Wolfram Scheurlen

19.9k total citations · 1 hit paper
46 papers, 3.1k citations indexed

About

Wolfram Scheurlen is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Wolfram Scheurlen has authored 46 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Genetics and 11 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Wolfram Scheurlen's work include Glioma Diagnosis and Treatment (9 papers), Hedgehog Signaling Pathway Studies (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Wolfram Scheurlen is often cited by papers focused on Glioma Diagnosis and Treatment (9 papers), Hedgehog Signaling Pathway Studies (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Wolfram Scheurlen collaborates with scholars based in Germany, United Kingdom and United States. Wolfram Scheurlen's co-authors include Lutz Gissmann, Harald zur Hausen, Hans Ikenberg, Michael Boshart, Andreas Kleinheinz, Andreas von Deimling, Jan Mollenhauer, Klaus K. Wilgenbus, Annemarie Poustka and Stefan Wiemann and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Wolfram Scheurlen

45 papers receiving 3.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer.

1984 1.0k citations Michael Boshart, Lutz Gissmann et al. The EMBO Journal profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wolfram Scheurlen Germany	25	1.5k	1.0k	752	512	504	46	3.1k
Patrick Saulnier France	28	1.1k 0.7×	349 0.3×	652 0.9×	480 0.9×	396 0.8×	48	2.5k
Akira Hangaishi Japan	28	1.1k 0.7×	361 0.3×	499 0.7×	583 1.1×	497 1.0×	86	2.7k
Jeffrey Sklar United States	28	1.8k 1.2×	577 0.6×	494 0.7×	2.6k 5.0×	373 0.7×	54	5.2k
Giuseppe Torelli Italy	42	913 0.6×	1.5k 1.4×	712 0.9×	2.2k 4.2×	175 0.3×	172	4.9k
Charles Crawley United Kingdom	26	875 0.6×	406 0.4×	961 1.3×	753 1.5×	181 0.4×	64	3.4k
A K Ghosh United Kingdom	19	983 0.7×	433 0.4×	345 0.5×	1.2k 2.3×	275 0.5×	31	4.1k
Carole Yee United States	29	1.3k 0.9×	1.9k 1.8×	563 0.7×	1.3k 2.5×	962 1.9×	59	4.1k
Lloyd Hutchinson United States	26	725 0.5×	903 0.9×	183 0.2×	634 1.2×	392 0.8×	80	2.4k
S Poppema Netherlands	36	1.0k 0.7×	522 0.5×	752 1.0×	1.7k 3.3×	156 0.3×	93	4.6k
Jean‐Claude Brouet France	33	1.3k 0.9×	566 0.5×	1.2k 1.6×	887 1.7×	336 0.7×	81	5.3k

Countries citing papers authored by Wolfram Scheurlen

Since Specialization

Citations

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

Fields of papers citing papers by Wolfram Scheurlen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfram Scheurlen

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfram Scheurlen. A scholar is included among the top collaborators of Wolfram Scheurlen 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 Scheurlen. Wolfram Scheurlen 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

Karremann, Michael, Marion Hoffmann, Maria Wiese, et al.. (2017). Haematological malignancies following temozolomide treatment for paediatric high-grade glioma. European Journal of Cancer. 81. 1–8. 4 indexed citations

Remke, Marc, Thomas Hielscher, Paul A. Northcott, et al.. (2011). Adult Medulloblastoma Comprises Three Major Molecular Variants. Journal of Clinical Oncology. 29(19). 2717–2723. 160 indexed citations

Traenka, Christopher, Marc Remke, Andrey Korshunov, et al.. (2010). Role of LIM and SH3 Protein 1 (LASP1) in the Metastatic Dissemination of Medulloblastoma. Cancer Research. 70(20). 8003–8014. 55 indexed citations

Pfister, Stefan M., Marc Remke, Axel Benner, et al.. (2009). Outcome Prediction in Pediatric Medulloblastoma Based on DNA Copy-Number Aberrations of Chromosomes 6q and 17q and the MYC and MYCN Loci. Journal of Clinical Oncology. 27(10). 1627–1636. 198 indexed citations

