Sabrina A. Suckiel

1.2k total citations
23 papers, 467 citations indexed

About

Sabrina A. Suckiel is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Sabrina A. Suckiel has authored 23 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Sabrina A. Suckiel's work include Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (15 papers) and Cancer Genomics and Diagnostics (4 papers). Sabrina A. Suckiel is often cited by papers focused on Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (15 papers) and Cancer Genomics and Diagnostics (4 papers). Sabrina A. Suckiel collaborates with scholars based in United States, United Kingdom and Australia. Sabrina A. Suckiel's co-authors include Saskia C. Sanderson, Michael D. Linderman, George A. Díaz, Eric E. Schadt, Andrew Kasarskis, Randi E. Zinberg, Melissa Wasserstein, Eimear E. Kenny, Noura S. Abul‐Husn and Micol Zweig and has published in prestigious journals such as SHILAP Revista de lepidopterología, Patient Education and Counseling and Genetics in Medicine.

In The Last Decade

Sabrina A. Suckiel

21 papers receiving 460 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sabrina A. Suckiel United States	13	323	142	92	60	48	23	467
Denise Lautenbach United States	9	363 1.1×	114 0.8×	60 0.7×	99 1.6×	36 0.8×	10	499
Tiffany Boughtwood Australia	11	342 1.1×	189 1.3×	117 1.3×	58 1.0×	54 1.1×	29	611
Randi E. Zinberg United States	13	311 1.0×	196 1.4×	76 0.8×	48 0.8×	80 1.7×	24	467
Katherine S. Hunt United States	11	283 0.9×	113 0.8×	80 0.9×	111 1.9×	80 1.7×	17	565
Sherry Grumet United States	6	322 1.0×	81 0.6×	49 0.5×	59 1.0×	84 1.8×	13	428
Belinda Rahman Australia	13	434 1.3×	128 0.9×	101 1.1×	82 1.4×	115 2.4×	27	633
Karen Powell United States	15	374 1.2×	150 1.1×	48 0.5×	39 0.7×	64 1.3×	22	565
Miranda L. G. Hallquist United States	10	201 0.6×	83 0.6×	30 0.3×	29 0.5×	42 0.9×	14	311
Margaret M. McGovern United States	9	257 0.8×	88 0.6×	39 0.4×	55 0.9×	39 0.8×	13	344
Anne‐Marie Laberge Canada	15	230 0.7×	148 1.0×	85 0.9×	30 0.5×	215 4.5×	55	604

Countries citing papers authored by Sabrina A. Suckiel

Since Specialization

Citations

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

Fields of papers citing papers by Sabrina A. Suckiel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabrina A. Suckiel

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

All Works

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20 of 20 papers shown

Biesecker, Barbara B., Sara Ackerman, Kyle B. Brothers, et al.. (2025). Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results. Genetics in Medicine. 27(4). 101363–101363.

Scollon, Sarah, Jill O. Robinson, Sabrina A. Suckiel, et al.. (2024). Satisfaction with mode of delivery of genomic sequencing results in a diverse national sample of research participants through the Clinical Sequencing Evidence-Generating Research Consortium. Genetics in Medicine. 26(9). 101176–101176.

Wand, Hannah, Sarah S. Kalia, Benjamin M. Helm, et al.. (2023). Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors. Journal of Genetic Counseling. 32(3). 558–575. 18 indexed citations

Suckiel, Sabrina A., et al.. (2022). Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores. Genetics in Medicine. 24(6). 1217–1226. 12 indexed citations

Suckiel, Sabrina A., et al.. (2022). Elective genetic testing: Genetics professionals’ perspectives and practices. Journal of Genetic Counseling. 32(3). 607–617. 1 indexed citations

Suckiel, Sabrina A., Julianne O’Daniel, Katie M. Gallagher, et al.. (2021). Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium. Journal of Personalized Medicine. 11(3). 202–202. 6 indexed citations

Dolan, Siobhan M., Dana Watnick, Katie M. Gallagher, et al.. (2021). Hope versus reality: Parent expectations of genomic testing. Patient Education and Counseling. 104(8). 2073–2079. 15 indexed citations

Abul‐Husn, Noura S., Emily R. Soper, Jessica Rodriguez, et al.. (2021). Implementing genomic screening in diverse populations. Genome Medicine. 13(1). 17–17. 39 indexed citations

Linderman, Michael D., Sabrina A. Suckiel, Nathan A. Thompson, et al.. (2021). Development and Validation of a Comprehensive Genomics Knowledge Scale. Public Health Genomics. 24(5-6). 291–303. 5 indexed citations

10.

Watnick, Dana, Jacqueline A. Odgis, Sabrina A. Suckiel, et al.. (2021). “Is that something that should concern me?”: a qualitative exploration of parent understanding of their child’s genomic test results. SHILAP Revista de lepidopterología. 2(2). 100027–100027. 7 indexed citations

11.

Pearson, Nathaniel M., Christian Stolte, Kevin Shi, et al.. (2021). GenomeDiver: a platform for phenotype-guided medical genomic diagnosis. Genetics in Medicine. 23(10). 1998–2002. 5 indexed citations

12.

Ang, Celina, Sabrina A. Suckiel, Emily R. Soper, et al.. (2020). Lynch Syndrome–Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank. JCO Precision Oncology. 4(4). 1429–1444. 13 indexed citations

13.

Biesecker, Barbara B., Sarah E. Lillie, Laura M. Amendola, et al.. (2020). A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research. Journal of Genetic Counseling. 30(1). 42–50. 9 indexed citations

14.

Abul‐Husn, Noura S., Emily R. Soper, Jacqueline A. Odgis, et al.. (2019). Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank. Genome Medicine. 12(1). 2–2. 70 indexed citations

15.

Linderman, Michael D., Saskia C. Sanderson, Ali Bashir, et al.. (2018). Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years. BMC Medical Genomics. 11(1). 5–5. 13 indexed citations

16.

Sanderson, Saskia C., Michael D. Linderman, Sabrina A. Suckiel, et al.. (2017). Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project. European Journal of Human Genetics. 25(3). 280–292. 49 indexed citations

17.

Linderman, Michael D., Ali Bashir, George A. Díaz, et al.. (2015). Preparing the next generation of genomicists: a laboratory-style course in medical genomics. BMC Medical Genomics. 8(1). 47–47. 14 indexed citations

18.

Sanderson, Saskia C., Michael D. Linderman, Sabrina A. Suckiel, et al.. (2015). Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project. European Journal of Human Genetics. 24(1). 14–20. 90 indexed citations

19.

Sanderson, Saskia C., Michael D. Linderman, Randi E. Zinberg, et al.. (2015). How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study. Genetics in Medicine. 17(11). 866–874. 21 indexed citations

20.

Sanderson, Saskia C., Sabrina A. Suckiel, Micol Zweig, et al.. (2015). Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public. Genetics in Medicine. 18(5). 501–512. 49 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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