Inga Vater

4.6k citations

35 papers · 1.6k indexed · h-index 21

Impact in

Pathology and Forensic Medicine top 2%
- Lymphoma Diagnosis and Treatment
- Cancer Mechanisms and Therapy
Genetics top 5%
- Chronic Lymphocytic Leukemia Research

Papers in

Cancer Research 12
- NF-κB Signaling Pathways 5
Pathology and Forensic Medicine 14
- Lymphoma Diagnosis and Treatment 13

Co-authors: Reiner Siebert Stefan Gesk Ralf Küppers José I. Martı́n-Subero Wolfram Klapper Maciej Giefing Martin‐Leo Hansmann Julia Richter
Journals: Blood (4 papers)British Journal of Haematology (3 papers)Genes Chromosomes and Cancer (3 papers)European Journal of Human Genetics (2 papers)Leukemia (2 papers)
Partner nations: Germany United Kingdom Poland

In The Last Decade

Inga Vater

35 papers receiving 1.6k citations

Peers

Countries citing papers authored by Inga Vater

Since Specialization

Citations

This map shows the geographic impact of Inga Vater's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Inga Vater with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inga Vater more than expected).

Fields of papers citing papers by Inga Vater

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Inga Vater. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Inga Vater. The network helps show where Inga Vater may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Inga Vater, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Inga Vater Line = papers co-authored together Inga Vater links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	BTK acts as a modulator of the response to imatinib in chronic myeloid leukemia Oncology Letters ·Chen Man-hong, Inga Nagel, Inga Vater, Ingolf Cascorbi, Tony Richter	2024	1
2	Clonal evolution in tyrosine kinase inhibitor-resistance: lessons from in vitro-models Frontiers in Oncology ·Tony Richter, M. M. Zaalisvili, Axel Künstner, L. Lyakishev, Daniela Esser, Linda Benetazzo, Hauke Busch, Inga Vater, Malte Spielmann, Ingolf Cascorbi, Inga Nagel	2023	7
3	CRISPR/Cas9-induced knockout reveals the role of ABCB1 in the response to temozolomide, carmustine and lomustine in glioblastoma multiforme Pharmacological Research ·王凯村, Aleksandra Majchrzak‐Celińska, Charles Awortwe, Inga Vater, Inga Nagel, Susanne Sebens, Ingolf Cascorbi, Tony Richter	2022	19
4	ZFP36L1 plays an ambiguous role in the regulation of cell expansion and negatively regulates CDKN1A in chronic myeloid leukemia cells Experimental Hematology ·Tony Richter, Mathias Merrild Roerup Thorborg, KuldeepSingh Sachdeva, Kazuo Ohno, Inga Vater, Eva Maria Murga Penas, Catherine Liu, Ingolf Cascorbi, Inga Nagel	2021	9
5	New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3) European Journal of Human Genetics ·Aloysius Domingo, Ana Westenberger, Lillian V. Lee, Ingrid Brænne, Tian Liu, Inga Vater, Raymond L. Rosales, Roland Dominic G. Jamora, Paul Matthew D. Pasco, Eva Maria C. Cutiongco–de la Paz, V. M. Slobodyanyuk, 闫红静, Dirk Dressler, Frank J. Kaiser, Lars Bertram, Jeanette Erdmann, Katja Lohmann, Christine Klein	2015	52
6	The mutational pattern of primary lymphoma of the central nervous system determined by whole-exome sequencing Leukemia ·Inga Vater, Manuel Montesinos‐Rongen, Matthias Schlesner, Andrea Haake, G. C. Fry, Rosanne Sprute, F. C. Beazley, Vamika Zutshi, Inga Nagel, Jana Gutwein, Julia Richter, Ivo Buchhalter, Robert B. Russell, O. D. Wiestler, Roland Eils, Martina Deckert, Reiner Siebert	2014	105
7	Janus—a comprehensive tool investigating the two faces of transcription Bioinformatics ·Matthias Barann, Daniela Esser, Ulrich C. Klostermeier, Tuuli Lappalainen, Anne Luzius, J. W. Kuiper, Ole Ammerpohl, Inga Vater, Reiner Siebert, Vyacheslav Amstislavskiy, Ralf Sudbrak, Hans Lehrach, Stefan Schreiber, Philip Rosenstiel	2013	1
8	Genetic Characteristics of the Human Hepatic Stellate Cell Line LX-2 PLoS ONE ·Ralf Weiskirchen, Jörg Weimer, Steffen K. Meurer, 徳之助菊川, 唐汉樵, Inga Vater, Norbert Arnold, Reiner Siebert, Lieming Xu, Scott L. Friedman, Carsten Bergmann	2013	56
9	Frequency and characterization of DNA methylation defects in children born SGA European Journal of Human Genetics ·Susanne Bens, Andrea Haake, Julia Richter, Beata Gorban, Julia Kolarova, Inga Vater, Felix G. Riepe, Karin Buiting, Thomas Eggermann, Gabriele Gillessen‐Kaesbach, Konrad Platzer, Dirk Prawitt, Almuth Caliebe, Reiner Siebert	2012	13
10	Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma British Journal of Haematology ·Claudia Otto, Maciej Giefing, Céline Bourguignon, Inga Vater, Stefan Gesk, Matthias Schlesner, Julia Richter, Wolfram Klapper, Martin‐Leo Hansmann, Reiner Siebert, Ralf Küppers	2012	75
