Michael Triebwasser

1.7k total citations · 1 hit paper
24 papers, 1.1k citations indexed

About

Michael Triebwasser is a scholar working on Immunology, Molecular Biology and Ophthalmology. According to data from OpenAlex, Michael Triebwasser has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Immunology, 7 papers in Molecular Biology and 7 papers in Ophthalmology. Recurrent topics in Michael Triebwasser's work include Complement system in diseases (10 papers), Retinal Diseases and Treatments (7 papers) and Pregnancy and preeclampsia studies (6 papers). Michael Triebwasser is often cited by papers focused on Complement system in diseases (10 papers), Retinal Diseases and Treatments (7 papers) and Pregnancy and preeclampsia studies (6 papers). Michael Triebwasser collaborates with scholars based in United States, United Kingdom and Finland. Michael Triebwasser's co-authors include John P. Atkinson, Soumya Raychaudhuri, Johanna M. Seddon, David Kavanagh, Mark J. Daly, Elizabeth C. Schramm, Yi Yu, Jane E. Salmon, Cara Heuser and Véronique Frémeaux‐Bacchi and has published in prestigious journals such as Science, Nature Genetics and Blood.

In The Last Decade

Michael Triebwasser

22 papers receiving 1.1k citations

Hit Papers

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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.

In vivo hematopoietic stem cell modification by mRNA delivery

2023 176 citations Laura Breda, Tyler E. Papp et al. Science profile →

Author Peers

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

Author						Papers	Cites
Michael Triebwasser	533	470	345	244	161	24	1.1k
Sara C. Nilsson	729 1.4×	130 0.3×	131 0.4×	76 0.3×	13 0.1×	28	940
C.–C. Chan	371 0.7×	864 1.8×	219 0.6×	245 1.0×	6 0.0×	19	1.3k
Fengqi An	734 1.4×	49 0.1×	102 0.3×	40 0.2×	10 0.1×	9	895
Thierry van den Bosch	245 0.5×	164 0.3×	208 0.6×	44 0.2×	17 0.1×	55	670
Judith S. Greengard	87 0.2×	134 0.3×	336 1.0×	77 0.3×	9 0.1×	26	976
Markus M. Valter	514 1.0×	18 0.0×	338 1.0×	53 0.2×	85 0.5×	25	1.2k
Michael J. Ombrello	332 0.6×	121 0.3×	292 0.8×	22 0.1×	4 0.0×	27	755
Edward Quinlan	60 0.1×	694 1.5×	331 1.0×	511 2.1×	16 0.1×	17	1.1k
Martina C. Herwig‐Carl	161 0.3×	331 0.7×	253 0.7×	153 0.6×	5 0.0×	89	824
Dmitry Yarilin	426 0.8×	8 0.0×	127 0.4×	26 0.1×	262 1.6×	17	800

Countries citing papers authored by Michael Triebwasser

Since Specialization

Citations

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

Fields of papers citing papers by Michael Triebwasser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Triebwasser

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Triebwasser. A scholar is included among the top collaborators of Michael Triebwasser 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 Michael Triebwasser. Michael Triebwasser 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

Lokki, A. Inkeri, Michael Triebwasser, Emma Daly, et al.. (2024). Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. Genes and Immunity. 26(1). 22–26. 2 indexed citations

Lokki, A. Inkeri, Zhen Ren, Michael Triebwasser, et al.. (2023). Identification of complement factor H variants that predispose to pre‐eclampsia: A genetic and functional study. BJOG An International Journal of Obstetrics & Gynaecology. 130(12). 1473–1482. 13 indexed citations

Breda, Laura, Tyler E. Papp, Michael Triebwasser, et al.. (2023). In vivo hematopoietic stem cell modification by mRNA delivery. Science. 381(6656). 436–443. 176 indexed citations breakdown →

