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Ofner-Ziegenfuss Lisa |

Publications

** = Publications listed in SCI/SSCI/Pubmed

2025

Case Report

** Peschaut, T; Michelitsch, M; Brandner, M; Kamper, S; Ofner-Ziegenfuss, L; Blatterer, J; Tichy, HA; Posch-Pertl, L An Unusual Retinal Presentation of a Novel COL11A1 Mutation: A Case Report
CASE REP OPHTHALMOL. 2025; 16(1): 62-67. Doi: 10.1159/000542708 (- Case Report) [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

2020

Full paper/article (Journal)

** Baghdasaryan, A; Ofner-Ziegenfuß, L; Lackner, C; Fickert, P; Resch, B; Morris, NM; Deutschmann, A Histological demonstration of BSEP/ABCB11 inhibition in transient neonatal cholestasis: a case report.
BMC Pediatr. 2020; 20(1):340-340 Doi: 10.1186/s12887-020-02201-x (- Case Report) [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

2017

Full paper/article (Journal)

** Jüngst, C; Stadlbauer, V; Reichert, MC; Zimmer, V; Weber, SN; Ofner-Ziegenfuß, L; Voigtländer, T; Spindelböck, W; Fickert, P; Kirchner, GI; Lammert, F; Lankisch, TO; Krawczyk, M NOD2 gene variants confer risk for secondary sclerosing cholangitis in critically ill patients.
Sci Rep. 2017; 7(1):7026-7026 Doi: 10.1038/s41598-017-06268-y [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

Short report/Letter

** Stampfer, L; Sperl, D; Fickert, P; Lackner, H; Sovinz, P; Ofner-Ziegenfuß, L; Strenger, V; Urban, C; Jahnel, J; Seidel, MG Life-threatening sinusoidal obstruction syndrome after high-dose chemotherapy linked to compound heterozygous mutations in ABCB11.
Pediatr Blood Cancer. 2017; 64(12): Doi: 10.1002/pbc.26666
Web of Science PubMed FullText FullText_MUG

Abstract (Journal)

** Jungst, C; Stadlbauer, V; Reichert, M; Weber, S; Ofner-Ziegenfuss, L; Voigtlander, T; Spindelbock, W; Fickert, P; Kirchner, G; Lammert, F; Lankisch, TO; Krawczyk, M NOD2 variants as novel genetic risk factors for secondary sclerosing cholangitis in critically ill patients
J HEPATOL. 2017; 66(1):S358-S358.-International Liver Congress / 52nd Annual Meeting of the European-Association-for-the-Study-of-the-Liver; APR 19-23, 2017; Amsterdam, NETHERLANDS. [Poster]
Web of Science

2016

Full paper/article (Journal)

** Tomaschitz, A; Verheyen, N; Meinitzer, A; Pieske, B; Belyavskiy, E; Brussee, H; Haas, J; März, W; Pieske-Kraigher, E; Verheyen, S; Ofner-Ziegenfuss, L; Hartaigh, BÓ; Schwetz, V; Aberer, F; Grübler, M; Lang, F; Alesutan, I; Voelkl, J; Gaksch, M; Horina, JH; Dimai, HP; Rus-Machan, J; Stiegler, C; Ritz, E; Fahrleitner-Pammer, A; Pilz, S Effect of eplerenone on parathyroid hormone levels in patients with primary hyperparathyroidism: results from the EPATH randomized, placebo-controlled trial.
J Hypertens. 2016; 34(7):1347-56 Doi: 10.1097/HJH.0000000000000927
Web of Science PubMed FullText FullText_MUG

Abstract (Journal)

** Jungst, C; Stadlbauer, V; Reichert, MC; Ofner-Ziegenfuss, L; Voigtlander, T; Spindelboeck, W; Fickert, P; Kirchner, GI; Lammert, F; Lankisch, T; Krawczyk, M NOD2 confers risk for sclerosing cholangitis in critically ill patients: genetic study in two independent cohorts
HEPATOLOGY. 2016; 63(1 SUPP):191A-192A.-67th Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases (AASLD); NOV 11-15, 2016; Boston, MA. [Poster]
Web of Science

2011

Full paper/article (Journal)

