Marija Tadin‐Strapps

1.1k total citations
19 papers, 596 citations indexed

About

Marija Tadin‐Strapps is a scholar working on Molecular Biology, Surgery and Urology. According to data from OpenAlex, Marija Tadin‐Strapps has authored 19 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Surgery and 4 papers in Urology. Recurrent topics in Marija Tadin‐Strapps's work include Hair Growth and Disorders (4 papers), RNA Interference and Gene Delivery (4 papers) and Skin and Cellular Biology Research (3 papers). Marija Tadin‐Strapps is often cited by papers focused on Hair Growth and Disorders (4 papers), RNA Interference and Gene Delivery (4 papers) and Skin and Cellular Biology Research (3 papers). Marija Tadin‐Strapps collaborates with scholars based in United States, Mexico and France. Marija Tadin‐Strapps's co-authors include Jyoti Disa, Sarah Jinn, Robert E. Drolet, Paige E. Cramer, Dawn Toolan, Bhavya Voleti, Galya Vassileva, David J. Stone, Dorothy Warburton and Angela M. Christiano and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Journal of Lipid Research.

In The Last Decade

Marija Tadin‐Strapps

19 papers receiving 584 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marija Tadin‐Strapps United States 14 255 110 81 80 76 19 596
Claudia A. Benavente United States 15 376 1.5× 73 0.7× 54 0.7× 42 0.5× 33 0.4× 24 709
Midhat S. Farooqi United States 11 318 1.2× 50 0.5× 92 1.1× 127 1.6× 35 0.5× 31 595
Rei Nakamura United States 13 621 2.4× 54 0.5× 91 1.1× 110 1.4× 14 0.2× 17 1.1k
Emanuela Bottani Italy 14 585 2.3× 29 0.3× 77 1.0× 74 0.9× 43 0.6× 25 810
Nicolas Kuperwasser France 11 554 2.2× 112 1.0× 171 2.1× 35 0.4× 16 0.2× 14 848
Ginat Narkis Israel 14 528 2.1× 107 1.0× 50 0.6× 38 0.5× 72 0.9× 23 836
Zongxiang Zhou China 16 481 1.9× 63 0.6× 44 0.5× 37 0.5× 20 0.3× 25 785
Risa Nonaka Japan 16 219 0.9× 171 1.6× 59 0.7× 36 0.5× 42 0.6× 22 598
Ching-Fang Chang Taiwan 12 285 1.1× 80 0.7× 33 0.4× 43 0.5× 9 0.1× 18 571
Shun-Ai Li Japan 14 643 2.5× 188 1.7× 98 1.2× 59 0.7× 32 0.4× 17 1.0k

Countries citing papers authored by Marija Tadin‐Strapps

Since Specialization
Citations

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

Fields of papers citing papers by Marija Tadin‐Strapps

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marija Tadin‐Strapps. 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 Marija Tadin‐Strapps. The network helps show where Marija Tadin‐Strapps may publish in the future.

