Britta Kluge

417 total citations
12 papers, 315 citations indexed

About

Britta Kluge is a scholar working on Molecular Biology, Surgery and Neurology. According to data from OpenAlex, Britta Kluge has authored 12 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Surgery and 2 papers in Neurology. Recurrent topics in Britta Kluge's work include Cancer-related gene regulation (2 papers), Pregnancy and preeclampsia studies (1 paper) and Moyamoya disease diagnosis and treatment (1 paper). Britta Kluge is often cited by papers focused on Cancer-related gene regulation (2 papers), Pregnancy and preeclampsia studies (1 paper) and Moyamoya disease diagnosis and treatment (1 paper). Britta Kluge collaborates with scholars based in Germany, Austria and United States. Britta Kluge's co-authors include Simone Wagner, James A. Koziol, Sabine Heiland, Simon Nagel, Julia E. Weigand, Beatrix Suess, Marc Vogel, Manuel Grez, Franco Laccone and Stefan Schwab and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Circulation Research.

In The Last Decade

Britta Kluge

12 papers receiving 311 citations

Peers

Countries citing papers authored by Britta Kluge

Since Specialization

Citations

This map shows the geographic impact of Britta Kluge'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 Britta Kluge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Britta Kluge more than expected).

Fields of papers citing papers by Britta Kluge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Britta Kluge. 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 Britta Kluge. The network helps show where Britta Kluge may publish in the future.

Co-authorship network of co-authors of Britta Kluge

This figure shows the co-authorship network connecting the top 25 collaborators of Britta Kluge. A scholar is included among the top collaborators of Britta Kluge based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Britta Kluge. Britta Kluge is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern 2019 ·Birth Defects Research ·Katharina Schoner, Martina Witsch‐Baumgartner, (unknown), (unknown), R. Bald, Susanne Gerit Kircher, Annette Ramaswamy, Britta Kluge, (unknown), Ralf Schmitz, Bárbara Fritz, Johannes Zschocke, Franco Laccone, Helga Rehder	14
2	A small, portable RNA device for the control of exon skipping in mammalian cells 2018 ·Nucleic Acids Research ·Marc Vogel, Julia E. Weigand, Britta Kluge, Manuel Grez, Beatrix Suess	46
3	Acanthocytosis and the c.680 A>G Mutation in the PANK2 Gene: A Study Enrolling a Cohort of PKAN Patients from the Dominican Republic 2015 ·PLoS ONE ·(unknown), (unknown), Franco Laccone, Britta Kluge, Alexander Tichy, Euripedes de Almeida Ribeiro, Rainer Prohaska, Peter Stoeter, (unknown), Ulrich Salzer	16
4	Jmjd3 Controls Mesodermal and Cardiovascular Differentiation of Embryonic Stem Cells 2013 ·Circulation Research ·Kisho Ohtani, Cong Zhao, Gergana Dobreva, Yosif Manavski, Britta Kluge, Thomas Braun, Michael A. Rieger, Andreas M. Zeiher, Stefanie Dimmeler	63
5	Klinefelter twins presenting with discordant aneuploidies, acardia, forked umbilical cord and with different gonadal sex despite monozygosity 2012 ·Prenatal Diagnosis ·Helga Rehder, Katharina Schoner, Britta Kluge, Frank Louwen, E. Schwinger, Jürgen Neesen	8
6	Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene 2011 ·European Journal of Human Genetics ·Franco Laccone, Katharina Schoner, Birgit Krabichler, Britta Kluge, (unknown), (unknown), Johannes Zschocke, Helga Rehder	21
7	Variations of frataxin protein levels in normal individuals 2010 ·Neurological Sciences ·(unknown), Barbara Scheiber‐Mojdehkar, Britta Kluge, Hans Goldenberg, Franco Laccone, Brigitte Sturm	15
8	DNA repair polymorphisms associated with cytogenetic subgroups in B‐cell chronic lymphocytic leukemia 2009 ·Genes Chromosomes and Cancer ·Christina Ganster, Jürgen Neesen, Sonja Zehetmayer, Ulrich Jäger, Harald Esterbauer, Christine Mannhalter, Britta Kluge, Christa Fonatsch	21
9	Determination of the Minimal Distance between the Matrix and Transmembrane Domains of the Large Hepatitis B Virus Envelope Protein 2005 ·Journal of Virology ·Britta Kluge, (unknown), (unknown), Volker Bruss	17
10	Volumetric evaluation of the ischemic lesion size with serial MRI in a transient MCAO model of the rat: comparison of DWI and T1WI 2004 ·Brain Research Protocols ·Simon Nagel, Simone Wagner, James A. Koziol, Britta Kluge, Sabine Heiland	22
11	MMP-9 Polymorphisms Are Not Associated With Spontaneous Cervical Artery Dissection 2004 ·Stroke ·Simone Wagner, Britta Kluge, James A. Koziol, Armin Grau, Caspar Grond‐Ginsbach	20
12	Topographically graded postischemic presence of metalloproteinases is inhibited by hypothermia 2003 ·Brain Research ·Simone Wagner, Simon Nagel, Britta Kluge, Stefan Schwab, Sabine Heiland, James A. Koziol, Humphrey Gardner, Werner Hacke	52

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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