Amanda P. Cline

1.8k total citations
23 papers, 1.6k citations indexed

About

Amanda P. Cline is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Amanda P. Cline has authored 23 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Physiology. Recurrent topics in Amanda P. Cline's work include RNA Interference and Gene Delivery (8 papers), Virus-based gene therapy research (7 papers) and Erythrocyte Function and Pathophysiology (6 papers). Amanda P. Cline is often cited by papers focused on RNA Interference and Gene Delivery (8 papers), Virus-based gene therapy research (7 papers) and Erythrocyte Function and Pathophysiology (6 papers). Amanda P. Cline collaborates with scholars based in United States, France and Poland. Amanda P. Cline's co-authors include David M. Bodine, Arthur W. Nienhuis, Stephen J. Brandt, Michael M. Gottesman, Ira Pastan, Brian P. Sorrentino, Stacie M. Anderson, R. Keith Humphries, Nancy E. Seidel and Donald Orlic and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Amanda P. Cline

23 papers receiving 1.5k citations

Peers

Amanda P. Cline
Éric Milot Canada
Esther R. Allay United States
Dan A. Wiginton United States
Allen Coleman United States
R.P. Creagan United States
N Odartchenko Switzerland
Kathrin M. Bernt United States
Patricia M. Rosten Canada
Lisa J. McReynolds United States
Alan J. Kinniburgh United States
Éric Milot Canada
Amanda P. Cline
Citations per year, relative to Amanda P. Cline Amanda P. Cline (= 1×) peers Éric Milot

Countries citing papers authored by Amanda P. Cline

Since Specialization
Citations

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

Fields of papers citing papers by Amanda P. Cline

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amanda P. Cline. 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 Amanda P. Cline. The network helps show where Amanda P. Cline may publish in the future.

Co-authorship network of co-authors of Amanda P. Cline

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda P. Cline. A scholar is included among the top collaborators of Amanda P. Cline 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 Amanda P. Cline. Amanda P. Cline 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.
Steiner, Laurie A., Nancy E. Seidel, Amanda P. Cline, et al.. (2012). A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter. Blood. 120(17). 3586–3593. 10 indexed citations
2.
Gallagher, Patrick G., Laurie A. Steiner, Robert I. Liem, et al.. (2010). Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis. Journal of Clinical Investigation. 120(12). 4453–4465. 24 indexed citations
3.
Markham, Nicholas O., Erin M. Parry, Lisa Garrett‐Beal, et al.. (2007). An 11-amino acid β-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes. Proceedings of the National Academy of Sciences. 104(35). 13972–13977. 26 indexed citations
4.
Nemeth, Michael J., Amanda P. Cline, Stacie M. Anderson, Lisa Garrett‐Beal, & David M. Bodine. (2004). Hmgb3 deficiency deregulates proliferation and differentiation of common lymphoid and myeloid progenitors. Blood. 105(2). 627–634. 54 indexed citations
5.
6.
Nemeth, Michael J., David J. Curtis, Martha Kirby, et al.. (2003). Hmgb3: an HMG-box family member expressed in primitive hematopoietic cells that inhibits myeloid and B-cell differentiation. Blood. 102(4). 1298–1306. 90 indexed citations
7.
Boulanger, Laurent, Denise E. Sabatino, Ellice Wong, et al.. (2002). Erythroid Expression of the Human α-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins. Journal of Biological Chemistry. 277(44). 41563–41570. 19 indexed citations
8.
Sabatino, Denise E., Nancy E. Seidel, Amanda P. Cline, et al.. (2001). Development of a Stable Retrovirus Vector Capable of Long‐Term Expression of γ‐Globin mRNA in Mouse Erythrocytes. Annals of the New York Academy of Sciences. 938(1). 246–261. 6 indexed citations
9.
Gallagher, Patrick G., Denise E. Sabatino, Daniela S. Daniela Sanchez Bassères, et al.. (2001). Erythrocyte Ankyrin Promoter Mutations Associated with Recessive Hereditary Spherocytosis Cause Significant Abnormalities in Ankyrin Expression. Journal of Biological Chemistry. 276(45). 41683–41689. 24 indexed citations
10.
Sabatino, Denise E., Nancy E. Seidel, Amanda P. Cline, et al.. (2000). Long-term expression of γ-globin mRNA in mouse erythrocytes from retrovirus vectors containing the human γ-globin gene fused to the ankyrin-1 promoter. Proceedings of the National Academy of Sciences. 97(24). 13294–13299. 38 indexed citations
11.
Sabatino, Denise E., Clara Wong, Amanda P. Cline, et al.. (2000). A Minimal Ankyrin Promoter Linked to a Human γ-Globin Gene Demonstrates Erythroid Specific Copy Number Dependent Expression with Minimal Position or Enhancer Dependence in Transgenic Mice. Journal of Biological Chemistry. 275(37). 28549–28554. 39 indexed citations
12.
Gallagher, Patrick G., Denise E. Sabatino, Marc Romana, et al.. (1999). A Human β-Spectrin Gene Promoter Directs High Level Expression in Erythroid but Not Muscle or Neural Cells. Journal of Biological Chemistry. 274(10). 6062–6073. 27 indexed citations
13.
Orlic, Donald, et al.. (1999). Isolation of Stem Cell‐Specific cDNAs from Hematopoietic Stem Cell Populations. Annals of the New York Academy of Sciences. 872(1). 243–255. 6 indexed citations
14.
Bodine, David M., Cynthia E. Dunbar, Nancy E. Seidel, et al.. (1998). Improved Amphotropic Retrovirus‐Mediated Gene Transfer into Hematopoietic Stem Cells. Annals of the New York Academy of Sciences. 850(1). 139–150. 18 indexed citations
15.
Orlic, Donald, Luc Girard, Craig T. Jordan, et al.. (1996). The level of mRNA encoding the amphotropic retrovirus receptor in mouse and human hematopoietic stem cells is low and correlates with the efficiency of retrovirus transduction.. Proceedings of the National Academy of Sciences. 93(20). 11097–11102. 205 indexed citations
16.
17.
Sorrentino, Brian P., Stephen J. Brandt, David M. Bodine, et al.. (1992). Selection of Drug-Resistant Bone Marrow Cells in Vivo After Retroviral Transfer of Human MDR 1. Science. 257(5066). 99–103. 401 indexed citations
18.
Browning, Philip J., et al.. (1986). "Replacement" of COOH-terminal truncation of v-fms with c-fms sequences markedly reduces transformation potential.. Proceedings of the National Academy of Sciences. 83(20). 7800–7804. 41 indexed citations
19.
Shimada, Takashi, A D Moulton, Amanda P. Cline, et al.. (1984). The functional human dihydrofolate reductase gene.. Journal of Biological Chemistry. 259(6). 3933–3943. 232 indexed citations
20.
Goldsmith, Merrill E., R. Keith Humphries, Timothy J. Ley, et al.. (1983). "Silent" nucleotide substitution in a beta+-thalassemia globin gene activates splice site in coding sequence RNA.. Proceedings of the National Academy of Sciences. 80(8). 2318–2322. 77 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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