Zoya Shapovalova

1.6k total citations
20 papers, 843 citations indexed

About

Zoya Shapovalova is a scholar working on Molecular Biology, Hematology and Immunology. According to data from OpenAlex, Zoya Shapovalova has authored 20 papers receiving a total of 843 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Hematology and 3 papers in Immunology. Recurrent topics in Zoya Shapovalova's work include Pluripotent Stem Cells Research (10 papers), CRISPR and Genetic Engineering (9 papers) and Acute Myeloid Leukemia Research (5 papers). Zoya Shapovalova is often cited by papers focused on Pluripotent Stem Cells Research (10 papers), CRISPR and Genetic Engineering (9 papers) and Acute Myeloid Leukemia Research (5 papers). Zoya Shapovalova collaborates with scholars based in Canada, United States and Australia. Zoya Shapovalova's co-authors include Mickie Bhatia, Allison L. Boyd, Tony Collins, Anargyros Xenocostas, Borko Tanasijevic, Ryan R. Mitchell, Lili Aslostovar, Yannick D. Benoit, Jennifer Reid and Brian Leber and has published in prestigious journals such as Cell, Nature Communications and Nature Cell Biology.

In The Last Decade

Zoya Shapovalova

20 papers receiving 835 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zoya Shapovalova Canada 15 526 299 122 113 99 20 843
Danny A. Stark United States 11 482 0.9× 276 0.9× 127 1.0× 174 1.5× 98 1.0× 16 890
Knut Niß United States 10 362 0.7× 266 0.9× 86 0.7× 214 1.9× 80 0.8× 11 756
Shoichiro Takeishi Japan 12 534 1.0× 275 0.9× 125 1.0× 124 1.1× 298 3.0× 16 940
Eva Vertes United States 5 290 0.6× 322 1.1× 202 1.7× 157 1.4× 216 2.2× 6 813
Steven J. Staats United States 6 465 0.9× 251 0.8× 128 1.0× 76 0.7× 59 0.6× 7 822
Vionnie W.C. Yu United States 13 571 1.1× 419 1.4× 308 2.5× 120 1.1× 161 1.6× 22 1.0k
Deidre Daria United States 10 392 0.7× 424 1.4× 304 2.5× 134 1.2× 124 1.3× 14 859
Elisa Tomellini Canada 10 336 0.6× 196 0.7× 132 1.1× 105 0.9× 111 1.1× 13 629
Michael D. Bettess Australia 8 883 1.7× 253 0.8× 159 1.3× 120 1.1× 202 2.0× 8 1.2k
Patricia Sousa United States 10 507 1.0× 163 0.5× 138 1.1× 69 0.6× 77 0.8× 22 721

Countries citing papers authored by Zoya Shapovalova

Since Specialization
Citations

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

Fields of papers citing papers by Zoya Shapovalova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zoya Shapovalova

