Christopher C. Oakes

5.7k total citations
67 papers, 2.5k citations indexed

About

Christopher C. Oakes is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Christopher C. Oakes has authored 67 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 26 papers in Genetics and 21 papers in Immunology. Recurrent topics in Christopher C. Oakes's work include Chronic Lymphocytic Leukemia Research (25 papers), Epigenetics and DNA Methylation (20 papers) and Lymphoma Diagnosis and Treatment (16 papers). Christopher C. Oakes is often cited by papers focused on Chronic Lymphocytic Leukemia Research (25 papers), Epigenetics and DNA Methylation (20 papers) and Lymphoma Diagnosis and Treatment (16 papers). Christopher C. Oakes collaborates with scholars based in United States, Germany and Canada. Christopher C. Oakes's co-authors include Jacquetta M. Trasler, Bernard Robaire, Christoph Plass, Sophie La Salle, Dominic J. Smiraglia, John C. Byrd, Guido Marcucci, Rainer Claus, William Blum and Thorsten Zenz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Christopher C. Oakes

64 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christopher C. Oakes United States	27	1.7k	698	410	344	309	67	2.5k
Genta Nagae Japan	24	2.6k 1.5×	503 0.7×	225 0.5×	386 1.1×	183 0.6×	48	3.4k
Aliza Amiel Israel	27	814 0.5×	236 0.3×	306 0.7×	613 1.8×	258 0.8×	159	2.6k
Lucio H. Castilla United States	23	2.2k 1.3×	311 0.4×	790 1.9×	651 1.9×	383 1.2×	46	3.2k
Marcos R. Estecio United States	34	3.0k 1.7×	596 0.9×	231 0.6×	425 1.2×	464 1.5×	76	4.0k
Tomáš Stopka Czechia	28	1.6k 0.9×	560 0.8×	413 1.0×	210 0.6×	296 1.0×	78	2.5k
Nianxiang Zhang United States	25	1.6k 0.9×	328 0.5×	121 0.3×	176 0.5×	155 0.5×	47	2.1k
Thomas Mikeska Australia	22	2.0k 1.2×	543 0.8×	195 0.5×	443 1.3×	314 1.0×	45	2.7k
François Gaudet United States	16	3.5k 2.0×	468 0.7×	105 0.3×	708 2.1×	280 0.9×	23	4.1k
Luke B. Hesson Australia	29	2.4k 1.4×	494 0.7×	105 0.3×	284 0.8×	173 0.6×	66	3.0k
Sridhar Rao United States	27	2.5k 1.5×	341 0.5×	142 0.3×	372 1.1×	606 2.0×	89	3.5k

Countries citing papers authored by Christopher C. Oakes

Since Specialization

Citations

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

Fields of papers citing papers by Christopher C. Oakes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher C. Oakes. 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 Christopher C. Oakes. The network helps show where Christopher C. Oakes may publish in the future.

Co-authorship network of co-authors of Christopher C. Oakes

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher C. Oakes. A scholar is included among the top collaborators of Christopher C. Oakes 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 Christopher C. Oakes. Christopher C. Oakes 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

Giacopelli, Brian, Kari G. Rabe, Yue-Zhong Wu, et al.. (2024). Prediction of outcomes for high-count monoclonal B lymphocytosis using an epigenetic and immunogenetic signature. Blood. 143(17). 1752–1757. 2 indexed citations

Huber, Sandra, Franziska R. Traube, Marc Seifert, et al.. (2024). Analysis of 3760 hematologic malignancies reveals rare transcriptomic aberrations of driver genes. Genome Medicine. 16(1). 70–70. 1 indexed citations

Chapiro, Élise, Ferran Nadeu, Thorsten Zenz, et al.. (2024). Epigenetic features support the diagnosis of B-cell prolymphocytic leukemia and identify 2 clinicobiological subtypes. Blood Advances. 8(24). 6297–6307. 1 indexed citations

Kohlschmidt, Jessica, Krzysztof Mrózek, Deedra Nicolet, et al.. (2023). Association of social deprivation with survival in younger adult patients with AML: an Alliance study. Blood Advances. 7(15). 4019–4023. 5 indexed citations

Stiff, Andrew, et al.. (2023). Effects of epigenetic therapy on natural killer cell function and development in hematologic malignancy. Journal of Leukocyte Biology. 113(5). 518–524. 2 indexed citations

Mrózek, Krzysztof, Jessica Kohlschmidt, James S. Blachly, et al.. (2023). Outcome prediction by the 2022 European LeukemiaNet genetic-risk classification for adults with acute myeloid leukemia: an Alliance study. Leukemia. 37(4). 788–798. 31 indexed citations

Broughton, Megan, Karilyn Larkin, Christopher C. Oakes, et al.. (2023). Type 3 Innate Lymphoid Cells Promote Acute Myeloid Leukemia Immune Evasion and Expansion. Blood. 142(Supplement 1). 5390–5390.

