien; Mary, Sandrine; Scalais, Emmanuel; Selim, Laila; Van Coster, Rudy; Lagae, Lieven; Nikanorova, Marina; Hjalgrim, Helle; Korenke, G. Christoph; Trivisano, Marina; Specchio, Nicola; Ceulemans, Berten; Dorn, Thomas; Helbig, Katherine L.; Hardies, Katia; Stamberger, Hannah; de Jonghe, Peter; Weckhuysen, Sarah; Lemke, Johannes R.; Kraegeloh-Mann, Ingeborg; Helbig, Ingo; Kluger, Gerhard; Lerche, Holger; Moller, Rikke S. (2017)
  • Genetic and physical interaction of Meis2, Pax3 and Pax7 during dorsal midbrain development
    Agoston, Zsuzsa; Li, Naixin; Haslinger, Anja; Wizenmann, Andrea; Schulte, Dorothea (2012)
  • Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9-year period
    Weisschuh, Nicole; Obermaier, Carolin D.; Battke, Florian; Bernd, Antje; Kuehlewein, Laura; Nasser, Fadi; Zobor, Ditta; Zrenner, Eberhart; Weber, Eva; Wissinger, Bernd; Biskup, Saskia; Stingl, Katarina; Kohl, Susanne (2020)
  • Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research
    Rajan, Roopa; Divya, K. P.; Kandadai, Rukmini Mridula; Yadav, Ravi; Satagopam, Venkata P.; Madhusoodanan, U. K.; Agarwal, Pankaj; Kumar, Niraj; Ferreira, Teresa; Kumar, Hrishikesh; Prasad, A. V. Sreeram; Shetty, Kuldeep; Mehta, Sahil; Desai, Soaham; Kumar, Suresh; Prashanth, L. K.; Bhatt, Mohit; Wadia, Pettarusp; Ramalingam, Sudha; Wali, G. M.; Pandey, Sanjay; Bartusch, Felix; Hannussek, Maximilian; Krueger, Jens; Kumar-Sreelatha, Ashwin; Grover, Sandeep; Lichtner, Peter; Sturm, Marc; Roeper, Jochen; Busskamp, Volker; Chandak, Giriraj R.; Schwamborn, Jens; Seth, Pankaj; Gasser, Thomas; Riess, Olaf; Goyal, Vinay; Pal, Pramod Kumar; Borgohain, Rupam; Krueger, Rejko; Kishore, Asha; Sharma, Manu (2020)
  • Genetic assessment of familial and early-onset Parkinson's disease in a Greek population
    Bozi, M.; Papadimitriou, D.; Antonellou, R.; Moraitou, M.; Maniati, M.; Vassilatis, D. K.; Papageorgiou, S. G.; Leonardos, A.; Tagaris, G.; Malamis, G.; Theofilopoulos, D.; Kamakari, S.; Stamboulis, E.; Hadjigeorgiou, G. M.; Athanassiadou, A.; Michelakakis, H.; Papadimitriou, A.; Gasser, T.; Stefanis, L. (2014)
  • Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behcet's Disease
    Ortiz Fernandez, Lourdes; Coit, Patrick; Yilmaz, Vuslat; Yentur, Sibel P.; Alibaz-Oner, Fatma; Aksu, Kenan; Erken, Eren; Duzgun, Nursen; Keser, Gokhan; Cefle, Ayse; Yazici, Ayten; Ergen, Andac; Alpsoy, Erkan; Salvarani, Carlo; Casali, Bruno; Kisacik, Bunyamin; Kotter, Ina; Henes, Jorg; cinar, Muhammet; Schaefer, Arne; Nohutcu, Rahime M.; Zhernakova, Alexandra; Wijmenga, Cisca; Takeuchi, Fujio; Harihara, Shinji; Kaburaki, Toshikatsu; Messedi, Meriam; Song, Yeong-Wook; Kasifoglu, Timucin; Carmona, F. David; Guthridge, Joel M.; James, Judith A.; Martin, Javier; Gonzalez Escribano, Maria Francisca; Saruhan-Direskeneli, Guher; Direskeneli, Haner; Sawalha, Amr H. (2021)
  • Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
