2005

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ZORA note on the authors' stated information

In the exportable list, publications with less than 30 authors are transferred 1:1 to ZORA. No author names are deleted. --> Reason: complete metadata per publication, also for further use (e.g. in Swisscovery).
For publications with more (>30) authors, the authors are automatically truncated to the number 30 during import. In the same step, an "et al" is created. If this leaves out UZH authors, they were added at the end, after "et al".
More information: Varia | University Library Zurich | UZH
For the complete listing of authors in order of publication, please use the authors list at the original publication. Or alternatively use the text file at the bottom of this page.

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Zeitz, Christina; van Genderen, Maria; Neidhardt, John; Luhmann, Ulrich F O; Hoeben, Frank; Forster, Ursula; Wycisk, Katharina Agnes; Matyas, Gabor; Hoyng, Carel B; Riemslag, Frans; Meire, Francoise; Cremers, Frans P M; Berger, Wolfgang (2005). Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram. Investigative Ophthalmology & Visual Science, 46(11):4328-4335.
Luhmann, Ulrich F O; Lin, Jihong; Acar, Niyazi; Lammel, Stefanie; Feil, Silke; Grimm, Christian; Seeliger, Mathias W; Hammes, Hans-Peter; Berger, Wolfgang (2005). Role of the Norrie Disease Pseudoglioma Gene in Sprouting Angiogenesis during Development of the Retinal Vasculature. Investigative Ophthalmology & Visual Science, 46(9):3372-3382.
Luhmann, Ulrich F O; Meunier, Dominique; Shi, Wei; Lüttges, Angela; Pfarrer, Christiane; Fundele, Reinald; Berger, Wolfgang (2005). Fetal loss in homozygous mutant Norrie disease mice: A new role of Norrin in reproduction. Genesis, 42(4):253-262.
Vermeesch, Joris Robert; Melotte, Cindy; Salden, Ivo; Riegel, Mariluce; Trifnov, Vladimir; Polityko, Anna; Rumyantseva, Natalia; Naumchik, Irina; Starke, Heike; Matthijs, Gert; Schinzel, Albert; Fryns, Jean-Pierre; Liehr, Thomas (2005). Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. European Journal of Medical Genetics, 48(3):319-327.
Schinzel, Albert (2005). Chromosome Aberrations. In: Panteliadis, Christos P; Korinthenberg, Rudolf. Paediatric Neurology : Theory and Practice. Stuttgart, New York: Georg Thieme Verlag, 235-251.
Riegel, Mariluce; Baumer Wolz, Alessandra; Süss, Jochen; Schinzel, Albert (2005). An unusual reciprocal translocation detected by subtelomeric FISH: interstitial and not terminal. American Journal of Medical Genetics. Part A, 135(1):86-90.
Riegel, Mariluce; Hargreaves, P; Baumer Wolz, Alessandra; Guc-Scekic, M; Ignjatovic, M; Schinzel, Albert (2005). Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21. European Journal of Medical Genetics, 48(2):167-174.
Descipio, Cheryl; Schneider, Lori; Young, Terri L; et al; Schinzel, Albert A G L (2005). Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome. American Journal of Medical Genetics. Part A, 134A(1):3-11.
Roelfsema, Jeroen H; White, Stefan J; Ariyürek, Yavuz; Bartholdi, Deborah; Niedrist, Dunja; Papadia, Francesco; Bacino, Carlos A; den Dunnen, Johan T; van Ommen, Gert-Jan B; Breuning, Martijn H; Hennekam, Raoul C; Peters, Dorien J M (2005). Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. American Journal of Human Genetics, 76(4):572-80.
Zeitz, Christina; Minotti, Roberta; Feil, Silke; Matyas, Gabor; Cremers, Frans P M; Hoyng, Carel B; Berger, Wolfgang (2005). Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness. Molecular Vision, 11:179-183.
So, Joyce; Suckow, Vanessa; Kijas, Zofia; et al; Schinzel, Albert (2005). Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics. Part A, 132A(1):1-7.
Cetin, Z; Berker Karaüzüm, S; Yakut, S; Mihci, Ercan; Baumer Wolz, Alessandra; Wey, E; Taçoy, S; Bagci, Gulseren; Lüleci, Güven (2005). M-FISH applications in clinical genetics. Genetic Counseling, 16(3):257-68.
Manguoğlu, E; Berker-Karaüzüm, S; Baumer Wolz, Alessandra; Mihci, Ercan; Taçoy, S; Lüleci, Güven; Schinzel, Albert (2005). A case with de novo interstitial deletion of chromosome 7q21.1-q22. Genetic Counseling, 16(2):155-9.

Textfile

So J, Suckow V, Kijas Z, Kalscheuer V, Moser B, Winter J, Baars M, Firth H, Lunt P, Hamel B, Meinecke P, Moraine C, Odent S, Schinzel A, van der Smagt JJ, Devriendt K, Albrecht B, Gillessen-Kaesbach G, van der Burgt I, Petrij F, Faivre L, McGaughranJ, McKenzie F, Opitz JM, Cox T, Schweiger S Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations Am J Med Genet 2005; 132A: 1-7

Wey E, Bartholdi D, Riegel M, Nazlican H, Horsthemke B, Schinzel A, Baumer A Mosaic Imprinting defect in a patient with an almost typical expression of the Prader-Willi syndrome Eur J Hum Genet 2005; 13:273-277

Roelfsema JH, White SJ, Ariyürek Y, Bartholdi D, Niedrist D, Papadia F, Bacino CA, den Dunnen JT, van Ommen G-JB, Breuning MH, Hennekam RC, Peters DJM Genetic heterogeneity in Rubinstein-Taybi syndrome: Mutations in both the CBP and EP300 genes cause disease Am J Hum Genet 2005;76:572-580

Schinzel A Chromosome Aberrations pp. 235-251, in: Paediatric Neurology. Theory and Practice. Ed. Christos P. Panteliadis and Rudolf Korinthenberg, 2005. Georg Thieme, Stuttgart-New York

De Scipio C, Schneider L, Young TL, Wassermann N, Yaeger D, Lu F, Wheeler PG, Williams MS, Bason L, Jukofsky L, Menon A, Geschwindt R, Chudley AE, Saraiva J, Schinzel AGL, Guichet A, Dobyns WE, Toutain A, Spinner NB, Krantz ID Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome Am J Med Genet 2005;134A:3-11

Riegel M, Hargreaves P, Baumer A, Guc-Scekic M, Ignjatovic M, Schinzel A Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21 Eur J Med Genet 2005;48:167-174

Riegel M, Baumer A, Süss J, Schinzel A An unusual reciprocal translocation detected by subtelomeric FISH: Interstitial and not terminal Am J Med Genet 2005; 135A:86-90

Kloeckener-Gruissem B, Betts DR, Zankl A, Berger W, Güngör T A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9 Am J Med Genet 2005; 136A/138A:31-37/19

Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns J-P, Liehr T Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype Eur J Med Genet 2005; 48:319-327

Manguoglu E, Berker-Karaüzüm S, Baumer A, Mihçi E, Taçoy S, Lüleci G, Schinzel A A case with de novo interstitial deletion of chromosome 7q21.1-q22 Genet Couns 2005;16:155-159

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