Rolf Koehler

4.8k total citations
26 papers, 1.1k citations indexed

About

Rolf Koehler is a scholar working on Public Health, Environmental and Occupational Health, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rolf Koehler has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Public Health, Environmental and Occupational Health, 11 papers in Hematology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rolf Koehler's work include Acute Lymphoblastic Leukemia research (19 papers), Acute Myeloid Leukemia Research (6 papers) and Childhood Cancer Survivors' Quality of Life (6 papers). Rolf Koehler is often cited by papers focused on Acute Lymphoblastic Leukemia research (19 papers), Acute Myeloid Leukemia Research (6 papers) and Childhood Cancer Survivors' Quality of Life (6 papers). Rolf Koehler collaborates with scholars based in Germany, United States and Austria. Rolf Koehler's co-authors include Martin Stanulla, Claus R. Bartram, Martin Schrappe, M Zimmermann, André Schrauder, Bart Janssen, Jochen Harbott, Kari Hemminki, Obul Reddy Bandapalli and Andreas E. Kulozik and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Journal of the American College of Cardiology.

In The Last Decade

Rolf Koehler

25 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rolf Koehler Germany	16	699	523	315	277	216	26	1.1k
ER van Wering Netherlands	12	649 0.9×	719 1.4×	238 0.8×	317 1.1×	47 0.2×	16	1.1k
JR Downing United States	9	434 0.6×	534 1.0×	102 0.3×	331 1.2×	133 0.6×	9	823
Pearl Leavitt United States	10	534 0.8×	561 1.1×	251 0.8×	268 1.0×	50 0.2×	13	1.1k
Phillip Barnette United States	11	254 0.4×	178 0.3×	119 0.4×	189 0.7×	146 0.7×	26	672
Marı́a Sara Felice Argentina	15	497 0.7×	401 0.8×	238 0.8×	140 0.5×	36 0.2×	46	736
Marry van den Heuvel‐Eibrink Netherlands	13	151 0.2×	257 0.5×	243 0.8×	618 2.2×	225 1.0×	32	956
S Richards United Kingdom	14	498 0.7×	305 0.6×	316 1.0×	111 0.4×	62 0.3×	20	828
Markéta Kalinová Czechia	13	296 0.4×	232 0.4×	86 0.3×	300 1.1×	71 0.3×	38	581
TJ Vietti United States	12	673 1.0×	546 1.0×	184 0.6×	168 0.6×	38 0.2×	20	853
SE Sallan United States	10	483 0.7×	377 0.7×	240 0.8×	93 0.3×	47 0.2×	17	753

Countries citing papers authored by Rolf Koehler

Since Specialization

Citations

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

Fields of papers citing papers by Rolf Koehler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rolf Koehler

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

Hinze, Laura, Stefanie V. Junk, Norman W. Klein, et al.. (2017). Genome-Wide Association Study (GWAS) of High-Risk Minimal Residual Disease and Relapse in B-Cell Acute Lymphoblastic Leukemia on Trial AIEOP-BFM ALL 2000. Blood. 130. 3981–3981. 1 indexed citations

Zuna, Jan, Anja Moericke, Rolf Koehler, et al.. (2016). Implications of delayed bone marrow aspirations at the end of treatment induction for risk stratification and outcome in children with acute lymphoblastic leukaemia. British Journal of Haematology. 173(5). 742–748. 3 indexed citations

Dalgaard, Marlene, Rachita Yadav, K Rasmussen, et al.. (2014). Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients. Leukemia. 29(2). 297–303. 14 indexed citations

Bandapalli, Obul Reddy, Markus Zimmermann, M. Stanulla, et al.. (2013). NOTCH1 activation clinically antagonizes the unfavorable effect of PTEN inactivation in BFM-treated children with precursor T-cell acute lymphoblastic leukemia. Haematologica. 98(6). 928–936. 51 indexed citations

Dörge, Petra, Barbara Meissner, M Zimmermann, et al.. (2012). IKZF1 deletion is an independent predictor of outcome in pediatric acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocol. Haematologica. 98(3). 428–432. 102 indexed citations