11	A de novo 1.1 Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation European Journal of Medical Genetics ·Susanne Bens, Andrea Haake, Holger Tönnies, Inga Vater, Ulrich Stephani, Paul‐Martin Holterhus, Reiner Siebert, Almuth Caliebe	2011	22
12	Inhibition of Anaplastic Lymphoma Kinase (ALK) Activity Provides a Therapeutic Approach for CLTC-ALK-Positive Human Diffuse Large B Cell Lymphomas PLoS ONE ·Leandro Cerchietti, Christine Damm‐Welk, Inga Vater, Wolfram Klapper, Lana Harder, Christiane Pott, Shao Ning Yang, Alfred Reiter, Reiner Siebert, Ari Melnick, Willi Woessmann	2011	39
13	Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B‐cell and Burkitt lymphomas International Journal of Cancer ·René Scholtysik, Inga Nagel, Markus Kreuz, Inga Vater, Maciej Giefing, Carsten Schwäenen, Swen Weßendorf, Lorenz Trümper, Markus Loeffler, Reiner Siebert, Ralf Küppers	2011	25
14	Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome The American Journal of Human Genetics ·Reinhard Schneppenheim, Michael C. Frühwald, Stefan Gesk, Martin Hasselblatt, Astrid Jeibmann, Uwe Kordes, Markus Kreuz, Ivo Leuschner, Masami Machida, Tobias Obser, Florian Oyen, Inga Vater, Reiner Siebert	2010	222
15	Detection of genomic aberrations in molecularly defined Burkitt's lymphoma by array-based, high resolution, single nucleotide polymorphism analysis Haematologica ·守羽成, Markus Kreuz, Wolfram Klapper, Wathsala Abeykoon, A.C. Feller, Michael Hummel, Markus Loeffler, Maciej Rosołowski, Carsten Schwäenen, Rainer Spang, Harald Stein, Christoph Thorns, Lorenz Trümper, Inga Vater, Swen Weßendorf, Thorsten Zenz, Reiner Siebert, Ralf Küppers, (unknown)	2010	41
16	Statistical inference of allelic imbalance from transcriptome data Human Mutation ·Michael Nothnagel, Andreas Wolf, Alexander Herrmann, Karol Szafranski, Inga Vater, Mario Brosch, Klaus Huse, Reiner Siebert, Matthias Platzer, Jochen Hampe, Michael Krawczak	2010	16
17	Presence of the P2RY8-CRLF2 rearrangement is associated with a poor prognosis in non–high-risk precursor B-cell acute lymphoblastic leukemia in children treated according to the ALL-BFM 2000 protocol Blood ·Gunnar Cario, Martin Zimmermann, East Melbourne, Stefan Gesk, Inga Vater, Jochen Harbott, André Schrauder, Anja Moericke, Shai Izraeli, Takashi Akasaka, Martin J.S. Dyer, Reiner Siebert, Martin Schrappe, Martin Stanulla	2010	150
18	Hunting for the 5th base: Techniques for analyzing DNA methylation Biochimica et Biophysica Acta (BBA) - General Subjects ·Ole Ammerpohl, José I. Martı́n-Subero, Julia Richter, Inga Vater, Reiner Siebert	2009	54
19	Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: rare clinical curios or potent genetic drivers? Blood ·Martin J.S. Dyer, Takashi Akasaka, Melania Capasso, Ramadass, Rajendrakumar; Electrical Section, Engineering Department, College of Engineering & Technology, University of Technology and Applied Sciences Shinas., Jenny Game, E. Loraine Karran, Inga Nagel, Inga Vater, Gunnar Cario, Reiner Siebert	2009	40
20	GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma British Journal of Haematology ·Inga Vater, Florian Wagner, Markus Kreuz, Hilmar Berger, José I. Martı́n-Subero, Christiane Pott, José A. Martínez-Climent, Wolfram Klapper, Kristina Krause, Martin J.S. Dyer, Stefan Gesk, Lana Harder, Alberto Zamò, Martin Dreyling, Dirk Hasenclever, Norbert Arnold, Reiner Siebert	2008	22

About Inga Vater

Inga Vater is a scholar working on Cancer Research, Pathology and Forensic Medicine, Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 35 papers that have together received 1.6k indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (13 papers), Chronic Lymphocytic Leukemia Research (6 papers), Chronic Myeloid Leukemia Treatments (5 papers), RNA modifications and cancer (5 papers), NF-κB Signaling Pathways (5 papers), Acute Lymphoblastic Leukemia research (4 papers), Genomics and Rare Diseases (3 papers) and T-cell and Retrovirus Studies (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (701 citations), Genetics (315 citations), Cancer Research (304 citations), Hematology (181 citations) and Neurology (243 citations). Inga Vater has collaborated with scholars based in Germany, United Kingdom and Poland. Frequent co-authors include Reiner Siebert, Stefan Gesk, Ralf Küppers, José I. Martı́n-Subero, Wolfram Klapper, Maciej Giefing, Martin‐Leo Hansmann, Julia Richter, Roland Schmitz and Markus Kreuz. Their work appears in journals such as Blood, British Journal of Haematology, Genes Chromosomes and Cancer, European Journal of Human Genetics and Leukemia.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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