Günter Assum

1.4k total citations
33 papers, 819 citations indexed

About

Günter Assum is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Günter Assum has authored 33 papers receiving a total of 819 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 11 papers in Genetics and 10 papers in Neurology. Recurrent topics in Günter Assum's work include Neurofibromatosis and Schwannoma Cases (10 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Chromatin Dynamics (7 papers). Günter Assum is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (10 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Chromatin Dynamics (7 papers). Günter Assum collaborates with scholars based in Germany, United States and Austria. Günter Assum's co-authors include W. Krone, Ingrid Eisenbarth, Walther Vogel, Hildegard Kehrer‐Sawatzki, Sven Hoffmeyer, Dieter Kaufmann, Gudrun Wöhr, Kim S. Beyer, Johannes Stökl and Tod F. Stuessy and has published in prestigious journals such as Nucleic Acids Research, Nature Biotechnology and Genetics.

In The Last Decade

Günter Assum

32 papers receiving 802 citations

Peers

Countries citing papers authored by Günter Assum

Since Specialization

Citations

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

Fields of papers citing papers by Günter Assum

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Günter Assum

This figure shows the co-authorship network connecting the top 25 collaborators of Günter Assum. A scholar is included among the top collaborators of Günter Assum 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 Günter Assum. Günter Assum 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	Analysis of short tandem repeat expansions and their methylation state with nanopore sequencing 2019 ·Nature Biotechnology ·Pay Gießelmann, Björn Brändl, Etienne Raimondeau, Rebecca Bowen, (unknown), Rashmi Tandon, Helene Kretzmer, Günter Assum, Christina Galonska, Reiner Siebert, Ole Ammerpohl, Andrew Heron, Susanne A. Schneider, Julia Ladewig, Philipp Koch, Bernhard Schuldt, James E. Graham, Alexander Meissner, Frank Müller	117
2	Genetic and environmental risk factors for submucous cleft palate 2012 ·European Journal Of Oral Sciences ·Rudolf Reiter, Sibylle Brosch, (unknown), (unknown), (unknown), Anja Pickhard, Günter Assum, Anke Schwandt, Walther Vogel, Josef Högel, Christiane Maier	18
3	Scent variation and hybridization cause the displacement of a sexually deceptive orchid species 2008 ·American Journal of Botany ·Johannes Stökl, Philipp M. Schlüter, Tod F. Stuessy, Hannes F. Paulus, Günter Assum, Manfred Ayasse	62
4	A Comparison of the Variability Spectra of Two Genomic Loci in a European Group of Individuals Reveals Fundamental Differences Pointing to Selection or a Population Bottleneck 2007 ·Annals of Human Genetics ·(unknown), Josef Hoegel, Walther Vogel, Günter Assum	1
5	Isochores and replication time zones: a perfect match 2007 ·Cytogenetic and Genome Research ·(unknown), H. Hameister, Walther Vogel, Günter Assum	25
6	Genetic variability in a genomic region with long-range linkage disequilibrium reveals traces of a bottleneck in the history of the European population 2005 ·Human Genetics ·(unknown), Josef Hoegel, Walther Vogel, Günter Assum	15
7	Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene 2001 ·The American Journal of Human Genetics ·Dieter Kaufmann, Ralf Müller-Xing, Britta Bartelt‐Kirbach, Michael Wolf, (unknown), C. Oliver Hanemann, Raimund Fahsold, (unknown), (unknown), Günter Assum	21
8	An Isochore Transition in the NF1 Gene Region Coincides with a Switch in the Extent of Linkage Disequilibrium 2000 ·The American Journal of Human Genetics ·Ingrid Eisenbarth, G Vogel, W. Krone, Walther Vogel, Günter Assum	49
9	Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients with Neurofibromatosis Type 1 2000 ·The American Journal of Human Genetics ·Ingrid Eisenbarth, Kim S. Beyer, W. Krone, Günter Assum	61
10	Characterization of an Alphoid Subfamily Located Near P-arm Sequences on Human Chromosome 22 1999 ·Chromosome Research ·Ingrid Eisenbarth, (unknown), Gudrun Wöhr, (unknown), Günter Assum	2
11	Concerted evolution of members of the multisequence family chAB4 located on various nonhomologous chromosomes 1998 ·Mammalian Genome ·Günter Assum, Juan J. Pasantes, (unknown), W. Schempp, Gudrun Wöhr	7
12	The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions 1997 ·Human Genetics ·Hildegard Kehrer‐Sawatzki, J Häussler, W. Krone, Harald Bode, Dieter E. Jenne, Karl Mehnert, (unknown), Günter Assum	69
13	A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2 1997 ·Human Genetics ·Hildegard Kehrer‐Sawatzki, (unknown), Günter Assum, Mariano Rocchi, W. Krone	21
14	Mutational analysis and expression studies of the neurofibromatosis type 2 (NF2) gene in a patient with a ring chromosome 22 and NF2 1997 ·Human Genetics ·Hildegard Kehrer‐Sawatzki, Martin Udart, W. Krone, (unknown), Raimund Fahsold, Gilles Thomas, (unknown), Günter Assum	18
15	Clonal Origin of Tumor Cells in a Plexiform Neurofibroma with LOH in NF1 Intron 38 and in Dermal Neurofibromas without LOH of the NF1 Gene 1997 ·Biochemical and Biophysical Research Communications ·(unknown), Günter Assum, Ingrid Eisenbarth, W. Krone, Sven Hoffmeyer, (unknown), B Heymer, Hildegard Kehrer‐Sawatzki	49
16	Evidence for the Presence of the Second Allele of the Neurofibromatosis Type 1 Gene in Melanocytes Derived from Café au Lait Macules of NF1 Patients 1997 ·Biochemical and Biophysical Research Communications ·Ingrid Eisenbarth, Günter Assum, Dieter Kaufmann, W. Krone	19
17	A palindromic structure in the pericentromeric region of various human chromosomes. 1996 ·Genome Research ·Gudrun Wöhr, (unknown), Günter Assum	25
18	On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1 1995 ·Human Molecular Genetics ·Sven Hoffmeyer, Günter Assum, (unknown), Dieter Kaufmann, Peter Nürnberg, W. Krone	40
19	A deletion in the 5 ′-region of the neurofibromatosis type 1 (NF1) gene 1994 ·Human Genetics ·Sven Hoffmeyer, Günter Assum, Dieter Kaufmann, (unknown), W. Krone	11
20	Evolution of the chAB4 Multisequence Family in Primates 1994 ·Genomics ·Günter Assum, (unknown), W. Schempp, Gudrun Wöhr	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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