Dorothee Foernzler

1.9k total citations · 1 hit paper
20 papers, 1.6k citations indexed

About

Dorothee Foernzler is a scholar working on Molecular Biology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Dorothee Foernzler has authored 20 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Oncology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Dorothee Foernzler's work include Lung Cancer Treatments and Mutations (5 papers), Colorectal Cancer Treatments and Studies (3 papers) and Lung Cancer Research Studies (3 papers). Dorothee Foernzler is often cited by papers focused on Lung Cancer Treatments and Mutations (5 papers), Colorectal Cancer Treatments and Studies (3 papers) and Lung Cancer Research Studies (3 papers). Dorothee Foernzler collaborates with scholars based in United States, Switzerland and Germany. Dorothee Foernzler's co-authors include David R. Beier, Maureen A. Su, Cameron C. Trenor, Nancy C. Andrews, Mark D. Fleming, William F. Dietrich, Annick Thompson, John D. McPherson, U. Gatzemeier and Klaus Lindpaintner and has published in prestigious journals such as Science, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Dorothee Foernzler

19 papers receiving 1.5k citations

Hit Papers

align trajectories sort by overperformance

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.

Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene

1997 975 citations Mark D. Fleming, Cameron C. Trenor et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dorothee Foernzler United States	12	797	721	466	357	210	20	1.6k
Vladimír Divoký Czechia	22	755 0.9×	162 0.2×	657 1.4×	678 1.9×	113 0.5×	78	1.6k
Arlette Porteu France	20	651 0.8×	426 0.6×	496 1.1×	938 2.6×	177 0.8×	28	2.0k
Jens Stolte Germany	13	829 1.0×	509 0.7×	587 1.3×	483 1.4×	71 0.3×	21	1.5k
Joanne E. Levy United States	14	1.1k 1.3×	876 1.2×	841 1.8×	291 0.8×	27 0.1×	15	1.6k
Ruihong Wang United States	16	837 1.1×	378 0.5×	711 1.5×	838 2.3×	249 1.2×	29	2.1k
S E Bernstein United States	15	417 0.5×	187 0.3×	287 0.6×	360 1.0×	81 0.4×	30	1.0k
Tsutomu Toki Japan	21	537 0.7×	80 0.1×	272 0.6×	1.2k 3.3×	121 0.6×	66	1.8k
Çagatay Güneş Germany	20	92 0.1×	189 0.3×	39 0.1×	631 1.8×	182 0.9×	51	1.3k
Roberta Giuliani Italy	16	361 0.5×	50 0.1×	114 0.2×	590 1.7×	185 0.9×	25	1.1k
Thomas Moulton United States	15	116 0.1×	68 0.1×	142 0.3×	1.1k 3.0×	150 0.7×	27	1.6k

Countries citing papers authored by Dorothee Foernzler

Since Specialization

Citations

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

Fields of papers citing papers by Dorothee Foernzler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorothee Foernzler

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

Rolfe, P. Alexander, et al.. (2022). Comparison of Two Illumina Whole Transcriptome RNA Sequencing Library Preparation Methods Using Human Cancer FFPE Specimens. Technology in Cancer Research & Treatment. 21. 2213818192–2213818192. 8 indexed citations

Lambrechts, Diether, Paul Delmar, Ian Buysschaert, et al.. (2009). 16LBA VEGFR-1 polymorphisms as potential predictors of clinical outcome in bevacizumab-treated patients with metastatic pancreatic cancer. European Journal of Cancer Supplements. 7(3). 10–10. 10 indexed citations

Berrahmoune, Hind, Annick Thompson, Suzanne Droesch, et al.. (2008). Genetic Polymorphism ofCYP2C19Gene in the Stanislas Cohort. A link with Inflammation. Annals of Human Genetics. 72(2). 178–183. 32 indexed citations

Felip, Enriqueta, Federico Rojo, Martin Reck, et al.. (2008). A Phase II Pharmacodynamic Study of Erlotinib in Patients with Advanced Non–Small Cell Lung Cancer Previously Treated with Platinum-Based Chemotherapy. Clinical Cancer Research. 14(12). 3867–3874. 68 indexed citations