Breda, Laura, Tyler E. Papp, Michael Triebwasser, et al.. (2022). In Vivo Modification of Hematopoietic Stem Cells By Targeted Lipid Nanoparticles Encapsulating mRNA. Blood. 140(Supplement 1). 305–306. 1 indexed citations

Rivella, Stefano, Danuta Jarocha, Laura Breda, et al.. (2022). P1521: A SEVERE MOUSE MODEL OF ALPHA-THALASSEMIA SHOWS ABNORMAL IRON METABOLISM, ERYTHROPOIESIS AND COAGULATION, AND CAN BE RESCUED BY A NOVEL GENE THERAPY APPROACH. HemaSphere. 6. 1402–1403.

Triebwasser, Michael, et al.. (2021). Rescue of Murine IL-7 Receptor Deficiency with Human IL-7 Receptor Gene Therapy. Blood. 138(Supplement 1). 3131–3131. 3 indexed citations

Lokki, A. Inkeri, Laura Teirilä, Michael Triebwasser, et al.. (2021). Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre‐eclampsia: a genetic and functional study. BJOG An International Journal of Obstetrics & Gynaecology. 128(8). 1282–1291. 15 indexed citations

Triebwasser, Michael, et al.. (2020). Hemophagocytic Lymphohistiocytosis Presenting as Nephrotic Syndrome. Journal of the American Society of Nephrology. 31(10S). 569–570.

Triebwasser, Michael, Xiaobo Wu, Paula Bertram, et al.. (2018). Timing and mechanism of conceptus demise in a complement regulatory membrane protein deficient mouse. American Journal of Reproductive Immunology. 80(4). e12997–e12997. 3 indexed citations

10.

Lokki, A. Inkeri, Michael Triebwasser, Emma Daly, et al.. (2018). Rare mutations in factor H predispose to severe preeclampsia. Molecular Immunology. 102. 184–185. 1 indexed citations

11.

Wagner, Erin K., Soumya Raychaudhuri, Anuja Java, et al.. (2016). Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden and lower antigenic levels in familial AMD. Scientific Reports. 6(1). 31531–31531. 41 indexed citations

12.

Atkinson, John P., Erin K. Wagner, Soumya Raychaudhuri, et al.. (2016). Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD. Immunobiology. 221(10). 1205–1206. 2 indexed citations

13.

Kavanagh, David, Elizabeth C. Schramm, Michael Triebwasser, et al.. (2015). Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. Human Molecular Genetics. 24(13). 3861–70. 96 indexed citations

14.

Triebwasser, Michael, Elisha Roberson, Yi Yu, et al.. (2015). Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 56(11). 6873–6873. 54 indexed citations

15.

Triebwasser, Michael. (2015). Excessive Complement Activation Due to Genetic Haploinsufficiency of Regulators in Multiple Human Diseases. Open Scholarship Institutional Repository (Washington University in St. Louis). 1 indexed citations

16.

Schramm, Elizabeth C., Simon J. Clark, Michael Triebwasser, et al.. (2014). Genetic variants in the complement system predisposing to age-related macular degeneration: A review. Molecular Immunology. 61(2). 118–125. 95 indexed citations

17.

Yu, Yi, Michael Triebwasser, Edwin Wong, et al.. (2014). Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. Human Molecular Genetics. 23(19). 5283–5293. 82 indexed citations

18.

Lyzogubov, Valeriy V., Xiaobo Wu, Purushottam Jha, et al.. (2014). Complement Regulatory Protein CD46 Protects against Choroidal Neovascularization in Mice. American Journal Of Pathology. 184(9). 2537–2548. 32 indexed citations

19.

Seddon, Johanna M., Yi Yu, Elizabeth C. Miller, et al.. (2013). Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration. Nature Genetics. 45(11). 1366–1370. 262 indexed citations

20.

Salmon, Jane E., Cara Heuser, Michael Triebwasser, et al.. (2011). Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort. PLoS Medicine. 8(3). e1001013–e1001013. 221 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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