Dietmar Lohmann

11.5k total citations · 1 hit paper
98 papers, 3.8k citations indexed

About

Dietmar Lohmann is a scholar working on Ophthalmology, Oncology and Molecular Biology. According to data from OpenAlex, Dietmar Lohmann has authored 98 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Ophthalmology, 45 papers in Oncology and 42 papers in Molecular Biology. Recurrent topics in Dietmar Lohmann's work include Ocular Oncology and Treatments (67 papers), Cancer-related Molecular Pathways (42 papers) and Hedgehog Signaling Pathway Studies (14 papers). Dietmar Lohmann is often cited by papers focused on Ocular Oncology and Treatments (67 papers), Cancer-related Molecular Pathways (42 papers) and Hedgehog Signaling Pathway Studies (14 papers). Dietmar Lohmann collaborates with scholars based in Germany, Switzerland and Canada. Dietmar Lohmann's co-authors include Bernhard Horsthemke, Michael Zeschnigk, Norbert Bornfeld, Brenda L. Gallie, Eberhard Passarge, Petra Temming, Claudia H.D. Metz, Frank Tschentscher, Ludger Klein‐Hitpaß and Gerasimos Anastassiou and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Dietmar Lohmann

95 papers receiving 3.7k 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.

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

2013 369 citations Marcel Martin, Petra Temming et al. Nature Genetics profile →

Peers

Dietmar Lohmann

OPHTH

ONCOL

GENET

Joyce M. Rapaport United States

Catherine D. Van Raamsdonk Canada

Léonidas Zografos Switzerland

Lori A. Worley United States

Jeannette Bennicelli United States

Swapna S. Vemula United States

Elisabeth Mangold Germany

Cornelia M. Mooy Netherlands

Nicole C. Naus Netherlands

Alexandre Moulin Switzerland

Joyce M. Rapaport United States

Dietmar Lohmann

1.4k ×0.7

OPHTH

2.0k ×1.0

1.8k ×1.1

ONCOL

729 ×1.1

GENET

596 ×1.3

Citations per year, relative to Dietmar Lohmann Dietmar Lohmann (= 1×) peers Joyce M. Rapaport

Countries citing papers authored by Dietmar Lohmann

Since Specialization

Citations

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

Fields of papers citing papers by Dietmar Lohmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dietmar Lohmann

This figure shows the co-authorship network connecting the top 25 collaborators of Dietmar Lohmann. A scholar is included among the top collaborators of Dietmar Lohmann 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 Dietmar Lohmann. Dietmar Lohmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Lever, M. J., et al.. (2025). Presence of tumor DNA in aqueous humor is correlated with high risk uveal melanoma. Scientific Reports. 15(1). 19406–19406.

Afanasyeva, Elena, M. Schneider, Christopher Schröder, et al.. (2024). A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma. Communications Biology. 7(1). 919–919. 2 indexed citations

Busch, Maike, Eva Biewald, Nikolaos E. Bechrakis, et al.. (2022). TFF1 in Aqueous Humor—A Potential New Biomarker for Retinoblastoma. Cancers. 14(3). 677–677. 14 indexed citations

Kanber, Deniz, Alexandra Brenzel, Janine Altmüller, et al.. (2022). RB1-Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation. Cancers. 14(9). 2166–2166. 8 indexed citations

Munier, Francis L., Maja Beck‐Popovic, Guillermo Chantada, et al.. (2019). Conservative management of retinoblastoma: Challenging orthodoxy without compromising the state of metastatic grace. “Alive, with good vision and no comorbidity”. Progress in Retinal and Eye Research. 73. 100764–100764. 133 indexed citations

Weaver, K. Nicole, Kristin E. Noack Watt, Robert B. Hufnagel, et al.. (2015). Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction. The American Journal of Human Genetics. 96(5). 765–774. 54 indexed citations

Künkele, Annette, Dietmar Lohmann, Norbert Bornfeld, et al.. (2015). Neoadjuvant/adjuvant treatment of high-risk retinoblastoma: a report from the German Retinoblastoma Referral Centre. British Journal of Ophthalmology. 99(7). 949–953. 15 indexed citations

Bouguila, H., et al.. (2014). Genetic testing in Tunisian families with heritable retinoblastoma using a low cost approach permits accurate risk prediction in relatives and reveals incomplete penetrance in adults. Experimental Eye Research. 124. 48–55. 8 indexed citations

Martin, Marcel, Petra Temming, Sven Rahmann, et al.. (2013). Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3. Nature Genetics. 45(8). 933–936. 369 indexed citations breakdown →

10.

Kanber, Deniz, Karin Buiting, Christian Roos, et al.. (2013). The Origin of the RB1 Imprint. PLoS ONE. 8(11). e81502–e81502. 21 indexed citations

11.

Dauwerse, Johannes G., Jill Dixon, Saskia Seland, et al.. (2010). Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genetics. 43(1). 20–22. 243 indexed citations

12.

Balik, Vladimír, et al.. (2008). Meningioma 40 Years after Radiation Therapy for Retinoblastoma: Genetic and Phenotypic Analysis, and Minireview of Literature. Central European Neurosurgery - Zentralblatt für Neurochirurgie. 69(4). 194–199. 2 indexed citations

13.

Zeschnigk, Michael, et al.. (2006). Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome 3. Experimental Eye Research. 83(4). 858–864. 21 indexed citations

14.

Toedt, Grischa, Frank Mendrzyk, Daniel E. Stange, et al.. (2005). Detection of chromosomal imbalances in retinoblastoma by matrix‐based comparative genomic hybridization. Genes Chromosomes and Cancer. 43(3). 294–301. 85 indexed citations

15.

Grasemann, Corinna, Harald Stephan, Andreas Schüler, et al.. (2005). Gains and overexpression identify DEK and E2F3 as targets of chromosome 6p gains in retinoblastoma. Oncogene. 24(42). 6441–6449. 89 indexed citations

16.

Lohmann, Dietmar & Brenda L. Gallie. (2004). Retinoblastoma: Revisiting the model prototype of inherited cancer. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 129C(1). 23–28. 127 indexed citations

17.

Wieczorek, Dagmar, et al.. (2003). Two brothers with Burn-McKeown syndrome. Clinical Dysmorphology. 12(3). 171–174. 6 indexed citations

18.

Tschentscher, Frank, Gabriele Prescher, Michael Zeschnigk, Bernhard Horsthemke, & Dietmar Lohmann. (2000). Identification of chromosomes 3, 6, and 8 aberrations in uveal melanoma by microsatellite analysis in comparison to comparative genomic hybridization. Cancer Genetics and Cytogenetics. 122(1). 13–17. 84 indexed citations

19.

Rieder, Harald, et al.. (1998). Loss of Heterozygosity of the Retinoblastoma (RB1) Gene in Lipomas From a Retinoblastoma Patient. JNCI Journal of the National Cancer Institute. 90(4). 324–326. 11 indexed citations

20.

Lohmann, Dietmar, et al.. (1993). Identification of p53 gene mutations in gastrointestinal and pancreatic carcinoids by nonradioisotopic SSCA. Virchows Archiv B Cell Pathology Including Molecular Pathology. 64(1). 293–296. 56 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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