Eckert, Cornelia, T Flohr, Rolf Koehler, et al.. (2011). Very early/early relapses of acute lymphoblastic leukemia show unexpected changes of clonal markers and high heterogeneity in response to initial and relapse treatment. Leukemia. 25(8). 1305–1313. 22 indexed citations

Zimmermann, Martin, Anja Möricke, Barbara Meissner, et al.. (2011). Low platelet counts after induction therapy for childhood acute lymphoblastic leukemia are strongly associated with poor early response to treatment as measured by minimal residual disease and are prognostic for treatment outcome. Haematologica. 97(3). 402–409. 22 indexed citations

Kox, Corinne, M Zimmermann, Martin Stanulla, et al.. (2010). The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL–BFM 2000 protocol can be separated from FBXW7 loss of function. Leukemia. 24(12). 2005–2013. 95 indexed citations

Prasad, Rashmi B., Fay J. Hosking, Jayaram Vijayakrishnan, et al.. (2009). Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood. Blood. 115(9). 1765–1767. 91 indexed citations

10.

Kox, Corinne, Martin Zimmermann, Martin Stanulla, et al.. (2009). The Favorable Effect of Activating NOTCH1 Receptor Mutations On Long Term Outcome in T-ALL Is Treatment Related and Can Be Separated From NOTCH Pathway Activation by FBXW7 Loss of Function.. Blood. 114(22). 908–908. 2 indexed citations

11.

Flohr, T, André Schrauder, Giovanni Cazzaniga, et al.. (2008). Minimal residual disease-directed risk stratification using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the international multicenter trial AIEOP-BFM ALL 2000 for childhood acute lymphoblastic leukemia. Leukemia. 22(4). 771–782. 247 indexed citations

12.

Kawamata, Norihiko, Seishi Ogawa, Martin Zimmermann, et al.. (2007). Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high resolution single nucleotide polymorphism oligonucleotide microarray.. Cancer Research. 67. 389–389. 4 indexed citations

13.

Kawamata, Norihiko, Seishi Ogawa, Martin Zimmermann, et al.. (2007). Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood. 111(2). 776–784. 160 indexed citations

14.

Machado, Rajiv D., Rolf Koehler, Eric W. Glissmeyer, et al.. (2006). Genetic Association of the Serotonin Transporter in Pulmonary Arterial Hypertension. American Journal of Respiratory and Critical Care Medicine. 173(7). 793–797. 62 indexed citations

15.

Koehler, Rolf, Horst Olschewski, Marius M. Hoeper, Bart Janssen, & Ekkehard Grünig. (2005). Serotonin Transporter Gene Polymorphism in a Cohort of German Patients With Idiopathic Pulmonary Arterial Hypertension or Chronic Thromboembolic Pulmonary Hypertension. CHEST Journal. 128(6). 619S–619S. 15 indexed citations

16.

Grünig, Ekkehard, Christoph Dehnert, Derliz Mereles, et al.. (2005). Enhanced Hypoxic Pulmonary Vasoconstriction in Families of Adults or Children With Idiopathic Pulmonary Arterial Hypertension. CHEST Journal. 128(6). 630S–633S. 20 indexed citations

17.

Hofmann, Wera, Rolf Koehler, Bart Janssen, et al.. (2004). LargeBRCA1 gene deletions are found in 3% of German high-risk breast cancer families. Human Mutation. 24(6). 534–534. 69 indexed citations

18.

Koehler, Rolf, et al.. (2004). Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension. Journal of Medical Genetics. 41(12). e127–e127. 58 indexed citations

19.

Grünig, Ekkehard, Rolf Koehler, Gábriel Miltenberger-Miltényi, et al.. (2004). Primary Pulmonary Hypertension in Children May Have a Different Genetic Background Than in Adults. Pediatric Research. 56(4). 571–578. 34 indexed citations

20.

Grünig, Ekkehard, Rolf Koehler, Gábriel Miltenberger-Miltényi, et al.. (2003). Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31. Journal of the American College of Cardiology. 41(12). 2237–2244. 19 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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