Beth A. Tarini

3.5k total citations
74 papers, 2.1k citations indexed

About

Beth A. Tarini is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Beth A. Tarini has authored 74 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 26 papers in Pediatrics, Perinatology and Child Health and 19 papers in Clinical Biochemistry. Recurrent topics in Beth A. Tarini's work include Genomics and Rare Diseases (23 papers), BRCA gene mutations in cancer (21 papers) and Metabolism and Genetic Disorders (19 papers). Beth A. Tarini is often cited by papers focused on Genomics and Rare Diseases (23 papers), BRCA gene mutations in cancer (21 papers) and Metabolism and Genetic Disorders (19 papers). Beth A. Tarini collaborates with scholars based in United States, Canada and Vietnam. Beth A. Tarini's co-authors include Aaron J. Goldenberg, Dimitri Christakis, Ingrid A. Larson, Robert A. Saul, Matthew M. Davis, Marilyn C. Jones, Emily Chen, Debra Freedenberg, Joan M. Stoler and John B. Moeschler and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Vaccine.

In The Last Decade

Beth A. Tarini

71 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beth A. Tarini United States 26 933 549 461 289 264 74 2.1k
Michele A. Lloyd-Puryear United States 27 1.1k 1.1× 918 1.7× 335 0.7× 974 3.4× 677 2.6× 72 2.9k
Marie Y. Mann United States 21 506 0.5× 880 1.6× 140 0.3× 711 2.5× 328 1.2× 44 2.1k
Alison M. Elliott Canada 25 662 0.7× 344 0.6× 373 0.8× 33 0.1× 371 1.4× 117 2.5k
Ian Porter United Kingdom 23 307 0.3× 413 0.8× 233 0.5× 89 0.3× 272 1.0× 76 1.7k
Brian D. Gonzalez United States 28 156 0.2× 361 0.7× 396 0.9× 62 0.2× 302 1.1× 116 2.4k
Holly Etchegary Canada 22 476 0.5× 256 0.5× 323 0.7× 43 0.1× 115 0.4× 104 1.5k
Siobhan M. Dolan United States 27 382 0.4× 1.5k 2.8× 857 1.9× 51 0.2× 277 1.0× 93 3.2k
George A. Burghen United States 25 322 0.3× 576 1.0× 698 1.5× 68 0.2× 338 1.3× 58 2.8k
James R. Eckman United States 39 151 0.2× 1.1k 2.0× 258 0.6× 90 0.3× 497 1.9× 90 4.2k
Rajat Das Gupta United States 22 102 0.1× 308 0.6× 332 0.7× 77 0.3× 176 0.7× 115 1.7k

Countries citing papers authored by Beth A. Tarini

Since Specialization
Citations

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

Fields of papers citing papers by Beth A. Tarini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beth A. Tarini. 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 Beth A. Tarini. The network helps show where Beth A. Tarini may publish in the future.

