Susanna Bunge

1.7k citations

26 papers · 1.2k indexed · h-index 18

Co-authors: Andreas Gal Cordula Steglich John J. Hopwood Michael Beck E. Schwinger C. Phillip Morris Hamish S. Scott Wim J. Kleijer
Topics: Lysosomal Storage Disorders Research (23 papers)Trypanosoma species research and implications (16 papers)Glycogen Storage Diseases and Myoclonus (8 papers)
Cited by: Physiology Rheumatology Epidemiology
Journals: The American Journal of Human Genetics Human Molecular Genetics Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Partner nations: Germany Australia Netherlands

In The Last Decade

Susanna Bunge

26 papers receiving 1.2k citations

Peers

Countries citing papers authored by Susanna Bunge

Since Specialization

Citations

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

Fields of papers citing papers by Susanna Bunge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susanna Bunge

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical, biochemical and molecular findings in a two‐generation Morquio A family 1998 ·Clinical Genetics ·Anna Tylki‐Szymańska,Barbara Czartoryska,Susanna Bunge,Otto P. van Diggelen,Wim J. Kleijer,(unknown),J. G. M. Huijmans,(unknown)	17
2	Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type II 1998 ·European Journal of Human Genetics ·Susanna Bunge,(unknown),Cordula Steglich,Marie-Louise Bondeson,Anna Tylki‐Szymańska,Ewa Popowska,Andreas Gal	26
3	Genotype–phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studies 1998 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Susanna Bunge,Peter R. Clements,Sharon Byers,(unknown),Doug A. Brooks,John J. Hopwood	64
4	Identification of 16 sulfamidase gene mutations including the common R74C in patients with mucopolysaccharidosis type IIIA (Sanfilippo A) 1997 ·Human Mutation ·Susanna Bunge,Hüseyin İnce,Cordula Steglich,(unknown),Michael Beck,Jacek Zaremba,Otto P. van Diggelen,Birgit Weber,(unknown),Andreas Gal	51
5	Identification of 31 novel mutations in the N-acetylgalactosamine-6-sulfatase gene reveals excessive allelic heterogeneity among patients with Morquio A syndrome 1997 ·Human Mutation ·Susanna Bunge,Wim J. Kleijer,Anna Tylki‐Szymańska,Cordula Steglich,Michael Beck,Shunji Tomatsu,Seiji Fukuda,Ben J. H. M. Poorthuis,Barbara Czartoryska,Tadao Orii,Andreas Gal	58
6	Mucopolysaccharidosis type I: Identification of 13 novel mutations of the α-L-iduronidase gene 1995 ·Human Mutation ·Susanna Bunge,Wim J. Kleijer,Cordula Steglich,Michael Beck,E. Schwinger,Andreas Gal	40
7	Molecular genetics of muccpolysaccharidosis type I: Diagnostic, clinical, and biological implications 1995 ·Human Mutation ·Hamish S. Scott,Susanna Bunge,Andreas Gal,L. Clarke,C. Phillip Morris,John J. Hopwood	153
8	Common CFTR mutations are not likely to predispose to chronic bronchitis in Northern Germany 1995 ·Human Genetics ·A. Artlich,(unknown),Susanna Bunge,P. Entzian,Max Schlaak,E. Schwinger	18
9	Mutations of the iduronate-2-sulfatase gene in 12 Polish. Patients with mucopolysaccharidosis type II (Hunter syndrome) 1995 ·Human Mutation ·Ewa Popowska,(unknown),Anna Tylki‐Szymańska,Susanna Bunge,Cordula Steglich,E. Schwinger,Andreas Gal	30
10	Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28 1995 ·Human Genetics ·(unknown),Susanna Bunge,Cordula Steglich,E. Schwinger,Andreas Gal	38
11	Mutation {open_quotes}hot spots{close_quotes} in the iduronate-sulfatase gene, and evidence for a pseudogene 1994 ·The American Journal of Human Genetics ·(unknown),Susanna Bunge,A. Gal	1
12	Mucopolysaccharidosis type I. Identification of 93% of mutant alleles in a group of 70 patients 1994 ·The American Journal of Human Genetics ·Susanna Bunge,Cordula Steglich,Wim J. Kleijer	1
13	Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,xxy male heterozygous for a missense point mutation 1994 ·Prenatal Diagnosis ·Susanna Bunge,Cordula Steglich,Peter Lorenz,Michael Beck,Suying Xu,John J. Hopwood,Andreas Gal	5
14	Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common α-L-iduronidase mutations (W402X and Q70X) among European patients 1994 ·Human Molecular Genetics ·Susanna Bunge,Wim J. Kleijer,Cordula Steglich,Michael Beck,(unknown),C. Phillip Morris,E. Schwinger,John J. Hopwood,Hamish S. Scott,Andreas Gal	86
15	Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter gene 1993 ·Human Genetics ·Cordula Steglich,Susanna Bunge,Theo J.M. Hulsebos,Michael Beck,(unknown),E. Schwinger,(unknown),(unknown)	7
16	Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome) 1993 ·Human Molecular Genetics ·Susanna Bunge,Cordula Steglich,(unknown),Michael Beck,C. Phillip Morris,E. Schwinger,Albert Schinzel,John J. Hopwood,Andreas Gal	52
17	Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa 1993 ·Genomics ·Susanna Bunge,(unknown),D. David,(unknown),L.I. van den Born,C. Aulehla‐Scholz,(unknown),M Horn,J. Ott,E. Schwinger,Albert Schinzel,M. J. Denton,Andreas Gal	77
18	Molecular basis of mucopolysaccharidosis type II: Mutations in the iduronate-2-sulphatase gene 1993 ·Human Mutation ·John J. Hopwood,Susanna Bunge,C. Phillip Morris,Peter J. Wilson,Cordula Steglich,Michael Beck,E. Schwinger,Andreas Gal	105
19	Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome) 1992 ·Human Molecular Genetics ·Susanna Bunge,Cordula Steglich,Michael Beck,W Rosenkranz,E. Schwinger,John J. Hopwood,Andreas Gal	52
20	A comparison of leaf thionin sequences of barley cultivars and wild barley species 1992 ·Molecular and General Genetics MGG ·Susanna Bunge,J. Wolters,Klaus Apel	23

About Susanna Bunge

Susanna Bunge is a scholar working on Physiology, Rheumatology and Epidemiology, having authored 26 papers that have together received 1.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (23 papers), Trypanosoma species research and implications (16 papers) and Glycogen Storage Diseases and Myoclonus (8 papers). The work is most often cited by research in Physiology (1.0k citations), Rheumatology (286 citations) and Epidemiology (559 citations). Susanna Bunge has collaborated with scholars based in Germany, Australia and Netherlands. Frequent co-authors include Andreas Gal, Cordula Steglich, John J. Hopwood, Michael Beck, E. Schwinger, C. Phillip Morris, Hamish S. Scott, Wim J. Kleijer, Anna Tylki‐Szymańska and L. Clarke. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

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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