Trigemino-cardiac reflex may be refractory to conventional management in adults von Schaller, B., Filis, A., Sandu, N., Rasper, J., Noethen, C., Buchfelder, M.

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Functional Outcome Changes in Surgery for Pituitary Adenomas After Intraoperative Occurrence of the Trigeminocardiac Reflex: First Description in a Retrospective Observational Stud... von Chowdhury, T., Nöthen, C., Filis, A., Sandu, N., Buchfelder, M., Schaller, Bernhard

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Cerebral hemodynamic changes during the trigeminocardiac reflex: description of a new animal model protocol von Sandu, N, Cornelius, J, Filis, A, Nöthen, C, Rasper, J, Kulinsky, V I, Schaller, B J

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Trigemino-cardiac reflex: The trigeminal depressor responses during skull base surgery von Schaller, B, Sandu, N, Filis, A, Ottaviani, G, Rasper, J, Nöethen, C, Buchfelder, M

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Le Dictionaire Imperial, Representant Les quatre Langues principales de L'Europe von Sieur de Veneroni, mzk2008464106

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Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study von Beaty, T. H., Taub, M. A., Scott, A. F., Murray, J. C., Marazita, M. L., Schwender, H., Parker, M. M., Hetmanski, J. B., Balakrishnan, P., Mansilla, M. A., Mangold, E., Ludwig, K. U., Noethen, M. M., Rubini, M., Elcioglu, N., Ruczinski, I.

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Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task von Walter, H, Schnell, K, Erk, S, Arnold, C, Kirsch, P, Esslinger, C, Mier, D, Schmitgen, M M, Rietschel, M, Witt, S H, Nöthen, M M, Cichon, S, Meyer-Lindenberg, A

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Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III von Björkqvist, Jenny, de Maat, Steven, Lewandrowski, Urs, Di Gennaro, Antonio, Oschatz, Chris, Schönig, Kai, Nöthen, Markus M, Drouet, Christian, Braley, Hal, Nolte, Marc W, Sickmann, Albert, Panousis, Con, Maas, Coen, Renné, Thomas

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High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences von Rivera, Natalia V, Ronninger, Marcus, Shchetynsky, Klementy, Franke, Andre, Nöthen, Markus M, Müller-Quernheim, Joachim, Schreiber, Stefan, Adrianto, Indra, Karakaya, Bekir, van Moorsel, Coline H M, Navratilova, Zdenka, Kolek, Vitezslav, Rybicki, Benjamin A, Iannuzzi, Michael C, Petrek, Martin, Grutters, Jan C, Montgomery, Courtney, Fischer, Annegret, Eklund, Anders, Padyukov, Leonid, Grunewald, Johan

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G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth von Pasternack, Sandra M, von Kügelgen, Ivar, Aboud, Khalid Al, Lee, Young-Ae, Rüschendorf, Franz, Voss, Katrin, Hillmer, Axel M, Molderings, Gerhard J, Franz, Thomas, Ramirez, Alfredo, Nürnberg, Peter, Nöthen, Markus M, Betz, Regina C

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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies von Yu, Dongmei, Sul, Jae Hoon, Tsetsos, Fotis, Nawaz, Muhammad S, Huang, Alden Y, Zelaya, Ivette, Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M, Hirschtritt, Matthew E, Greenberg, Erica, Muller-Vahl, Kirsten R, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L, Grados, Marco, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, Hinney, Anke, King, Robert A, Fernandez, Thomas V, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L, Rizzo, Renata, Lyon, Gholson J, McMahon, William M, Batterson, James R, Cath, Danielle C, Malaty, Irene A, Okun, Michael S, Berlin, Cheston, Woods, Douglas W, Lee, Paul C, Jankovic, Joseph, Robertson, Mary M, Gilbert, Donald L, Brown, Lawrence W, Coffey, Barbara J, Dietrich, Andrea, Hoekstra, Pieter J, Kuperman, Samuel, Zinner, Samuel H, Luðvigsson, Pétur, Sæmundsen, Evald, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Wagner, Michael, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N, Pato, Michele T, Knowles, James A, Roffman, Joshua L, Smoller, Jordan W, Buckner, Randy L, Willsey, A. Jeremy, Tischfield, Jay A, Heiman, Gary A, Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Cox, Nancy J, Pauls, David L, Freimer, Nelson B, Neale, Benjamin M, Davis, Lea K, Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A, Scharf, Jeremiah M

