David Siemieniak

3.7k total citations · 2 hit papers
35 papers, 2.6k citations indexed

About

David Siemieniak is a scholar working on Molecular Biology, Hematology and Immunology. According to data from OpenAlex, David Siemieniak has authored 35 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Hematology and 7 papers in Immunology. Recurrent topics in David Siemieniak's work include Protease and Inhibitor Mechanisms (6 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Platelet Disorders and Treatments (4 papers). David Siemieniak is often cited by papers focused on Protease and Inhibitor Mechanisms (6 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Platelet Disorders and Treatments (4 papers). David Siemieniak collaborates with scholars based in United States, Canada and Netherlands. David Siemieniak's co-authors include William C. Nichols, Beth McGee, David Ginsburg, Angela Yang, Tatiana Foroud, Jeanette N. McClintick, Eric E. Bouhassira, Jefferson D. Upshaw, Visalam Chandrasekaran and Eric C.‐Y. Lian and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

David Siemieniak

34 papers receiving 2.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

2001 1.3k citations Gallia G. Levy, William C. Nichols et al. Nature profile →
Isolation of a partial candidate gene for Menkes disease by positional cloning

1993 545 citations Julian F. B. Mercer, Bryan Hall et al. Nature Genetics profile →

Author Peers

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

Author						Papers	Cites
David Siemieniak	1.1k	951	644	473	455	35	2.6k
Yoshihito Yawata	282 0.3×	662 0.7×	795 1.2×	127 0.3×	157 0.3×	113	2.3k
J P Kushner	228 0.2×	698 0.7×	990 1.5×	379 0.8×	42 0.1×	35	2.5k
Martha P. Mims	635 0.6×	452 0.5×	928 1.4×	179 0.4×	37 0.1×	82	2.7k
Julie A. Vrana	395 0.4×	358 0.4×	2.6k 4.0×	311 0.7×	974 2.1×	69	3.6k
Ramin Radpour	565 0.5×	322 0.3×	1.3k 2.0×	77 0.2×	166 0.4×	72	2.7k
AF LoBuglio	836 0.7×	240 0.3×	575 0.9×	119 0.3×	44 0.1×	45	2.4k
Nicola Pozzi	228 0.2×	579 0.6×	468 0.7×	87 0.2×	91 0.2×	73	1.5k
Anneke Geurts‐Moespot	481 0.4×	822 0.9×	804 1.2×	281 0.6×	20 0.0×	75	2.9k
Bart Claes	414 0.4×	211 0.2×	816 1.3×	85 0.2×	204 0.4×	38	2.4k
Jean Paul Fermand	159 0.1×	603 0.6×	1.5k 2.4×	55 0.1×	415 0.9×	36	1.9k

Countries citing papers authored by David Siemieniak

Since Specialization

Citations

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

Fields of papers citing papers by David Siemieniak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Siemieniak

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

All Works

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20 of 20 papers shown

Holding, Matthew L., et al.. (2025). Thermodynamics and selection of the plasminogen activator inhibitor-1 latency transition. Journal of Biological Chemistry. 301(12). 110896–110896.

Holding, Matthew L., et al.. (2025). High‐throughput amino acid‐level characterization of the interactions of plasminogen activator inhibitor‐1 with variably divergent proteases. Protein Science. 34(4). e70088–e70088. 3 indexed citations

Tang, Vi T., Bolin Xu, Yawei Wang, et al.. (2022). Hepatic inactivation of murine Surf4 results in marked reduction in plasma cholesterol. eLife. 11. 19 indexed citations

Yee, Andrew, et al.. (2022). Deep mutational scanning and massively parallel kinetics of plasminogen activator inhibitor-1 functional stability to probe its latency transition. Journal of Biological Chemistry. 298(12). 102608–102608. 7 indexed citations

Yee, Andrew, Manhong Dai, Stacy E. Croteau, et al.. (2021). Phage display broadly identifies inhibitor‐reactive regions in von Willebrand factor. Journal of Thrombosis and Haemostasis. 19(11). 2702–2709. 3 indexed citations

