Publications 2010

  • Berger W, Kloeckener-Gruissem B, Neidhardt J (2010) The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res 29:335-375
  • Brunner S, Skosyrski S, Kirschner-Schwabe R, Knobeloch KP, Neidhardt J, Feil S, Glaus E, Luhmann UF, Rüther K, Berger W (2010) Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgrounds. Invest Ophthalmol Vis Sci 51:1106-1115
  • Curjuric I, Imboden M, Schindler C, Downs SH, Hersberger M, Liu SL, Matyas G, Russi EW, Schwartz J, Thun GA, Postma DS, Rochat T, and Probst-Hensch NM (2010) HMOX1 and GST variants modify attenuation of FEF25-75% decline due to PM10 reduction. Eur Respir J 35:505-514
  • Hersberger M, Thun GA, Imboden M, Brandstätter A, Waechter V, Summerer M, Schmid-Grendelmeier P, Bircher A, Rohrer L, Berger W, Russi EW, Rochat T, Kronenberg F, Probst-Hensch N (2010) Association of STR polymorphisms in CMA1 and IL-4 with asthma and atopy: the SAPALDIA cohort. Hum Immunol 71:1154-1160
  • Meienberg J, Rohrbach M, Neuenschwander S, Spanaus K, Giunta C, Alonso S, Arnold E, Henggeler C, Regenass S, Patrignani A, Azzarello-Burri S, Steiner B, Nygren AOH, Carrel T, Steinmann B, Mátyás G (2010) Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: A lesson for and from true haploinsufficiency. Eur J Hum Genet 18:1315-1321
  • Meier ID, Bernreuther C, Tilling T, Neidhardt J, Wee WY, Schulze C, Streichert T, Schachner M (2010) Short DNA sequences inserted for gene targeting can accidentally interfere with off-target gene expression. FASEB J 24:1714-1724
  • Poloschek CM, Bach M, Lagrèze WA, Glaus E, Lemke JR, Berger W, Neidhardt J (2010) ABCA4 and ROM1: Implications for modification of the PRPH2-associated macular dystrophy phenotype. Invest Ophthalmol Vis Sci 51:4253-4265
  • Schmid F, Glaus E, Cremers FPM, Kloeckener-Gruissem B, Berger W, Neidhardt J (2010) Mutation- and tissue-specific alterations of RPGR transcripts. Invest Ophthalmol Vis Sci 51:1628-1635
  • Zuercher J, Neidhardt J, Magyar I, Labs S, Moore AT, Tanner FC, Waseem N, Schorderet DF, Munier FL, Bhattacharya S, Berger W, Kloeckener-Gruissem B (2010) Alterations of the 5’untranslated leader region of SLC16A12 lead to age-related cataract. Invest Ophthalmol Vis Sci 51:3354-3361