Publications by authors named "Inga Vater"

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The role of the lysine histone methylase KMT2D in chronic myeloid leukemia.
Lina Schlemminger, Inga Nagel, Inga Vater, Ingolf Cascorbi, Meike Kaehler

Front Pharmacol· October 2025

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Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis.
Daniel Kaschta, Christina Post, Franziska Gaass, Milad Al-Tawil, Vincent Arriens, Inga Vater

Genome Med· September 2025

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BTK acts as a modulator of the response to imatinib in chronic myeloid leukemia.
Lena Schmidlechner, Inga Nagel, Inga Vater, Ingolf Cascorbi, Meike Kaehler

Oncol Lett· September 2024

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Clonal evolution in tyrosine kinase inhibitor-resistance: lessons from -models.
Meike Kaehler, Pia Osteresch, Axel Künstner, Stella Juliane Vieth, Daniela Esser, Inga Vater

Front Oncol· June 2023

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CRISPR/Cas9-induced knockout reveals the role of ABCB1 in the response to temozolomide, carmustine and lomustine in glioblastoma multiforme.
Lena Radtke, Aleksandra Majchrzak-Celińska, Charles Awortwe, Inga Vater, Inga Nagel

Pharmacol Res· November 2022

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Molecular characterization of Burkitt lymphoma in the breast or ovary.
Shaymaa Elgaafary, Cristina López, Inga Nagel, Inga Vater, Susanne Bens

Leuk Lymphoma· September 2021

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Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Inga Vater

PLoS Genet· September 2021

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Genome sequencing in families with congenital limb malformations.
Jonas Elsner, Martin A Mensah, Manuel Holtgrewe, Jakob Hertzberg, Stefania Bigoni, Inga Vater

Hum Genet· August 2021

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ZFP36L1 plays an ambiguous role in the regulation of cell expansion and negatively regulates CDKN1A in chronic myeloid leukemia cells.
Meike Kaehler, Maike Dworschak, Julian Phillip Rodin, Johanna Ruemenapp, Inga Vater

Exp Hematol· July 2021

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Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Inga Vater

PLoS Genet· July 2021

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Mucopolysaccharidosis type I due to maternal uniparental disomy of chromosome 4 with partial isodisomy of 4p16.3p15.2.
Kloth Katja, Vater Inga, Lindschau Ramona, Caliebe Almuth, Muschol Nicole Maria

Mol Genet Metab Rep· December 2020

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Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study.
Sümeyye Cöktü, Claudia Spix, Melanie Kaiser, Jasmin Beygo, Stephanie Kleinle, Inga Vater

Br J Cancer· August 2020

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Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage.
Ana C Queirós, Renée Beekman, Roser Vilarrasa-Blasi, Martí Duran-Ferrer, Guillem Clot, Inga Vater

Cancer Cell· November 2016

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Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).
Mariela C Coccé, Balca R Mardin, Susanne Bens, Adrian M Stütz, Fabiana Lubieniecki, Inga Vater

Genes Chromosomes Cancer· September 2016

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Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.
Susanne Bens, Julia Kolarova, Jasmin Beygo, Karin Buiting, Almuth Caliebe, Inga Vater

Epigenomics· June 2016

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Genotype/phenotype correlation in a female patient with 21q22.3 and 12p13.33 duplications.
Mona K Mekkawy, Inas M Mazen, Alaa K Kamel, Inga Vater, Maha S Zaki

Am J Med Genet A· April 2016

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A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis.
René Santer, Marcel du Moulin, Tatevik Shahinyan, Inga Vater, Esther Maier

Orphanet J Rare Dis· April 2016

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DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control.
Helene Kretzmer, Stephan H Bernhart, Wei Wang, Andrea Haake, Marc A Weniger, Inga Vater

Nat Genet· November 2015

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New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).
Aloysius Domingo, Ana Westenberger, Lillian V Lee, Ingrid Brænne, Tian Liu, Inga Vater

Eur J Hum Genet· October 2015

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Genetic characteristics of the human hepatic stellate cell line LX-2.
Ralf Weiskirchen, Jörg Weimer, Steffen K Meurer, Anja Kron, Barbara Seipel, Inga Vater

PLoS One· June 2014

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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Frank J Kaiser, Morad Ansari, Diana Braunholz, María Concepción Gil-Rodríguez, Christophe Decroos, Inga Vater

Hum Mol Genet· June 2014

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A familial disorder of altered DNA-methylation.
Almuth Caliebe, Julia Richter, Ole Ammerpohl, Deniz Kanber, Jasmin Beygo, Inga Vater

J Med Genet· June 2014

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Recurrent mutation of JAK3 in T-cell prolymphocytic leukemia.
Anke K Bergmann, Sina Schneppenheim, Marc Seifert, Matthew J Betts, Andrea Haake, Inga Vater

Genes Chromosomes Cancer· April 2014

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A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.
Itziar Salaverria, Idoia Martin-Guerrero, Rabea Wagener, Markus Kreuz, Christian W Kohler, Inga Vater

Blood· February 2014

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Frequent triple-hit expression of MYC, BCL2, and BCL6 in primary lymphoma of the central nervous system and absence of a favorable MYC(low)BCL2 (low) subgroup may underlie the inferior prognosis as compared to systemic diffuse large B cell lymphomas.
Anna Brunn, Inga Nagel, Manuel Montesinos-Rongen, Wolfram Klapper, Inga Vater

Acta Neuropathol· October 2013

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