A study on multi-GNSS phase-only positioning von Khodabandeh, A, Zaminpardaz, S, Nadarajah, N

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Landscape of genetic lesions in 944 patients with myelodysplastic syndromes von Haferlach, T, Nagata, Y, Grossmann, V, Okuno, Y, Bacher, U, Nagae, G, Schnittger, S, Sanada, M, Kon, A, Alpermann, T, Yoshida, K, Roller, A, Nadarajah, N, Shiraishi, Y, Shiozawa, Y, Chiba, K, Tanaka, H, Koeffler, H P, Klein, H-U, Dugas, M, Aburatani, H, Kohlmann, A, Miyano, S, Haferlach, C, Kern, W, Ogawa, S

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Landscape of TET2 mutations in acute myeloid leukemia von Weissmann, S, Alpermann, T, Grossmann, V, Kowarsch, A, Nadarajah, N, Eder, C, Dicker, F, Fasan, A, Haferlach, C, Haferlach, T, Kern, W, Schnittger, S, Kohlmann, A

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Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML von Stengel, A, Kern, W, Meggendorfer, M, Nadarajah, N, Perglerovà, K, Haferlach, T, Haferlach, C

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IMM Forward Filtering and Backward Smoothing for Maneuvering Target Tracking von Nadarajah, N., Tharmarasa, R., McDonald, M., Kirubarajan, T.

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Landmark analysis of DNMT3A mutations in hematological malignancies von Roller, A, Grossmann, V, Bacher, U, Poetzinger, F, Weissmann, S, Nadarajah, N, Boeck, L, Kern, W, Haferlach, C, Schnittger, S, Haferlach, T, Kohlmann, A

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IRNSS/NavIC and GPS: a single- and dual-system L5 analysis von Zaminpardaz, S., Teunissen, P. J. G., Nadarajah, N.

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Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease von Kohlmann, A, Nadarajah, N, Alpermann, T, Grossmann, V, Schindela, S, Dicker, F, Roller, A, Kern, W, Haferlach, C, Schnittger, S, Haferlach, T

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Multitarget Passive Coherent Location with Transmitter-Origin and Target-Altitude Uncertainties von Tharmarasa, R., Subramaniam, M., Nadarajah, N., Kirubarajan, T., McDonald, M.

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WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups von Krauth, M-T, Alpermann, T, Bacher, U, Eder, C, Dicker, F, Ulke, M, Kuznia, S, Nadarajah, N, Kern, W, Haferlach, C, Haferlach, T, Schnittger, S

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High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome von Krauth, M-T, Eder, C, Alpermann, T, Bacher, U, Nadarajah, N, Kern, W, Haferlach, C, Haferlach, T, Schnittger, S

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Using reciprocity to derive the far field displacements due to buried sources and scatterers von Rose, L. R. Francis, Chiu, W. K., Nadarajah, N., Vien, B. S.

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Single-frequency L5 attitude determination from IRNSS/NavIC and GPS: a single- and dual-system analysis von Zaminpardaz, S., Teunissen, P. J. G., Nadarajah, N.

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Multitarget Tracking using Probability Hypothesis Density Smoothing von Nadarajah, N., Kirubarajan, T., Lang, T., Mcdonald, M., Punithakumar, K.

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Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia von Meggendorfer, Manja, de Albuquerque, Andreia, Nadarajah, Niroshan, Alpermann, Tamara, Kern, Wolfgang, Steuer, Kimberly, Perglerová, Karolína, Haferlach, Claudia, Schnittger, Susanne, Haferlach, Torsten

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Aberrations identified by genomic arrays in normal karyotype CMML can be detected in 40% of patients, but do not add prognostic information to molecular mutations von Vetro, C, Haferlach, C, Haferlach, T, Zenger, M, Nadarajah, N, Kern, W, Meggendorfer, M

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Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPN von Jeromin, S, Kohlmann, A, Meggendorfer, M, Schindela, S, Perglerová, K, Nadarajah, N, Kern, W, Haferlach, C, Haferlach, T, Schnittger, S

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Instantaneous GPS/Galileo/QZSS/SBAS Attitude Determination: A Single-Frequency (L1/E1) Robustness Analysis under Constrained Environments von Nadarajah, N., Teunissen, P. J. G.

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Robustness of comprehensive DNA- and RNA-based assays at diagnosis of acute myeloid leukemia using blood and bone marrow stored on filter cards von Haferlach, T, Weber, S, Konietschke, R, Nadarajah, N, Stengel, A, Kern, W, Haferlach, C, Meggendorfer, M

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BAALC expression: a suitable marker for prognostic risk stratification and detection of residual disease in cytogenetically normal acute myeloid leukemia von Weber, S, Alpermann, T, Dicker, F, Jeromin, S, Nadarajah, N, Eder, C, Fasan, A, Kohlmann, A, Meggendorfer, M, Haferlach, C, Kern, W, Haferlach, T, Schnittger, S

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