Stephen Arnovitz

3.6k total citations
17 papers, 343 citations indexed

About

Stephen Arnovitz is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Stephen Arnovitz has authored 17 papers receiving a total of 343 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Hematology and 5 papers in Genetics. Recurrent topics in Stephen Arnovitz's work include Acute Myeloid Leukemia Research (7 papers), Epigenetics and DNA Methylation (4 papers) and DNA Repair Mechanisms (3 papers). Stephen Arnovitz is often cited by papers focused on Acute Myeloid Leukemia Research (7 papers), Epigenetics and DNA Methylation (4 papers) and DNA Repair Mechanisms (3 papers). Stephen Arnovitz collaborates with scholars based in United States, China and Australia. Stephen Arnovitz's co-authors include Zejuan Li, Jianjun Chen, Akinola Olumide Emmanuel, Fotini Gounari, Priya Mathur, Jasmin Quandt, Khashayarsha Khazaie, Chuan He, Mary Beth Neilly and Marei Dose and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Nature Immunology.

In The Last Decade

Stephen Arnovitz

14 papers receiving 343 citations

Peers

Stephen Arnovitz

IMMUN

GENET

ONCOL

HEMAT

Giorgia Montano Sweden

Višnja Radulović Sweden

Sabine Jurado Australia

Tamara C. Pereboom Netherlands

Roberto Tirado-Magallanes Singapore

Himalee S. Sabnis United States

Katharine Hodby United Kingdom

Maud Bizot France

Alix Rousseau France

Candace J. Poole United States

Giorgia Montano Sweden

Stephen Arnovitz

319 ×1.4

78 ×0.9

IMMUN

45 ×0.7

GENET

49 ×0.9

ONCOL

35 ×0.8

HEMAT

Citations per year, relative to Stephen Arnovitz Stephen Arnovitz (= 1×) peers Giorgia Montano

Countries citing papers authored by Stephen Arnovitz

Since Specialization

Citations

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

Fields of papers citing papers by Stephen Arnovitz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephen Arnovitz

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

All Works

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17 of 17 papers shown

Puppala, Anupama K., Maureen Regan, Georgina Mancinelli, et al.. (2025). Programmable multistep CRISPR gene activation via control of RNA polymerase III termination. Science Advances. 11(49). eadt1532–eadt1532.

Stubbins, Ryan J., Stephen Arnovitz, Imo J. Akpan, et al.. (2025). Predisposition to hematopoietic malignancies by deleterious germline CHEK2 variants. Leukemia. 39(7). 1702–1713.

Emmanuel, Akinola Olumide, et al.. (2024). Stabilization of β-Catenin Directs HEB to Limit Thymic Selection. The Journal of Immunology. 213(5). 641–650.

Arnovitz, Stephen, Priya Mathur, Jasmin Quandt, et al.. (2022). Tcf-1 promotes genomic instability and T cell transformation in response to aberrant β-catenin activation. Proceedings of the National Academy of Sciences. 119(32). e2201493119–e2201493119. 8 indexed citations

Quandt, Jasmin, Stephen Arnovitz, Priya Mathur, et al.. (2021). Wnt–β-catenin activation epigenetically reprograms Treg cells in inflammatory bowel disease and dysplastic progression. Nature Immunology. 22(4). 471–484. 69 indexed citations

Jiang, Xi, Gang Greg Wang, Stephen Arnovitz, et al.. (2020). PBX3 and MEIS1 Cooperate in Hematopoietic Cells to Drive Acute Myeloid Leukemias Characterized by a Core Transcriptome of the MLL-Rearranged Disease. UNC Libraries. 3 indexed citations

Emmanuel, Akinola Olumide, Stephen Arnovitz, Priya Mathur, et al.. (2018). TCF-1 and HEB cooperate to establish the epigenetic and transcription profiles of CD4+CD8+ thymocytes. Nature Immunology. 19(12). 1366–1378. 46 indexed citations

Li, Zejuan, Ping Chen, Rui Su, et al.. (2016). PBX3 and MEIS1 Cooperate in Hematopoietic Cells to Drive Acute Myeloid Leukemias Characterized by a Core Transcriptome of the MLL -Rearranged Disease. Cancer Research. 76(3). 619–629. 48 indexed citations

Huang, Hao, Xi Jiang, Jinhua Wang, et al.. (2016). Identification of MLL-fusion/MYC⊣miR-26⊣TET1 signaling circuit in MLL-rearranged leukemia. Cancer Letters. 372(2). 157–165. 23 indexed citations

10.

Li, Zejuan, Lucia Guidugli, Amy Knight Johnson, et al.. (2015). A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings. Journal of Human Genetics. 60(7). 363–369. 27 indexed citations

11.

Moen, Erika L., Stephen Arnovitz, Xu Zhang, et al.. (2015). Characterization of CpG sites that escape methylation on the inactive human X-chromosome. Epigenetics. 10(9). 810–818. 7 indexed citations

12.

Vasanthakumar, Aparna, Stephen Arnovitz, Rafael Márquez, et al.. (2015). Brca1 deficiency causes bone marrow failure and spontaneous hematologic malignancies in mice. Blood. 127(3). 310–313. 38 indexed citations

13.

Vasanthakumar, Aparna, Stephen Arnovitz, Rafael Márquez, et al.. (2015). Brca1 Deficiency Causes Bone Marrow Failure and Spontaneous Hematologic Malignancies in Mice. Blood. 126(23). 295–295. 3 indexed citations

14.

Zhao, Lei, Ming-an Sun, Zejuan Li, et al.. (2014). The dynamics of DNA methylation fidelity during mouse embryonic stem cell self-renewal and differentiation. Genome Research. 24(8). 1296–1307. 60 indexed citations

15.

Huang, Hao, Xi Jiang, Jinhua Wang, et al.. (2014). Identification of MLL-Fusion/Myc⊣miR-26a/Mir-29a⊣Tet1 Signaling Circuit in MLL-Rearranged Leukemia. Blood. 124(21). 1011–1011. 2 indexed citations

16.

He, Miao, Ping Chen, Stephen Arnovitz, et al.. (2012). Two isoforms of HOXA9 function differently but work synergistically in human MLL-rearranged leukemia. Blood Cells Molecules and Diseases. 49(2). 102–106. 8 indexed citations

17.

Price, Colles, Zejuan Li, Yuanyuan Li, et al.. (2011). MLL-Rearrangements Result in Upregulation of Mir-9 and Subsequent Inhibition of the Tumor Suppressor TGFBI. Blood. 118(21). 2453–2453. 1 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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