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2022
Li, Jeany Q., Kellner, Ulrich, Lorenz, Birgit, Stahl, Andreas and Krohne, Tim U. (2022). Retina, Vitreous Humor, Ocular Fundus Prenatal Retinopathy. Augenheilkund. Up2date, 12 (1). S. 13 - 33. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1616-9735
Li, Jeany Q., Kellner, Ulrich, Lorenz, Birgit, Stahl, Andreas and Krohne, Tim U. (2022). Retinopathy of Prematurity Update on Classification, Screening, and Therapy. Klinische Monatsblat. Augenheilkunde, 239 (3). S. 346 - 364. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3999
Maier, Rolf F., Hummler, Helmut, Kellner, Ulrich, Krohne, Tim U. 
ORCID: 0000-0003-2280-925X, Lawrenz, Burkhard, Lorenz, Birgit, Mitschdoerfer, Barbara, Roll, Claudia and Stahl, Andreas
(2022).
National guideline for ophthalmological screening of premature infants in Germany (S2k level, AWMF guidelines register no. 024/010, March 2020).
Ophthalmologie, 119.
S. 123 - 137.
HEIDELBERG:
SPRINGER HEIDELBERG.
ISSN 2731-7218
2021
Li, Jeany Q., Kellner, Ulrich, Lorenz, Birgit, Stahl, Andreas and Krohne, Tim U. (2021). Screening for retinopathy of prematurity-the most important changes in the new German guidelines 2020. Ophthalmologe, 118 (12). S. 1240 - 1245. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1433-0423
Volk, Alexander E., Hedergott, Andrea ORCID: 0000-0002-6398-3919, Preising, Markus, Rading, Sebastian, Fricke, Julia, Herkenrath, Peter, Nurnberg, Peter, Altmueller, Janine, von Ameln, Simon, Lorenz, Birgit, Neugebauer, Antje, Karsak, Meliha and Kubisch, Christian
(2021).
Biallelic mutations in l-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism.
Hum. Genet., 140 (8).
S. 1157 - 1169.
NEW YORK:
SPRINGER.
ISSN 1432-1203
Wabbels, Bettina ORCID: 0000-0002-7767-114X, Fricke, Julia, Schittkowski, Michael, Graf, Michael, Lorenz, Birgit, Bau, Viktoria, Nentwich, Martin M., Atili, Abed, Eckstein, Anja, Sturm, Veit, Beisse, Christina, Sterker, Ina, Neppert, Birte and Mauschitz, Matthias M.
(2021).
Yokoyama procedure for esotropia associated with high myopia: real-world data from a large-scale multicentre analysis.
Acta Ophthalmol., 99 (8).
S. E1340 - 8.
HOBOKEN:
WILEY.
ISSN 1755-3768
Wilms, Vlada, Jaeger, Melanie, Schlamann, Marc, Weber, Damien Charles and Lorenz, Birgit (2021). Rhabdoid Tumour of the Orbit in a Child. Laryngo-Rhino-Otol., 100 (2). S. 130 - 132. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1438-8685
2020
Koss, Michael Janusz, Bolz, Matthias, Augustin, Albert J., Koch, Frank, Szurman, Peter, Stanzel, Boris, Fauser, Sascha, Mennel, Stefan, Vossmerbaeumer, Urs, de Smet, Marc D., Hoehn, Fabian, Kuechle, Michael, Lorenz, Birgit ORCID: 0000-0002-9737-8127, Lueke, Mathias, Lytvynchuk, Lyubomyr, Meyer, Carsten H. ORCID: 0000-0002-0530-5298, Paul, Christoph, Rodrigues, Eduardo B., Schrage, Norbert and Zehnder, Claus
(2020).
Safety, Efficacy and Protective Aspects of an Add-on Paracentesis during Intravitreal Injections.
Klinische Monatsblat. Augenheilkunde, 237 (1).
S. 90 - 95.
STUTTGART:
GEORG THIEME VERLAG KG.
ISSN 1439-3999
Wilms, Vlada, Jaeger, Melanie, Schlamann, Marc, Weber, Damien Charles and Lorenz, Birgit ORCID: 0000-0002-9737-8127
(2020).
Rhabdoid Tumour of the Orbit in a Child.
Klinische Monatsblat. Augenheilkunde, 237 (2).
S. 205 - 207.
STUTTGART:
GEORG THIEME VERLAG KG.
