Brigitte Pabst

539 total citations
29 papers, 374 citations indexed

About

Brigitte Pabst is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Brigitte Pabst has authored 29 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Surgery. Recurrent topics in Brigitte Pabst's work include Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers) and Chromosomal and Genetic Variations (3 papers). Brigitte Pabst is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Congenital heart defects research (3 papers) and Chromosomal and Genetic Variations (3 papers). Brigitte Pabst collaborates with scholars based in Germany, United States and Switzerland. Brigitte Pabst's co-authors include Jörg Schmidtke, Julianne Behnke, Barbara Zoll, I. Hansmann, Mine Arslan‐Kirchner, U. Braun, Martin Hermann, Doris Steinemann, Irmgard Nippert and Konstantin Miller and has published in prestigious journals such as PLoS ONE, Hepatology and Transplantation.

In The Last Decade

Brigitte Pabst

29 papers receiving 363 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Brigitte Pabst Germany 12 137 109 65 59 56 29 374
Ana Francés United States 14 95 0.7× 110 1.0× 72 1.1× 80 1.4× 33 0.6× 21 1.2k
Krishna K. Yelavarthi United States 12 134 1.0× 90 0.8× 97 1.5× 171 2.9× 73 1.3× 13 957
H.F.L. Mark United States 13 157 1.1× 156 1.4× 58 0.9× 30 0.5× 30 0.5× 38 375
Souichi Yoshida Japan 16 196 1.4× 108 1.0× 54 0.8× 100 1.7× 23 0.4× 23 1.1k
Susanne Michel Germany 11 208 1.5× 125 1.1× 72 1.1× 20 0.3× 22 0.4× 18 405
Miyuki Tsumura Japan 17 175 1.3× 165 1.5× 29 0.4× 109 1.8× 26 0.5× 39 566
Liesbeth van Emst Netherlands 13 268 2.0× 92 0.8× 44 0.7× 38 0.6× 35 0.6× 28 562
Isabel Ferreirós-Vidal Spain 12 227 1.7× 229 2.1× 37 0.6× 101 1.7× 19 0.3× 23 638
Cushla McKinney New Zealand 13 218 1.6× 157 1.4× 22 0.3× 40 0.7× 37 0.7× 15 488
Katsuji Kokawa Japan 16 227 1.7× 81 0.7× 72 1.1× 103 1.7× 12 0.2× 27 920

