Simone Schuffenhauer

3.7k total citations
42 papers, 1.7k citations indexed

About

Simone Schuffenhauer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Simone Schuffenhauer has authored 42 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 29 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Simone Schuffenhauer's work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (11 papers) and Genetic Syndromes and Imprinting (8 papers). Simone Schuffenhauer is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (11 papers) and Genetic Syndromes and Imprinting (8 papers). Simone Schuffenhauer collaborates with scholars based in Germany, Australia and United Kingdom. Simone Schuffenhauer's co-authors include Thomas Meitinger, Peter Lichtner, Jan Murken, Peter Groenen, J P Fryns, I. M. Holdaway, Rudolf W. Bilous, Wim Van de Ven, Rolf Beetz and Rajesh V. Thakker and has published in prestigious journals such as Nature, Nature Genetics and Molecular Cell.

In The Last Decade

Simone Schuffenhauer

42 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simone Schuffenhauer Germany 23 1.0k 964 308 181 151 42 1.7k
Holger Tönnies Germany 23 927 0.9× 833 0.9× 179 0.6× 221 1.2× 136 0.9× 55 1.6k
Jean‐Pierre Fryns Belgium 21 1.2k 1.2× 909 0.9× 202 0.7× 73 0.4× 174 1.2× 25 2.0k
Marie McDonald United States 19 749 0.7× 1.1k 1.1× 188 0.6× 94 0.5× 158 1.0× 45 1.7k
Roberto Mendoza‐Londono Canada 26 1.0k 1.0× 1.2k 1.2× 151 0.5× 86 0.5× 166 1.1× 85 2.1k
M.H. Breuning Netherlands 16 1.4k 1.3× 1.7k 1.8× 207 0.7× 160 0.9× 118 0.8× 26 2.1k
Steven Van Vooren Belgium 16 1.2k 1.1× 1.3k 1.4× 247 0.8× 187 1.0× 57 0.4× 25 2.0k
Sung‐Hae Kang United States 20 737 0.7× 925 1.0× 348 1.1× 180 1.0× 65 0.4× 30 1.4k
Jacqueline Schoumans Sweden 29 1.2k 1.1× 1.6k 1.6× 442 1.4× 458 2.5× 162 1.1× 73 2.5k
Małgorzata Krajewska‐Walasek Poland 23 1.4k 1.3× 1.0k 1.0× 329 1.1× 69 0.4× 142 0.9× 110 2.2k
P. Pearson Netherlands 21 879 0.9× 710 0.7× 144 0.5× 276 1.5× 81 0.5× 50 1.6k

Countries citing papers authored by Simone Schuffenhauer

Since Specialization
Citations

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

Fields of papers citing papers by Simone Schuffenhauer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Schuffenhauer

This figure shows the co-authorship network connecting the top 25 collaborators of Simone Schuffenhauer. A scholar is included among the top collaborators of Simone Schuffenhauer 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 Simone Schuffenhauer. Simone Schuffenhauer 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.
Kuhn, Klaus A., Raffael Bild, Gabriele Anton, Simone Schuffenhauer, & H‐Erich Wichmann. (2016). Vernetzung von Biobanken großer europäischer Kohorten (EU-Projekt BBMRI-LPC). Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 59(3). 385–389. 3 indexed citations
2.
Merino-Martinez, Roxana, David van Enckevort, Gabriele Anton, et al.. (2016). Toward Global Biobank Integration by Implementation of the Minimum Information About BIobank Data Sharing (MIABIS 2.0 Core). Biopreservation and Biobanking. 14(4). 298–306. 52 indexed citations
3.
Callen, David F., Helen J. Eyre, Shannon K. McDonnell, Simone Schuffenhauer, & Kapil N. Bhalla. (2002). A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction. Chromosoma. 111(3). 170–175. 8 indexed citations
4.
5.
Uhrig, Sabine, Simone Schuffenhauer, Christine Fauth, et al.. (1999). Multiplex-FISH for Pre- and Postnatal Diagnostic Applications. The American Journal of Human Genetics. 65(2). 448–462. 72 indexed citations
6.
Schuffenhauer, Simone, Peter Lichtner, Jan Murken, et al.. (1998). Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2). European Journal of Human Genetics. 6(3). 213–225. 64 indexed citations
7.
8.
Hewett, D., Oliva Handt, Lynne Hobson, et al.. (1998). FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis. Molecular Cell. 1(6). 773–781. 73 indexed citations
9.
Wissinger, Bernd, Frank Müller, Ingo Weyand, et al.. (1997). Cloning, Chromosomal Localization and Functional Expression of the Gene Encoding the α‐Subunit of the cG‐MP‐Gated Channel in Human Cone Photoreceptors. European Journal of Neuroscience. 9(12). 2512–2521. 31 indexed citations
10.
Deckert, Jürgen, Markus M. Nöthen, Simone Schuffenhauer, et al.. (1997). Mapping of the human adenosine A 2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region. Human Genetics. 99(3). 326–328. 31 indexed citations
11.
Robinson, Wendy P., Sylvie Langlois, Simone Schuffenhauer, et al.. (1996). CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15. Prenatal Diagnosis. 16(9). 837–844. 50 indexed citations
12.
Schuffenhauer, Simone, Tina Buchholz, S. Stengel‐Rutkowski, et al.. (1996). A familial deletion in the Prader-Willi syndrome region including the imprinting control region. Human Mutation. 8(3). 288–292. 6 indexed citations
13.
Schuffenhauer, Simone, Astrid Golla, Peter Lichtner, et al.. (1996). Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p. American Journal of Medical Genetics. 63(1). 177–184. 14 indexed citations
14.
Schindelhauer, Dirk, Simone Schuffenhauer, Thomas Gasser, Alexander Steinkasserer, & Thomas Meitinger. (1995). The Gene Coding for Glial Cell Line Derived Neurotrophic Factor (GDNF) Maps to Chromosome 5p12-p13.1. Genomics. 28(3). 605–607. 19 indexed citations
15.
Schuffenhauer, Simone, Oliver Bartsch, Markus Stümm, et al.. (1995). DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor. Human Genetics. 96(5). 562–571. 46 indexed citations
16.
Schirren, Carl Georg, et al.. (1994). Dyskeratosis congenita bei monozygoten Zwillingen. Der Hautarzt. 45(4). 249–255. 1 indexed citations
17.
Brilliant, Murray H., Richard A. King, Uta Francke, et al.. (1994). The Mouse Pink‐Eyed Dilution Gene: Association with Hypopigmentation in Prader‐Willi and Angelman Syndromes and with Human OCA2. Pigment Cell Research. 7(6). 398–402. 23 indexed citations
18.
Daumer‐Haas, Cornelia, et al.. (1994). Tetrasomy 21 pter→q22.1 and Down syndrome: Molecular definition of the region. American Journal of Medical Genetics. 53(4). 359–365. 19 indexed citations
19.
Robinson, Wendy P., Isabel Lorda‐Sánchez, S Malcolm, et al.. (1993). Increased Parental Ages and Uniparental Disomy 15: A Paternal Age Effect?. European Journal of Human Genetics. 1(4). 280–286. 42 indexed citations
20.
Schuffenhauer, Simone, et al.. (1992). De novo interstitial deletion 16(q12. 1q13) of paternal origin in a 10‐year‐old boy. Clinical Genetics. 42(5). 246–250. 12 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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