Publications of Ralf Sudbrak

Journal Article (38)

1.
Journal Article
Willems, T.; Gymrek, M.; Highnam, G.; The 1000 Genomes Project, C.; Herwig, R.; Lehrach, H.; Sudbrak, R.; Timmermann, B.; Mittelman, D.; Erlich, Y.: The landscape of human STR variation. Genome Research 24 (11), pp. 1894 - 1904 (2014)
2.
Journal Article
Colonna, V.; Ayub, Q.; Chen, Y.; Pagani, L.; Luisi, P.; Pybus, M.; Garrison, E.; Xue, Y.; Tyler-Smith, C.; 1000 Genomes Project, C. et al.: Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biology: Biology for the Post-Genomic Era 15 (6), R88 (2014)
3.
Journal Article
Khurana, E.; Fu, Y.; Colonna, V.; Mu, X. J.; Kang, H. M.; Lappalainen, T.; Sboner, A.; Lochovsky, L.; Chen, J.; Harmanci, A. et al.: Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 342 (6154), p. 1235587 - 1235587 (2013)
4.
Journal Article
Zazzu, V.; Regierer, B.; Kühn, A.; Sudbrak, R.; Lehrach, H.: IT Future of Medicine: from molecular analysis to clinical diagnosis and improved treatment. New Biotechnology 30 (4), pp. 362 - 365 (2013)
5.
Journal Article
Barann, M.; Esser, D.; Klostermeier, U. C.; Lappalainen, T.; Luzius, A.; Kuiper, J. W. P.; Ammerpohl, O.; Vater, I.; Siebert, R.; Amstislavskiy, V. et al.: Janus-a comprehensive tool investigating the two faces of transcription. Bioinformatics 29 (13), pp. 1600 - 1606 (2013)
6.
Journal Article
Lappalainen, T.; Sammeth, M.; Friedlander, M. R.; 't Hoen, P. A. C.; Monlong, J.; Rivas, M. A.; Gonzalez-Porta, M.; Kurbatova, N.; Griebel, T.; Ferreira, P. G. et al.: Transcriptome and genome sequencing uncovers functional variation in humans. Nature 501 (7468), pp. 506 - 511 (2013)
7.
Journal Article
Abecasis, G. R.; Auton, A.; Brooks, L. D.; DePristo, M. A.; Durbin, R. M.; Handsaker, R. E.; Kang, H. M.; Marth, G. T.; McVean, G. A.; The 1000 Genomes Project Consortium et al.: An integrated map of genetic variation from 1,092 human genomes. Nature 491 (7422), pp. 56 - 65 (2012)
8.
Journal Article
The 1000 Genomes Project Consortium; Sudbrak, R.; Albrecht, M.; Amstislavskiy, V.; Borodina, T. A.; Dahl, A.; Davydov, A.; Herwig, R.; Marquardt, P.; Mertes, F. et al.: The 1000 Genomes Project: data management and community access. Nature methods 9 (5), pp. 459 - 462 (2012)
9.
Journal Article
MacArthur, D. G.; Balasubramanian, S.; Frankish, A.; 1000 Genomes Project, C.; Sudbrak, R.; Albrecht , M. W.; Amstislavskiy, V.; Borodina, T. A.; Dahl, A.; Davydov, A. et al.: A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 335 (6070), pp. 823 - 828 (2012)
10.
Journal Article
Hornef, N.; Olbrich, H.; Horvath, J.; Zariwala, M. A.; Fliegauf, M.; Loges, N. T.; Wildhaber, J.; Noone, P. G.; Kennedy, M.; Antonarakis, S. E. et al.: DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects. American Journal of Respiratory and Critical Care Medicine: an Official Journal of the American Thoracic Society, Medical Section of the Lung Association 174 (2), pp. 120 - 126 (2006)
11.
Journal Article
Hornef, N.; Olbrich, H.; Horvath, J.; Zariwala, M. A.; Fliegauf, M.; Loges, N. T.; Wildhaber, J.; Noone, P. G.; Kennedy, M.; Antonarakis, S. E. et al.: DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects. American Journal of Respiratory and Critical Care Medicine: an Official Journal of the American Thoracic Society, Medical Section of the Lung Association 174 (2), pp. 120 - 126 (2006)
12.
Journal Article
Muzny, D. M.; Scherer, S. E.; Kaul, R.; Wang, J.; Yu, J.; Sudbrak, R.; Buhay, C. J.; Chen, R.; Cree, A.; Ding, Y. et al.: The DNA sequence, annotation and analysis of human chromosome 3. Nature 440 (7088), pp. 1194 - 1198 (2006)
13.
Journal Article
Muzny, D. M.; Scherer, S. E.; Kaul, R.; Wang, J.; Yu, J.; Sudbrak, R.; Buhay, C. J.; Chen, R.; Cree, A.; Ding, Y. et al.: The DNA sequence, annotation and analysis of human chromosome 3. Nature 440 (7088), pp. 1194 - 1198 (2006)
14.
Journal Article
Muzny, D. M.; Scherer, S. E.; Kaul, R.; Wang, J.; Yu, J.; Sudbrak, R.; Buhay, C. J.; Chen, R.; Cree, A.; Ding, Y. et al.: The DNA sequence, annotation and analysis of human chromosome 3. Nature 440 (7088), pp. 1194 - 1198 (2006)
15.
Journal Article
Horváth, J.; Fliegauf, M.; Olbrich, H.; Kispert, A.; King, S. M.; Mitchison, H.; Zariwala, M. A.; Knowles, M. R.; Sudbrak, R.; Fekete, G. et al.: Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology 33 (1), pp. 41 - 47 (2005)
16.
Journal Article
Horváth, J.; Fliegauf, M.; Olbrich, H.; Kispert, A.; King, S. M.; Mitchison, H.; Zariwala, M. A.; Knowles, M. R.; Sudbrak, R.; Fekete, G. et al.: Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology 33 (1), pp. 41 - 47 (2005)
17.
Journal Article
Hoefele, J.; Sudbrak, R.; Reinhardt, R.; Lehrack, S.; Hennig, S.; Imm, A.; Muerb, U.; Utsch, B.; Attanasio, M.; O'Toole, J. F. et al.: Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis. Human Mutation 25 (4), p. 411 - 411 (2005)
18.
Journal Article
Hoefele, J.; Sudbrak, R.; Reinhardt, R.; Lehrack, S.; Hennig, S.; Imm, A.; Muerb, U.; Utsch, B.; Attanasio, M.; O'Toole, J. F. et al.: Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis. Human Mutation 25 (4), p. 411 - 411 (2005)
19.
Journal Article
Otto, E. A.; Loeys, B.; Khanna, H.; Hellemans, J.; Sudbrak, R.; Fan, S.; Muerb, U.; O'Toole, J. F.; Helou, J.; Attanasio, M. et al.: Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin. Nature Genetics 37 (3), pp. 282 - 288 (2005)
20.
Journal Article
Otto, E. A.; Loeys, B.; Khanna, H.; Hellemans, J.; Sudbrak, R.; Fan, S.; Muerb, U.; O'Toole, J. F.; Helou, J.; Attanasio, M. et al.: Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin. Nature Genetics 37 (3), pp. 282 - 288 (2005)
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