Logical Process Based Sequential Simulation Cloning von Peschlow, P., Geuer, M., Martini, P.

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Vergleich links- und rechtsventrikulärer Auswurf- und Füllungsparameter des Herzens mittels Cine MRT in Atemanhaltetechnik: klinische Studie an 42 Patienten mit Kardiomyopathie und... von Rominger, M. B., Bachmann, G. F., Geuer, M., Puzik, M., Ricken, W. W., Rau, W.S.

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Bestimmung des links- und rechtsventrikulären Auswurf- und Füllungsverhalten des Herzens mittels schneller Cine MRT in Atemanhaltetechnik an Probanden von Rominger, M. B., Bachmann, G. F., Geuer, M., Puzik, M., Pabst, W., Rau, W. S.

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Die ultraschallgeführte Oktantenbiopsie der Prostata. Wie kann sie die Therapie beeinflussen? von Meyer-Schwickerath, M, Lünzmann, M, Geuer, M, Heinke, T

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Comparison of left and right ventricular ejection and filling parameters of the heart using cine-MRI with breath holding technique. Clinical study of 42 patients with cardiomyopath... von Rominger, M B, Bachmann, G F, Geuer, M, Puzik, M, Ricken, W W, Rau, W S

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The determination of left and right ventricular ejection and filling functions of the heart by fast cine MRT in the breath-hold technic in subjects von Rominger, M B, Bachmann, G F, Geuer, M, Puzik, M, Pabst, W, Rau, W S

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Accuracy of right and left ventricular heart volume and left ventricular muscle mass determination with cine MRI in breath holding technique von Rominger, M B, Bachmann, G F, Geuer, M, Puzik, M, Boedeker, R H, Ricken, W W, Rau, W S

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Genauigkeit der rechts- und linksventrikulären Herzvolumen- und linksventrikulären Muskelmassenbestimmung mittels Cine MRT in Atemanhaltetechnik von ROMINGER, M. B, BACHMANN, G. F, GEUER, M, PUZIK, M, BOEDEKER, R.-H, RICKEN, W. W, RAU, W. S

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Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice von Kraft, Katerina, Geuer, Sinje, Will, Anja J., Chan, Wing Lee, Paliou, Christina, Borschiwer, Marina, Harabula, Izabela, Wittler, Lars, Franke, Martin, Ibrahim, Daniel M., Kragesteen, Bjørt K., Spielmann, Malte, Mundlos, Stefan, Lupiáñez, Darío G., Andrey, Guillaume

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De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome von Jansen, Sandra, Geuer, Sinje, Pfundt, Rolph, Brough, Rachel, Ghongane, Priyanka, Herkert, Johanna C., Marco, Elysa J., Willemsen, Marjolein H., Kleefstra, Tjitske, Hannibal, Mark, Shieh, Joseph T., Lynch, Sally Ann, Flinter, Frances, FitzPatrick, David R., Gardham, Alice, Bernhard, Birgitta, Ragge, Nicola, Newbury-Ecob, Ruth, Bernier, Raphael, Kvarnung, Malin, Magnusson, E.A. Helena, Wessels, Marja W., van Slegtenhorst, Marjon A., Monaghan, Kristin G., de Vries, Petra, Veltman, Joris A., Lord, Christopher J., Vissers, Lisenka E.L.M., de Vries, Bert B.A.

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Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidine von Wevers, R. A., Christensen, M., Engelke, U. F. H., Geuer, S., Coene, K. L. M., Kwast, J. T., Lund, A. M., Vissers, L. E. L. M.

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De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay von Vissers, Lisenka E.L.M., Kalvakuri, Sreehari, de Boer, Elke, Geuer, Sinje, Oud, Machteld, van Outersterp, Inge, Kwint, Michael, Witmond, Melde, Kersten, Simone, Polla, Daniel L., Weijers, Dilys, Begtrup, Amber, McWalter, Kirsty, Ruiz, Anna, Gabau, Elisabeth, Morton, Jenny E.V., Griffith, Christopher, Weiss, Karin, Gamble, Candace, Bartley, James, Vernon, Hilary J., Brunet, Kendra, Ruivenkamp, Claudia, Kant, Sarina G., Kruszka, Paul, Larson, Austin, Afenjar, Alexandra, Billette de Villemeur, Thierry, Nugent, Kimberly, Raymond, F. Lucy, Venselaar, Hanka, Demurger, Florence, Soler-Alfonso, Claudia, Li, Dong, Bhoj, Elizabeth, Hayes, Ian, Hamilton, Nina Powell, Ahmad, Ayesha, Fisher, Rachel, van den Born, Myrthe, Willems, Marjolaine, Sorlin, Arthur, Delanne, Julian, Moutton, Sebastien, Christophe, Philippe, Mau-Them, Frederic Tran, Vitobello, Antonio, Goel, Himanshu, Massingham, Lauren, Phornphutkul, Chanika, Schwab, Jennifer, Keren, Boris, Charles, Perrine, Vreeburg, Maaike, De Simone, Lenika, Hoganson, George, Iascone, Maria, Milani, Donatella, Evenepoel, Lucie, Revencu, Nicole, Ward, D. Isum, Burns, Kaitlyn, Krantz, Ian, Raible, Sarah E., Murrell, Jill R., Wood, Kathleen, Cho, Megan T., van Bokhoven, Hans, Muenke, Maximilian, Kleefstra, Tjitske, Bodmer, Rolf, de Brouwer, Arjan P.M.

