Publikationen von Ralf Sudbrak

Ralf Sudbrak, Alfred Beck, Katja Heitmann, Steffen Hennig, Sven Klages, Anna Kosiura, Ines Mueller, Richard Reinhardt, Hans Lehrach, and ... et al, "The DNA sequence of the human X chromosome," Nature 343 (7031), 325-337 (2005).

Ralf Sudbrak, Alfred Beck, Katja Heitmann, Steffen Hennig, Sven Klages, Anna Kosiura, Ines Mueller, Richard Reinhardt, Hans Lehrach, and et al, "The DNA sequence of the human X chromosome," Nature 343 (7031), 325-337 (2005).

E. Hammer, K. Kutsche, F. Haag, K. Ullrich, R. Sudbrak, R. P. Willig, T. Braulke, and B. Kubler, "Mono-allelic expression of the IGF-I receptor does not affect IGF responses in human fibroblasts," European Journal of Endocrinology 151 (4), 521-529 (2004).

Peter Hurt, Lutz Walter, Ralf Sudbrak, Sven Klages, Ines Mueller, Takashi Shiina, Hidetoshi Inoko, Hans Lehrach, Eberhard Guenther, Reinhard Reinhardt, and Heinz Himmelbauer, "The genomic sequence and comparative analysis of the rat major histocompatibility complex," Genome Research 14 (4), 631-639 (2004).

Enkhjargal Tsend-Ayush, Frank Grützner, Ying Yue, Bärbel Grossmann, Ulrike Hänsel, Ralf Sudbrak, and Thomas Haaf, "Plasticity of human chromosome 3 during primate evolution," Genomics 83 (2), 193-202 (2004).

Bernd Timmermann, Sascha Sauer, Heymut Omran, Ralf Sudbrak, and Richard Reinhardt, "Vergleichende Sequenzierung von Kandidatengenen: die Resequencing-Plattform am MPI-MG," GenomXPress: Informationen aus der Deutschen Genomforschung 2004 (1), 17-19 (2004).

J. Hoefele, Ralf Sudbrak, E. Otto, A. Imm, J. O'Toole, and F. Hildebrandt, "Mutational analysis in nephronophthisis type 4.," Journal of the American Society of Nephrology 14 (Suppl. S), 359A-359A (2003).

Heike Olbrich, Manfred Fliegauf, Julia Hoefele, Andreas Kispert, Edgar Otto, Andreas Volz, Matthias T. Wolf, Gürsel Sasmaz, Ute Trauer, Richard Reinhardt, Ralf Sudbrak, Corinne Antignac, Norbert Gretz, Gerd Walz, Bernhard Schermer, Thomas Benzing, Friedhelm Hildebrandt, and Heymut Omran, "Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis," Nature Genetics 34 (4), 455-459 (2003).

Ralf Sudbrak, Richard Reinhardt, Steffen Hennig, Hans Lehrach, Eberhard Gunther, and Lutz Walter, "Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region," Immunogenetics 54 (10), 699-704 (2003).

Ralf Sudbrak, Richard Reinhardt, Steffen Hennig, Eberhard Günther, and Lutz Walter, "Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region," Immunogenetics 54 (10), 699-704 (2002).

Edgar Otto, Julia Hoefele, Rainer Ruf, Adelheid M. Mueller, Karl S. Hiller, Matthias T. F. Wolf, Maria J. Schuermann, Achim Becker, Ralf Birkenhäger, Ralf Sudbrak, Hans C. Hennies, Peter Nürnberg, and Friedhelm Hildebrandt, "A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution," American Journal of Human Genetics 71 (5), 1161-1167 (2002).

Edgar Otto, Julia Hoefele, Rainer Ruf, Adelheid M. Mueller, Karl S. Hiller, Matthias T. F. Wolf, Maria J. Schuermann, Achim Becker, Ralf Birkenhäger, Ralf Sudbrak, Hans C. Hennies, Peter Nürnberg, and Friedhelm Hildebrandt, "A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution," American Journal of Human Genetics 71 (5), 1161-1167 (2002).

Lutz Walter, Peter Peter Hurt, Heinz Himmelbauer, Ralf Sudbrak, and Eberhard Günther, "Physical mapping of the major histocompatibility complex class II and class III regions of the rat," Immunogenetics 54 (4), 268-275 (2002).

Carol Dobson-Stone, Rebecca Fairclough, Eimear Dunne, Joanna Brown, Manel Dissanayake, Colin S. Munro, Tom Strachan, Susan Burge, Ralf Sudbrak, Anthony P. Monaco, and Alain Hovnanian, "Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene," Journal of Investigative Dermatology 118 (2), 338-343 (2002).

Heike Olbrich, Karsten Häffner, Andreas Kispert, Alexander Völkel, Andreas Volz, Gürsel Sasmaz, Richard Reinhardt, Steffen Hennig, Hans Lehrach, Nikolaus Konietzko, Maimoona Zariwala, Peadar G. Noone, Michael Knowles, Hannah M. Mitchison, Maggie Meeks, Eddie M. K. Chung, Friedhelm Hildebrandt, Ralf Sudbrak, and Heymut Omran, "Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry," Nature Genetics 30 (2), 143-144 (2002).

Heike Olbrich, Karsten Häffner, Andreas Kispert, Alexander Völkel, Andreas Volz, Gürsel Sasmaz, Richard Reinhardt, Steffen Hennig, Hans Lehrach, Nikolaus Konietzko, Maimoona Zariwala, Peadar G. Noone, Michael Knowles, Hannah M. Mitchison, Maggie Meeks, Eddie M. K. Chung, Friedhelm Hildebrandt, Ralf Sudbrak, and Heymut Omran, "Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry," Nature Genetics 30 (2), 143-144 (2002).

Heike Olbrich, Karsten Häffner, Andreas Kispert, Alexander Völkel, Andreas Volz, Gürsel Sasmaz, Richard Reinhardt, Steffen Hennig, Hans Lehrach, Nikolaus Konietzko, Maimoona Zariwala, Peadar G. Noone, Michael Knowles, Hannah M. Mitchison, Maggie Meeks, Eddie M. K. Chung, Friedhelm Hildebrandt, Ralf Sudbrak, and Heymut Omran, "Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry," Nature Genetics 30 (2), 143-144 (2002).

Jörg Schickel, Katharina Stahn, Klaus-Peter Zimmer, Ralf Sudbrak, Tim M. Størm, Matthias Dürst, Michael Kiehntopf, and Thomas Deufel, "Gene for integrin-associated protein (IAP, CD47): physical mapping, genomic structure, and expression studies in skeletal muscle.," Biochemistry and Cell Biology 80 (2), 169-176 (2002).

B. Regierer, V. Zazzu, R. Sudbrak, A. Kühn, and H. Lehrach, "Future of Medicine: Models in Predictive Diagnostics and Personalized Medicine", in Advances in Biochemical Engineering/Biotechnology, edited by H. Seitz and S. Schuhmacher (Springer, Berlin Heidelberg, 2013), Vol. 133, pp. 15-33.

R. Sudbrak and H. Lehrach, "IT Future of Medicine (ITFoM)", in Proceedings Iwbbio 2013: International Work-Conference on Bioinformatics and Biomedical Engineering, (2013), pp. 335-335.