Co-authorship network of co-authors of Beth A. Tarini

This figure shows the co-authorship network connecting the top 25 collaborators of Beth A. Tarini. A scholar is included among the top collaborators of Beth A. Tarini 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 Beth A. Tarini. Beth A. Tarini 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.
Heo, Moonseong, Corinna J. Rea, Tammy M. Brady, et al.. (2025). Racial and Ethnic Disparities in Pediatric Counseling on Nutrition, Lifestyle, and Weight. JAMA Network Open. 8(1). e2456238–e2456238.
2.
Peshkin, Beth N., Jada G. Hamilton, Mingqian Liu, et al.. (2025). Parental Communication With their Children about Cancer Risk and DTC Cascade Genetic Testing: Implications for Genetic Education and Counseling. American Journal of Medical Genetics Part A. 197(9). e64115–e64115.
3.
Peshkin, Beth N., Jada G. Hamilton, Jamie Brower, et al.. (2023). Measuring high‐risk parents' opinions about direct‐to‐consumer genetic testing for adult‐onset inherited cancer syndromes in their adolescent and young adult children. Journal of Genetic Counseling. 32(4). 768–777. 2 indexed citations
4.
Tarini, Beth A., et al.. (2023). The Krabbe Conundrum Is Really a Newborn Screening Conundrum. JAMA Pediatrics. 177(10). 1007–1007. 1 indexed citations
5.
Soranno, Danielle E., Tamara D. Simon, Samudragupta Bora, et al.. (2023). Justice, Equity, Diversity, and Inclusion in the Pediatric Faculty Research Workforce: Call to Action. PEDIATRICS. 152(3). 3 indexed citations
6.
Williams, Kirsten M., A. Desirée LaBeaud, Robert F. Sidonio, et al.. (2021). COVID-19 Cliff Notes: A COVID-19 Multidisciplinary Care Compendium. Transplantation and Cellular Therapy. 27(6). 474.e1–474.e3. 1 indexed citations
7.
Tarini, Beth A., et al.. (2019). Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result. Journal of Community Genetics. 10(4). 447–451. 3 indexed citations
8.
Tarini, Beth A., et al.. (2019). Vaccine administration error rates at a large academic medical center and its affiliated clinics – Familiarity matters. Vaccine. 37(36). 5390–5396. 5 indexed citations
9.
Childerhose, Janet E., et al.. (2017). Adolescent bariatric surgery: a systematic review of recommendation documents. Surgery for Obesity and Related Diseases. 13(10). 1768–1779. 15 indexed citations
10.
Tarini, Beth A., et al.. (2016). Biobank participant support of newborn screening for disorders with variable treatment and intervention options. Journal of Community Genetics. 7(4). 291–302. 1 indexed citations
11.
Lillie, Sarah E., Beth A. Tarini, Nancy K. Janz, & Brian J. Zikmund‐Fisher. (2015). Framing optional genetic testing in the context of mandatory newborn screening tests. BMC Medical Informatics and Decision Making. 15(1). 50–50. 5 indexed citations
12.
Larson, Ingrid A., et al.. (2014). Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature. Genetics in Medicine. 17(3). 169–176. 190 indexed citations
13.
Goldenberg, Aaron J., et al.. (2013). Parents’ interest in whole-genome sequencing of newborns. Genetics in Medicine. 16(1). 78–84. 77 indexed citations
14.
Tarini, Beth A., Laura Konczal, Aaron J. Goldenberg, Edward B. Goldman, & Shawn E. McCandless. (2013). The Perils of SNP Microarray Testing: Uncovering Unexpected Consanguinity. Pediatric Neurology. 49(1). 50–53. 5 indexed citations
15.
Lee, Joyce M., et al.. (2013). Screening Practices for Identifying Type 2 Diabetes in Adolescents. Journal of Adolescent Health. 54(2). 139–143. 24 indexed citations
16.
Prosser, Lisa A., Scott D. Grosse, Alex R. Kemper, Beth A. Tarini, & James M. Perrin. (2012). Decision analysis, economic evaluation, and newborn screening: challenges and opportunities. Genetics in Medicine. 14(8). 703–712. 34 indexed citations
17.
Burke, Wylie, et al.. (2011). Genetic Screening. Epidemiologic Reviews. 33(1). 148–164. 52 indexed citations
18.
Lee, Joyce M., et al.. (2010). Diagnosis of Diabetes using Hemoglobin A1c: Should Recommendations in Adults Be Extrapolated to Adolescents?. The Journal of Pediatrics. 158(6). 947–952.e3. 71 indexed citations
19.
Tarini, Beth A.. (2007). The Current Revolution in Newborn Screening. Archives of Pediatrics and Adolescent Medicine. 161(8). 767–767. 46 indexed citations
20.
Tarini, Beth A., Michelle M. Garrison, & Dimitri Christakis. (2007). Institutional variation in ordering complete blood counts for children hospitalized with bronchiolitis. Journal of Hospital Medicine. 2(2). 69–73. 7 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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