Co-authorship network of co-authors of Marija Tadin‐Strapps

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

All Works

19 of 19 papers shown
1.
Murphy, Beth, Marija Tadin‐Strapps, Kristian K. Jensen, et al.. (2017). siRNA-mediated inhibition of SREBP cleavage-activating protein reduces dyslipidemia in spontaneously dysmetabolic rhesus monkeys. Metabolism. 71. 202–212. 9 indexed citations
2.
Jinn, Sarah, Robert E. Drolet, Paige E. Cramer, et al.. (2017). TMEM175 deficiency impairs lysosomal and mitochondrial function and increases α-synuclein aggregation. Proceedings of the National Academy of Sciences. 114(9). 2389–2394. 177 indexed citations
3.
Khan, Tayeba, Hans Weber, Jillian DiMuzio, et al.. (2016). Silencing Myostatin Using Cholesterol-conjugated siRNAs Induces Muscle Growth. Molecular Therapy — Nucleic Acids. 5(8). e342–e342. 71 indexed citations
4.
Wood, Harold B., Jiayi Xu, Wayne M. Geissler, et al.. (2016). Preclinical and translational evaluation of coagulation factor IXa as a novel therapeutic target. Pharmacology Research & Perspectives. 4(1). e00207–e00207. 14 indexed citations
5.
Cai, Tian‐Quan, Weizhen Wu, Myung K. Shin, et al.. (2015). Factor XII full and partial null in rat confers robust antithrombotic efficacy with no bleeding. Blood Coagulation & Fibrinolysis. 26(8). 893–902. 20 indexed citations
6.
Hamza, Mohamed Sabry, Walter Strapps, M. Robinson, et al.. (2015). Alterations in the hepatic transcriptional landscape after RNAi mediated ApoB silencing in cynomolgus monkeys. Atherosclerosis. 242(2). 383–395. 6 indexed citations
7.
Tadin‐Strapps, Marija, et al.. (2015). Development of Lipoprotein(a) siRNAs for Mechanism of Action Studies in Non-Human Primate Models of Atherosclerosis. Journal of Cardiovascular Translational Research. 8(1). 44–53. 15 indexed citations
8.
DeStefano, Gina M., Mazen Kurban, Kwame Anyane‐Yeboa, et al.. (2014). Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth. PLoS Genetics. 10(5). e1004333–e1004333. 39 indexed citations
9.
Olearczyk, J, Sheng Gao, Marianne Eybye, et al.. (2013). Targeting of hepatic angiotensinogen using chemically modified siRNAs results in significant and sustained blood pressure lowering in a rat model of hypertension. Hypertension Research. 37(5). 405–412. 39 indexed citations
10.
DeStefano, Gina M., Katherine A. Fantauzzo, Lynn Petukhova, et al.. (2013). Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis. Proceedings of the National Academy of Sciences. 110(19). 7790–7795. 39 indexed citations
11.
Tep, Samnang, Victoria Pickering, Marija Tadin‐Strapps, et al.. (2012). Rescue of Mtp siRNA-induced hepatic steatosis by DGAT2 siRNA silencing. Journal of Lipid Research. 53(5). 859–867. 14 indexed citations
12.
Ason, Brandon, Samnang Tep, Yiming Xu, et al.. (2011). Improved efficacy for ezetimibe and rosuvastatin by attenuating the induction of PCSK9. Journal of Lipid Research. 52(4). 679–687. 36 indexed citations
13.
Castro‐Perez, José, Thomas P. Roddy, Vinit Shah, et al.. (2011). Attenuation of Slc27a5 Gene Expression Followed by LC–MS Measurement of Bile Acid Reconjugation Using Metabolomics and a Stable Isotope Tracer Strategy. Journal of Proteome Research. 10(10). 4683–4691. 5 indexed citations
14.
Ason, Brandon, José Castro‐Perez, Samnang Tep, et al.. (2011). ApoB siRNA‐induced Liver Steatosis is Resistant to Clearance by the Loss of Fatty Acid Transport Protein 5 (Fatp5). Lipids. 46(11). 991–1003. 34 indexed citations
15.
Fantauzzo, Katherine A., Marija Tadin‐Strapps, Yu You, et al.. (2008). A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice. Human Molecular Genetics. 17(22). 3539–3551. 42 indexed citations
16.
Tadin‐Strapps, Marija, et al.. (2004). Fishing for new genes in skin biology: impact of cytogenetics on gene discovery. Clinical Genetics. 66(2). 94–106. 1 indexed citations
17.
Tadin‐Strapps, Marija, Dorothy Warburton, F. A. M. Baumeister, et al.. (2004). Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenetic and Genome Research. 107(1-2). 68–76. 17 indexed citations
18.
Tadin‐Strapps, Marija, et al.. (2003). Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X‐linked trait. Clinical Genetics. 63(5). 418–422. 13 indexed citations
19.
Horev, Liran, Amalia Martı́nez-Mir, Marija Tadin‐Strapps, et al.. (2003). Identification of mutations in theCOL7A1gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency. Clinical and Experimental Dermatology. 28(1). 80–84. 5 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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