Richard A. Voit

1.2k total citations · 1 hit paper
17 papers, 783 citations indexed

About

Richard A. Voit is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Richard A. Voit has authored 17 papers receiving a total of 783 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Hematology. Recurrent topics in Richard A. Voit's work include Hemoglobinopathies and Related Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers) and Acute Myeloid Leukemia Research (2 papers). Richard A. Voit is often cited by papers focused on Hemoglobinopathies and Related Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers) and Acute Myeloid Leukemia Research (2 papers). Richard A. Voit collaborates with scholars based in United States and Canada. Richard A. Voit's co-authors include Matthew H. Porteus, Vijay G. Sankaran, Jian Xu, Stuart H. Orkin, Zhen Shao, Guo‐Cheng Yuan, Jeff Vierstra, J Stamatoyannopoulos, Sophia C. Kamran and Matthew C. Canver and has published in prestigious journals such as Science, Cell and Nucleic Acids Research.

In The Last Decade

Richard A. Voit

15 papers receiving 774 citations

Hit Papers

An Erythroid Enhancer of BCL11A Subject to Genetic Variat... 2013 2026 2017 2021 2013 100 200 300 400

Peers

Richard A. Voit
Divya S. Vinjamur United States
Christopher T. Lux United States
David J. Young United States
Mirosława Siatecka United States
NP Anagnou United States
Jason E. Farrar United States
Tatjana Kilo Australia
AD Auerbach United States
Jingmin Shu United States
Divya S. Vinjamur United States
Richard A. Voit
Citations per year, relative to Richard A. Voit Richard A. Voit (= 1×) peers Divya S. Vinjamur

Countries citing papers authored by Richard A. Voit

Since Specialization
Citations

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

Fields of papers citing papers by Richard A. Voit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard A. Voit. 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 Richard A. Voit. The network helps show where Richard A. Voit may publish in the future.

Co-authorship network of co-authors of Richard A. Voit

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

All Works

17 of 17 papers shown
1.
Nguyen, Trieu, Takeshi Iwasaki, Susan Kales, et al.. (2026). Systematic functional dissection of germline noncoding risk variants impacting clonal hematopoiesis. bioRxiv (Cold Spring Harbor Laboratory).
3.
Voit, Richard A. & Vijay G. Sankaran. (2023). MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development. Journal of Clinical Immunology. 43(6). 1052–1066. 7 indexed citations
4.
Voit, Richard A., Liming Tao, Fulong Yu, et al.. (2022). A genetic disorder reveals a hematopoietic stem cell regulatory network co-opted in leukemia. Nature Immunology. 24(1). 69–83. 24 indexed citations
5.
Hou, Lifei, Richard A. Voit, Sophia Koutsogiannaki, et al.. (2022). CD11c regulates neutrophil maturation. Blood Advances. 7(7). 1312–1325. 17 indexed citations
6.
Voit, Richard A., Xiaotian Liao, Myriam Armant, et al.. (2022). Regulated Expression of GATA1 As a Gene Therapy Cure for Diamond-Blackfan Anemia. Blood. 140(Supplement 1). 986–987. 4 indexed citations
7.
Wahlster, Lara, Jeffrey M. Verboon, Leif S. Ludwig, et al.. (2021). Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript. The Journal of Experimental Medicine. 218(6). 10 indexed citations
8.
Shen, Yong, et al.. (2021). Pathogenic BCL11A variants provide insights into the mechanisms of human fetal hemoglobin silencing. PLoS Genetics. 17(10). e1009835–e1009835. 13 indexed citations
9.
Shen, Yong, Jeffrey M. Verboon, Yuannyu Zhang, et al.. (2021). A unified model of human hemoglobin switching through single-cell genome editing. Nature Communications. 12(1). 4991–4991. 15 indexed citations
10.
Hou, Lifei, Richard A. Voit, Vijay G. Sankaran, Timothy A. Springer, & Koichi Yuki. (2020). CD11c regulates hematopoietic stem and progenitor cells under stress. Blood Advances. 4(24). 6086–6097. 13 indexed citations
11.
Voit, Richard A. & Vijay G. Sankaran. (2020). Stabilizing HIF to Ameliorate Anemia. Cell. 180(1). 6–6. 48 indexed citations
12.
Voit, Richard A. & Rachael F. Grace. (2020). Pyruvate kinase deficiency in a newborn with extramedullary hematopoiesis in the skin. Blood. 136(6). 770–770. 1 indexed citations
13.
Fine, Eli J., Zhilan Zheng, Richard A. Voit, et al.. (2014). SAPTA: a new design tool for improving TALE nuclease activity. Nucleic Acids Research. 42(6). e47–e47. 41 indexed citations
14.
Voit, Richard A., Ayal Hendel, Shondra M. Pruett‐Miller, & Matthew H. Porteus. (2013). Nuclease-mediated gene editing by homologous recombination of the human globin locus. Nucleic Acids Research. 42(2). 1365–1378. 76 indexed citations
15.
Voit, Richard A., Moira A. McMahon, Sara L. Sawyer, & Matthew H. Porteus. (2013). Generation of an HIV Resistant T-cell Line by Targeted “Stacking” of Restriction Factors. Molecular Therapy. 21(4). 786–795. 63 indexed citations
16.
Bauer, Daniel E., Sophia C. Kamran, Samuel Lessard, et al.. (2013). Fine-Mapping and Genome Editing Reveal An Essential Erythroid Enhancer At The HbF-Associated BCL11A Locus. Blood. 122(21). 437–437.
17.
Bauer, Daniel E., Sophia C. Kamran, Samuel Lessard, et al.. (2013). An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level. Science. 342(6155). 253–257. 450 indexed citations breakdown →

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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