Bianca Miterski

1.9k total citations
19 papers, 778 citations indexed

About

Bianca Miterski is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Immunology. According to data from OpenAlex, Bianca Miterski has authored 19 papers receiving a total of 778 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 4 papers in Immunology. Recurrent topics in Bianca Miterski's work include Mitochondrial Function and Pathology (2 papers), RNA regulation and disease (2 papers) and Multiple Sclerosis Research Studies (2 papers). Bianca Miterski is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), RNA regulation and disease (2 papers) and Multiple Sclerosis Research Studies (2 papers). Bianca Miterski collaborates with scholars based in Germany, United Kingdom and Luxembourg. Bianca Miterski's co-authors include Jörg T. Epplen, Wolfram Klein, Sebastian Schimrigk, M. Haupts, E. Sindern, Ludger Sch�ls, C. Epplen, Eduardo José Melo dos Santos, Lüdger Schöls and Stefan Böhringer and has published in prestigious journals such as Nature Genetics, Neurology and Electrophoresis.

In The Last Decade

Bianca Miterski

19 papers receiving 765 citations

Peers

Countries citing papers authored by Bianca Miterski

Since Specialization

Citations

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

Fields of papers citing papers by Bianca Miterski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bianca Miterski

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function 2010 ·Haematologica ·Vytautas Ivaškevičius, Arijit Biswas, Carville G. Bevans, Verena Schroeder, H Köhler, H. Rott, Susan Halimeh, Petro E. Petrides, H. Lenk, (unknown), Bianca Miterski, Ursula Harbrecht, Johannes Oldenburg	36
2	New Mutations of EXT1 and EXT2 Genes in German Patients with Multiple Osteochondromas 2009 ·Annals of Human Genetics ·Wolfram Heinritz, Ulrike Hüffmeier, (unknown), Bianca Miterski, Christiane Zweier, (unknown), Axel Bohring, Beate Mitulla, (unknown), Ursula G. Froster	24
3	Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis 2005 ·Journal of Molecular Medicine ·(unknown), (unknown), Bianca Miterski, Ralf Gold, Antje Kroner, Dirk Koczan, (unknown), Peter Rieckmann, Jörg T. Epplen, Saleh Ibrahim	59
4	Complex genetic predisposition in adult and juvenile rheumatoid arthritis 2004 ·BMC Genetics ·Bianca Miterski, Susanne Drynda, (unknown), Wolfram Klein, (unknown), Jörn Kekow, Jörg T. Epplen	62
5	Numerous genetic predisposition factors for rheumatic arthritis in adults and juveniles. 2004 ·(unknown), Bianca Miterski, Susanne Drynda, (unknown), (unknown), Jörn Kekow, Jörg T. Epplen, S. G. Pandalai	3
6	Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data 2003 ·European Journal of Human Genetics ·Stefan Böhringer, Cornelia Hardt, Bianca Miterski, Ansgar Steland, Jörg T. Epplen	5
7	Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia 2003 ·Neurology ·Thorsten Schulte, Bianca Miterski, (unknown), H. Przuntek, Jörg T. Epplen, Lüdger Schöls	28
8	Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene 2002 ·Nature Genetics ·Tamio Suzuki, Wei Li, Qing Zhang, Amna Karim, Edward K. Novak, Elena V. Sviderskaya, Simon P. Hill, Dorothy C. Bennett, Alex V. Levin, H. Karel Nieuwenhuis, Chin‐To Fong, Claudio Castellan, Bianca Miterski, Richard T. Swank, Richard A. Spritz	141
9	PTPRC(CD45) is not associated with multiple sclerosis in a large cohort of German patients 2002 ·BMC Medical Genetics ·Bianca Miterski, E. Sindern, M. Haupts, Sebastian Schimrigk, Jörg T. Epplen	26
10	A genome screen for linkage disequilibrium in HLA-DRB115-positive Germans with multiple sclerosis based on 4666 microsatellite markers 2002 ·Human Genetics* ·(unknown), Stephen Sawcer, Stefan Böehringer, Bianca Miterski, E. Sindern, M. Haupts, Sebastian Schimrigk, Alastair Compston, Jörg T. Epplen	31
11	Inhibitors in the NFκB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations 2002 ·Genes and Immunity ·Bianca Miterski, Stefan Böhringer, Wolfram Klein, E. Sindern, M. Haupts, Sebastian Schimrigk, Jörg T. Epplen	74
12	Mutation analysis and association studies of nuclear factor-κB1 in sporadic Parkinson's disease patients 2002 ·Journal of Neural Transmission ·Philip Wintermeyer, (unknown), Lüdger Schöls, H. Przuntek, Bianca Miterski, Jörg T. Epplen, Rejko Krüger	12
13	Mutation analysis of thespastingene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia 2002 ·Human Mutation ·Simone M. Sauter, Bianca Miterski, Sven Klimpe, Dominikus Bönsch, Lüdger Schöls, (unknown), (unknown), H. C. Hopf, Wolfgang Engel, Thomas Deufel, Jörg T. Epplen, Jürgen Neesen	74
14	On the genetic contribution to selected multifactorial diseases with autoimmune characteristics. 2002 ·PubMed ·Bianca Miterski, Jörg T. Epplen, Martin Genčík	5
15	Does the tuberous sclerosis complex include clivus chordoma? A case report 2001 ·European Journal of Pediatrics ·Jan Börgel, (unknown), (unknown), Bianca Miterski, Jörg T. Epplen	27
16	PCR/SSCP Detects Reliably and Efficiently DNA Sequence Variations in Large Scale Screening Projects 2000 ·Combinatorial Chemistry & High Throughput Screening ·Bianca Miterski, Rejko Krüger, Philip Wintermeyer, Jörg T. Epplen	9
17	The interferon gene cluster: a candidate region for MS predisposition? 1999 ·Genes and Immunity ·Bianca Miterski, (unknown), Jörg T. Epplen, Dieter Pöhlau, Cornelia Hardt, (unknown)	19
18	Polymerase chain reaction—single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes 1998 ·Electrophoresis ·(unknown), Jörg T. Epplen, Marion Kauth, Bianca Miterski, Frank Tschentscher, Cornelia Epplen	48
19	Differential stability of the (GAA) n tract in the Friedreich ataxia (STM7) gene 1997 ·Human Genetics ·C. Epplen, Jörg T. Epplen, (unknown), Bianca Miterski, Eduardo José Melo dos Santos, Ludger Sch�ls	95

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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