Michelle Moksa

5.5k total citations
35 papers, 734 citations indexed

About

Michelle Moksa is a scholar working on Molecular Biology, Hematology and Immunology. According to data from OpenAlex, Michelle Moksa has authored 35 papers receiving a total of 734 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 8 papers in Hematology and 7 papers in Immunology. Recurrent topics in Michelle Moksa's work include Epigenetics and DNA Methylation (9 papers), Single-cell and spatial transcriptomics (7 papers) and Acute Myeloid Leukemia Research (6 papers). Michelle Moksa is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), Single-cell and spatial transcriptomics (7 papers) and Acute Myeloid Leukemia Research (6 papers). Michelle Moksa collaborates with scholars based in Canada, United States and France. Michelle Moksa's co-authors include Martin Hirst, Connie J. Eaves, Samuel Aparício, Annaïck Carles, David J. H. F. Knapp, Misha Bilenky, Davide Pellacani, Nagarajan Kannan, Long Nguyen and Alireza Heravi‐Moussavi and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Michelle Moksa

33 papers receiving 730 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michelle Moksa Canada 16 518 194 166 83 69 35 734
Osama E. Demerdash United States 11 478 0.9× 134 0.7× 296 1.8× 39 0.5× 49 0.7× 15 754
Adnan Derti United States 16 1.1k 2.1× 183 0.9× 108 0.7× 117 1.4× 60 0.9× 20 1.3k
Bethan Lloyd‐Lewis United Kingdom 17 523 1.0× 108 0.6× 416 2.5× 79 1.0× 53 0.8× 26 953
Jean‐Pascal Capp France 16 531 1.0× 195 1.0× 212 1.3× 118 1.4× 35 0.5× 47 766
Luigi Grassi Italy 14 559 1.1× 237 1.2× 74 0.4× 104 1.3× 115 1.7× 41 859
Mario Cepeda Canada 10 356 0.7× 140 0.7× 99 0.6× 50 0.6× 20 0.3× 19 628
Stefanie Böhm Sweden 18 892 1.7× 98 0.5× 131 0.8× 92 1.1× 21 0.3× 31 1.0k
Jason A. Hanna United States 11 576 1.1× 223 1.1× 171 1.0× 47 0.6× 17 0.2× 19 829
Alka A. Potdar United States 14 480 0.9× 111 0.6× 74 0.4× 69 0.8× 31 0.4× 27 736
Luis M. Soares United States 12 1.3k 2.5× 112 0.6× 133 0.8× 90 1.1× 38 0.6× 12 1.5k

Countries citing papers authored by Michelle Moksa

Since Specialization
Citations

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

Fields of papers citing papers by Michelle Moksa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michelle Moksa

