CGHPRO – A comprehensive data analysis tool for array CGH

Por Chen, Wei, Erdogan, Fikret, Ropers, H-Hilger, Lenzner, Steffen, Ullmann, Reinhard
Publicado em 2005

Genomic Structure and Comparative Analysis of Nine Fugu Genes: Conservation of Synteny with Human Chromosome Xp22.2–p22.1

Por Brunner, Bodo, Todt, Tilman, Lenzner, Steffen, Stout, Karen, Schulz, Ute, Ropers, Hans-Hilger, Kalscheuer, Vera M.
Publicado em 1999

Mutations in the FTSJ1 Gene Coding for a Novel S-Adenosylmethionine–Binding Protein Cause Nonsyndromic X-Linked Mental Retardation

Por Freude, Kristine, Hoffmann, Kirsten, Jensen, Lars-Riff, Delatycki, Martin B., des Portes, Vincent, Moser, Bettina, Hamel, Ben, van Bokhoven, Hans, Moraine, Claude, Fryns, Jean-Pierre, Chelly, Jamel, Gécz, Jozef, Lenzner, Steffen, Kalscheuer, Vera M., Ropers, Hans-Hilger
Publicado em 2004

CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling

Por Starokadomskyy, Petro, Gluck, Nathan, Li, Haiying, Chen, Baozhi, Wallis, Mathew, Maine, Gabriel N., Mao, Xicheng, Zaidi, Iram W., Hein, Marco Y., McDonald, Fiona J., Lenzner, Steffen, Zecha, Agnes, Ropers, Hans-Hilger, Kuss, Andreas W., McGaughran, Julie, Gecz, Jozef, Burstein, Ezra
Publicado em 2013

Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation

Por Jensen, Lars Riff, Amende, Marion, Gurok, Ulf, Moser, Bettina, Gimmel, Verena, Tzschach, Andreas, Janecke, Andreas R., Tariverdian, Gholamali, Chelly, Jamel, Fryns, Jean-Pierre, Van Esch, Hilde, Kleefstra, Tjitske, Hamel, Ben, Moraine, Claude, Gécz, Jozef, Turner, Gillian, Reinhardt, Richard, Kalscheuer, Vera M., Ropers, Hans-Hilger, Lenzner, Steffen
Publicado em 2005