Patrick J. Heizer

653 total citations
18 papers, 444 citations indexed

About

Patrick J. Heizer is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Patrick J. Heizer has authored 18 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 5 papers in Cell Biology. Recurrent topics in Patrick J. Heizer's work include Lipid metabolism and disorders (7 papers), RNA Research and Splicing (6 papers) and Nuclear Structure and Function (6 papers). Patrick J. Heizer is often cited by papers focused on Lipid metabolism and disorders (7 papers), RNA Research and Splicing (6 papers) and Nuclear Structure and Function (6 papers). Patrick J. Heizer collaborates with scholars based in United States, Australia and Denmark. Patrick J. Heizer's co-authors include Loren G. Fong, Stephen G. Young, Thomas A. Weston, Rachel S. Jung, Yiping Tu, Paul H. Kim, Christopher M. Allan, Anne P. Beigneux, Natalie Chen and Haibo Jiang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cell Metabolism and Scientific Reports.

In The Last Decade

Patrick J. Heizer

17 papers receiving 442 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick J. Heizer United States 11 245 131 88 80 62 18 444
Rachel S. Jung United States 12 177 0.7× 182 1.4× 125 1.4× 95 1.2× 83 1.3× 21 462
Xuchen Hu United States 9 117 0.5× 82 0.6× 47 0.5× 65 0.8× 31 0.5× 15 258
Vi T. Tang United States 10 196 0.8× 155 1.2× 30 0.3× 80 1.0× 24 0.4× 19 406
Clémence Merlen Canada 11 254 1.0× 118 0.9× 48 0.5× 35 0.4× 17 0.3× 26 414
Ashwini Dhume United States 8 178 0.7× 115 0.9× 21 0.2× 45 0.6× 40 0.6× 8 338
Ryan Reed United States 13 349 1.4× 90 0.7× 34 0.4× 36 0.5× 70 1.1× 17 604
Tatsuo Shinagawa United States 10 209 0.9× 180 1.4× 91 1.0× 49 0.6× 34 0.5× 15 455
John A. Parente United States 7 244 1.0× 80 0.6× 44 0.5× 149 1.9× 22 0.4× 8 395
Xiaoxue Fan China 13 230 0.9× 197 1.5× 20 0.2× 80 1.0× 21 0.3× 33 534
Masayuki Suda Japan 9 176 0.7× 83 0.6× 37 0.4× 143 1.8× 21 0.3× 10 378

Countries citing papers authored by Patrick J. Heizer

Since Specialization
Citations

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

Fields of papers citing papers by Patrick J. Heizer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick J. Heizer

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick J. Heizer. A scholar is included among the top collaborators of Patrick J. Heizer 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 J. Heizer. Patrick J. Heizer 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.
2.
McMurphy, Travis, et al.. (2024). AAV-mediated co-expression of an immunogenic transgene plus PD-L1 enables sustained expression through immunological evasion. Scientific Reports. 14(1). 28853–28853. 2 indexed citations
3.
Song, Wenxin, Patrick J. Heizer, Yiping Tu, et al.. (2023). Intracapillary LPL levels in brown adipose tissue, visualized with an antibody-based approach, are regulated by ANGPTL4 at thermoneutral temperatures. Proceedings of the National Academy of Sciences. 120(8). e2219833120–e2219833120. 10 indexed citations
4.
Chen, Natalie, Paul H. Kim, Yiping Tu, et al.. (2021). Increased expression of LAP2β eliminates nuclear membrane ruptures in nuclear lamin–deficient neurons and fibroblasts. Proceedings of the National Academy of Sciences. 118(25). 6 indexed citations
5.
Kim, Paul H., Natalie Chen, Patrick J. Heizer, et al.. (2021). Nuclear membrane ruptures underlie the vascular pathology in a mouse model of Hutchinson-Gilford progeria syndrome. JCI Insight. 6(16). 22 indexed citations
6.
Heizer, Patrick J., Yiping Tu, Paul H. Kim, et al.. (2020). Deficiency in ZMPSTE24 and resulting farnesyl–prelamin A accumulation only modestly affect mouse adipose tissue stores. Journal of Lipid Research. 61(3). 413–421. 8 indexed citations
7.
He, Cuiwen, Haibo Jiang, Wenxin Song, et al.. (2020). Cultured macrophages transfer surplus cholesterol into adjacent cells in the absence of serum or high-density lipoproteins. Proceedings of the National Academy of Sciences. 117(19). 10476–10483. 27 indexed citations
8.
Chen, Natalie, Thomas A. Weston, Jason N. Belling, et al.. (2019). An absence of lamin B1 in migrating neurons causes nuclear membrane ruptures and cell death. Proceedings of the National Academy of Sciences. 116(51). 25870–25879. 63 indexed citations
9.
Hu, Xuchen, Thomas A. Weston, Cuiwen He, et al.. (2019). Release of cholesterol-rich particles from the macrophage plasma membrane during movement of filopodia and lamellipodia. eLife. 8. 27 indexed citations
10.
Beigneux, Anne P., Christopher M. Allan, Norma P. Sandoval, et al.. (2019). Lipoprotein lipase is active as a monomer. Proceedings of the National Academy of Sciences. 116(13). 6319–6328. 62 indexed citations
11.
Kim, Paul H., Patrick J. Heizer, Yiping Tu, et al.. (2018). Disrupting the LINC complex in smooth muscle cells reduces aortic disease in a mouse model of Hutchinson-Gilford progeria syndrome. Science Translational Medicine. 10(460). 58 indexed citations
12.
Allan, Christopher M., Patrick J. Heizer, Yiping Tu, et al.. (2018). Impaired thermogenesis and sharp increases in plasma triglyceride levels in GPIHBP1-deficient mice during cold exposure. Journal of Lipid Research. 59(4). 706–713. 10 indexed citations
13.
He, Cuiwen, Thomas A. Weston, Rachel S. Jung, et al.. (2018). NanoSIMS Analysis of Intravascular Lipolysis and Lipid Movement across Capillaries and into Cardiomyocytes. Cell Metabolism. 27(5). 1055–1066.e3. 42 indexed citations
14.
Allan, Christopher M., Patrick J. Heizer, Yiping Tu, et al.. (2018). An upstream enhancer regulates Gpihbp1 expression in a tissue-specific manner. Journal of Lipid Research. 60(4). 869–879. 6 indexed citations
15.
He, Cuiwen, Xuchen Hu, Thomas A. Weston, et al.. (2018). NanoSIMS imaging reveals unexpected heterogeneity in nutrient uptake by brown adipocytes. Biochemical and Biophysical Research Communications. 504(4). 899–902. 8 indexed citations
16.
He, Cuiwen, Xuchen Hu, Thomas A. Weston, et al.. (2018). Macrophages release plasma membrane-derived particles rich in accessible cholesterol. Proceedings of the National Academy of Sciences. 115(36). E8499–E8508. 37 indexed citations
17.
Allan, Christopher M., Mikael Larsson, Patrick J. Heizer, et al.. (2017). Mutating a conserved cysteine in GPIHBP1 reduces amounts of GPIHBP1 in capillaries and abolishes LPL binding. Journal of Lipid Research. 58(7). 1453–1461. 13 indexed citations
18.
Larsson, Mikael, Christopher M. Allan, Rachel S. Jung, et al.. (2017). Apolipoprotein C-III inhibits triglyceride hydrolysis by GPIHBP1-bound LPL. Journal of Lipid Research. 58(9). 1893–1902. 43 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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