    Aung, Tin; Ozaki, Mineo; Lee, Mei Chin; Schlotzer-Schrehardt, Ursula; Thorleifsson, Gudmar; Mizoguchi, Takanori; Igo, Robert P., Jr.; Haripriya, Aravind; Williams, Susan E.; Astakhov, Yury S.; Orr, Andrew C.; Burdon, Kathryn P.; Nakano, Satoko; Mori, Kazuhiko; Abu-Amero, Khaled; Hauser, Michael; Li, Zheng; Prakadeeswari, Gopalakrishnan; Bailey, Jessica N. Cooke; Cherecheanu, Alina Popa; Kang, Jae H.; Nelson, Sarah; Hayashi, Ken; Manabe, Shin-ichi; Kazama, Shigeyasu; Zarnowski, Tomasz; Inoue, Kenji; Irkec, Murat; Coca-Prados, Miguel; Sugiyama, Kazuhisa; Jarvela, Irma; Schlottmann, Patricio; Lerner, S. Fabian; Lamari, Hasnaa; Nilgun, Yildirim; Bikbov, Mukharram; Park, Ki Ho; Cha, Soon Cheol; Yamashiro, Kenji; Zenteno, Juan C.; Jonas, Jost B.; Kumar, Rajesh S.; Perera, Shamira A.; Chan, Anita S. Y.; Kobakhidze, Nino; George, Ronnie; Vijaya, Lingam; Do, Tan; Edward, Deepak P.; de Juan Marcos, Lourdes; Pakravan, Mohammad; Moghimi, Sasan; Ideta, Ryuichi; Bach-Holm, Daniella; Kappelgaard, Per; Wirostko, Barbara; Thomas, Samuel; Gaston, Daniel; Bedard, Karen; Greer, Wenda L.; Yang, Zhenglin; Chen, Xueyi; Huang, Lulin; Sang, Jinghong; Jia, Hongyan; Jia, Liyun; Qiao, Chunyan; Zhang, Hui; Liu, Xuyang; Zhao, Bowen; Wang, Ya-Xing; Xu, Liang; Leruez, Stephanie; Reynier, Pascal; Chichua, George; Tabagari, Sergo; Uebe, Steffen; Zenkel, Matthias; Berner, Daniel; Mossboeck, Georg; Weisschuh, Nicole; Hoja, Ursula; Welge-Luessen, Ulrich-Christoph; Mardin, Christian; Founti, Panayiota; Chatzikyriakidou, Anthi; Pappas, Theofanis; Anastasopoulos, Eleftherios; Lambropoulos, Alexandros; Ghosh, Arkasubhra; Shetty, Rohit; Porporato, Natalia; Saravanan, Vijayan; Venkatesh, Rengaraj; Shivkumar, Chandrashekaran; Kalpana, Narendran; Sarangapani, Sripriya; Kanavi, Mozhgan R.; Beni, Afsaneh Naderi; Yazdani, Shahin; Lashay, Alireza (2017)
  • Genetic authentication: Differentiation of hazelnut cultivars using polymorphic sites of the chloroplast genome
    Lang, Christina; Weber, Nico; Moeller, Maya; Schramm, Lisa; Schelm, Stefanie; Kohlbacher, Oliver; Fischer, Markus (2021)
  • Genetic basis of neurodevelopmental disorders in 103 Jordanian families
    Froukh, Tawfiq; Nafie, Omar; Al Hait, Sana' A. S.; Laugwitz, Lucia; Sommerfeld, Julia; Sturm, Marc; Baraghiti, Aya; Issa, Tala; Al-Nazer, Anis; Koch, Philipp A.; Hanselmann, Johannes; Kootz, Beate; Bauer, Peter; Al-Ameri, Wael; Abou Jamra, Rami; Alfrook, Ayman J.; Hamadallah, Moath; Sofan, Linda; Riess, Angelika; Haack, Tobias B.; Riess, Olaf; Buchert, Rebecca (2020)
  • Genetic Biomarkers in Epilepsy
    Weber, Yvonne G.; Nies, Anne T.; Schwab, Matthias; Lerche, Holger (2014)
  • Genetic characterization of advanced conjunctival melanoma and response to systemic treatment
    Lodde, Georg C.; Jansen, Philipp; Moeller, Inga; Sucker, Antje; Hassel, Jessica C.; Forschner, Andrea; Eckardt, Julia; Meier, Friedegund; Reinhardt, Lydia; Kaehler, Katharina C.; Ziemer, Mirjana; Schlaak, Max; Rahimi, Farnaz; Schatton, Kerstin; Meiss, Frank; Gutzmer, Ralf; Pfoehler, Claudia; Terheyden, Patrick; Schilling, Bastian; Sachse, Michael; Heppt, Markus, V; Sindrilaru, Anca; Leiter, Ulrike; Zaremba, Anne; Thielmann, Carl M.; Ugurel, Selma; Zimmer, Lisa; Hadaschik, Eva; Bechrakis, Nikolaos E.; Schadendorf, Dirk; Westekemper, Henrike; Livingstone, Elisabeth; Griewank, Klaus G. (2022)
  • Genetic comorbidities in Parkinson's disease
    Nalls, Mike A.; Saad, Mohamad; Noyce, Alastair J.; Keller, Margaux F.; Schrag, Anette; Bestwick, Jonathan P.; Traynor, Bryan J.; Gibbs, J. Raphael; Hernandez, Dena G.; Cookson, Mark R.; Morris, Huw R.; Williams, Nigel; Gasser, Thomas; Heutink, Peter; Wood, Nick; Hardy, John; Martinez, Maria; Singleton, Andrew B. (2014)