Countries citing papers authored by Brigitte Pabst

Since Specialization
Citations

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

Fields of papers citing papers by Brigitte Pabst

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brigitte Pabst

This figure shows the co-authorship network connecting the top 25 collaborators of Brigitte Pabst. A scholar is included among the top collaborators of Brigitte Pabst 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 Brigitte Pabst. Brigitte Pabst is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Pfeffer, Tobias J., Bernd Auber, Brigitte Pabst, et al.. (2023). Prevalence of HSPB6 gene variants in peripartum cardiomyopathy: Data from the German PPCM registry. International Journal of Cardiology. 379. 96–99. 2 indexed citations
2.
Kloth, Katja, Doris Steinemann, Brigitte Pabst, et al.. (2019). 16p13.11 microdeletion uncovers loss‐of‐function of a MYH11 missense variant in a patient with megacystis‐microcolon‐intestinal‐hypoperistalsis syndrome. Clinical Genetics. 96(1). 85–90. 20 indexed citations
3.
Golas, Monika M., Bernd Auber, Tim Ripperger, et al.. (2019). Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. American Journal of Medical Genetics Part A. 179(7). 1383–1389. 9 indexed citations
4.
Wappenschmidt, Barbara, Brigitte Pabst, Saki Chan, et al.. (2018). A tandem duplication of BRCA1 exons 1–19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome. Breast Cancer Research and Treatment. 172(3). 561–569. 11 indexed citations
5.
Vogt, J., Tim Ripperger, Brigitte Pabst, et al.. (2016). PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1. European Journal of Human Genetics. 24(11). 1598–1604. 7 indexed citations
6.
Schwemmle, C., Mine Arslan‐Kirchner, Brigitte Pabst, & M. Ptok. (2012). Tetrasomie 18p und Innenohrschwerhörigkeit. HNO. 60(10). 901–905. 1 indexed citations
7.
Borchers, Sylvia, Melanie Bremm, Thomas Lehrnbecher, et al.. (2012). Sequential Anti-Cytomegalovirus Response Monitoring May Allow Prediction of Cytomegalovirus Reactivation after Allogeneic Stem Cell Transplantation. PLoS ONE. 7(12). e50248–e50248. 27 indexed citations
8.
Ripperger, Tim, Marcel Tauscher, Brigitte Pabst, et al.. (2011). Constitutional trisomy 8p11.21‐q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia. British Journal of Haematology. 155(2). 209–217. 25 indexed citations
9.
Ehmer, Ursula, Sandra Kalthoff, Brigitte Pabst, et al.. (2011). Gilbert syndrome redefined: A complex genetic haplotype influences the regulation of glucuronidation. Hepatology. 55(6). 1912–1921. 34 indexed citations
10.
Bohnhorst, Bettina, I. Luhmer, Susanne Morlot, et al.. (2010). Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome. European Journal of Medical Genetics. 53(5). 280–285. 14 indexed citations
11.
Warnecke, G., M. Avşar, Jens Gottlieb, et al.. (2009). Correlation of Donor Leukocyte Chimerism With Pulmonary Allograft Survival After Immunosuppressive Drug Withdrawal in a Porcine Model. Transplantation. 87(10). 1468–1477. 6 indexed citations
12.
Sieberer, Marcel, et al.. (2006). Das neuropsychiatrische Spektrum des Velokardiofazialen Syndroms (Deletion 22q11.2). Fortschritte der Neurologie · Psychiatrie. 74(5). 263–274. 2 indexed citations
13.
Schmidtke, Jörg, Brigitte Pabst, & Irmgard Nippert. (2005). DNA-based Genetic Testing Is Rising Steeply in a National Health Care System with Open Access to Services: A Survey of Genetic Test Use in Germany, 1996–2002. Genetic Testing. 9(1). 80–84. 16 indexed citations
14.
Sieberer, Marcel, et al.. (2005). Basal ganglia calcification and psychosis in 22q11.2 deletion syndrome. European Psychiatry. 20(8). 567–569. 13 indexed citations
15.
Pabst, Brigitte, et al.. (2003). The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature. Cytogenetic and Genome Research. 103(1-2). 3–7. 4 indexed citations
16.
Pabst, Brigitte, Mine Arslan‐Kirchner, A. Eckardt, et al.. (2003). Search for deletion 22q11.2 in interphase nuclei of buccal mucosa of patients ascertained by isolated cleft palate: a new diagnostic approach. International Journal of Oral and Maxillofacial Surgery. 32(2). 198–200. 8 indexed citations
17.
Miller, Konstantin, Brigitte Pabst, Peter Nürnberg, et al.. (2003). Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin. Human Genetics. 112(4). 343–347. 12 indexed citations
18.
Pabst, Brigitte, et al.. (2002). Reciprocal translocation between Y chromosome long arm euchromatin and the short arm of chromosome 1. Annales de Génétique. 45(1). 5–8. 8 indexed citations
19.
Behnke, Julianne, et al.. (1995). Distribution of epidermal growth factor receptor gene amplification in brain tumours and correlation to prognosis. Journal of Neurology. 242(10). 683–688. 65 indexed citations
20.
Hansmann, I. & Brigitte Pabst. (1992). Nondisjunction by failures in the molecular control of oocyte maturation. Annals of Anatomy - Anatomischer Anzeiger. 174(6). 485–490. 13 indexed citations

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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