This figure shows the co-authorship network connecting the top 25 collaborators of Michelle Moksa. A scholar is included among the top collaborators of Michelle Moksa 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 Michelle Moksa. Michelle Moksa 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.
Lee, Joon S., Genny Trigo‐Gonzalez, Michelle Moksa, et al.. (2024). Genome-Wide CRISPR Screen Identifies KEAP1 Perturbation as a Vulnerability of ARID1A-Deficient Cells. Cancers. 16(17). 2949–2949. 1 indexed citations
2.
Hirst, Martin, Michelle Moksa, Annaïck Carles, et al.. (2024). tp53 R217H and R242H mutant zebrafish exhibit dysfunctional p53 hallmarks and recapitulate Li-Fraumeni syndrome phenotypes. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1871(3). 167612–167612. 1 indexed citations
3.
Jenkins, Catherine E., Qi Cao, Jasper Wong, et al.. (2023). RUNX1 colludes with NOTCH1 to reprogram chromatin in T cell acute lymphoblastic leukemia. iScience. 26(6). 106795–106795. 3 indexed citations
4.
Lorzadeh, Alireza, Colin A. Hammond, David J. H. F. Knapp, et al.. (2022). Polycomb contraction differentially regulates terminal human hematopoietic differentiation programs. BMC Biology. 20(1). 104–104. 5 indexed citations
5.
Rajan, Vinothkumar, Sergey V. Prykhozhij, Michelle Moksa, et al.. (2021). Stress hematopoiesis induces a proliferative advantage in TET2 deficiency. Leukemia. 36(3). 809–820. 2 indexed citations
6.
Carles, Annaïck, Genny Trigo‐Gonzalez, Qi Cao, et al.. (2020). The Pathognomonic FOXL2 C134W Mutation Alters DNA-Binding Specificity. Cancer Research. 80(17). 3480–3491. 19 indexed citations
7.
Pellacani, Davide, Naoto Nakamichi, Colin A. Hammond, et al.. (2020). MYC-induced human acute myeloid leukemia requires a continuing IL-3/GM-CSF costimulus. Blood. 136(24). 2764–2773. 18 indexed citations
8.
Souza, Camila P. E. de, Mirela Andronescu, Tehmina Masud, et al.. (2020). Epiclomal: Probabilistic clustering of sparse single-cell DNA methylation data. PLoS Computational Biology. 16(9). e1008270–e1008270. 15 indexed citations
9.
Sloma, Ivan, Philip Beer, Christophe Desterke, et al.. (2020). Epigenetic and functional changes imposed by NUP98-HOXA9 in a genetically engineered model of chronic myeloid leukemia progression. Haematologica. 106(3). 881–885. 1 indexed citations
10.
Nguyen, Long, Maisam Makarem, Nagarajan Kannan, et al.. (2018). Clonal Analysis of Mouse Mammary Luminal Epithelial Cell Transplants. Stem Cells and Development. 28(5). 353–355.
11.
Knapp, David J. H. F., Colin A. Hammond, Nima Aghaeepour, et al.. (2018). Single-cell analysis identifies a CD33+ subset of human cord blood cells with high regenerative potential. Nature Cell Biology. 20(6). 710–720. 40 indexed citations
12.
Cao, Qi, Kieran O’Neill, Colin A. Hammond, et al.. (2018). High-Resolution Single-Cell DNA Methylation Measurements Reveal Epigenetically Distinct Hematopoietic Stem Cell Subpopulations. Stem Cell Reports. 11(2). 578–592. 62 indexed citations
13.
Lorzadeh, Alireza, et al.. (2017). Generation of Native Chromatin Immunoprecipitation Sequencing Libraries for Nucleosome Density Analysis. Journal of Visualized Experiments. 4 indexed citations
14.
Lorzadeh, Alireza, et al.. (2017). Generation of Native Chromatin Immunoprecipitation Sequencing Libraries for Nucleosome Density Analysis. Journal of Visualized Experiments.
15.
Eaves, Connie J., David J. H. F. Knapp, Colin A. Hammond, et al.. (2017). Molecular and biological analysis of human hematopoietic stem cells at single-cell resolution. Experimental Hematology. 53. S24–S24. 1 indexed citations
16.
Lee, Lisa, Nikolay Stoynov, Michelle Moksa, et al.. (2017). The [PSI +] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI +] cells can promote aneuploidy. Scientific Reports. 7(1). 8442–8442. 10 indexed citations
17.
Pellacani, Davide, Misha Bilenky, Nagarajan Kannan, et al.. (2016). Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks. Cell Reports. 17(8). 2060–2074. 59 indexed citations
18.
Nguyen, Long, Davide Pellacani, Sylvain Lefort, et al.. (2015). Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells. Nature. 528(7581). 267–271. 86 indexed citations
19.
Pon, Julia R., Jackson Wong, Saeed Saberi, et al.. (2015). MEF2B mutations in non-Hodgkin lymphoma dysregulate cell migration by decreasing MEF2B target gene activation. Nature Communications. 6(1). 7953–7953. 41 indexed citations
20.
Baross, Ágnes, Yaron S.N. Butterfield, Shaun Coughlin, et al.. (2004). Systematic Recovery and Analysis of Full-ORF Human cDNA Clones. Genome Research. 14(10b). 2083–2092. 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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