An identical HMGIC-LPP fusion transcript is consistently expressed in pulmonary chondroid hamartomas with t(3;12)(q27-28;q14-15) von Rogalla, Piere, Lemke, Inga, Kazmierczak, Bernd, Bullerdiek, Jörn

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An identicalHMGIC-LPP fusion transcript is consistently expressed in pulmonary chondroid hamartomas with t(3;12)(q27-28;q14-15) von Rogalla, Piere, Lemke, Inga, Kazmierczak, Bernd, Bullerdiek, J rn

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Unübersetzbar‹, ›unspielbar‹…? Racines »Phädra« als Exempel: Einblicke in die europäische Dramaturgie- und Theatergeschichte von Lemke, Inga

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'Unübersetzbar', 'unspielbar'. Racines "Phädra" als Exempel. Einblicke in die europäische Dramaturgie- und Theatergeschichte von Lemke, Inga

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Absence of HMGIC-LHFP fusion in pulmonary chondroid hamartomas with aberrations involving chromosomal regions 12q13∼q15 and 13q12∼q14 von Rogalla, Piere, Lemke, Inga, Bullerdiek, Jörn

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Absence of HMGIC-LHFP fusion in pulmonary chondroid hamartomas with aberrations involving chromosomal regions 12q13 through 15 and 13q12 through q14 von Rogalla, Piere, Lemke, Inga, Bullerdiek, Jörn

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Large deletion of part of the HMGIC locus accompanying a t(3;12)(q27∼q28;q14∼q15) in a lipoma von Lemke, Inga, Rogalla, Piere, Bullerdiek, Jörn

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Expression of the HMGA2-LPP fusion transcript in only 1 of 61 karyotypically normal pulmonary chondroid hamartomas von Lemke, Inga, Rogalla, Piere, Grundmann, Felix, Kunze, Wolf-Peter, Haupt, Rolf, Bullerdiek, Jörn

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De novo variants in neurodevelopmental disorders with epilepsy von Heyne, Henrike O., Singh, Tarjinder, Stamberger, Hannah, Abou Jamra, Rami, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Guerrini, Renzo, Helbig, Katherine L., Koeleman, Bobby P. C., Kosmicki, Jack A., Linnankivi, Tarja, May, Patrick, Muhle, Hiltrud, Møller, Rikke S., Neubauer, Bernd A., Palotie, Aarno, Pendziwiat, Manuela, Striano, Pasquale, Tang, Sha, Wu, Sitao, Poduri, Annapurna, Weber, Yvonne G., Weckhuysen, Sarah, Sisodiya, Sanjay M., Daly, Mark J., Helbig, Ingo, Lal, Dennis, Lemke, Johannes R.

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Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies von Schröter, Julian, Popp, Bernt, Brennenstuhl, Heiko, Döring, Jan H, Donze, Stephany H, Bijlsma, Emilia K, van Haeringen, Arie, Huhle, Dagmar, Jestaedt, Leonie, Merkenschlager, Andreas, Arelin, Maria, Gräfe, Daniel, Neuser, Sonja, Oates, Stephanie, Pal, Deb K, Parker, Michael J, Lemke, Johannes R, Hoffmann, Georg F, Kölker, Stefan, Harting, Inga, Syrbe, Steffen

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Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies von Johannesen, Katrine, Marini, Carla, Pfeffer, Siona, Møller, Rikke S, Dorn, Thomas, Niturad, Christina, Gardella, Elena, Weber, Yvonne, Søndergård, Marianne, Hjalgrim, Helle, Nikanorova, Mariana, Becker, Felicitas, Larsen, Line H.G, Dahl, Hans A, Maier, Oliver, Mei, Davide, Biskup, Saskia, Klein, Karl M, Reif, Philipp S, Rosenow, Felix, Elias, Abdallah F, Hudson, Cindy, Helbig, Katherine L, Schubert-Bast, Susanne, Scordo, Maria R, Craiu, Dana, Djémié, Tania, Hoffman-Zacharska, Dorota, Caglayan, Hande, Helbig, Ingo, Serratosa, Jose, Striano, Pasquale, De Jonghe, Peter, Weckhuysen, Sarah, Suls, Arvid, Muru, Kai, Talvik, Inga, Talvik, Tiina, Muhle, Hiltrud, Borggraefe, Ingo, Rost, Imma, Guerrini, Renzo, Lerche, Holger, Lemke, Johannes R, Rubboli, Guido, Maljevic, Snezana