Yee, Andrew, Colin A. Kretz, Matthew L. Holding, et al.. (2021). Deep mutational scanning of the plasminogen activator inhibitor-1 functional landscape. Scientific Reports. 11(1). 18827–18827. 11 indexed citations

Cleuren, Audrey, Martijn A. van der Ent, Hui Jiang, et al.. (2019). The in vivo endothelial cell translatome is highly heterogeneous across vascular beds. Proceedings of the National Academy of Sciences. 116(47). 23618–23624. 103 indexed citations

Tomberg, Kärt, Randal J. Westrick, Audrey Cleuren, et al.. (2018). Whole exome sequencing of ENU-induced thrombosis modifier mutations in the mouse. PLoS Genetics. 14(9). e1007658–e1007658. 2 indexed citations

Westrick, Randal J., Kärt Tomberg, Guojing Zhu, et al.. (2017). Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci. Proceedings of the National Academy of Sciences. 114(36). 9659–9664. 9 indexed citations

10.

Kretz, Colin A., Manhong Dai, Onuralp Söylemez, et al.. (2015). Massively parallel enzyme kinetics reveals the substrate recognition landscape of the metalloprotease ADAMTS13. Proceedings of the National Academy of Sciences. 112(30). 9328–9333. 24 indexed citations

11.

Levy, Gallia G., William C. Nichols, Eric C.‐Y. Lian, et al.. (2001). Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 413(6855). 488–494. 1254 indexed citations breakdown →

12.

Srinivasan, Jannavi, et al.. (1998). Genotyping of Apolipoprotein E by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Rapid Communications in Mass Spectrometry. 12(16). 1045–1050. 22 indexed citations

13.

Nichols, William C., Daniel L. Koller, Bonnie Slovis, et al.. (1997). Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32. Nature Genetics. 15(3). 277–280. 201 indexed citations

14.

Liu, Yan‐Hui, Yongdong Zhu, Xiaoli Liang, et al.. (1995). Rapid screening of genetic polymorphisms using buccal cell DNA with detection by matrix‐assisted laser desorption/ionization mass spectrometry. Rapid Communications in Mass Spectrometry. 9(9). 735–743. 48 indexed citations

15.

Liu, Yan‐Hui, et al.. (1994). Matrix‐assisted laser desorption/ionization mass sectrometry of restriction enzyme‐digested plasmid DNA using an active nafion substrate. Rapid Communications in Mass Spectrometry. 8(9). 687–691. 34 indexed citations

16.

Slightom, Jerry L., David Siemieniak, Leang C. Sieu, Ben F. Koop, & L Hood. (1994). Nucleotide Sequence Analysis of 77.7 kb of the Human Vβ T-Cell Receptor Gene Locus: Direct Primer-Walking Using Cosmid Template DNAs. Genomics. 20(2). 149–168. 33 indexed citations

17.

Mercer, Julian F. B., Bryan Hall, Jennifer A. Paynter, et al.. (1993). Isolation of a partial candidate gene for Menkes disease by positional cloning. Nature Genetics. 3(1). 20–25. 545 indexed citations breakdown →

18.

Thompson, Gary A., David Siemieniak, Leang C. Sieu, Jerry L. Slightom, & Brian A. Larkins. (1992). Sequence analysis of linked maize 22 kDa ?-zein genes. Plant Molecular Biology. 18(4). 827–833. 16 indexed citations

19.

Siemieniak, David, Leang C. Sieu, & Jerry L. Slightom. (1991). Strategy and methods for directly sequencing cosmid clones. Analytical Biochemistry. 192(2). 441–448. 13 indexed citations

20.

Siemieniak, David, et al.. (1990). Nucleotide sequence of Streptomyces fradiae transposable element Tn4556: a class-II transposon related to Tn3. Gene. 86(1). 1–9. 30 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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