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Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome von Willemsen, Michèl A, Vissers, Lisenka Elm, Verbeek, Marcel M, van Bon, Bregje W, Geuer, Sinje, Gilissen, Christian, Klepper, Joerg, Kwint, Michael P, Leen, Wilhelmina G, Pennings, Maartje, Wevers, Ron A, Veltman, Joris A, Kamsteeg, Erik-Jan

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Target-Site Investigation for the Plasma Prolactin Response: Mechanism-Based Pharmacokinetic-Pharmacodynamic Analysis of Risperidone and Paliperidone in the Rat von Shimizu, Shinji, den Hoedt, Sandra M., Mangas-Sanjuan, Victor, Cristea, Sinziana, Geuer, Jana K., van den Berg, Dirk-Jan, Hartman, Robin, Bellanti, Francisco, de Lange, Elizabeth C.M.

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Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy von Voisin, Norine, Schnur, Rhonda E., Douzgou, Sofia, Hiatt, Susan M., Rustad, Cecilie F., Brown, Natasha J., Earl, Dawn L., Keren, Boris, Levchenko, Olga, Geuer, Sinje, Verheyen, Sarah, Johnson, Diana, Zarate, Yuri A., Hančárová, Miroslava, Amor, David J., Bebin, E. Martina, Blatterer, Jasmin, Brusco, Alfredo, Cappuccio, Gerarda, Charrow, Joel, Chatron, Nicolas, Cooper, Gregory M., Courtin, Thomas, Dadali, Elena, Delafontaine, Julien, Del Giudice, Ennio, Doco, Martine, Douglas, Ganka, Eisenkölbl, Astrid, Funari, Tara, Giannuzzi, Giuliana, Gruber-Sedlmayr, Ursula, Guex, Nicolas, Heron, Delphine, Holla, Øystein L., Hurst, Anna C.E., Juusola, Jane, Kronn, David, Lavrov, Alexander, Lee, Crystle, Lorrain, Séverine, Merckoll, Else, Mikhaleva, Anna, Norman, Jennifer, Pradervand, Sylvain, Prchalová, Darina, Rhodes, Lindsay, Sanders, Victoria R., Sedláček, Zdeněk, Seebacher, Heidelis A., Sellars, Elizabeth A., Sirchia, Fabio, Takenouchi, Toshiki, Tanaka, Akemi J., Taska-Tench, Heidi, Tønne, Elin, Tveten, Kristian, Vitiello, Giuseppina, Vlčková, Markéta, Uehara, Tomoko, Nava, Caroline, Yalcin, Binnaz, Kosaki, Kenjiro, Donnai, Dian, Mundlos, Stefan, Brunetti-Pierri, Nicola, Chung, Wendy K., Reymond, Alexandre

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Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis von Coman, David, Vissers, Lisenka E.L.M., Riley, Lisa G., Kwint, Michael P., Hauck, Roxanna, Koster, Janet, Geuer, Sinje, Hopkins, Sarah, Hallinan, Barbra, Sweetman, Larry, Engelke, Udo F.H., Burrow, T. Andrew, Cardinal, John, McGill, James, Inwood, Anita, Gurnsey, Christine, Waterham, Hans R., Christodoulou, John, Wevers, Ron A., Pitt, James

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InfEval: Application for Object Detection Analysis von Bogomasov, Kirill, Geuer, Tim, Conrad, Stefan

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De novo variants in CNOT1, a central component of the CCR4-NOT complex involved in gene expression and RNA and protein stability, cause neurodevelopmental delay von Vissers, L.E.L.M., Kalvakuri, S., Boer, E. de, Geuer, S., Oud, M., Outersterp, I. van, Kwint, M., Witmond, M., Kersten, S., Polla, D.L., Weijers, D., Begtrup, A., McWalter, K., Ruiz, A., Gabau, E., Morton, J.E.V., Griffith, C., Weiss, K., Gamble, C., Bartley, J., Vernon, H.J., Brunet, K., Ruivenkamp, C., Kant, S.G., Kruszka, P., Larson, A., Afenjar, A., Villemeur, T.B. de, Nugent, K., Raymond, F.L., Venselaar, H., Demurger, F., Soler-Alfonso, C., Li, D., Bhoj, E., Hayes, I., Hamilton, N.P., Ahmad, A., Fisher, R., Born, M. van den, Willems, M., Sorlin, A., Delanne, J., Moutton, S., Christophe, P., Mau-Them, F.T., Vitobello, A., Goel, H., Massingham, L., Phornphutkul, C., Schwab, J., Keren, B., Charles, P., Vreeburg, M., Simone, L. de, Hoganson, G., Iascone, M., Milani, D., Evenepoel, L., Revencu, N., Ward, D.I., Burns, K., Krantz, I., Raible, S.E., Murrell, J.R., Wood, K., Cho, M.T., Bokhoven, H. van, Muenke, M., Kleefstra, T., Bodmer, R., Brouwer, A.P.M. de

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A High Resolution Spectrograph for the 72 cm Waltz Telescope at Landessternwarte, Heidelberg von Tala, M, Heeren, P, Grill, M, Harris, R J, Stürmer, J, Schwab, C, Gutcke, T, Reffert, S, Quirrenbach, A, Seifert, W, Mandel, H, Geuer, L, Schäffner, L, Thimm, G, Seemann, U, Tietz, J, Wagner, K

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Stahl, Eisen, Eisenlegierungen von Schließmann, O., Bogatzki, G., Pinsl, H., Bischof, E., Geuer, G., Swenigorodskaja, W. M., Weihrich, R., Schwarz, W., Stepin, W. W., Musowskaja, N. W., Tscherny, A. T., Diepschlag, E., Stadler, L. G., Bessonow, I. M., Sweschnikow, A. T., Boretzkaja, T. W., Ssossnowski, B. A., Ishii, R., Bogdantschenko, A. G., Schkotowa, S. N., Quadratund, O., Vcělák, Vl, Mischoinsniky, S.

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