Tara Maga

1.7k total citations
21 papers, 874 citations indexed

About

Tara Maga is a scholar working on Immunology, Nephrology and Genetics. According to data from OpenAlex, Tara Maga has authored 21 papers receiving a total of 874 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Immunology, 9 papers in Nephrology and 9 papers in Genetics. Recurrent topics in Tara Maga's work include Renal Diseases and Glomerulopathies (9 papers), Complement system in diseases (9 papers) and BRCA gene mutations in cancer (7 papers). Tara Maga is often cited by papers focused on Renal Diseases and Glomerulopathies (9 papers), Complement system in diseases (9 papers) and BRCA gene mutations in cancer (7 papers). Tara Maga collaborates with scholars based in United States, France and Philippines. Tara Maga's co-authors include Richard J. Smith, Carla Nishimura, Amy E. Weaver, Kathy L. Frees, Carla Nester, Nicole C. Meyer, Christie P. Thomas, Fengxiao Bu, Kai Wang and Yuzhou Zhang and has published in prestigious journals such as Blood, Cancer and Cancer Research.

In The Last Decade

Tara Maga

20 papers receiving 859 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tara Maga United States 11 661 465 300 159 110 21 874
Andrew W. Pawluczkowycz United States 9 490 0.7× 49 0.1× 115 0.4× 95 0.6× 28 0.3× 17 773
Urs Wirthmueller Switzerland 11 467 0.7× 45 0.1× 84 0.3× 184 1.2× 8 0.1× 14 654
Elisabeth T Korthof Netherlands 13 208 0.3× 21 0.0× 605 2.0× 383 2.4× 14 0.1× 18 1.1k
Chiara Gentilini Germany 14 605 0.9× 22 0.0× 252 0.8× 177 1.1× 6 0.1× 24 932
Alexandra Croockewit Netherlands 12 367 0.6× 66 0.1× 396 1.3× 366 2.3× 2 0.0× 20 801
Lisa P. Chu United States 6 348 0.5× 36 0.1× 260 0.9× 243 1.5× 3 0.0× 8 786
Wim P.M. Tamboer Netherlands 10 210 0.3× 98 0.2× 42 0.1× 286 1.8× 3 0.0× 15 565
R. Leo Germany 8 283 0.4× 9 0.0× 347 1.2× 125 0.8× 10 0.1× 9 573
DA Carson United States 13 426 0.6× 15 0.0× 218 0.7× 338 2.1× 82 0.7× 16 1.3k
Paul Guglielmi France 14 415 0.6× 28 0.1× 116 0.4× 278 1.7× 2 0.0× 23 758

Countries citing papers authored by Tara Maga

Since Specialization
Citations

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

Fields of papers citing papers by Tara Maga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tara Maga

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

All Works

20 of 20 papers shown
1.
Maga, Tara, et al.. (2024). Risk-reducing salpingo-oophorectomy among diverse patients with BRCA mutations at an urban public hospital: a mixed methods study. BMJ Open. 14(6). e082608–e082608. 1 indexed citations
2.
Reizine, Natalie, et al.. (2023). Alternative model to deliver germline genetic testing to patients with advanced prostate cancer (PCa).. JCO Oncology Practice. 19(11_suppl). 123–123.
3.
Henderson, Vida, Jessica M. Madrigal, Jennifer Newsome, et al.. (2022). Pilot study of a culturally sensitive intervention to promote genetic counseling for breast cancer risk. BMC Health Services Research. 22(1). 826–826. 6 indexed citations
4.
Henderson, Vida, Ravneet Kaur, Jennifer Newsome, et al.. (2021). Development of a culturally sensitive narrative intervention to promote genetic counseling among African American women at risk for hereditary breast cancer. Cancer. 127(14). 2535–2544. 15 indexed citations
5.
Maga, Tara, et al.. (2020). Parental attitudes regarding the need for genetic services in a pediatric brain tumor survivorship program. Journal of Genetic Counseling. 30(2). 533–543. 2 indexed citations
6.
Singhal, Rishi, et al.. (2020). An Eye on Trafficking Genes: Identification of Four Eye Color Mutations in Drosophila. UNC Libraries. 1 indexed citations
7.
Maga, Tara, et al.. (2020). Adopted individuals’ interest in elective genomic testing. Journal of Medical Genetics. 59(2). 197–203. 5 indexed citations
8.
Postula, Kristen J. Vogel, et al.. (2020). Genetic counselors’ perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome. Journal of Genetic Counseling. 30(1). 158–169. 9 indexed citations
9.
Maga, Tara, et al.. (2017). Advantages and Some Remaining Challenges in Hereditary Gastrointestinal Cancer Panel Testing. Clinical and Translational Gastroenterology. 8(5). e92–e92. 3 indexed citations
10.
Maga, Tara, et al.. (2016). An Eye on Trafficking Genes: Identification of Four Eye Color Mutations inDrosophila. G3 Genes Genomes Genetics. 6(10). 3185–3196. 11 indexed citations
11.
Schramm, Elizabeth C., Lubka T. Roumenina, Tania Rybkine, et al.. (2015). Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome. Blood. 125(15). 2359–2369. 87 indexed citations
12.
Bu, Fengxiao, Tara Maga, Nicole C. Meyer, et al.. (2014). Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome. Japanese journal of pediatric nephrology. 27(1). 43–44. 3 indexed citations
13.
Bu, Fengxiao, Tara Maga, Nicole C. Meyer, et al.. (2013). Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology. 25(1). 55–64. 161 indexed citations
14.
Feng, Shuju, Yuzhou Zhang, Tara Maga, et al.. (2013). Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome. Blood. 122(8). 1487–1493. 58 indexed citations
15.
Nishimura, Carla, Kathy Frees, Michael P. Jones, et al.. (2011). Allelic Variants of Complement Genes Associated with Dense Deposit Disease. Journal of the American Society of Nephrology. 22(8). 1551–1559. 73 indexed citations
16.
Maga, Tara, Adam P. DeLuca, Kyle R. Taylor, et al.. (2011). Targeted-genomic capture and high-throughput sequencing for genetic testing and new gene discovery in atypical hemolytic uremic syndrome. Molecular Immunology. 48(14). 1666–1666. 1 indexed citations
17.
Maga, Tara, et al.. (2010). A novel mutation in the Complement Factor B gene (CFB) and atypical hemolytic uremic syndrome. Pediatric Nephrology. 25(5). 947–951. 39 indexed citations
18.
Maga, Tara, Carla Nishimura, Amy E. Weaver, Kathy L. Frees, & Richard J. Smith. (2010). Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Human Mutation. 31(6). E1445–E1460. 244 indexed citations
19.
Maga, Tara, Nicole C. Meyer, Craig W. Belsha, et al.. (2010). A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome. Nephrology Dialysis Transplantation. 26(2). 739–741. 41 indexed citations
20.
Horak, Christine E., Jong‐Heun Lee, Abdel Elkahloun, et al.. (2007). Nm23-H1 Suppresses Tumor Cell Motility by Down-regulating the Lysophosphatidic Acid Receptor EDG2. Cancer Research. 67(15). 7238–7246. 99 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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