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Mutations in GABRB3: From febrile seizures to epileptic encephalopathies von Møller, Rikke S, Wuttke, Thomas V, Helbig, Ingo, Marini, Carla, Johannesen, Katrine M, Brilstra, Eva H, Vaher, Ulvi, Borggraefe, Ingo, Talvik, Inga, Talvik, Tiina, Kluger, Gerhard, Francois, Laurence L, Lesca, Gaetan, de Bellescize, Julitta, Blichfeldt, Susanne, Chatron, Nicolas, Holert, Nils, Jacobs, Julia, Swinkels, Marielle, Betzler, Cornelia, Syrbe, Steffen, Nikanorova, Marina, Myers, Candace T, Larsen, Line H.G, Vejzovic, Sabina, Pendziwiat, Manuela, von Spiczak, Sarah, Hopkins, Sarah, Dubbs, Holly, Mang, Yuan, Mukhin, Konstantin, Holthausen, Hans, van Gassen, Koen L, Dahl, Hans A, Tommerup, Niels, Mefford, Heather C, Rubboli, Guido, Guerrini, Renzo, Lemke, Johannes R, Lerche, Holger, Muhle, Hiltrud, Maljevic, Snezana

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Normal and Time-Compressed Speech von Anne Schlueter, Ulrike Lemke, Birger Kollmeier, Inga Holube

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Intelligibility of time-compressed speech: the effect of uniform versus non-uniform time-compression algorithms von Schlueter, Anne, Lemke, Ulrike, Kollmeier, Birger, Holube, Inga

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Normal and Time-Compressed Speech: How Does Learning Affect Speech Recognition Thresholds in Noise? von Schlueter, Anne, Lemke, Ulrike, Kollmeier, Birger, Holube, Inga

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Changes in the pattern of suicides and suicide attempt admissions in relation to the COVID-19 pandemic von Reif-Leonhard, Christine, Lemke, Dorothea, Holz, Franziska, Ahrens, Kira F., Fehr, Christoph, Steffens, Markus, Grube, Michael, Freitag, Christine M., Kölzer, Sarah C., Schlitt, Sabine, Gebhardt, Rebekka, Gädeke, Theresa, Schmidt, Helga, Gerlach, Ferdinand M., Wolff, Kira, Stäblein, Michael, Hauschild, Nora, Beig, Inga, Wagner, Louisa, Müller, Juliane, Verhoff, Marcel A., Schlang, Christiane, Reif, Andreas

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Speech perception at positive signal-to-noise ratios using adaptive adjustment of time compression von Schlueter, Anne, Brand, Thomas, Lemke, Ulrike, Nitzschner, Stefan, Kollmeier, Birger, Holube, Inga

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Applicability of a Novel Formula (Bogossian formula) for Evaluation of the QT‐Interval in Heart Failure and Left Bundle Branch Block Due to Right Ventricular Pacing von FROMMEYER, GERRIT, BOGOSSIAN, HARILAOS, PECHLIVANIDOU, ELENI, CONZEN, PHILIPP, GEMEIN, CHRISTOPHER, WEIPERT, KAY, HELMIG, INGA, CHASAN, RITVAN, JOHNSON, VICTORIA, ECKARDT, LARS, HAMM, CHRISTIAN W, SEYFARTH, MELCHIOR, LEMKE, BERND, ZARSE, MARKUS, SCHMITT, JÖRN, ERKAPIC, DAMIR

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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome von Suls, Arvid, Jaehn, Johanna A, Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C, Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M, Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S, Giraldez, Beatriz G, Serratosa, José, Lemke, Johannes R, Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S, Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D, Lehesjoki, Anna-Elina, de Witte, Peter A.M, Palotie, Aarno, Lerche, Holger, Esguerra, Camila V, De Jonghe, Peter, Helbig, Ingo, the EuroEPINOMICS RES Consortium

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Mutations in GABRB3 von Møller, Rikke S, Wuttke, Thomas V, Helbig, Ingo, Marini, Carla, Johannesen, Katrine M, Brilstra, Eva H, Vaher, Ulvi, Borggraefe, Ingo, Talvik, Inga, Talvik, Tiina, Kluger, Gerhard, Francois, Laurence L, Lesca, Gaetan, Bellescize, Julitta de, Blichfeldt, Susanne, Chatron, Nicolas, Holert, Nils, Jacobs, Julia, Swinkels, Marielle, Betzler, Cornelia, Syrbe, Steffen, Nikanorova, Marina, Myers, Candace T, Larsen, Line H. G, Vejzovic, Sabina, Pendziwiat, Manuela, Spiczak, Sarah von, Hopkins, Sarah, Dubbs, Holly, Mang, Yuan, Mukhin, Konstantin, Holthausen, Hans, Gassen, Koen L. van, Dahl, Hans A, Tommerup, Niels, Mefford, Heather C, Rubboli, Guido, Guerrini, Renzo, Lemke, Johannes R, Lerche, Holger, Muhle, Hiltrud, Maljevic, Snezana

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