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GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores von Mullins, Niamh, Bigdeli, Tim B, Børglum, Anders D, Coleman, Jonathan R.I, Demontis, Ditte, Mehta, Divya, Ripke, Stephan, Stahl, Eli A, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan R, Forstner, Andreas J, Reif, Andreas, Koller, Anna C, Świątkowska, Beata, Baune, Bernhard T, Müller-Myhsok, Bertram, Penninx, Brenda W.J.H, Pato, Carlos, Rujescu, Dan, Hougaard, David M, Quested, Digby, Levinson, Douglas F, Binder, Elisabeth B, Byrne, Enda M, Agerbo, Esben, Streit, Fabian, Mayoral, Fermin, Bellivier, Frank, Degenhardt, Franziska, Breen, Gerome, Morken, Gunnar, Turecki, Gustavo, Rouleau, Guy A, Grabe, Hans J, Jones, Ian, Agartz, Ingrid, Lawrence, Jacob, Walters, James T.R, Strohmaier, Jana, Shi, Jianxin, Hauser, Joanna, Biernacka, Joanna M, Vincent, John B, Kelsoe, John, Strauss, John S, Smoller, Jordan W, Guzman-Parra, José, Berger, Klaus, Scott, Laura J, Jones, Lisa A, Azevedo, M. Helena, Trzaskowski, Maciej, Kogevinas, Manolis, Rietschel, Marcella, Boks, Marco, Ising, Marcus, Grigoroiu-Serbanescu, Maria, Hamshere, Marian L, Leboyer, Marion, Nöthen, Markus M, Preisig, Martin, Boehnke, Michael, O’Donovan, Michael C, Owen, Michael J, Pato, Michele T, Renteria, Miguel E, Budde, Monika, Weissman, Myrna M, Wray, Naomi R, Bass, Nicholas, Craddock, Nicholas, Smeland, Olav B, Mors, Ole, Gejman, Pablo V, Sklar, Pamela, McGrath, Patrick, Hoffmann, Per, McGuffin, Peter, Lee, Phil H, Mortensen, Preben Bo, Kahn, René S, Ophoff, Roel A, Adolfsson, Rolf, Van der Auwera, Sandra, Djurovic, Srdjan, Heilmann-Heimbach, Stefanie, Jamain, Stéphane, Hamilton, Steven P, Lucae, Susanne, Schulze, Thomas G, Hansen, Thomas, Werge, Thomas, Air, Tracy M, Nimgaonkar, Vishwajit, Appadurai, Vivek, Cahn, Wiepke, McQuillin, Andrew, Lewis, Cathryn M

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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts von Bureau, Alexandre, Parker, Margaret M, Ruczinski, Ingo, Taub, Margaret A, Marazita, Mary L, Murray, Jeffrey C, Mangold, Elisabeth, Noethen, Markus M, Ludwig, Kirsten U, Hetmanski, Jacqueline B, Bailey-Wilson, Joan E, Cropp, Cheryl D, Li, Qing, Szymczak, Silke, Albacha-Hejazi, Hasan, Alqosayer, Khalid, Field, L Leigh, Wu-Chou, Yah-Huei, Doheny, Kimberly F, Ling, Hua, Scott, Alan F, Beaty, Terri H

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis von Adam, Ronja, Spier, Isabel, Zhao, Bixiao, Kloth, Michael, Marquez, Jonathan, Hinrichsen, Inga, Kirfel, Jutta, Tafazzoli, Aylar, Horpaopan, Sukanya, Uhlhaas, Siegfried, Stienen, Dietlinde, Friedrichs, Nicolaus, Altmüller, Janine, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Kayser, Katrin, Thiele, Holger, Holinski-Feder, Elke, Marra, Giancarlo, Kristiansen, Glen, Nöthen, Markus M., Büttner, Reinhard, Möslein, Gabriela, Betz, Regina C., Brieger, Angela, Lifton, Richard P., Aretz, Stefan

