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Profil bibliographique

L. van’t Veer

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

8Publications signalées
390Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Cancer Genomics and DiagnosticsGenetic factors in colorectal cancerCancer Immunotherapy and BiomarkersGenomics and Chromatin DynamicsPancreatic and Hepatic Oncology Research

Les publications récentes

Accès ouvert 2023 erratum OpenAlex

Author Correction: The landscape of viral associations in human cancers

Marc Zapatka, Daniel S. Brewer, Adam T. Grundhoff, Holger Sültmann et autres

In the published version of this paper, the members of the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium were listed in the Supplementary Information; however, these members should have been included in the main paper. The original Article has been corrected to …

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1 citation Nature Genetics
Accès ouvert 2023 erratum OpenAlex

Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

Esther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, Jeremiah A. Wala et autres

Correction to: Nature Published online 5 February 2020 In the published version of this paper, the members of the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium were listed in the Supplementary Information; however, these members should have been included in the main …

us, dk, gb, de, es, ca, ch, jp, se, kr, pl, ee (code pays fourni par la source)

12 citations Nature
Accès ouvert 2023 erratum OpenAlex

Author Correction: The evolutionary history of 2,658 cancers

Moritz Gerstung, Clemency Jolly, Ignaty Leshchiner, Stefan C. Dentro et autres

In the published version of this paper, the members of the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium were listed in the Supplementary Information; however, these members should have been included in the main paper. The original Article has been corrected to …

gb, ru, de, us, ca, si, au, be, fi, kr (code pays fourni par la source)

5 citations Nature
Accès ouvert 2022 erratum OpenAlex

Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours

Vinayak Bhandari, Constance H. Li, Robert Glen Bristow, Paul Christopher Boutros et autres

In the published version of this paper, the members of the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium were listed in the Supplementary Information; however, these members should have been included in the main paper. The original Article has been corrected to …

ca, us, gb, fi, jp, kr, sa, es, de, au, no, cn, il, dk, mx, in (code pays fourni par la source)

1 citation Nature Communications
Accès ouvert 2022 erratum OpenAlex

Author Correction: Inferring structural variant cancer cell fraction

Marek Cmero, Ke Yuan, Cheng Soon Ong, Jan Schröder et autres

In the published version of this paper, the members of the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium were listed in the Supplementary Information; however, these members should have been included in the main paper. The original article has been corrected to …

au, gb, us, ca, de, be, si, kr, fi, no, jp, sa, es (code pays fourni par la source)

0 citations Nature Communications
Accès ouvert 2022 erratum OpenAlex

Author Correction: Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig

Yulia Rubanova, Caitlin F. Harrigan, Roujia Li, Jeff A. Wintersinger et autres

In the published version of this paper, the members of the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium were listed in the Supplementary Information; however, these members should have been included in the main paper. The original Article has been corrected to …

ca, gb, us, de, au, be, si, kr, fi, jp, no, sa, es (code pays fourni par la source)

0 citations Nature Communications
Accès ouvert 2020 article OpenAlex

Inferring structural variant cancer cell fraction

Marek Cmero, Ke Yuan, Cheng Soon Ong, Jan Schröder et autres

We present SVclone, a computational method for inferring the cancer cell fraction of structural variant (SV) breakpoints from whole-genome sequencing data. SVclone accurately determines the variant allele frequencies of both SV breakends, then simultaneously estimates the cancer cell fraction and SV copy …

au, gb, us, ca, de, be, si, kr, fi, no, jp, sa, es (code pays fourni par la source)

56 citations Nature Communications
Accès ouvert 2020 article OpenAlex

Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer

Kadir Caner Akdemir, Victoria T. Le, Sahaana Chandran, Roel G.W. Verhaak et autres

Chromatin is folded into successive layers to organize linear DNA. Genes within the same topologically associating domains (TADs) demonstrate similar expression and histone-modification profiles, and boundaries separating different domains have important roles in reinforcing the stability of these features. Indeed, domain disruptions …

us, gb, es, ca, au, de, il, ru, kr, jp, dk (code pays fourni par la source)

315 citations Nature Genetics

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