** Beraza, N; Ofner-Ziegenfuss, L; Ehedego, H; Boekschoten, M; Bischoff, SC; Mueller, M; Trauner, M; Trautwein, C Nor-ursodeoxycholic acid reverses hepatocyte-specific nemo-dependent steatohepatitis.
Gut. 2011; 60(3):387-396 Doi: 10.1136/gut.2010.223834
Web of Science PubMed FullText FullText_MUG Google Scholar

2010

Full paper/article (Journal)

** Sánchez-Soriano, N; Gonçalves-Pimentel, C; Beaven, R; Haessler, U; Ofner-Ziegenfuss, L; Ballestrem, C; Prokop, A Drosophila growth cones: a genetically tractable platform for the analysis of axonal growth dynamics.
Dev Neurobiol. 2010; 70(1):58-71 Doi: 10.1002/dneu.20762 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

Abstract (Journal)

** Beraza, N; Ofner-Ziegenfuss, L; Ehedego, H; Boekschoten, M; Mueller, M; Trauner, M; Trautwein, C NOR-UDCA ATTENUATES PROGRESSION OF NASH
J HEPATOL. 2010; 52: S304-S304. Doi: 10.1016/S0168-8278(10)60783-0 [Poster]
Web of Science FullText FullText_MUG

2009

Abstract (Journal)

** Beraza, N; Ofner-Ziegenfuss, L; Ehedego, H; Boekschoten, MV; Muller, M; Trauner, M; Trautwein, C THERAPEUTIC EFFECT OF A NOR-UDCA BASED DIET ON NASH PROGRESSION IN THE CHRONIC DISEASE MODEL OF HEPATOCYTE-SPECIFIC NEMO DELETION
HEPATOLOGY. 2009; 50(4):1920- [Oral Communication]
Web of Science

2008

Full paper/article (Journal)

** Windpassinger, C; Schoser, B; Straub, V; Hochmeister, S; Noor, A; Lohberger, B; Farra, N; Petek, E; Schwarzbraun, T; Ofner, L; Löscher, WN; Wagner, K; Lochmüller, H; Vincent, JB; Quasthoff, S An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1.
Am J Hum Genet. 2008; 82(1): 88-99. Doi: 10.1016/j.ajhg.2007.09.004 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

2007

Full paper/article (Journal)

** Schwarzbraun, T; Ofner, L; Gillessen-Kaesbach, G; Schaperdoth, B; Preisegger, KH; Windpassinger, C; Wagner, K; Petek, E; Kroisel, PM A new 3p interstitial deletion including the entire MITF gene causes a variation of Tietz/Waardenburg type IIA syndromes.
Am J Med Genet A. 2007; 143(6): 619-624. Doi: 10.1002/ajmg.a.31627 (- Case Report)
Web of Science PubMed FullText FullText_MUG

2006

Full paper/article (Journal)

** Ofner, L; Raedle, J; Windpassinger, C; Schwarzbraun, T; Kroisel, PM; Wagner, K; Petek, E Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene.
J HUM GENET. 2006; 51(2): 141-146. Doi: 10.1007/s10038-005-0333-x [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

** Schwarzbraun, T; Ullmann, R; Schubert, M; Ledinegg, M; Ofner, L; Windpassinger, C; Wagner, K; Kroisel, PM; Petek, E Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development.
Cytogenet Genome Res. 2006; 115(1):84-89 Doi: 10.1159/000094804 (- Case Report)
Web of Science PubMed FullText FullText_MUG

** Schwarzbraun, T; Windpassinger, C; Ofner, L; Vincent, JB; Cheung, J; Scherer, SW; Wagner, K; Kroisel, PM; Petek, E Genomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS).
EUR J MED GENET. 2006; 49(4): 338-345. Doi: 10.1016/j.ejmg.2005.10.133
Web of Science PubMed FullText FullText_MUG

2004

Full paper/article (Journal)

** Schwarzbraun, T; Vincent, JB; Schumacher, A; Geschwind, DH; Oliveira, J; Windpassinger, C; Ofner, L; Ledinegg, MK; Kroisel, PM; Wagner, K; Petek, E Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue.
Genomics. 2004; 84(3):577-586 Doi: 10.1016/j.ygeno.2004.04.013
Web of Science PubMed FullText FullText_MUG

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