Wolfram Henn

1.1k total citations
27 papers, 540 citations indexed

About

Wolfram Henn is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Wolfram Henn has authored 27 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Epidemiology. Recurrent topics in Wolfram Henn's work include Genomics and Chromatin Dynamics (6 papers), Meningioma and schwannoma management (5 papers) and Neuroblastoma Research and Treatments (4 papers). Wolfram Henn is often cited by papers focused on Genomics and Chromatin Dynamics (6 papers), Meningioma and schwannoma management (5 papers) and Neuroblastoma Research and Treatments (4 papers). Wolfram Henn collaborates with scholars based in Germany, Poland and Netherlands. Wolfram Henn's co-authors include K. D. Zang, W. Feiden, I. Niedermayer, Nikolaus Blin, Cornelius Welter, Gerhard Seitz, Ralf Ketter, Patrick Müller, W. I. Steudel and Karlheinz Holzmann and has published in prestigious journals such as Nucleic Acids Research, Cancer Letters and Investigative Ophthalmology & Visual Science.

In The Last Decade

Wolfram Henn

27 papers receiving 507 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wolfram Henn Germany 12 190 145 117 94 89 27 540
Paige K. Bradley United States 6 187 1.0× 128 0.9× 40 0.3× 95 1.0× 171 1.9× 8 510
P Balestrazzi Italy 12 92 0.5× 170 1.2× 51 0.4× 43 0.5× 129 1.4× 31 410
Ruth A. Heim United States 13 155 0.8× 117 0.8× 57 0.5× 54 0.6× 111 1.2× 21 643
Victoria Parker United Kingdom 10 274 1.4× 174 1.2× 55 0.5× 367 3.9× 92 1.0× 25 774
Rossella Capolino Italy 18 449 2.4× 369 2.5× 146 1.2× 92 1.0× 39 0.4× 56 825
Cecilie F. Rustad Norway 11 210 1.1× 116 0.8× 111 0.9× 37 0.4× 170 1.9× 18 491
P Bouloux United Kingdom 6 159 0.8× 146 1.0× 181 1.5× 35 0.4× 87 1.0× 7 466
Manuela Fanciulli Italy 11 241 1.3× 367 2.5× 64 0.5× 21 0.2× 24 0.3× 13 726
E. Vámos Belgium 11 156 0.8× 205 1.4× 17 0.1× 78 0.8× 65 0.7× 23 420
B. G. A. ter Haar Netherlands 15 212 1.1× 160 1.1× 30 0.3× 59 0.6× 23 0.3× 20 423

Countries citing papers authored by Wolfram Henn

Since Specialization
Citations

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

Fields of papers citing papers by Wolfram Henn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfram Henn

