Paula M. Jacobi

595 total citations
18 papers, 427 citations indexed

About

Paula M. Jacobi is a scholar working on Hematology, Genetics and Immunology. According to data from OpenAlex, Paula M. Jacobi has authored 18 papers receiving a total of 427 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Hematology, 6 papers in Genetics and 5 papers in Immunology. Recurrent topics in Paula M. Jacobi's work include Platelet Disorders and Treatments (11 papers), Blood groups and transfusion (7 papers) and Complement system in diseases (5 papers). Paula M. Jacobi is often cited by papers focused on Platelet Disorders and Treatments (11 papers), Blood groups and transfusion (7 papers) and Complement system in diseases (5 papers). Paula M. Jacobi collaborates with scholars based in United States, France and Canada. Paula M. Jacobi's co-authors include Sandra L. Haberichter, Robert R. Montgomery, Veronica H. Flood, Kenneth D. Friedman, Joan Cox Gill, Raymond G. Hoffmann, Pamela A. Christopherson, Alan T. Nurden, Elizabeth P. Merricks and Timothy C. Nichols and has published in prestigious journals such as Nature Communications, Blood and Journal of Pharmacology and Experimental Therapeutics.

In The Last Decade

Paula M. Jacobi

18 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paula M. Jacobi United States 10 316 103 85 62 49 18 427
Simon Stritt Germany 10 107 0.3× 21 0.2× 79 0.9× 63 1.0× 49 1.0× 15 345
S.J. Shattil United States 6 198 0.6× 16 0.2× 75 0.9× 38 0.6× 72 1.5× 7 356
S. Krey Germany 7 325 1.0× 64 0.6× 63 0.7× 63 1.0× 59 1.2× 7 395
F Velasco Spain 7 127 0.4× 39 0.4× 42 0.5× 83 1.3× 43 0.9× 13 321
Alan T. Nurden France 7 197 0.6× 11 0.1× 98 1.2× 73 1.2× 29 0.6× 7 312
Taishi Yamashita Japan 7 102 0.3× 48 0.5× 218 2.6× 148 2.4× 23 0.5× 8 448
Alessandro Bucalossi Italy 11 218 0.7× 20 0.2× 88 1.0× 31 0.5× 26 0.5× 26 379
Y Takimoto Japan 11 97 0.3× 26 0.3× 157 1.8× 50 0.8× 22 0.4× 48 355
Keita Horitani Japan 9 201 0.6× 30 0.3× 107 1.3× 77 1.2× 16 0.3× 20 359

Countries citing papers authored by Paula M. Jacobi

Since Specialization
Citations

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

Fields of papers citing papers by Paula M. Jacobi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paula M. Jacobi. 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 Paula M. Jacobi. The network helps show where Paula M. Jacobi may publish in the future.

Co-authorship network of co-authors of Paula M. Jacobi

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

All Works

18 of 18 papers shown
1.
Jacobi, Paula M., Roxanne Cofiell, C‐Hong Chang, Sung-Kwon Kim, & Sarah E. Sartain. (2022). Complement Activation Is Associated with Endothelial Damage in Hematopoietic Stem Cell Transplant Associated-Thrombotic Microangiopathy. Blood. 140(Supplement 1). 5522–5524. 2 indexed citations
2.
Desch, Karl C., Ayse Bilge Ozel, Matthew Halvorsen, et al.. (2020). Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood. 136(5). 533–541. 31 indexed citations
3.
Ma, Qianyi, Paula M. Jacobi, Brian T. Emmer, et al.. (2017). Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels. Blood Advances. 1(15). 1037–1046. 17 indexed citations
4.
White‐Adams, Tara C., Christopher J. Ng, Paula M. Jacobi, Sandra L. Haberichter, & Jorge A. Di Paola. (2016). Mutations in the D′D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF. Thrombosis Research. 145. 112–118. 13 indexed citations
5.
Desch, Karl C., Ayse Bilge Ozel, Matthew Halvorsen, et al.. (2016). Exome Sequencing in Venous Thromboembolic Disease Identifies Excess Mutation Burden in PROS1, PROC, SERPINC1 and STAB2. Blood. 128(22). 3794–3794. 4 indexed citations
6.
Chen, Junmei, Jesse Hinckley, Sandra L. Haberichter, et al.. (2015). Variable content of von Willebrand factor mutant monomer drives the phenotypic variability in a family with von Willebrand disease. Blood. 126(2). 262–269. 12 indexed citations
7.
Flood, Veronica H., Sandra L. Haberichter, Paula M. Jacobi, et al.. (2015). Crucial role for the VWF A1 domain in binding to type IV collagen. Blood. 125(14). 2297–2304. 67 indexed citations
8.
Flood, Veronica H., et al.. (2013). VWF Interaction With Type IV Collagen Is Mediated Through Critical VWF A1 Domain Residues. Blood. 122(21). 29–29. 1 indexed citations
9.
Nurden, Paquita, Alan T. Nurden, Timothy C. Nichols, et al.. (2013). Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A. Nature Communications. 4(1). 2773–2773. 93 indexed citations
10.
Flood, Veronica H., Joan Cox Gill, Kenneth D. Friedman, et al.. (2013). Collagen Binding Provides a Sensitive Screen for Variant von Willebrand Disease. Clinical Chemistry. 59(4). 684–691. 48 indexed citations
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Haberichter, Sandra L., Paula M. Jacobi, Veronica H. Flood, et al.. (2011). Quantitative Analysis of VWF Multimer Structure: Discrimination Between VWD Subtypes. Blood. 118(21). 1215–1215. 3 indexed citations
14.
Lameh, Jelveh, Fabio Bertozzi, Nicholas M. Kelly, et al.. (2010). Neuropeptide FF Receptors Have Opposing Modulatory Effects on Nociception. Journal of Pharmacology and Experimental Therapeutics. 334(1). 244–254. 39 indexed citations
15.
Merricks, Elizabeth P., Paquita Nurden, Eric S. Jensen, et al.. (2010). De Novo Synthesis & Storage of Human Factor VIII In Platelets Reduces Bleeding In Canine Hemophilia A. Blood. 116(21). 2198–2198. 1 indexed citations
16.
Nichols, Timothy C., Sandra L. Haberichter, Paula M. Jacobi, et al.. (2009). Platelet-Targeted Expression of Human BDD-FVIII Reduces Bleeding in Canine Hemophilia A.. Blood. 114(22). 691–691. 3 indexed citations
17.
Jacobi, Paula M., Joan Cox Gill, Kenneth D. Friedman, Robert R. Montgomery, & Sandra L. Haberichter. (2008). Intersection of Mechanisms of Type 2A Von Willebrand Disease through Defects in Von Willebrand Factor Multimerization, Secretion, ADAMTS-13 Susceptibility, and Regulated Storage. Blood. 112(11). 588–588. 1 indexed citations
18.
Haberichter, Sandra L., Paula M. Jacobi, & Robert R. Montgomery. (2003). Critical independent regions in the VWF propeptide and mature VWF that enable normal VWF storage. Blood. 101(4). 1384–1391. 41 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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