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High risk neuroblastoma (HR-NB) with MNA and age <18 months: Results from the HR-NBL1/SIOPEN trial
High risk neuroblastoma (HR-NB) with MNA and age <18 months: Results from the HR-NBL1/SIOPEN trial
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High risk neuroblastoma (HR-NB) with MNA and age <18 months: Results from the HR-NBL1/SIOPEN trial

Ladenstein, Ruth Lydia ; Poetschger, Ulrike ; Valteau Couanet, Dominique ; Ash, Shifra ; Beck Popovic, Maja ; Balwierz, Walentyna ; Boterberg, Tom ; Chan, Godfrey Chi-Fung ; Elliott, Martin ; Kogner, Per ; Lode, Holger N. ; Laureys, Genevieve ; Luksch, Roberto ; Malis, Josef ; Owens, Cormac ; Papadakis, Vassilios ; Sarnacki, Sabine ; Taschner-Mandl, Sabine ; Schleiermacher, Gudrun ; Canete, Adela

JOURNAL OF CLINICAL ONCOLOGY, 2023, Vol.41 (16_suppl), p.10000-10000 [Periódico revisado por pares]

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2
Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)
Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)
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Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)

Bellini, Angela ; Pötschger, Ulrike ; Bernard, Virginie ; Lapouble, Eve ; Baulande, Sylvain ; Ambros, Peter F ; Auger, Nathalie ; Beiske, Klaus ; Bernkopf, Marie ; Betts, David R ; Bhalshankar, Jaydutt ; Bown, Nick ; de Preter, Katleen ; Clément, Nathalie ; Combaret, Valérie ; Font de Mora, Jaime ; George, Sally L ; Jiménez, Irene ; Jeison, Marta ; Marques, Barbara ; Martinsson, Tommy ; Mazzocco, Katia ; Morini, Martina ; Mühlethaler-Mottet, Annick ; Noguera, Rosa ; Pierron, Gaelle ; Rossing, Maria ; Taschner-Mandl, Sabine ; Van Roy, Nadine ; Vicha, Ales ; Chesler, Louis ; Balwierz, Walentyna ; Castel, Victoria ; Elliott, Martin ; Kogner, Per ; Laureys, Geneviève ; Luksch, Roberto ; Malis, Josef ; Popovic-Beck, Maja ; Ash, Shifra ; Delattre, Olivier ; Valteau-Couanet, Dominique ; Tweddle, Deborah A ; Ladenstein, Ruth ; Schleiermacher, Gudrun

Journal of clinical oncology, 2021-10, Vol.39 (30), p.3377-3390 [Periódico revisado por pares]

United States: American Society of Clinical Oncology

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3
HIGH RISK NEUROBLASTOMA (HR-NB) WITH MNA AND AGE
HIGH RISK NEUROBLASTOMA (HR-NB) WITH MNA AND AGE
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Ata de Congresso 		Adicionar ao Meu Espaço

HIGH RISK NEUROBLASTOMA (HR-NB) WITH MNA AND AGE

Ladenstein, R ; Potschger, U ; Valteau-Couanet, D ; Ash, S ; Beck-Popovic, M ; Balwierz, W ; Boterberg, T ; Chan, GCF ; Elliott, M ; Kogner, P ; Lode, H ; Laureys, G ; Luksch, R ; Malis, J ; Owens, C ; Papadakis, V ; Sarnacki, S ; Taschner-Mandl, S ; Schleiermacher, G ; Canete, A

PEDIATRIC BLOOD & CANCER, 2023, Vol.70, p.S89 [Periódico revisado por pares]

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4
RISK FACTORS IN HIGH RISK NEUROBLASTOMA PATIENTS OVER 5 YEARS: RESULTS FROM THE HR-NBL1/SIOPEN TRIAL
RISK FACTORS IN HIGH RISK NEUROBLASTOMA PATIENTS OVER 5 YEARS: RESULTS FROM THE HR-NBL1/SIOPEN TRIAL
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RISK FACTORS IN HIGH RISK NEUROBLASTOMA PATIENTS OVER 5 YEARS: RESULTS FROM THE HR-NBL1/SIOPEN TRIAL

Ladenstein, R ; Valteau-Couanet, D ; Elliott, M ; Luksch, R ; Castel, V ; Ash, S ; Balwierz, W ; Laureys, G ; Beiske, K ; Kogner, P ; Papadakis, V ; Beck-Popovic, M ; Malis, J ; Brok, JS ; Vettenranta, K ; Bician, P ; Trahair, T ; Chan, GCF ; Owens, C ; Lacerda, A ; Sarnacki, S ; Boterberg, T ; Taschner-Mandl, S ; Schleiermacher, G ; Lode, H ; Potschger, U

PEDIATRIC BLOOD & CANCER, 2023, Vol.70 [Periódico revisado por pares]

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5
HGVS Recommendations for the Description of Sequence Variants: 2016 Update
HGVS Recommendations for the Description of Sequence Variants: 2016 Update
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HGVS Recommendations for the Description of Sequence Variants: 2016 Update

den Dunnen, Johan T. ; Dalgleish, Raymond ; Maglott, Donna R. ; Hart, Reece K. ; Greenblatt, Marc S. ; McGowan-Jordan, Jean ; Roux, Anne-Francoise ; Smith, Timothy ; Antonarakis, Stylianos E. ; Taschner, Peter E.M.

Human mutation, 2016-06, Vol.37 (6), p.564-569 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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6
Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker
Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker
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Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker

Wildeman, Martin ; van Ophuizen, Ernest ; den Dunnen, Johan T ; Taschner, Peter E.M

Human mutation, 2008-01, Vol.29 (1), p.6-13 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Neuroblastoma and the epigenome
Neuroblastoma and the epigenome
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Neuroblastoma and the epigenome

Fetahu, Irfete S. ; Taschner-Mandl, Sabine

Cancer and metastasis reviews, 2021-03, Vol.40 (1), p.173-189 [Periódico revisado por pares]

New York: Springer US

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8
DNA segment capture by Smc5/6 holocomplexes
DNA segment capture by Smc5/6 holocomplexes
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DNA segment capture by Smc5/6 holocomplexes

Taschner, Michael ; Gruber, Stephan

Nature structural & molecular biology, 2023-05, Vol.30 (5), p.619-628 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications
Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications
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Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications

Soussi, Thierry ; Taschner, Peter E.M. ; Samuels, Yardena

Human mutation, 2017-04, Vol.38 (4), p.339-342 [Periódico revisado por pares]

United States: Hindawi Limited

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10
Recommendations for Analyzing and Reporting TP53 Gene Variants in the High-Throughput Sequencing Era
Recommendations for Analyzing and Reporting TP53 Gene Variants in the High-Throughput Sequencing Era
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Recommendations for Analyzing and Reporting TP53 Gene Variants in the High-Throughput Sequencing Era

Soussi, Thierry ; Leroy, Bernard ; Taschner, Peter E.M.

Human mutation, 2014-06, Vol.35 (6), p.766-778 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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