Gambier, Nicolas, Jean‐Brice Marteau, Anne‐Marie Batt, et al.. (2006). Interaction between CYP1A1 T3801C and AHR G1661A polymorphisms according to smoking status on blood pressure in the Stanislas cohort. Journal of Hypertension. 24(11). 2199–2205. 20 indexed citations

Rojo, Federico, Dorothee Foernzler, Barbara Klughammer, et al.. (2005). Phase II pharmacodynamic trial of erlotinib in advanced non-small cell lung cancer (NSCLC) patients previously treated with platinum-based chemotherapy: preliminary results. Journal of Clinical Oncology. 23(16_suppl). 7100–7100. 1 indexed citations

Lumsden, Amanda L., Ulf P. Guenther, Dorothee Foernzler, et al.. (2005). Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations inABCC6. Human Mutation. 26(3). 235–248. 75 indexed citations

Gatzemeier, U., Dorothee Foernzler, Joachim Moecks, et al.. (2005). Exploratory analyses EGFR, kRAS mutations and other molecular markers in tumors of NSCLC patients (pts) treated with chemotherapy +/- erlotinib (TALENT). Journal of Clinical Oncology. 23(16_suppl). 7028–7028. 39 indexed citations

Felip, Enriqueta, Federico Rojo, Dorothee Foernzler, et al.. (2005). P-949 Phase II pharmacodynamic trial of erlotinib in advancednon-small cell lung cancer (NSCLC) patients previously treated with platinum-based chemotherapy. Lung Cancer. 49. S369–S369. 1 indexed citations

10.

Reck, Martin, Dorothee Foernzler, Joachim Moecks, et al.. (2005). PD-155 Molecular markers such as EGFR and kRAS mutations aspredictors of sensitivity to erlotinib in patients (pts) with NSCLC: Exploratory subanalyses of TALENT, a phase III trial. Lung Cancer. 49. S112–S112. 2 indexed citations

11.

Liao, Guochun, Jianmei Wang, John Allard, et al.. (2004). In Silico Genetics: Identification of a Functional Element Regulating H2 - E α Gene Expression. Science. 306(5696). 690–695. 89 indexed citations

12.

Foernzler, Dorothee, Stacie K. Loftus, Shanming Liu, et al.. (2003). A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation. Development. 130(19). 4665–4672. 63 indexed citations

13.

Balemans, Wendy, Dorothee Foernzler, Martin Ebeling, et al.. (2002). Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms. Bone. 31(4). 515–519. 35 indexed citations

14.

Acuña, Gonzalo, Dorothee Foernzler, Diane U. Leong, et al.. (2002). Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity. The Pharmacogenomics Journal. 2(5). 327–334. 57 indexed citations

15.

Lehnert, Valerie, et al.. (2001). A semi-automated system for analysis and storage of SNPs. Human Mutation. 17(4). 243–254. 6 indexed citations

16.

Heinimann, Karl, Annick Thompson, Rémy Meier, et al.. (2001). Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis. PubMed. 61(20). 7616–22. 42 indexed citations

17.

Marks, Peter, et al.. (1999). The spontaneous coat color mutant white nose ( wn ) maps to murine Chromosome 15. Mammalian Genome. 10(7). 750–752. 2 indexed citations

18.

Davidson, Alan J., John H. Postlethwait, Yi‐Lin Yan, et al.. (1999). Isolation of Zebrafish gdf7 and Comparative Genetic Mapping of Genes Belonging to the Growth/Differentiation Factor 5, 6, 7 Subgroup of the TGF-β Superfamily. Genome Research. 9(2). 121–129. 25 indexed citations

19.

Foernzler, Dorothee & David R. Beier. (1998). Chapter 11 Gene Mapping in Zebrafish Using Single-Strand Conformation Polymorphism Analysis. Methods in cell biology. 60. 185–193. 3 indexed citations

20.

Fleming, Mark D., Cameron C. Trenor, Maureen A. Su, et al.. (1997). Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nature Genetics. 16(4). 383–386. 975 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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