David B. Sykes

6.7k total citations · 1 hit paper
118 papers, 3.5k citations indexed

About

David B. Sykes is a scholar working on Molecular Biology, Immunology and Hematology. According to data from OpenAlex, David B. Sykes has authored 118 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 35 papers in Immunology and 28 papers in Hematology. Recurrent topics in David B. Sykes's work include Acute Myeloid Leukemia Research (17 papers), Biochemical and Molecular Research (14 papers) and Immune cells in cancer (14 papers). David B. Sykes is often cited by papers focused on Acute Myeloid Leukemia Research (17 papers), Biochemical and Molecular Research (14 papers) and Immune cells in cancer (14 papers). David B. Sykes collaborates with scholars based in United States, Sweden and Germany. David B. Sykes's co-authors include Mark P. Kamps, Martina P. Pasillas, Katherine R. Calvo, David T. Scadden, Gang Greg Wang, Hans Häcker, Christopher K. Glass, Borja Sáez, Youmna Kfoury and Laure Escoubet‐Lozach and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

David B. Sykes

110 papers receiving 3.4k 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.

Dissecting the immune suppressive human prostate tumor microenvironment via integrated single-cell and spatial transcriptomic analyses

2023 126 citations Taghreed Hirz, Shenglin Mei et al. Nature Communications profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David B. Sykes United States	30	1.7k	1.1k	649	599	467	118	3.5k
Takeshi Kondo Japan	30	1.7k 1.0×	1.1k 1.0×	1.0k 1.6×	706 1.2×	327 0.7×	168	3.9k
William F. C. Rigby United States	39	1.9k 1.1×	1.5k 1.4×	577 0.9×	872 1.5×	351 0.8×	102	5.2k
Ryuta Nishikomori Japan	34	1.7k 1.0×	2.2k 2.0×	438 0.7×	491 0.8×	298 0.6×	148	4.0k
Claudia Wickenhauser Germany	37	1.4k 0.8×	1.1k 1.0×	1.1k 1.7×	588 1.0×	649 1.4×	199	4.3k
Masaki Inoue Japan	33	1.1k 0.6×	1.1k 1.0×	768 1.2×	463 0.8×	368 0.8×	93	3.2k
Nobutaka Kiyokawa Japan	35	1.7k 1.0×	794 0.7×	628 1.0×	663 1.1×	191 0.4×	186	4.0k
Adalberto Benito Spain	19	1.3k 0.7×	1.2k 1.1×	553 0.9×	738 1.2×	415 0.9×	37	3.3k
Robert M. Verdijk Netherlands	36	1.2k 0.7×	1.4k 1.3×	1.0k 1.6×	321 0.5×	248 0.5×	194	4.7k
Harald Burkhardt Germany	38	1.0k 0.6×	1.8k 1.6×	620 1.0×	487 0.8×	346 0.7×	160	4.7k
Reinhold Munker United States	31	1.4k 0.8×	1.1k 1.0×	767 1.2×	1.2k 1.9×	599 1.3×	119	3.7k

Countries citing papers authored by David B. Sykes

Since Specialization

Citations

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

Fields of papers citing papers by David B. Sykes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David B. Sykes. 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 David B. Sykes. The network helps show where David B. Sykes may publish in the future.

Co-authorship network of co-authors of David B. Sykes

This figure shows the co-authorship network connecting the top 25 collaborators of David B. Sykes. A scholar is included among the top collaborators of David B. Sykes 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 David B. Sykes. David B. Sykes 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

Kumar, Roshan, David B. Sykes, Victor I. Band, et al.. (2025). Gut sulfide metabolism modulates behavior and brain bioenergetics. Proceedings of the National Academy of Sciences. 122(25). e2503677122–e2503677122. 2 indexed citations

He, Lingli, Ting Zhao, Wei Zhong Leong, et al.. (2024). AML Stem Cell Clearance By Inhibiting Selenoprotein Biosynthesis That Causes Cgas-Sting Activation and Ferroptosis. Blood. 144(Supplement 1). 1354–1354. 1 indexed citations

Zhang, Manqi, et al.. (2023). Regulation of EZH2 Expression by INPP4B in Normal Prostate and Primary Prostate Cancer. Cancers. 15(22). 5418–5418. 1 indexed citations

Rhee, Catherine, Elizabeth W. Scadden, Lai Ping Wong, et al.. (2023). Limited plasticity of monocyte fate and function associated with epigenetic scripting at the level of progenitors. Blood. 142(7). 658–674. 5 indexed citations

Leković, Danijela, et al.. (2023). Comprehensive Next-Generation Sequencing Testing in a Patient with TEMPI Syndrome. Laboratory Medicine. 54(5). 546–549.

