Donald Lavelle

2.2k total citations
69 papers, 1.6k citations indexed

About

Donald Lavelle is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Donald Lavelle has authored 69 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Genetics, 49 papers in Molecular Biology and 28 papers in Hematology. Recurrent topics in Donald Lavelle's work include Hemoglobinopathies and Related Disorders (52 papers), Epigenetics and DNA Methylation (39 papers) and Prenatal Screening and Diagnostics (15 papers). Donald Lavelle is often cited by papers focused on Hemoglobinopathies and Related Disorders (52 papers), Epigenetics and DNA Methylation (39 papers) and Prenatal Screening and Diagnostics (15 papers). Donald Lavelle collaborates with scholars based in United States and Italy. Donald Lavelle's co-authors include Joseph DeSimone, Yogen Saunthararajah, Robert E. Molokie, Kestis Vaitkus, Nadim Mahmud, Mabel Koshy, Linda R. Bressler, Louise Dorn, Yi-Hsiang Chen and Hiroto Araki and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

Donald Lavelle

66 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Donald Lavelle United States 24 1.1k 762 672 218 174 69 1.6k
Jianqiong Zhu United States 16 402 0.4× 269 0.4× 198 0.3× 53 0.2× 71 0.4× 35 935
Kumiko Goi Japan 21 665 0.6× 148 0.2× 341 0.5× 54 0.2× 34 0.2× 78 1.2k
Francesca Arruga Italy 20 502 0.4× 550 0.7× 394 0.6× 23 0.1× 42 0.2× 60 1.3k
Jette Ford Australia 19 470 0.4× 125 0.2× 248 0.4× 92 0.4× 31 0.2× 40 896
Francesco Paolo Tambaro United States 16 789 0.7× 262 0.3× 294 0.4× 29 0.1× 26 0.1× 40 1.3k
Allison Mayle United States 10 788 0.7× 134 0.2× 462 0.7× 23 0.1× 50 0.3× 13 1.1k
Timothy J. Hoy United Kingdom 19 504 0.4× 374 0.5× 189 0.3× 31 0.1× 28 0.2× 34 896
Jorge DiMartino United States 14 829 0.7× 140 0.2× 588 0.9× 27 0.1× 17 0.1× 42 1.2k
Yosuke Minami Japan 22 802 0.7× 355 0.5× 812 1.2× 17 0.1× 24 0.1× 103 1.6k
SM Watt United Kingdom 13 394 0.3× 141 0.2× 559 0.8× 22 0.1× 62 0.4× 20 1.1k

Countries citing papers authored by Donald Lavelle

Since Specialization
Citations

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

Fields of papers citing papers by Donald Lavelle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Donald Lavelle

This figure shows the co-authorship network connecting the top 25 collaborators of Donald Lavelle. A scholar is included among the top collaborators of Donald Lavelle 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 Donald Lavelle. Donald Lavelle 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.
Molokie, Robert E., Santosh L. Saraf, Michael Pacini, et al.. (2023). Translating an HPFH-Mechanism into Oral Small Molecule Therapy for Beta-Hemoglobinopathies: Clinical Proof-of-Principle. Blood. 142(Supplement 1). 2524–2524.
2.
Jagadeeswaran, Ramasamy, et al.. (2021). Nicotinamide Improves Anemia and Decreases Reactive Oxygen Species in Sickle Cell Disease Mice. Blood. 138(Supplement 1). 2019–2019. 2 indexed citations
3.
Chambers, Christopher B., Jeffrey Gross, Katherine L. Pratt, et al.. (2020). The mRNA-Binding Protein IGF2BP1 Restores Fetal Hemoglobin in Cultured Erythroid Cells from Patients with β-Hemoglobin Disorders. Molecular Therapy — Methods & Clinical Development. 17. 429–440. 16 indexed citations
4.
Jagadeeswaran, Ramasamy, et al.. (2019). Selenium Deficiency in a Mouse Model of Sickle Cell Disease Resulted in Increased Oxygen Consumption and Aberrant Mitochondrial Retention (OR11-05-19). Current Developments in Nutrition. 3. nzz044.OR11–5. 2 indexed citations
5.
Rivers, Angela, Kestis Vaitkus, Ramasamy Jagadeeswaran, et al.. (2018). Oral administration of the LSD1 inhibitor ORY-3001 increases fetal hemoglobin in sickle cell mice and baboons. Experimental Hematology. 67. 60–64.e2. 18 indexed citations
6.
7.
Rivers, Angela, Kestis Vaitkus, Ramasamy Jagadeeswaran, et al.. (2017). Oral Administration of the LSD1 Inhibitor OG-S1335 Increases Fetal Hemoglobin in Humanized Transgenic Sickle Cell Disease Mice and in Baboons. Blood. 130. 356–356. 1 indexed citations
8.
Mahmud, Nadim, Benjamin J. Petro, Sudhakar Baluchamy, et al.. (2014). Differential Effects of Epigenetic Modifiers on the Expansion and Maintenance of Human Cord Blood Stem/Progenitor Cells. Biology of Blood and Marrow Transplantation. 20(4). 480–489. 38 indexed citations
9.
Lavelle, Donald, Maria Armila Ruiz, Vinzon Ibañez, et al.. (2012). Effect of AGM and Fetal Liver-Derived Stromal Cell Lines on Globin Expression in Adult Baboon (P. anubis) Bone Marrow-Derived Erythroid Progenitors. PLoS ONE. 7(5). e36846–e36846. 6 indexed citations
10.
Lavelle, Donald, Kestis Vaitkus, Yonghua Ling, et al.. (2011). Effects of tetrahydrouridine on pharmacokinetics and pharmacodynamics of oral decitabine. Blood. 119(5). 1240–1247. 72 indexed citations
11.
Akpan, Imo J., et al.. (2010). Decitabine increases fetal hemoglobin in Papio anubis by increasing γ-globin gene transcription. Experimental Hematology. 38(11). 989–993.e1. 21 indexed citations
12.
Lavelle, Donald, Kestis Vaitkus, Sanjeev Redkar, et al.. (2007). Oral decitabine reactivates expression of the methylated γ‐globin gene in Papio anubis. American Journal of Hematology. 82(11). 981–985. 28 indexed citations
13.
Lavelle, Donald, et al.. (2006). Developmental changes in DNA methylation and covalent histone modifications of chromatin associated with the ε-, γ-, and β-globin gene promoters in Papio anubis. Blood Cells Molecules and Diseases. 36(2). 269–278. 19 indexed citations
15.
Saunthararajah, Yogen, Donald Lavelle, & Joseph DeSimone. (2004). DNA hypo‐methylating agents and sickle cell disease. British Journal of Haematology. 126(5). 629–636. 30 indexed citations
16.
Uddin, Shahab, Dolores Mahmud, Donald Lavelle, et al.. (2002). Regulation of myeloma cell growth through Akt/Gsk3/forkhead signaling pathway. Biochemical and Biophysical Research Communications. 297(4). 760–764. 35 indexed citations
17.
18.
Chen, Yi-Hsiang, et al.. (1997). Modulation of Interleukin-6/Interleukin-6 Receptor Cytokine Loop in the Treatment of Multiple Myeloma. Leukemia & lymphoma. 27(1-2). 11–23. 14 indexed citations
20.
Lavelle, Donald, et al.. (1986). On the mechanism of Hb F elevations in the baboon by erythropoietic stress and pharmacologic manipulation. Blood. 67(4). 1083–1089. 25 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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