Wolfram Henn

72 papers receiving 2.6k citations

Wolfram Henn's Hit Papers

Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia 1997 · 1.2k citations
1.2k0+9+19Years since publication4008001.2k

Peers

Wolfram Henn
Comparison fields: 5 of 114
  • Genetics 267
  • Cancer Research 349
  • Rheumatology 325
  • Molecular Biology 1.4k
  • Oncology 511
Replace Alessandro De Luca with:
Alessandro De Luca Italy
Mark J. Pettenati United States
Anne H. Child United Kingdom
R. Neil Schimke United States
David Walterhouse United States
Franck Bourdeaut France
Athena M. Cherry United States
Sally Ann Lynch Ireland
Hans Kristian Ploos van Amstel Netherlands
B S Emanuel United States
Wolfram Henn relative to Alessandro De Luca Italy Alessandro De Luca's profile →
Citations per field
00.5×2.6×
Alessandro De Luca · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Wolfram Henn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Wolfram Henn Line = papers co-authored together Wolfram Henn links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 78 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
Hit paper breakdown →
19971217
2 199589
3 199988
4 200184
5 200576
6 200573
7 198664
8 200761
9 200657
10 200852
11 199647
12 199742
13 200140
14 200738
15 200937
16 199333
17
Modulation of the cellular and humoral immune responses of tumor patients by mistletoe therapy.
199829
18 199528
19 199327
20 201427

About Wolfram Henn

Wolfram Henn is a scholar working on Molecular Biology, Epidemiology, Pediatrics, Perinatology and Child Health, Genetics and Genetics, having authored 78 papers that have together received 2.7k indexed citations. Recurring topics across this work include Meningioma and schwannoma management (17 papers), Ethics and Legal Issues in Pediatric Healthcare (13 papers), Glioma Diagnosis and Treatment (9 papers), Prenatal Screening and Diagnostics (8 papers), Neurofibromatosis and Schwannoma Cases (7 papers), Medical and Health Sciences Research (7 papers), Cancer Genomics and Diagnostics (7 papers) and Bone Tumor Diagnosis and Treatments (6 papers). The work is most often cited by research in Genetics (267 citations), Cancer Research (349 citations), Rheumatology (325 citations), Molecular Biology (1.4k citations) and Oncology (511 citations). Wolfram Henn has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include K. D. Zang, Stefan Mundlos, Roland Mertelsmann, F Otto, Joan H.M. Knoll, William G. Cole, Bernhard Zabel, John B. Mulliken, Bjørn R. Olsen and Dick Lindhout. Their work appears in journals such as Human Genetics, Nature Reviews Genetics, International Journal of Cancer, Clinical Genetics and Journal of Medical Ethics.

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