Loges, Niki T., Heike Olbrich, Cornelia Klein, et al.. (2007). Further Evidence for a Somatic KRAS Mutation in a Pilocytic Astrocytoma. Neuropediatrics. 38(2). 61–63. 51 indexed citations

Ebinger, Martin, et al.. (2006). Screening molekularbiologischer Marker zur Risikostratifizierung bei Medulloblastomen. Klinische Pädiatrie. 218(3). 139–142. 3 indexed citations

Scheurlen, Wolfram, et al.. (2005). Neonatal Mastocytosis with Pachydermic Bullous Skin without c-Kit 816 Mutation. Dermatology. 212(1). 70–72. 18 indexed citations

Ebinger, Martin, et al.. (2004). NO ABERRANT METHYLATION OF NEUROFIBROMATOSIS 1 GENE (NF1) PROMOTER IN PILOCYTIC ASTROCYTOMA IN CHILDHOOD. Pediatric Hematology and Oncology. 22(1). 83–87. 5 indexed citations

Ebinger, Martin, et al.. (2004). Promoter methylation pattern of caspase-8, P16INK4A, MGMT, TIMP-3, and E-cadherin in medulloblastoma. Pathology & Oncology Research. 10(1). 17–21. 38 indexed citations

10.

Mollenhauer, Jan, Hanna Müller, Stefan Lyer, et al.. (2002). The SRCR/SID region of DMBT1 defines a complex multi‐allele system representing the major basis for its variability in cancer. Genes Chromosomes and Cancer. 35(3). 242–255. 36 indexed citations

11.

Höglund, Pia, Markus Sormaala, Siru Haila, et al.. (2001). Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea. Human Mutation. 18(3). 233–242. 26 indexed citations

12.

Girschick, Hermann, Rüdiger Klein, Wolfram Scheurlen, & Joachim Kühl. (2001). Cytogenetic and histopathologic studies of congenital supratentorial primitive neuroectodermal tumors: A case report. Pathology & Oncology Research. 7(1). 67–71. 10 indexed citations

13.

Scheurlen, Wolfram, et al.. (2001). Chronic autoimmune thrombopenia/neutropenia in a boy with persistent parvovirus B19 infection. Journal of Clinical Virology. 20(3). 173–178. 36 indexed citations

14.

Mechtersheimer, Gunhild, S. Öhl, Klaus K. Wilgenbus, et al.. (2000). Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics. Cytogenetic and Genome Research. 90(1-2). 86–92. 42 indexed citations

15.

Scheurlen, Wolfram, Jürgen Krauß, Stanislas du Manoir, et al.. (1996). Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization. Genes Chromosomes and Cancer. 16(3). 196–203. 71 indexed citations

16.

Nanan, Ralph, et al.. (1995). Severe low-titer cold-hemagglutinin disease responsive to steroid pulse therapy. Annals of Hematology. 71(2). 101–102. 1 indexed citations

17.

Scheurlen, Wolfram, Jürgen Krauß, & Joachim Kühl. (1995). No preferential loss of one parental allele of chromosome 17p13.3 in childhood medulloblastoma. International Journal of Cancer. 63(3). 372–374. 10 indexed citations

18.

Scheurlen, Wolfram, et al.. (1995). Analysis of the gap‐related domain of the neurofibromatosis type 1 (NF1) gene in childhood brain tumors. International Journal of Cancer. 64(4). 234–238. 12 indexed citations

19.

Scheurlen, Wolfram, et al.. (1992). Polymerase chain reaction-amplification of urease genes: rapid screening for ureaplasma urealyticum infection in endotracheal aspirates of ventilated newborns. European Journal of Pediatrics. 151(10). 740–742. 9 indexed citations

20.

Boshart, Michael, Lutz Gissmann, Hans Ikenberg, et al.. (1984). A new type of papillomavirus DNA, its presence in genital cancer biopsies and in cell lines derived from cervical cancer.. The EMBO Journal. 3(5). 1151–1157. 1039 indexed citations breakdown →

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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