Elissa Levin

805 total citations
6 papers, 72 citations indexed

About

Elissa Levin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Economics and Econometrics. According to data from OpenAlex, Elissa Levin has authored 6 papers receiving a total of 72 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Economics and Econometrics. Recurrent topics in Elissa Levin's work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (2 papers). Elissa Levin is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (3 papers) and Prenatal Screening and Diagnostics (2 papers). Elissa Levin collaborates with scholars based in United States. Elissa Levin's co-authors include James T. Lu, Sara Riordan, David Bick, Keith W. Dunaway, Sarah T. South, Kimberly A. Strong, Jill Hagenkord, Nicole Washington, Erick Loomis and Hyunseok P. Kang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics in Medicine and Journal of Molecular Diagnostics.

In The Last Decade

Elissa Levin

6 papers receiving 72 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elissa Levin United States	6	54	23	12	11	11	6	72
Sian Greening Australia	5	51 0.9×	16 0.7×	9 0.8×	17 1.5×	14 1.3×	6	78
Amanda L. Lazzeri United States	4	80 1.5×	20 0.9×	24 2.0×	7 0.6×	11 1.0×	4	111
Gemma R. Brett Australia	7	126 2.3×	42 1.8×	14 1.2×	11 1.0×	34 3.1×	10	163
Minh Thu Nguyen Canada	6	55 1.0×	38 1.7×	7 0.6×	11 1.0×	23 2.1×	11	107
Rachel Barnett United States	3	57 1.1×	16 0.7×	3 0.3×	3 0.3×	19 1.7×	5	68
Caroline McGowan United States	4	29 0.5×	7 0.3×	3 0.3×	5 0.5×	15 1.4×	7	60
Samantha Ayres Australia	4	66 1.2×	13 0.6×	4 0.3×	5 0.5×	32 2.9×	8	74
Sylvia Mann Au United States	5	50 0.9×	22 1.0×	7 0.6×	12 1.1×	54 4.9×	8	125
Kate Brunstrom United Kingdom	2	33 0.6×	8 0.3×	5 0.4×	3 0.3×	12 1.1×	2	39
Alyson Krokosky United States	5	41 0.8×	13 0.6×	3 0.3×	6 0.5×	7 0.6×	10	63

Countries citing papers authored by Elissa Levin

Since Specialization

Citations

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

Fields of papers citing papers by Elissa Levin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elissa Levin

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

All Works

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6 of 6 papers shown

1.

Allen, Caitlin G., Daniel P. Judge, Elissa Levin, et al.. (2022). A pragmatic implementation research study for In Our DNA SC: a protocol to identify multi-level factors that support the implementation of a population-wide genomic screening initiative in diverse populations. SHILAP Revista de lepidopterología. 3(1). 48–48. 11 indexed citations

2.

Allen, Caitlin G., Leslie Lenert, Kelly J. Hunt, et al.. (2022). Lessons Learned from the Pilot Phase of a Population-Wide Genomic Screening Program: Building the Base to Reach a Diverse Cohort of 100,000 Participants. Journal of Personalized Medicine. 12(8). 1228–1228. 7 indexed citations

3.

Barrett, Kelly M. Schiabor, Alexandre Bolze, Yunyun Ni, et al.. (2021). Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records. Genetics in Medicine. 23(12). 2300–2308. 8 indexed citations

4.

Dunaway, Keith W., Erick Loomis, Stephen Riffle, et al.. (2019). Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world. Journal of Genetic Counseling. 28(2). 456–465. 18 indexed citations

5.

Lu, James T., Matthew J. Ferber, Jill Hagenkord, et al.. (2018). Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing. Journal of Molecular Diagnostics. 21(1). 3–12. 18 indexed citations

6.

Levin, Elissa, et al.. (2012). Genetic Counseling for Personal Genomic Testing: Optimizing Client Uptake of Post‐Test Telephonic Counseling Services. Journal of Genetic Counseling. 21(3). 462–468. 10 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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