Bhatnagar, Bhavana, Jessica Kohlschmidt, Shelley Orwick, et al.. (2023). Framework of clonal mutations concurrent with WT1 mutations in adults with acute myeloid leukemia: Alliance for Clinical Trials in Oncology study. Blood Advances. 7(16). 4671–4675. 1 indexed citations

Masle‐Farquhar, Etienne, Timothy J. Peters, Lisa A. Miosge, et al.. (2022). Uncontrolled CD21low age-associated and B1 B cell accumulation caused by failure of an EGR2/3 tolerance checkpoint. Cell Reports. 38(3). 110259–110259. 15 indexed citations

10.

Koenig, Michael J., Jacob M. Kaufman, Walter Wang, et al.. (2021). STK11/LKB1 Loss of Function Is Associated with Global DNA Hypomethylation and S -Adenosyl-Methionine Depletion in Human Lung Adenocarcinoma. Cancer Research. 81(16). 4194–4204. 10 indexed citations

11.

Roos‐Weil, Damien, Brian Giacopelli, Marine Armand, et al.. (2020). Identification of two DNA methylation subtypes of Waldenström's macroglobulinemia with plasma and memory B cell features. Blood. 136(5). 585–595. 6 indexed citations

12.

Herling, Carmen, Kevin R. Coombes, Axel Benner, et al.. (2019). Time-to-progression after front-line fludarabine, cyclophosphamide, and rituximab chemoimmunotherapy for chronic lymphocytic leukaemia: a retrospective, multicohort study. The Lancet Oncology. 20(11). 1576–1586. 15 indexed citations

13.

Eisfeld, Ann‐Kathrin, Jessica Kohlschmidt, Krzysztof Mrózek, et al.. (2016). Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality. Cancer Research. 77(1). 207–218. 16 indexed citations

14.

Hotz‐Wagenblatt, Agnes, Jennifer Hüllein, Leopold Sellner, et al.. (2015). p53-dependent non-coding RNA networks in chronic lymphocytic leukemia. Leukemia. 29(10). 2015–2023. 140 indexed citations

15.

Mleczko‐Sanecka, Katarzyna, Flavia D’Alessio, Anan Ragab, et al.. (2014). Unbiased RNAi screen for hepcidin regulators links hepcidin suppression to proliferative Ras/RAF and nutrient-dependent mTOR signaling. Blood. 123(10). 1574–1585. 59 indexed citations

16.

Arab, Khelifa, Yoon Jung Park, Anders M. Lindroth, et al.. (2014). Long Noncoding RNA TARID Directs Demethylation and Activation of the Tumor Suppressor TCF21 via GADD45A. Molecular Cell. 55(4). 604–614. 222 indexed citations

17.

Oakes, Christopher C., Rainer Claus, Lei Gu, et al.. (2013). Evolution of DNA Methylation Is Linked to Genetic Aberrations in Chronic Lymphocytic Leukemia. Cancer Discovery. 4(3). 348–361. 110 indexed citations

18.

Niles, Kirsten M., Donovan Chan, Sophie La Salle, Christopher C. Oakes, & Jacquetta M. Trasler. (2011). Critical Period of Nonpromoter DNA Methylation Acquisition during Prenatal Male Germ Cell Development. PLoS ONE. 6(9). e24156–e24156. 24 indexed citations

19.

Oakes, Christopher C., Sophie La Salle, Dominic J. Smiraglia, Bernard Robaire, & Jacquetta M. Trasler. (2007). Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells. Developmental Biology. 307(2). 368–379. 175 indexed citations

20.

Salle, Sophie La, et al.. (2007). Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L. BMC Developmental Biology. 7(1). 104–104. 73 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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