ISSN 1439-3999
2019
Larsen, Petra P., Thiele, Sarah, Krohne, Tim U., Ziemssen, Focke, Krummenauer, Frank, Holz, Frank G., Finger, Robert P., Kohnen, Thomas ORCID: 0000-0002-6933-9585, Naycheva, Lubka, Jochem, Maximilian, Reinhard, Thomas, Boehringer, Daniel, Engesser, Diana, Lagreze, Wolf, Mueller, Claudia, Wolff, Carolin, Schmitz, Jessica, Lorenz, Birgit, Papadopoulou-Laiou, Chrysanthi, Holve, Kerstin, Schweinfurth, Silke, Hoerauf, Hans, Schwarz, Wiebke, Spitzer, Martin, Wagenfeld, Lars, Bertram, Paul, Auffarth, Gerd, Gavrilovic, Branka, Cursiefen, Claus, Schaub, Friederike, Lentzsch, Anna, Welsandt, Gerhard, Thieme, Hagen, Weigel, Melanie, Hidaya, Diyala, Ehmer, Angela, Priglinger, Siegfried, von Livonius, Bettina, Drexler, Carina, Semmelsberger, Jessica, Eter, Nicole, Alten, Florian, Sigleur, Annika, Sieber, Dorothee, Braeutigam, Andrea, Haerter, Friederike, Adorf, Adeline, Pauleikhoff, Daniel, Robering, Angela, Helbig, Horst, Brandl, Caroline, Ziemssen, Focke, Roeck, Daniel, Krummenauer, Frank, Tulka, Sabrina, Wabbels, Bettina, Kupitz, David. G., Goebel, Arno P., Steinberg, Julia, Larsen, Petra P., Schnetzer, Anne, Kobialka, Bianka, Prinz, Beate, Kutten, Danielle, Schneider, Pia, Toczko, Olivia and Yoganathan, Thanushiya
(2019).
Visual impairment and blindness in institutionalized elderly in Germany.
Graefes Arch. Clin. Exp. Ophthalmol., 257 (2).
S. 363 - 371.
NEW YORK:
SPRINGER.
ISSN 1435-702X
Preising, Markus N., Goerg, Boris, Friedburg, Christoph, Qvartskhava, Natalia, Budde, Birgit S., Bonus, Michele, Toliat, Mohammad R., Pfleger, Christopher, Altmueller, Janine, Herebian, Diran ORCID: 0000-0002-8528-0122, Beyer, Mila, Zoellner, Helge J., Wittsack, Hans-Joerg, Schaper, Joerg, Klee, Dirk, Zechner, Ulrich, Nuernberg, Peter, Schipper, Joerg, Schnitzler, Alfons, Gohlke, Holger, Lorenz, Birgit ORCID: 0000-0002-9737-8127, Haeussinger, Dieter and Bolz, Hanno J.
(2019).
Biallelic mutation of human SLC6A6 encoding the taurine transporter TAUT is linked to early retinal degeneration.
Faseb J., 33 (10).
S. 11507 - 11528.
BETHESDA:
FEDERATION AMER SOC EXP BIOL.
ISSN 1530-6860
2017
Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Mueller-Hofstede, Cornelie, Issa, Peter Charbel ORCID: 0000-0002-0351-6673, Heller, Raoul, Beck, Bodo, Ruether, Klaus, Mitter, Diana, Rohrschneider, Klaus, Steinhauer, Ute, Korbmacher, Heike M., Huhle, Dagmar, Elsayed, Solaf M., Taha, Hesham M., Baig, Shahid M., Stoehr, Heidi, Preising, Markus, Markus, Susanne, Moeller, Fabian, Lorenz, Birgit, Nagel-Wolfrum, Kerstin, Khan, Arif O. and Bolz, Hanno J.
(2017).
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome.
Mol. Genet. Genom. Med., 5 (5).
S. 531 - 553.
HOBOKEN:
WILEY.
ISSN 2324-9269
2013
Eisenberger, Tobias, Neuhaus, Christine, Khan, Arif O., Decker, Christian, Preising, Markus N., Friedburg, Christoph, Bieg, Anika, Gliem, Martin, Issa, Peter Charbel ORCID: 0000-0002-0351-6673, Holz, Frank G., Baig, Shahid M., Hellenbroich, Yorck, Galvez, Alberto, Platzer, Konrad ORCID: 0000-0001-6127-6308, Wollnik, Bernd, Laddach, Nadja, Ghaffari, Saeed Reza, Rafati, Maryam, Botzenhart, Elke, Tinschert, Sigrid, Boerger, Doris, Bohring, Axel, Schreml, Julia, Koertge-Jung, Stefani, Schell-Apacik, Chayim, Bakur, Khadijah ORCID: 0000-0002-0668-1762, Al-Aama, Jumana Y., Neuhann, Teresa, Herkenrath, Peter, Nuernberg, Gudrun, Nuernburg, Peter, Davis, John S., Gal, Andreas, Bergmann, Carsten, Lorenz, Birgit and Bolz, Hanno J.
(2013).
Increasing the Yield in Targeted Next-Generation Sequencing by Implicating CNV Analysis, Non-Coding Exons and the Overall Variant Load: The Example of Retinal Dystrophies.
PLoS One, 8 (11).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203