Kfoury, Youmna, Fei Ji, Esha Jain, et al.. (2023). The bone marrow stroma in human myelodysplastic syndrome reveals alterations that regulate disease progression. Blood Advances. 7(21). 6608–6623. 7 indexed citations

Sykes, David B., Nithin Gupta, C. Rory Goodwin, et al.. (2023). How dimensions can guide surgical planning and training: a systematic review of Kambin’s triangle. Neurosurgical FOCUS. 54(1). E6–E6. 3 indexed citations

Milosevic, Jelena, Abirami Kugadas, Xiaoxiao Lu, et al.. (2023). Prenylcysteine oxidase 1 like protein is required for neutrophil bactericidal activities. Nature Communications. 14(1). 2761–2761. 9 indexed citations

Chaudagar, Kiranj, Shenglin Mei, Taghreed Hirz, et al.. (2023). 1537 Androgen blockade primes NLRP3 inflammasome in macrophages to induce tumor cell phagocytosis. SHILAP Revista de lepidopterología. A1760–A1762. 1 indexed citations

10.

Olsen, Thale Kristin, Cecilia Dyberg, Jelena Milosevic, et al.. (2022). DHODH is an independent prognostic marker and potent therapeutic target in neuroblastoma. JCI Insight. 7(17). 21 indexed citations

11.

Kfoury, Youmna, Ninib Baryawno, Nicolas Sévère, et al.. (2021). Human prostate cancer bone metastases have an actionable immunosuppressive microenvironment. Cancer Cell. 39(11). 1464–1478.e8. 148 indexed citations

12.

Cabal‐Hierro, Lucía, Peter van Galen, Miguel A. Prado, et al.. (2020). Chromatin accessibility promotes hematopoietic and leukemia stem cell activity. Nature Communications. 11(1). 1406–1406. 39 indexed citations

13.

Ameri, Amir H., Brian R. Curtis, & David B. Sykes. (2019). Immune neutropenia mediated by micafungin. American Journal of Hematology. 94(7). 830–832. 2 indexed citations

14.

Fites, J. Scott, John F. Kernien, Zeina Dagher, et al.. (2018). An unappreciated role for neutrophil-DC hybrids in immunity to invasive fungal infections. PLoS Pathogens. 14(5). e1007073–e1007073. 47 indexed citations

15.

Kalaitzidis, Demetrios, Dongjun Lee, Alejo Efeyan, et al.. (2017). Amino acid–insensitive mTORC1 regulation enables nutritional stress resilience in hematopoietic stem cells. Journal of Clinical Investigation. 127(4). 1405–1413. 24 indexed citations

16.

Mercier, François, Jiantao Shi, David B. Sykes, et al.. (2017). A Genome-Wide, In Vivo, Dropout CRISPR Screen in Acute Myeloid Leukemia Identifies an Essential Role for Beta-Galactosylation in Leukemic Cell Homing. Blood. 130. 2493–2493. 2 indexed citations

17.

Hahm, Eunsil, Changli Wei, Isabel Cuesta Fernández, et al.. (2016). Bone marrow-derived immature myeloid cells are a main source of circulating suPAR contributing to proteinuric kidney disease. Nature Medicine. 23(1). 100–106. 101 indexed citations

18.

Yoon, Kyoung Wan, Sanguine Byun, Eun‐Jeong Kwon, et al.. (2015). Control of signaling-mediated clearance of apoptotic cells by the tumor suppressor p53. Science. 349(6247). 1261669–1261669. 174 indexed citations

19.

Sykes, David B., et al.. (2015). Hormones and the Bone Marrow: Panhypopituitarism and Pancytopenia in a Man with a Pituitary Adenoma. Journal of General Internal Medicine. 30(5). 692–696. 8 indexed citations

20.

Mansour, Michael K., Jenny M. Tam, Nida S. Khan, et al.. (2013). Dectin-1 Activation Controls Maturation of β-1,3-Glucan-containing Phagosomes. Journal of Biological Chemistry. 288(22). 16043–16054. 61 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.

Explore authors with similar magnitude of impact