Patrick G. Gallagher

14.2k total citations · 1 hit paper
234 papers, 9.4k citations indexed

About

Patrick G. Gallagher is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Patrick G. Gallagher has authored 234 papers receiving a total of 9.4k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Physiology, 74 papers in Molecular Biology and 68 papers in Genetics. Recurrent topics in Patrick G. Gallagher's work include Erythrocyte Function and Pathophysiology (123 papers), Hemoglobinopathies and Related Disorders (67 papers) and Blood properties and coagulation (46 papers). Patrick G. Gallagher is often cited by papers focused on Erythrocyte Function and Pathophysiology (123 papers), Hemoglobinopathies and Related Disorders (67 papers) and Blood properties and coagulation (46 papers). Patrick G. Gallagher collaborates with scholars based in United States, France and China. Patrick G. Gallagher's co-authors include Narla Mohandas, Matthew J. Bizzarro, Vincent Schulz, Bernard G. Forget, Robert S. Baltimore, Silverio Perrotta, Yelena Maksimova, Richard A. Ehrenkranz, Laurie A. Steiner and Craig Raskind and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Patrick G. Gallagher

227 papers receiving 9.2k citations

Hit Papers

Red cell membrane: past, ... 2008 2026 2014 2020 2008 250 500 750

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Patrick G. Gallagher 4.2k 3.3k 2.1k 1.8k 1.4k 234 9.4k
Steven L. Spitalnik 2.1k 0.5× 2.5k 0.7× 447 0.2× 823 0.5× 530 0.4× 188 7.9k
David Allan 1.4k 0.3× 3.7k 1.1× 635 0.3× 1.2k 0.7× 573 0.4× 277 7.8k
Karl S. Lang 2.2k 0.5× 3.0k 0.9× 1.2k 0.6× 433 0.2× 662 0.5× 200 9.2k
Martin R. Pollak 1.2k 0.3× 5.5k 1.6× 933 0.4× 2.1k 1.2× 359 0.3× 189 14.6k
Lawrence B. Schwartz 6.1k 1.5× 5.0k 1.5× 3.4k 1.6× 1.9k 1.1× 144 0.1× 263 22.2k
Leo Koenderman 3.4k 0.8× 5.2k 1.5× 2.4k 1.1× 595 0.3× 177 0.1× 324 17.5k
Laurence A. Boxer 1.5k 0.4× 2.3k 0.7× 624 0.3× 562 0.3× 375 0.3× 218 9.2k
Lawrence M. Lichtenstein 12.0k 2.9× 3.3k 1.0× 3.1k 1.5× 2.0k 1.1× 268 0.2× 397 26.0k
William C. Aird 1.4k 0.3× 6.3k 1.9× 1.2k 0.6× 576 0.3× 240 0.2× 169 14.1k
Tadashi Matsuda 1.1k 0.3× 5.0k 1.5× 799 0.4× 904 0.5× 315 0.2× 276 14.6k

Countries citing papers authored by Patrick G. Gallagher

Since Specialization
Citations

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

Fields of papers citing papers by Patrick G. Gallagher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick G. Gallagher. 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 Patrick G. Gallagher. The network helps show where Patrick G. Gallagher may publish in the future.

Co-authorship network of co-authors of Patrick G. Gallagher

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick G. Gallagher. A scholar is included among the top collaborators of Patrick G. Gallagher 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 Patrick G. Gallagher. Patrick G. Gallagher 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.
Leduc, Marjorie, Julien Papoin, Hongxia Yan, et al.. (2025). Comprehensive phenotypic and proteomic analyses of human reticulocyte maturation. PubMed. 1(2). 100012–100012.
2.
McGrath, Kathleen E., Anne D. Koniski, Kristin Murphy, et al.. (2025). BMI1 regulates human erythroid self-renewal through both gene repression and gene activation. Nature Communications. 16(1). 7619–7619.
3.
Gu, Sean X., Vincent Schulz, Henry M. Rinder, et al.. (2024). Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studies. Blood Cells Molecules and Diseases. 110. 102893–102893.
4.
Feinn, Richard, et al.. (2024). Joint bleeds in mild hemophilia: Prevalence and clinical characteristics. Haemophilia. 30(2). 331–335. 2 indexed citations
5.
Papoin, Julien, Hongxia Yan, Marjorie Leduc, et al.. (2023). Phenotypic and proteomic characterization of the human erythroid progenitor continuum reveal dynamic changes in cell cycle and in metabolic pathways. American Journal of Hematology. 99(1). 99–112. 8 indexed citations
6.
Gallagher, Patrick G.. (2022). Anemia in the pediatric patient. Blood. 140(6). 571–593. 36 indexed citations
7.
Sriswasdi, Sira, Sandra L. Harper, Hsin‐Yao Tang, Patrick G. Gallagher, & David W. Speicher. (2014). Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometry. Proceedings of the National Academy of Sciences. 111(5). 1801–1806. 15 indexed citations
8.
An, Xiuli, Vincent Schulz, Jie Li, et al.. (2014). Global transcriptome analyses of human and murine terminal erythroid differentiation. Blood. 123(22). 3466–3477. 243 indexed citations
9.
Deng, Changwang, Ying Li, Kairong Cui, et al.. (2013). USF1 and hSET1A Mediated Epigenetic Modifications Regulate Lineage Differentiation and HoxB4 Transcription. PLoS Genetics. 9(6). e1003524–e1003524. 50 indexed citations
10.
Su, Mack Y., Laurie A. Steiner, Tejaswini Mishra, et al.. (2013). Identification of Biologically Relevant Enhancers in Human Erythroid Cells. Journal of Biological Chemistry. 288(12). 8433–8444. 40 indexed citations
11.
Zarychanski, Ryan, Vincent Schulz, Brett L. Houston, et al.. (2012). Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis. Blood. 120(9). 1908–1915. 307 indexed citations
12.
X, Li, Shaohua Wang, Ying Li, et al.. (2011). Chromatin boundaries require functional collaboration between the hSET1 and NURF complexes. Blood. 118(5). 1386–1394. 30 indexed citations
13.
Yang, Mary Qu, Clara Wong, Laurie A. Steiner, et al.. (2010). Functional Analysis of a Novel cis -Acting Regulatory Region within the Human Ankyrin Gene ( ANK-1 ) Promoter. Molecular and Cellular Biology. 30(14). 3493–3502. 1 indexed citations
14.
Steiner, Laurie A., Yelena Maksimova, Vincent Schulz, et al.. (2009). Chromatin Architecture and Transcription Factor Binding Regulate Expression of Erythrocyte Membrane Protein Genes. Molecular and Cellular Biology. 29(20). 5399–5412. 27 indexed citations
15.
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
16.
Zhou, Dewang, et al.. (2006). Alterations in Expression and Chromatin Configuration of the Alpha Hemoglobin-Stabilizing Protein Gene in Erythroid Kruppel-Like Factor-Deficient Mice. Molecular and Cellular Biology. 26(11). 4368–4377. 45 indexed citations
18.
Gallagher, Patrick G., et al.. (1999). Fast, effortless and accurate measurement of glomerular filtration rate in conscious monkeys. Seminars in Hematology. 36(4). 328–39. 3 indexed citations
19.
Gallagher, Patrick G., Mary Jane Petruzzi, Scott A. Weed, et al.. (1997). Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.. Journal of Clinical Investigation. 99(2). 267–277. 31 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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