Cordula Steglich

1.1k total citations
24 papers, 805 citations indexed

About

Cordula Steglich is a scholar working on Physiology, Epidemiology and Rheumatology. According to data from OpenAlex, Cordula Steglich has authored 24 papers receiving a total of 805 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Physiology, 18 papers in Epidemiology and 6 papers in Rheumatology. Recurrent topics in Cordula Steglich's work include Lysosomal Storage Disorders Research (20 papers), Trypanosoma species research and implications (18 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Cordula Steglich is often cited by papers focused on Lysosomal Storage Disorders Research (20 papers), Trypanosoma species research and implications (18 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). Cordula Steglich collaborates with scholars based in Germany, Australia and Netherlands. Cordula Steglich's co-authors include Andreas Gal, Susanna Bunge, E. Schwinger, Michael Beck, John J. Hopwood, Wim J. Kleijer, C. Phillip Morris, Michael Beck, Anna Tylki‐Szymańska and Peter J. Wilson and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Genomics.

In The Last Decade

Cordula Steglich

24 papers receiving 790 citations

Peers

Countries citing papers authored by Cordula Steglich

Since Specialization

Citations

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

Fields of papers citing papers by Cordula Steglich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cordula Steglich

This figure shows the co-authorship network connecting the top 25 collaborators of Cordula Steglich. A scholar is included among the top collaborators of Cordula Steglich 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 Cordula Steglich. Cordula Steglich 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	Dried Blood Spots Allow Targeted Screening to Diagnose Mucopolysaccharidosis and Mucolipidosis 2014 ·JIMD Reports ·(unknown), Cordula Steglich, René Santer, Zoltán Lukács, Andreas Gal	16
2	The Mutation p.Ser298Pro in the sulphamidase gene (SGSH) is associated with a slowly progressive clinical phenotype in mucopolysaccharidosis type IIIA (Sanfilippo A Syndrome) 2008 ·Human Mutation ·(unknown), (unknown), Andreas Gal, Cordula Steglich, Chris Mühlhausen, Kurt Ullrich, Thomas Braulke, Nicole Muschol	31
3	First pregnancy and life after preimplantation genetic diagnosis by polar body analysis for mucopolysaccharidosis type I 2006 ·Reproductive BioMedicine Online ·(unknown), A. Schultze-Mosgau, Juliane Eckhold, (unknown), S. Al‐Hasani, Cordula Steglich, Andreas Gal, R Axt-Fliedner, E. Schwinger, Klaus Diedrich, Georg Griesinger	15
4	Seventeen novelPLP1mutations in patients with Pelizaeus-Merzbacher disease 2005 ·Human Mutation ·Christian A. Hübner, Ulrike Orth, (unknown), Cordula Steglich, Alfried Kohlschütter, Rudolf Korinthenberg, Andreas Gal	31
5	Intronic mutations in theL1CAMgene may cause X-linked hydrocephalus by aberrant splicing 2004 ·Human Mutation ·Christian A. Hübner, Barbara Utermann, Sigrid Tinschert, Gabriele Krüger, (unknown), Cordula Steglich, Albert Schinzel, Andreas Gal	12
6	LETM1, a gene deleted in Wolf–Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein 2003 ·Genomics ·(unknown), Abhay Moghekar, Jeremy C. Simpson, Cordula Steglich, Richard O’Brien, Andreas Winterpacht, Sabine Endele	80
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
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	Deletion of the hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type II 1992 ·American Journal of Medical Genetics ·Michael Beck, Cordula Steglich, Bernhard Zabel, Niklas Dahl, E. Schwinger, John J. Hopwood, Andreas Gal	12

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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