
Publications of Ralf Sudbrak
All genres
Journal Article (38)
1.
Journal Article
24 (11), pp. 1894 - 1904 (2014)
The landscape of human STR variation. Genome Research 2.
Journal Article
15 (6), R88 (2014)
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biology: Biology for the Post-Genomic Era 3.
Journal Article
342 (6154), p. 1235587 - 1235587 (2013)
Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 4.
Journal Article
30 (4), pp. 362 - 365 (2013)
IT Future of Medicine: from molecular analysis to clinical diagnosis and improved treatment. New Biotechnology 5.
Journal Article
29 (13), pp. 1600 - 1606 (2013)
Janus-a comprehensive tool investigating the two faces of transcription. Bioinformatics 6.
Journal Article
501 (7468), pp. 506 - 511 (2013)
Transcriptome and genome sequencing uncovers functional variation in humans. Nature 7.
Journal Article
491 (7422), pp. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature 8.
Journal Article
9 (5), pp. 459 - 462 (2012)
The 1000 Genomes Project: data management and community access. Nature methods 9.
Journal Article
335 (6070), pp. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 10.
Journal Article
174 (2), pp. 120 - 126 (2006)
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 11.
Journal Article
174 (2), pp. 120 - 126 (2006)
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 12.
Journal Article
440 (7088), pp. 1194 - 1198 (2006)
The DNA sequence, annotation and analysis of human chromosome 3. Nature 13.
Journal Article
440 (7088), pp. 1194 - 1198 (2006)
The DNA sequence, annotation and analysis of human chromosome 3. Nature 14.
Journal Article
440 (7088), pp. 1194 - 1198 (2006)
The DNA sequence, annotation and analysis of human chromosome 3. Nature 15.
Journal Article
33 (1), pp. 41 - 47 (2005)
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology 16.
Journal Article
33 (1), pp. 41 - 47 (2005)
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology 17.
Journal Article
25 (4), p. 411 - 411 (2005)
Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis. Human Mutation 18.
Journal Article
25 (4), p. 411 - 411 (2005)
Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis. Human Mutation 19.
Journal Article
37 (3), pp. 282 - 288 (2005)
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin. Nature Genetics 20.
Journal Article
37 (3), pp. 282 - 288 (2005)
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin. Nature Genetics