Lori A. Reed

1.5k total citations
8 papers, 1.0k citations indexed

About

Lori A. Reed is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lori A. Reed has authored 8 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lori A. Reed's work include Congenital heart defects research (4 papers), Tracheal and airway disorders (3 papers) and RNA Interference and Gene Delivery (2 papers). Lori A. Reed is often cited by papers focused on Congenital heart defects research (4 papers), Tracheal and airway disorders (3 papers) and RNA Interference and Gene Delivery (2 papers). Lori A. Reed collaborates with scholars based in United States. Lori A. Reed's co-authors include Elaine H. Zackai, Donna M. McDonald‐McGinn, Deborah A. Driscoll, Beverly S. Emanuel, Elizabeth Goldmuntz, Abbas F. Jawad, Laura E. Mitchell, Bernard J. Clark, Bettina F. Cuneo and Ronald L. Stotish and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of the American College of Cardiology.

In The Last Decade

Lori A. Reed

8 papers receiving 1.0k citations

Peers

Lori A. Reed
Michael L. Nordlund United States
Michelle D. Combs United States
Tim C. McQuinn United States
Stephen Rainer Australia
Xuan Chi United States
Laura A. Dyer United States
C Camacho-Hübner United Kingdom
Michael L. Nordlund United States
Lori A. Reed
Citations per year, relative to Lori A. Reed Lori A. Reed (= 1×) peers Michael L. Nordlund

Countries citing papers authored by Lori A. Reed

Since Specialization
Citations

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

Fields of papers citing papers by Lori A. Reed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lori A. Reed

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

All Works

8 of 8 papers shown
1.
Burdick, Andrew D., Simone Sciabola, Srinivasa R. Mantena, et al.. (2014). Sequence motifs associated with hepatotoxicity of locked nucleic acid—modified antisense oligonucleotides. Nucleic Acids Research. 42(8). 4882–4891. 114 indexed citations
2.
Morton, Daniel, Lori A. Reed, Wenhu Huang, et al.. (2014). Toxicity of Hydroxyurea in Rats and Dogs. Toxicologic Pathology. 43(4). 498–512. 13 indexed citations
3.
Kakiuchi-Kiyota, Satoko, Petra Koza‐Taylor, Srinivasa R. Mantena, et al.. (2013). Comparison of Hepatic Transcription Profiles of Locked Ribonucleic Acid Antisense Oligonucleotides: Evidence of Distinct Pathways Contributing to Non-target Mediated Toxicity in Mice. Toxicological Sciences. 138(1). 234–248. 41 indexed citations
4.
Lee, Se‐Jin, Lori A. Reed, Monique V. Davies, et al.. (2005). Regulation of muscle growth by multiple ligands signaling through activin type II receptors. Proceedings of the National Academy of Sciences. 102(50). 18117–18122. 412 indexed citations
5.
Goldmuntz, Elizabeth, Bernard J. Clark, Laura E. Mitchell, et al.. (1998). Frequency of 22q11 deletions in patients with conotruncal defects. Journal of the American College of Cardiology. 32(2). 492–498. 373 indexed citations
6.
Sullivan, Kathleen E., Donna M. McDonald‐McGinn, Deborah A. Driscoll, et al.. (1997). Juvenile rheumatoid arthritis‐like polyarthritis in chromosome 22q11.2 deletion syndrome (digeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome). Arthritis & Rheumatism. 40(3). 430–436. 72 indexed citations
7.
Gripp, Karen W., Donna M. McDonald‐McGinn, Deborah A. Driscoll, et al.. (1997). Nasal dimple as part of the 22q11.2 deletion syndrome. American Journal of Medical Genetics. 69(3). 290–292. 11 indexed citations
8.
Gripp, Karen W., Donna M. McDonald‐McGinn, Deborah A. Driscoll, et al.. (1997). Nasal dimple as part of the 22q11.2 deletion syndrome. American Journal of Medical Genetics. 69(3). 290–292. 2 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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