Precipitation of Terephthalic Acid from Alkaline Solution: Influence of Temperature and Precipitation Acid von Müller, Clemens, Heck, Carina A., Stephan, Luca, Paschetag, Mandy, Scholl, Stephan

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SLC2A3 single‐nucleotide polymorphism and duplication influence cognitive processing and population‐specific risk for attention‐deficit/hyperactivity disorder von Merker, Sören, Reif, Andreas, Ziegler, Georg C., Weber, Heike, Mayer, Ute, Ehlis, Ann‐Christine, Conzelmann, Annette, Johansson, Stefan, Müller‐Reible, Clemens, Nanda, Indrajit, Haaf, Thomas, Ullmann, Reinhard, Romanos, Marcel, Fallgatter, Andreas J., Pauli, Paul, Strekalova, Tatyana, Jansch, Charline, Vasquez, Alejandro Arias, Haavik, Jan, Ribasés, Marta, Ramos‐Quiroga, Josep Antoni, Buitelaar, Jan K., Franke, Barbara, Lesch, Klaus‐Peter

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Measurement-induced population switching von Ferguson, Michael S., Camenzind, Leon C., Müller, Clemens, Biesinger, Daniel E. F., Scheller, Christian P., Braunecker, Bernd, Zumbühl, Dominik M., Zilberberg, Oded

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Correlating Decoherence in Transmon Qubits: Low Frequency Noise by Single Fluctuators von Schlör, Steffen, Lisenfeld, Jürgen, Müller, Clemens, Bilmes, Alexander, Schneider, Andre, Pappas, David P., Ustinov, Alexey V., Weides, Martin

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Dissipative Rabi model in the dispersive regime von Müller, Clemens

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Lebenszykluskosten Von Straen: Umsetzungsformen, Modulare Kalkulation, Optimierungspotentiale von Muller, Clemens

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A standardized framework for the validation and verification of clinical molecular genetic tests von Mattocks, Christopher J, Morris, Michael A, Matthijs, Gert, Swinnen, Elfriede, Corveleyn, Anniek, Dequeker, Els, Müller, Clemens R, Pratt, Victoria, Wallace, Andrew

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Screening of the Ryanodine 1 Gene for Malignant Hyperthermia Causative Mutations by High Resolution Melt Curve Analysis von Broman, Marcus, Heinecke, Kai, Islander, Gunilla, Schuster, Frank, Glahn, Klaus, Bodelsson, Mikael, Treves, Susan, Müller, Clemens

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Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication von Lippert, Juliane, Appenzeller, Silke, Liang, Raimunde, Sbiera, Silviu, Kircher, Stefan, Altieri, Barbara, Nanda, Indrajit, Weigand, Isabel, Gehrig, Andrea, Steinhauer, Sonja, Riemens, Renzo J M, Rosenwald, Andreas, Müller, Clemens R, Kroiss, Matthias, Rost, Simone, Fassnacht, Martin, Ronchi, Cristina L

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Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1 von Larsen, Mirjam, Rost, Simone, El Hajj, Nady, Ferbert, Andreas, Deschauer, Marcus, Walter, Maggie C, Schoser, Benedikt, Tacik, Pawel, Kress, Wolfram, Müller, Clemens R

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The genetic basis of resistance to anticoagulants in rodents von Pelz, Hans-Joachim, Rost, Simone, Hünerberg, Mirja, Fregin, Andreas, Heiberg, Ann-Charlotte, Baert, Kristof, MacNicoll, Alan D, Prescott, Colin V, Walker, Anne-Sophie, Oldenburg, Johannes, Müller, Clemens R

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Passive On-Chip Superconducting Circulator Using a Ring of Tunnel Junctions von Müller, Clemens, Guan, Shengwei, Vogt, Nicolas, Cole, Jared H, Stace, Thomas M

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Human Vitamin K 2,3-Epoxide Reductase Complex Subunit 1-like 1 (VKORC1L1) Mediates Vitamin K-dependent Intracellular Antioxidant Function von Westhofen, Philipp, Watzka, Matthias, Marinova, Milka, Hass, Moritz, Kirfel, Gregor, Müller, Jens, Bevans, Carville G., Müller, Clemens R., Oldenburg, Johannes

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Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2 von Oldenburg, Johannes, Rost, Simone, Fregin, Andreas, Ivaskevicius, Vytautas, Conzelmann, Ernst, Hörtnagel, Konstanze, Pelz, Hans-Joachim, Lappegard, Knut, Seifried, Erhard, Scharrer, Inge, Tuddenham, Edward G. D, Müller, Clemens R, Strom, Tim M

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Quantum Rifling: Protecting a Qubit from Measurement Back Action von Szombati, Daniel, Gomez Frieiro, Alejandro, Müller, Clemens, Jones, Tyler, Jerger, Markus, Fedorov, Arkady

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Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene von Bach, Elisa J., Wolf, Beat, Oldenburg, Johannes, Müller, Clemens R., Rost, Simone

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BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer von Weber-Lassalle, Nana, Hauke, Jan, Ramser, Juliane, Richters, Lisa, Groß, Eva, Blümcke, Britta, Gehrig, Andrea, Kahlert, Anne-Karin, Müller, Clemens R, Hackmann, Karl, Honisch, Ellen, Weber-Lassalle, Konstantin, Niederacher, Dieter, Borde, Julika, Thiele, Holger, Ernst, Corinna, Altmüller, Janine, Neidhardt, Guido, Nürnberg, Peter, Klaschik, Kristina, Schroeder, Christopher, Platzer, Konrad, Volk, Alexander E, Wang-Gohrke, Shan, Just, Walter, Auber, Bernd, Kubisch, Christian, Schmidt, Gunnar, Horvath, Judit, Wappenschmidt, Barbara, Engel, Christoph, Arnold, Norbert, Dworniczak, Bernd, Rhiem, Kerstin, Meindl, Alfons, Schmutzler, Rita K, Hahnen, Eric

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Endogenous regeneration after collagenase-induced knee joint damage in the adult newt Notophthalmus viridescens von Geyer, Matthias, Borchardt, Thilo, Schreiyäck, Carina, Wietelmann, Astrid, Müller-Schrobsdorff, Florian, Müller, Clemens, Müller-Ladner, Ulf, Dinser, Robert

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Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces von Czogalla, Katrin J., Biswas, Arijit, Wendeln, Ann-Christin, Westhofen, Philipp, Müller, Clemens R., Watzka, Matthias, Oldenburg, Johannes

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Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6 von Rost, Simone, Bach, Elisa, Neuner, Cordula, Nanda, Indrajit, Dysek, Sandra, Bittner, Reginald E, Keller, Alexander, Bartsch, Oliver, Mlynski, Robert, Haaf, Thomas, Müller, Clemens R, Kunstmann, Erdmute

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