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

All Works

20 of 20 papers shown
1.
Orlando, Luca, Borko Tanasijevic, Mio Nakanishi, et al.. (2021). Phosphorylation state of the histone variant H2A.X controls human stem and progenitor cell fate decisions. Cell Reports. 34(10). 108818–108818. 14 indexed citations
2.
Nakanishi, Mio, Ryan R. Mitchell, Yannick D. Benoit, et al.. (2019). Human Pluripotency Is Initiated and Preserved by a Unique Subset of Founder Cells. Cell. 177(4). 910–924.e22. 35 indexed citations
3.
Boyd, Allison L., Lili Aslostovar, Jennifer Reid, et al.. (2018). Identification of Chemotherapy-Induced Leukemic-Regenerating Cells Reveals a Transient Vulnerability of Human AML Recurrence. Cancer Cell. 34(3). 483–498.e5. 111 indexed citations
4.
Boyd, Allison L., Jennifer Reid, Lili Aslostovar, et al.. (2017). Acute myeloid leukaemia disrupts endogenous myelo-erythropoiesis by compromising the adipocyte bone marrow niche. Nature Cell Biology. 19(11). 1336–1347. 156 indexed citations
5.
Lee, Jong‐Hee, Tony Collins, Zoya Shapovalova, et al.. (2017). Lineage-Specific Differentiation Is Influenced by State of Human Pluripotency. Cell Reports. 19(1). 20–35. 44 indexed citations
6.
Benoit, Yannick D., Ryan R. Mitchell, Ruth M. Risueño, et al.. (2017). Sam68 Allows Selective Targeting of Human Cancer Stem Cells. Cell chemical biology. 24(7). 833–844.e9. 43 indexed citations
7.
Lee, Jong‐Hee, Jennifer Reid, Luca Orlando, et al.. (2017). Brief Report: Human Acute Myeloid Leukemia Reprogramming to Pluripotency Is a Rare Event and Selects for Patient Hematopoietic Cells Devoid of Leukemic Mutations. Stem Cells. 35(9). 2095–2102. 20 indexed citations
8.
Guezguez, Borhane, Yannick D. Benoit, Zoya Shapovalova, et al.. (2016). GSK3 Deficiencies in Hematopoietic Stem Cells Initiate Pre-neoplastic State that Is Predictive of Clinical Outcomes of Human Acute Leukemia. Cancer Cell. 29(1). 61–74. 51 indexed citations
9.
Lee, Jung Bok, Ryan R. Mitchell, Luca Orlando, et al.. (2015). Acquisition of pluripotency through continued environmental influence on OCT4-induced plastic human fibroblasts. Stem Cell Research. 15(1). 221–230. 5 indexed citations
10.
Lee, Jung Bok, Ryan R. Mitchell, Luca Orlando, et al.. (2015). Derivation of human induced pluripotent stem cells through continued exposure of OCT4-induced plastic human fibroblasts to reprogramming media. Stem Cell Research. 15(1). 240–242. 1 indexed citations
11.
Lee, Jung Bok, Monica Graham, Tony Collins, et al.. (2015). Reversible Lineage-Specific Priming of Human Embryonic Stem Cells Can Be Exploited to Optimize the Yield of Differentiated Cells. Stem Cells. 33(4). 1142–1152. 10 indexed citations
12.
Lee, Jong‐Hee, Ryan R. Mitchell, Jamie McNicol, et al.. (2015). Single Transcription Factor Conversion of Human Blood Fate to NPCs with CNS and PNS Developmental Capacity. Cell Reports. 11(9). 1367–1376. 65 indexed citations
13.
14.
McIntyre, Brendan A.S., et al.. (2014). Innate immune response of human pluripotent stem cell-derived airway epithelium. Innate Immunity. 21(5). 504–511. 1 indexed citations
15.
Mitchell, Ryan R., Éva Szabó, Zoya Shapovalova, et al.. (2014). Molecular Evidence for OCT4-Induced Plasticity in Adult Human Fibroblasts Required for Direct Cell Fate Conversion to Lineage Specific Progenitors. Stem Cells. 32(8). 2178–2187. 40 indexed citations
16.
Lee, Jong‐Hee, Jung Bok Lee, Zoya Shapovalova, et al.. (2014). Somatic transcriptome priming gates lineage-specific differentiation potential of human-induced pluripotent stem cell states. Nature Communications. 5(1). 5605–5605. 41 indexed citations
17.
Boyd, Allison L., et al.. (2013). Nonhematopoietic cells represent a more rational target of in vivo hedgehog signaling affecting normal or acute myeloid leukemia progenitors. Experimental Hematology. 41(10). 858–869.e4. 19 indexed citations
18.
Guezguez, Borhane, Clinton J.V. Campbell, Allison L. Boyd, et al.. (2013). Regional Localization within the Bone Marrow Influences the Functional Capacity of Human HSCs. Cell stem cell. 13(2). 175–189. 92 indexed citations
19.
Chun, Justin, Zoya Shapovalova, Selma Y. Dejgaard, John F. Presley, & Paul Melançon. (2008). Characterization of Class I and II ADP-Ribosylation Factors (Arfs) in Live Cells: GDP-bound Class II Arfs Associate with the ER-Golgi Intermediate Compartment Independently of GBF1. Molecular Biology of the Cell. 19(8). 3488–3500. 73 indexed citations
20.
Shapovalova, Zoya, et al.. (2007). The Fer tyrosine kinase regulates an axon retraction response to Semaphorin 3A in dorsal root ganglion neurons. BMC Developmental Biology. 7(1). 133–133. 21 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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