  • Genetic Correction of a LRRK2 Mutation in Human iPSCs Links Parkinsonian Neurodegeneration to ERK-Dependent Changes in Gene Expression
    Reinhardt, Peter; Schmid, Benjamin; Burbulla, Lena F.; Schoendorf, David C.; Wagner, Lydia; Glatza, Michael; Hoeing, Susanne; Hargus, Gunnar; Heck, Susanna A.; Dhingra, Ashutosh; Wu, Guangming; Mueller, Stephan; Brockmann, Kathrin; Kluba, Torsten; Maisel, Martina; Krueger, Rejko; Berg, Daniela; Tsytsyura, Yaroslav; Thiel, Cora S.; Psathaki, Olympia-Ekaterini; Klingauf, Juergen; Kuhlmann, Tanja; Klewin, Marlene; Mueller, Heiko; Gasser, Thomas; Schoeler, Hans R.; Sterneckert, Jared (2013)
  • Genetic deficiency of the tumor suppressor protein p53 influences erythrocyte survival
    Bissinger, Rosi; Lang, Elisabeth; Gonzalez-Menendez, Irene; Quintanilla-Martinez, Leticia; Ghashghaeinia, Mehrdad; Pelzl, Lisann; Sukkar, Basma; Bhuyan, Abdulla Al Mamun; Salker, Madhuri S.; Singh, Yogesh; Fehrenbacher, Birgit; Fakhri, Hajar; Umbach, Anja T.; Schaller, Martin; Qadri, Syed M.; Lang, Florian (2018)
  • Genetic deletion and pharmacological inhibition of PI3K gamma reduces neutrophilic airway inflammation and lung damage in mice with cystic fibrosis-like lung disease
    Galluzzo, Maria; Ciraolo, Elisa; Lucattelli, Monica; Hoxha, Eriola; Ulrich, Martina; Campa, Carlo Cosimo; Lungarella, Giuseppe; Doring, Gerd; Zhou-Suckow, Zhe; Mall, Marcus; Hirsch, Emilio; De Rose, Virginia (2015)
  • Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
    Rhodes, Christopher J.; Batai, Ken; Bleda, Marta; Haimel, Matthias; Southgate, Laura; Germain, Marine; Pauciulo, Michael W.; Hadinnapola, Charaka; Aman, Jurjan; Girerd, Barbara; Arora, Amit; Knight, Jo; Hanscombe, Ken B.; Karnes, Jason H.; Kaakinen, Marika; Gall, Henning; Ulrich, Anna; Harbaum, Lars; Cebola, Ines; Ferrer, Jorge; Lutz, Katie; Swietlik, Emilia M.; Ahmad, Ferhaan; Amouyel, Philippe; Archer, Stephen L.; Argula, Rahul; Austin, Eric D.; Badesch, David; Bakshi, Sahil; Barnett, Christopher; Benza, Raymond; Bhatt, Nitin; Bogaard, Harm J.; Burger, Charles D.; Chakinala, Murali; Church, Colin; Coghlan, John G.; Condliffe, Robin; Corris, Paul A.; Danesino, Cesare; Debette, Stephanie; Elliott, C. Gregory; Elwing, Jean; Eyries, Melanie; Fortin, Terry; Franke, Andre; Frantz, Robert P.; Frost, Adaani; Garcia, Joe G. N.; Ghio, Stefano; Ghofrani, Hossein-Ardeschir; Gibbs, J. Simon R.; Harley, John; He, Hua; Hill, Nicholas S.; Hirsch, Russel; Houweling, Arjan C.; Howard, Luke S.; Ivy, Dunbar; Kiely, David G.; Klinger, James; Kovacs, Gabor; Lahm, Tim; Laudes, Matthias; Machado, Rajiv D.; Ross, Robert V. MacKenzie; Marsolo, Keith; Martin, Lisa J.; Moledina, Shahin; Montani, David; Nathan, Steven D.; Newnham, Michael; Olschewski, Andrea; Olschewski, Horst; Oudiz, Ronald J.; Ouwehand, Willem H.; Peacock, Andrew J.; Pepke-Zaba, Joanna; Rehman, Zia; Robbins, Ivan; Roden, Dan M.; Rosenzweig, Erika B.; Saydain, Ghulam; Scelsi, Laura; Schilz, Robert; Seeger, Werner; Shaffer, Christian M.; Simms, Robert W.; Simon, Marc; Sitbon, Olivier; Suntharalingam, Jay; Tang, Haiyang; Tchourbanov, Alexander Y.; Thenappan, Thenappan; Torres, Fernando; Toshner, Mark R.; Treacy, Carmen M.; Noordegraaf, Anton Vonk; Waisfisz, Quinten; Walsworth, Anna K.; Walter, Robert E. (2019)