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GestaltMatcher facilitates rare disease matching using facial phenotype descriptors von Hsieh, Tzung-Chien, Bar-Haim, Aviram, Moosa, Shahida, Ehmke, Nadja, Gripp, Karen W., Pantel, Jean Tori, Danyel, Magdalena, Mensah, Martin Atta, Horn, Denise, Rosnev, Stanislav, Fleischer, Nicole, Bonini, Guilherme, Hustinx, Alexander, Schmid, Alexander, Knaus, Alexej, Javanmardi, Behnam, Klinkhammer, Hannah, Lesmann, Hellen, Sivalingam, Sugirthan, Kamphans, Tom, Meiswinkel, Wolfgang, Ebstein, Frédéric, Krüger, Elke, Küry, Sébastien, Bézieau, Stéphane, Schmidt, Axel, Peters, Sophia, Engels, Hartmut, Mangold, Elisabeth, Kreiß, Martina, Cremer, Kirsten, Perne, Claudia, Betz, Regina C., Bender, Tim, Grundmann-Hauser, Kathrin, Haack, Tobias B., Wagner, Matias, Brunet, Theresa, Bentzen, Heidi Beate, Averdunk, Luisa, Coetzer, Kimberly Christine, Lyon, Gholson J., Spielmann, Malte, Schaaf, Christian P., Mundlos, Stefan, Nöthen, Markus M., Krawitz, Peter M.

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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease von Schunkert, Heribert, Kathiresan, Sekar, Stewart, Alexandre F R, Barbalic, Maja, Absher, Devin, Aherrahrou, Zouhair, Allayee, Hooman, Anand, Sonia S, Anderson, Jeffrey L, Ardissino, Diego, Balmforth, Anthony J, Boerwinkle, Eric, Braund, Peter S, Brown, Morris J, Burnett, Mary Susan, Buysschaert, Ian, Carlquist, John F, Chen, Li, Cichon, Sven, Davies, Robert W, Dehghan, Abbas, Demissie, Serkalem, Do, Ron, Eifert, Sandra, Mokhtari, Nour Eddine El, Elosua, Roberto, Engert, James C, Epstein, Stephen E, Fischer, Marcus, Folsom, Aaron R, Freyer, Jennifer, Halperin, Eran, Hammond, Naomi, Hazen, Stanley L, Horne, Benjamin D, Illig, Thomas, Iribarren, Carlos, Kaiser, Michael A, Kaplan, Lee M, Kastelein, John J P, Laaksonen, Reijo, Leander, Karin, Lettre, Guillaume, Li, Mingyao, Loley, Christina, Lotery, Andrew J, Mannucci, Pier M, Maouche, Seraya, Martinelli, Nicola, Meisinger, Christa, Melander, Olle, Mooser, Vincent, Mühleisen, Thomas W, Münzel, Thomas, Musunuru, Kiran, Nelson, Christopher P, Nöthen, Markus M, Olivieri, Oliviero, Patel, Riyaz S, Patterson, Chris C, Peters, Annette, Peyvandi, Flora, Quyyumi, Arshed A, Rallidis, Loukianos S, Rice, Catherine, Rosendaal, Frits R, Salomaa, Veikko, Sampietro, M Lourdes, Schäfer, Arne, Schillert, Arne, Schreiber, Stefan, Schrezenmeir, Jürgen, Schwartz, Stephen M, Sivananthan, Mohan, Smith, Albert, Smith, Tamara B, Snoep, Jaapjan D, Soranzo, Nicole, Spertus, John A, Stark, Klaus, Stirrups, Kathy, Stoll, Monika, Tang, W H Wilson, Thorgeirsson, Gudmundur, Thorleifsson, Gudmar, van Rij, Andre M, Wells, George A, Wichmann, H-Erich, Wild, Philipp S, Willenborg, Christina, Zeller, Tanja, Ziegler, Andreas, Cambien, Francois, Hengstenberg, Christian, Blankenberg, Stefan, Ouwehand, Willem H, Hall, Alistair S, Thompson, John R, McPherson, Ruth, Erdmann, Jeanette

