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Titel/AutorZitiert von Jahr
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65
6912012
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65
3722011
Driver mutations in histone H3. 3 and chromatin remodelling genes in paediatric glioblastoma
J Schwartzentruber, A Korshunov, XY Liu, DTW Jones, E Pfaff, K Jacob, ...
Nature 482 (7384), 226-231
2992012
Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations
T Rausch, DTW Jones, M Zapatka, AM Stütz, T Zichner, J Weischenfeldt, ...
Cell 148 (1), 59-71
1632012
Dissecting the genomic complexity underlying medulloblastoma
DTW Jones, N Jäger, M Kool, T Zichner, B Hutter, M Sultan, YJ Cho, ...
Nature 488 (7409), 100-105
1462012
RazerS—fast read mapping with sensitivity control
D Weese, AK Emde, T Rausch, A Döring, K Reinert
Genome Research 19 (9), 1646-1654
1002009
SeqAn an efficient, generic C++ library for sequence analysis
A Döring, D Weese, T Rausch, K Reinert
BMC bioinformatics 9 (1), 11
942008
DELLY: structural variant discovery by integrated paired-end and split-read analysis
T Rausch, T Zichner, A Schlattl, AM Stütz, V Benes, JO Korbel
Bioinformatics 28 (18), i333-i339
442012
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.
J Richter, M Schlesner, S Hoffmann, M Kreuz, E Leich, B Burkhardt, ...
Nature genetics 44 (12)
402012
Segment-based multiple sequence alignment
T Rausch, AK Emde, D Weese, A Döring, C Notredame, K Reinert
Bioinformatics 24 (16), i187-i192
392008
The genomic and transcriptomic landscape of a HeLa cell line
JJM Landry, PT Pyl, T Rausch, T Zichner, MM Tekkedil, AM Stütz, A Jauch, ...
G3: Genes| Genomes| Genetics 3 (8), 1213-1224
352013
Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer
J Weischenfeldt, R Simon, L Feuerbach, K Schlangen, D Weichenhan, ...
Cancer Cell 23 (2), 159-170
352013
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short reads
T Rausch, S Koren, G Denisov, D Weese, AK Emde, A Döring, K Reinert
Bioinformatics 25 (9), 1118-1124
272009
Fast and adaptive variable order markov chain construction
M Schulz, D Weese, T Rausch, A Döring, K Reinert, M Vingron
Algorithms in Bioinformatics, 306-317
182008
A parallel genetic algorithm to discover patterns in genetic markers that indicate predisposition to multifactorial disease
T Rausch, A Thomas, NJ Camp, LA Cannon-Albright, JC Facelli
Computers in biology and medicine 38 (7), 826-836
132008
Impact of genomic structural variation in Drosophila melanogaster based on population-scale sequencing
T Zichner, DA Garfield, T Rausch, AM Stütz, E Cannavó, M Braun, ...
Genome research 23 (3), 568-579
102013
Whole-exome sequencing links caspase recruitment domain 11 (CARD11) inactivation to severe combined immunodeficiency
J Greil, T Rausch, T Giese, OR Bandapalli, V Daniel, I Bekeredjian-Ding, ...
Journal of Allergy and Clinical Immunology
92013
Robust consensus computation
T Rausch, AK Emde, K Reinert
BMC Bioinformatics 9 (Suppl 10), P4
52008
Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition
M Kool, DTW Jones, N Jäger, PA Northcott, TJ Pugh, V Hovestadt, ...
Cancer cell 25 (3), 393-405
22014
Identification of novel sequence variations in microRNAs in chronic lymphocytic leukemia
J Kminkova, M Mraz, K Zaprazna, V Navrkalova, B Tichy, K Plevova, ...
Carcinogenesis, bgt396
12013
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