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfram Henn. A scholar is included among the top collaborators of Wolfram Henn 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 Wolfram Henn. Wolfram Henn 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.
Faßbender, Klaus, et al.. (2011). Neurologische Manifestationen der AGel-Amyloidose (Meretoja-Syndrom) bei einer deutschen Familie. Fortschritte der Neurologie · Psychiatrie. 79(4). 238–241. 4 indexed citations
2.
Weiss, Jayne S., Howard S. Kruth, Helena Kuivaniemi, et al.. (2007). Mutations in theUBIAD1Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy. Investigative Ophthalmology & Visual Science. 48(11). 5007–5007. 81 indexed citations
3.
Henn, Wolfram, et al.. (2003). Monosomy 7p in meningiomas: a rare constituent of tumor progression. Cancer Genetics and Cytogenetics. 144(1). 65–68. 7 indexed citations
4.
Starke, Heike, Jörg Seidel, Wolfram Henn, et al.. (2002). Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements. European Journal of Human Genetics. 10(12). 790–800. 91 indexed citations
5.
Delb, W., et al.. (2001). Mandibulofacial dysostosis, microcephaly and thorax deformities in two brothers: a new recessive syndrome?. Clinical Dysmorphology. 10(2). 105–109. 5 indexed citations
6.
Kramer, Boris W., et al.. (2000). Lung hypoplasia in a patient with del(2)(q33-q35) demonstrated by chromosome microdissection. American Journal of Medical Genetics. 94(3). 184–188. 5 indexed citations
7.
Pahl, Stefan, et al.. (2000). Malignant odontogenic myxoma of the maxilla: case with cytogenetic confirmation. The Journal of Laryngology & Otology. 114(7). 533–535. 31 indexed citations
8.
Wullich, Bernd, et al.. (1997). Clonal chromosome aberrations in three of five sporadic angiomyolipomas of the kidney. Cancer Genetics and Cytogenetics. 96(1). 42–45. 11 indexed citations
9.
Niedermayer, I., et al.. (1997). Loss of alkaline phosphatase activity in meningiomas: a rapid histochemical technique indicating progression-associated deletion of a putative tumor suppressor gene on the distal part of the short arm of chromosome 1.. PubMed. 56(8). 879–86. 45 indexed citations
10.
Remberger, K., et al.. (1996). A novel site of DNA amplification on chromosome 1p32-33 in a rhabdomyosarcoma revealed by comparative genomic hybridization. Human Genetics. 97(1). 87–90. 11 indexed citations
11.
Henn, Wolfram, et al.. (1996). Early proliferation enhancement by monosomy 10 and intratumor heterogeneity in malignant human gliomas as revealed by smear preparations from biopsies. Genes Chromosomes and Cancer. 16(3). 180–184. 15 indexed citations
12.
Low, Malcolm J., et al.. (1995). Polysyndactyly and asymptomatic hypothalamic hamartoma in mother and son: a variant of Pallister‐Hall syndrome. Clinical Genetics. 48(4). 209–212. 17 indexed citations
13.
Holzmann, Karlheinz, Nikolaus Blin, Cornelius Welter, et al.. (1993). Telomeric associations and loss of telomeric DNA repeats in renal tumors. Genes Chromosomes and Cancer. 6(3). 178–181. 50 indexed citations
14.
Müller, Andreas, Wolfram Henn, & Gerhard Unteregger. (1991). Nuclear and DNA‐binding proteins in human brain tumors. Electrophoresis. 12(7-8). 515–523. 3 indexed citations
15.
Schrell, U., et al.. (1991). Loss of heterozygosity on chromosome 3, bands q24→qter, in a diploid meningioma. Cytogenetic and Genome Research. 57(2-3). 157–158. 2 indexed citations
16.
17.
Welter, Cornelius, Wolfram Henn, Birgit Theisinger, et al.. (1990). The cellular myb oncogene is amplified, rearranged and activated in human glioblastoma cell lines. Cancer Letters. 52(1). 57–62. 30 indexed citations
18.
Metzdorf, Reinhold, E. Göttert, Wolfram Henn, Ad Geurts van Kessel, & Nikolaus Blin. (1989). A polymorphic DNA probe from chromosome 19 (l9cen-q11). Nucleic Acids Research. 17(17). 7126–7126. 1 indexed citations
19.
Henn, Wolfram, E. Göttert, Birgit Theisinger, K. D. Zang, & Nikolaus Blin. (1989). Differential activity of two oncogenes from chromosome 7 in human glioblastoma cell lines. Cancer Genetics and Cytogenetics. 38(2). 172–172. 4 indexed citations
20.
Fischer, Hans, Annemieke van der Hout, Gerhard Unteregger, et al.. (1988). A human glioblastoma line with karyotypic nullisomy 13 containing several chromosome 13-specific sequences. Cancer Genetics and Cytogenetics. 33(1). 127–132. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Paige K. Bradley Breakdown of academic impact, for papers by P Balestrazzi Breakdown of academic impact, for papers by Ruth A. Heim Breakdown of academic impact, for papers by Victoria Parker Breakdown of academic impact, for papers by Rossella Capolino Breakdown of academic impact, for papers by Cecilie F. Rustad Breakdown of academic impact, for papers by P Bouloux Breakdown of academic impact, for papers by Manuela Fanciulli Breakdown of academic impact, for papers by E. Vámos Breakdown of academic impact, for papers by B. G. A. ter Haar
Rankless by CCL
2026