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Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1 von MCMAHON, Francis J, AKULA, Nirmala, MATTHEISEN, Manuel, MÜHLEISEN, Thomas W, MAIER, Wolfgang, NÖTHEN, Markus M, CICHON, Sven, FARMER, Anne, VINCENT, John B, HOLSBOER, Florian, PREISIG, Martin, RIETSCHEL, Marcella, SCHULZE, Thomas G, MUGLIA, Pierandrea, TOZZI, Federica, DETERA-WADLEIGH, Sevilla D, STEELE, C. J. M, BREUER, René, STROHMAIER, Jana, WENDLAND, Jens R

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Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III von Cichon, Sven, Martin, Ludovic, Hennies, Hans Christian, Müller, Felicitas, Van Driessche, Karen, Karpushova, Anna, Stevens, Wim, Colombo, Roberto, Renné, Thomas, Drouet, Christian, Bork, Konrad, Nöthen, Markus M.

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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease von Sims, Rebecca, Gerrish, Amy, Abraham, Richard, Hamshere, Marian L, Moskvina, Valentina, Jones, Nicola, Thomas, Charlene, Widdowson, Caroline, Chapman, Jade, Powell, John, Proitsi, Petroula, Lupton, Michelle K, Gill, Michael, Lawlor, Brian, Passmore, Peter A, Craig, David, McGuinness, Bernadette, Todd, Stephen, Mann, David, Smith, A David, Warden, Donald, Kehoe, Patrick G, Hardy, John, Mead, Simon, Collinge, John, Maier, Wolfgang, Schürmann, Britta, Heun, Reiner, Kölsch, Heike, van den Bussche, Hendrik, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Gallacher, John, Hüll, Michael, Rujescu, Dan, Giegling, Ina, Goate, Alison M, Kauwe, John S K, Nowotny, Petra, Morris, John C, Bettens, Karolien, Engelborghs, Sebastiaan, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E, Tsolaki, Magda, Guerreiro, Rita, Klopp, Norman, Wichmann, H-Erich, Barcikowska, Maria, Wszolek, Zbigniew K, Dickson, Dennis W, van Duijn, Cornelia M, Breteler, Monique M B, Ikram, M Arfan, Fitzpatrick, Annette L, Seshadri, Sudha, Berr, Claudine, Epelbaum, Jacques, Dartigues, Jean-François, Tzourio, Christophe, Feulner, Thomas M, Riehle, Caterina, Krawczak, Michael, Mayhaus, Manuel, Nicolhaus, S, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Snædal, Jon, Björnsson, Sigurbjörn, Chouraki, Vincent, Zelenika, Diana, Delepine, Marc, Pasquier, Florence, Porcellini, Elisa, Hanon, Olivier, Alvarez, Victoria, Bosco, Paolo, Siciliano, Gabriele, Solfrizzi, Vincenzo, Bossù, Paola, Piccardi, Paola, Seripa, Davide, Pilotto, Alberto, Scarpini, Elio, Brice, Alexis, Hannequin, Didier, Jones, Lesley, Holmans, Peter A, Jonsson, Thorlakur, Morgan, Kevin, Younkin, Steven G, Owen, Michael J, O'Donovan, Michael, Amouyel, Philippe, Williams, Julie

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LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding von Ludwig, Kerstin U., Schmithausen, Ricarda M., Li, David, Jacobs, Max L., Hollstein, Ronja, Blumenstock, Katja, Liebing, Jana, Słabicki, Mikołaj, Ben-Shmuel, Amir, Israeli, Ofir, Weiss, Shay, Ebert, Thomas S., Paran, Nir, Rüdiger, Wibke, Wilbring, Gero, Feldman, David, Lippke, Bärbel, Ishorst, Nina, Hochfeld, Lara M., Beins, Eva C., Kaltheuner, Ines H., Schmitz, Maximilian, Wöhler, Aliona, Döhla, Manuel, Sib, Esther, Jentzsch, Marius, Moench, Eva-Maria C., Borrajo, Jacob D., Strecker, Jonathan, Reinhardt, Julia, Cleary, Brian, Geyer, Matthias, Hölzel, Michael, Macrae, Rhiannon, Nöthen, Markus M., Hoffmann, Per, Exner, Martin, Regev, Aviv, Zhang, Feng, Schmid-Burgk, Jonathan L.

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