Ioana Cutcutache
Ioana Cutcutache
Principal Scientist, UCB Pharma
Bestätigte E-Mail-Adresse bei ucb.com
Titel
Zitiert von
Zitiert von
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Primer3—new capabilities and interfaces
A Untergasser, I Cutcutache, T Koressaar, J Ye, BC Faircloth, M Remm, ...
Nucleic acids research 40 (15), e115-e115, 2012
62132012
Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction
J Ye, G Coulouris, I Zaretskaya, I Cutcutache, S Rozen, TL Madden
BMC bioinformatics 13 (1), 1-11, 2012
36402012
Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes
ZJ Zang, I Cutcutache, SL Poon, SL Zhang, JR McPherson, J Tao, ...
Nature genetics 44 (5), 570-574, 2012
5932012
Exome sequencing of liver fluke–associated cholangiocarcinoma
CK Ong, C Subimerb, C Pairojkul, S Wongkham, I Cutcutache, W Yu, ...
Nature genetics 44 (6), 690-693, 2012
3792012
Exome sequencing identifies distinct mutational patterns in liver fluke–related and non-infection-related bile duct cancers
W Chan-On, ML Nairismägi, CK Ong, WK Lim, S Dima, C Pairojkul, ...
Nature genetics 45 (12), 1474, 2013
3422013
Whole-genome and epigenomic landscapes of etiologically distinct subtypes of cholangiocarcinoma
A Jusakul, I Cutcutache, CH Yong, JQ Lim, MN Huang, N Padmanabhan, ...
Cancer discovery 7 (10), 1116-1135, 2017
2572017
Genome-wide mutational signatures of aristolochic acid and its application as a screening tool
SL Poon, ST Pang, JR McPherson, W Yu, KK Huang, P Guan, WH Weng, ...
Science translational medicine 5 (197), 197ra101-197ra101, 2013
2322013
Janus kinase 3–activating mutations identified in natural killer/T-cell Lymphoma
GC Koo, SY Tan, T Tang, SL Poon, GE Allen, L Tan, SC Chong, WS Ong, ...
Cancer discovery 2 (7), 591-597, 2012
2252012
Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma
WK Lim, CK Ong, J Tan, AA Thike, CCY Ng, V Rajasegaran, SS Myint, ...
Nature genetics 46 (8), 877-880, 2014
1602014
Genomic landscapes of breast fibroepithelial tumors
J Tan, CK Ong, WK Lim, CCY Ng, AA Thike, LM Ng, V Rajasegaran, ...
Nature genetics 47 (11), 1341-1345, 2015
1232015
Whole-genome reconstruction and mutational signatures in gastric cancer
N Nagarajan, D Bertrand, AM Hillmer, ZJ Zang, F Yao, PÉ Jacques, ...
Genome biology 13 (12), 1-10, 2012
1202012
Ten-year outcomes after coronary artery bypass grafting according to age in patients with heart failure and left ventricular systolic dysfunction: an analysis of the extended …
MC Petrie, PS Jhund, L She, C Adlbrecht, T Doenst, JA Panza, JA Hill, ...
Circulation 134 (18), 1314-1324, 2016
872016
Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing
ZJ Zang, CK Ong, I Cutcutache, W Yu, SL Zhang, D Huang, LD Ler, ...
Cancer research 71 (1), 29-39, 2011
822011
JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma
ML Nairismägi, J Tan, JQ Lim, S Nagarajan, CCY Ng, V Rajasegaran, ...
Leukemia 30 (6), 1311-1319, 2016
802016
MSIseq: software for assessing microsatellite instability from catalogs of somatic mutations
MN Huang, JR McPherson, I Cutcutache, BT Teh, P Tan, SG Rozen
Scientific reports 5 (1), 1-10, 2015
742015
Pipa: Pipelined profiling and analysis on multicore systems
Q Zhao, I Cutcutache, WF Wong
ACM Transactions on Architecture and Code Optimization (TACO) 7 (3), 1-29, 2010
712010
Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance
AL Vettore, K Ramnarayanan, G Poore, K Lim, CK Ong, KK Huang, ...
Genome medicine 7 (1), 1-15, 2015
582015
Exome-wide sequencing shows low mutation rates and identifies novel mutated genes in seminomas
I Cutcutache, Y Suzuki, IB Tan, S Ramgopal, S Zhang, K Ramnarayanan, ...
European urology 68 (1), 77-83, 2015
492015
Microsatellite analysis of plaice (Pleuronectes platessa L.) in the NE Atlantic: weak genetic structuring in a milieu of high gene flow
A Was, E Gosling, G Hoarau
Marine Biology 157 (3), 447-462, 2010
282010
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
V Del Dotto, F Ullah, I Di Meo, P Magini, M Gusic, A Maresca, L Caporali, ...
The Journal of clinical investigation 130 (1), 108-125, 2020
222020
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