Tara Biagi

5.0k total citations
12 papers, 982 citations indexed

About

Tara Biagi is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Tara Biagi has authored 12 papers receiving a total of 982 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Tara Biagi's work include BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (3 papers) and Genetic factors in colorectal cancer (3 papers). Tara Biagi is often cited by papers focused on BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (3 papers) and Genetic factors in colorectal cancer (3 papers). Tara Biagi collaborates with scholars based in United States, Sweden and Norway. Tara Biagi's co-authors include Kerstin Lindblad‐Toh, Claire M. Wade, Henrik von Euler, Elinor K. Karlsson, Michael C. Zody, Eric S. Lander, Jill P. Mesirov, Edward J. Kulbokas, Nathan Anderson and Olle Kämpe and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Tara Biagi

12 papers receiving 950 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tara Biagi United States	8	534	359	138	130	89	12	982
Marjo K. Hytönen Finland	18	565 1.1×	481 1.3×	121 0.9×	60 0.5×	26 0.3×	67	1.1k
Laurent Tiret France	22	277 0.5×	880 2.5×	56 0.4×	86 0.7×	37 0.4×	71	1.6k
Heidi Anderson United States	15	266 0.5×	373 1.0×	48 0.3×	45 0.3×	17 0.2×	41	777
Henry J. Baker United States	28	391 0.7×	990 2.8×	74 0.5×	69 0.5×	58 0.7×	63	2.0k
Oliver P. Forman United Kingdom	18	321 0.6×	410 1.1×	59 0.4×	37 0.3×	31 0.3×	37	805
Leigh Anne Clark United States	16	342 0.6×	310 0.9×	50 0.4×	47 0.4×	45 0.5×	40	871
Vidhya Jagannathan Switzerland	25	1.1k 2.0×	1.2k 3.4×	80 0.6×	125 1.0×	34 0.4×	191	2.4k
R. Leiser Germany	24	330 0.6×	489 1.4×	161 1.2×	36 0.3×	18 0.2×	64	1.7k
Mark Barnett United Kingdom	20	433 0.8×	986 2.7×	31 0.2×	65 0.5×	34 0.4×	32	1.5k
Dianne Gerrelli United Kingdom	27	801 1.5×	1.4k 3.8×	223 1.6×	38 0.3×	33 0.4×	47	2.2k

Countries citing papers authored by Tara Biagi

Since Specialization

Citations

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

Fields of papers citing papers by Tara Biagi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tara Biagi

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

All Works

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12 of 12 papers shown

Biagi, Tara, et al.. (2020). Racial disparities in breast cancer hereditary risk assessment referrals. Journal of Genetic Counseling. 29(4). 587–593. 46 indexed citations

Biagi, Tara, et al.. (2019). Relationship Between Hereditary Cancer Syndromes and Oncotype DX Recurrence Score. Clinical Breast Cancer. 20(2). 125–130. 5 indexed citations

Peterson, J.R., et al.. (2019). Abstract PD6-12: Evaluating racial disparities in breast cancer referrals for hereditary risk assessment. Cancer Research. 79(4_Supplement). PD6–12. 1 indexed citations

Biagi, Tara, et al.. (2018). Effects of Cancer Genetic Panel Testing on at-Risk Individuals. Obstetrics and Gynecology. 131(6). 1103–1110. 4 indexed citations

McHenry, Allison, et al.. (2018). The Perils of Single-Site Genetic Testing for Hereditary Cancer Syndromes in the Era of Next-Generation Sequencing. The Oncologist. 23(4). 393–396. 2 indexed citations

Grabherr, Manfred, Evan Mauceli, Wolfgang Ernst, et al.. (2011). Exploiting Nucleotide Composition to Engineer Promoters. PLoS ONE. 6(5). e20136–e20136. 19 indexed citations

Wilbe, Maria, Päivi Jokinen, Katarina Truvé, et al.. (2010). Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex. Nature Genetics. 42(3). 250–254. 90 indexed citations

Våge, Jørn, Claire M. Wade, Tara Biagi, et al.. (2010). Association of dopamine‐ and serotonin‐related genes with canine aggression. Genes Brain & Behavior. 9(4). 372–378. 44 indexed citations

Awano, Tomoyuki, Gary S. Johnson, Claire M. Wade, et al.. (2009). Genome-wide association analysis reveals aSOD1mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences. 106(8). 2794–2799. 182 indexed citations

10.

Rivera, Patricio, Malin Melin, Tara Biagi, et al.. (2009). Mammary Tumor Development in Dogs Is Associated with BRCA1 and BRCA2. Cancer Research. 69(22). 8770–8774. 113 indexed citations

11.

Wade, Claire M., et al.. (2008). A deletion in nephronophthisis 4 (NPHP4) is associated with recessive cone-rod dystrophy in standard wire-haired dachshund. Genome Research. 18(9). 1415–1421. 64 indexed citations

12.

Karlsson, Elinor K., Claire M. Wade, Michael C. Zody, et al.. (2007). Efficient mapping of mendelian traits in dogs through genome-wide association. Nature Genetics. 39(11). 1321–1328. 412 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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