Tara Schmidlen

1.4k total citations
36 papers, 727 citations indexed

About

Tara Schmidlen is a scholar working on Genetics, Pharmacology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tara Schmidlen has authored 36 papers receiving a total of 727 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 8 papers in Pharmacology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tara Schmidlen's work include BRCA gene mutations in cancer (18 papers), Genomics and Rare Diseases (14 papers) and Pharmacogenetics and Drug Metabolism (8 papers). Tara Schmidlen is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Genomics and Rare Diseases (14 papers) and Pharmacogenetics and Drug Metabolism (8 papers). Tara Schmidlen collaborates with scholars based in United States, Switzerland and Canada. Tara Schmidlen's co-authors include Amy C. Sturm, Michael F. Christman, Erynn S. Gordon, M. Schwartz, H. Lester Kirchner, Neda Gharani, Laura Scheinfeldt, Margaret Keller, Catharine B. Stack and Norman P. Gerry and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Pharmaceutical Research.

In The Last Decade

Tara Schmidlen

35 papers receiving 711 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tara Schmidlen United States	17	433	130	111	97	78	36	727
Simon Sanderson United Kingdom	11	332 0.8×	92 0.7×	221 2.0×	110 1.1×	70 0.9×	18	1.0k
Katherine Johansen Taber United States	14	481 1.1×	233 1.8×	314 2.8×	328 3.4×	45 0.6×	31	1.1k
Marquitta J. White United States	16	210 0.5×	241 1.9×	27 0.2×	76 0.8×	126 1.6×	29	985
Joon‐Ho Yu United States	18	699 1.6×	349 2.7×	31 0.3×	114 1.2×	109 1.4×	38	1.1k
Rachel Mills United States	18	515 1.2×	265 2.0×	518 4.7×	372 3.8×	178 2.3×	51	1.2k
Eric Vermeulen Netherlands	17	216 0.5×	256 2.0×	24 0.2×	160 1.6×	119 1.5×	36	843
Monica Fujii United States	10	99 0.2×	107 0.8×	37 0.3×	42 0.4×	56 0.7×	28	561
Elisa J. F. Houwink Netherlands	21	855 2.0×	248 1.9×	310 2.8×	215 2.2×	141 1.8×	44	1.6k
Yixuan Song Japan	14	58 0.1×	60 0.5×	49 0.4×	69 0.7×	113 1.4×	22	954
Li‐Shiun Chen United States	17	260 0.6×	121 0.9×	14 0.1×	15 0.2×	93 1.2×	50	859

Countries citing papers authored by Tara Schmidlen

Since Specialization

Citations

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

Fields of papers citing papers by Tara Schmidlen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tara Schmidlen

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Rana, Huma Q., et al.. (2024). P517: Patient and clinician perspectives on a digital health platform for the longitudinal management of genetic cancer predisposition. SHILAP Revista de lepidopterología. 2. 101416–101416.

Kusic, Dara, Stefan Zajic, Neda Gharani, et al.. (2023). Genome-wide Association Study of Caffeine Consumption Using Coriell Personalized Medicine Collaborative Data. 5(1). 1 indexed citations

Campbell‐Salome, Gemme, Laney K. Jones, Ilene Ladd, et al.. (2023). Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia. BMC Health Services Research. 23(1). 340–340. 15 indexed citations

Savage, Sarah, et al.. (2023). Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study. SHILAP Revista de lepidopterología. 2. 100134–100134. 5 indexed citations

Schmidlen, Tara, et al.. (2022). Use of a chatbot to increase uptake of cascade genetic testing. Journal of Genetic Counseling. 31(5). 1219–1230. 43 indexed citations

Schmidlen, Tara, et al.. (2022). Implementing comprehensive pharmacogenomics in a community hospital–associated primary care setting. Journal of the American Pharmacists Association. 63(1). 188–192. 9 indexed citations

Ashcraft, Kristine, et al.. (2022). Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug–Gene, Drug–Drug–Gene, and Drug–Gene–Gene Interaction Risks in a Large Patient Population. Journal of Personalized Medicine. 12(12). 1972–1972. 4 indexed citations

Schmidlen, Tara, Sara L. Bristow, Kathryn E. Hatchell, et al.. (2022). The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives. Frontiers in Genetics. 13. 867226–867226. 21 indexed citations

Schmidlen, Tara, Amy C. Sturm, & Laura Scheinfeldt. (2020). Pharmacogenomic (PGx) Counseling: Exploring Participant Questions about PGx Test Results. Journal of Personalized Medicine. 10(2). 29–29. 7 indexed citations

10.

Hallquist, Miranda L. G., Michael N. Hallquist, Juliann M. Savatt, et al.. (2020). Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic. Genetics in Medicine. 22(8). 1348–1354. 28 indexed citations

11.

Schmidlen, Tara, et al.. (2019). Patient assessment of chatbots for the scalable delivery of genetic counseling. Journal of Genetic Counseling. 28(6). 1166–1177. 98 indexed citations

12.

Schmidlen, Tara, Amy C. Sturm, Shelly R. Hovick, et al.. (2018). Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Journal of Genetic Counseling. 27(5). 1111–1129. 22 indexed citations

13.

Sturm, Amy C., Tara Schmidlen, Laura Scheinfeldt, et al.. (2018). Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health. Journal of Personalized Medicine. 8(3). 25–25. 9 indexed citations

14.

Jones, Laney K., Tara Schmidlen, M. Schwartz, et al.. (2018). Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR. SHILAP Revista de lepidopterología. 6(1). 14–14. 12 indexed citations

15.

Sweet, Kevin, Amy C. Sturm, Tara Schmidlen, et al.. (2017). Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports. Journal of Genetic Counseling. 26(5). 980–998. 17 indexed citations

16.

Luzum, Jasmine A., Kevin Sweet, Philip F. Binkley, et al.. (2017). CYP2D6 Genetic Variation and Beta-Blocker Maintenance Dose in Patients with Heart Failure. Pharmaceutical Research. 34(8). 1615–1625. 22 indexed citations

17.

Sweet, Kevin, Shelly R. Hovick, Amy C. Sturm, et al.. (2016). Counselees’ Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study. Journal of Genetic Counseling. 26(4). 738–751. 16 indexed citations

18.

Scheinfeldt, Laura, Neda Gharani, Rachel Kasper, et al.. (2015). Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 168(8). 697–705. 28 indexed citations

19.

Gharani, Neda, Margaret Keller, Catharine B. Stack, et al.. (2013). The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system. Genome Medicine. 5(10). 93–93. 33 indexed citations

20.

Stack, Catharine B., Neda Gharani, Erynn S. Gordon, et al.. (2011). Genetic risk estimation in the Coriell Personalized Medicine Collaborative. Genetics in Medicine. 13(2). 131–139. 35 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.

Explore authors with similar magnitude of impact