Elizabeth T. Cirulli

19.5k total citations · 1 hit paper
50 papers, 2.8k citations indexed

About

Elizabeth T. Cirulli is a scholar working on Genetics, Molecular Biology and Pharmacology. According to data from OpenAlex, Elizabeth T. Cirulli has authored 50 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 18 papers in Molecular Biology and 7 papers in Pharmacology. Recurrent topics in Elizabeth T. Cirulli's work include Genetic Associations and Epidemiology (10 papers), Genomics and Rare Diseases (9 papers) and Genomic variations and chromosomal abnormalities (7 papers). Elizabeth T. Cirulli is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomics and Rare Diseases (9 papers) and Genomic variations and chromosomal abnormalities (7 papers). Elizabeth T. Cirulli collaborates with scholars based in United States, United Kingdom and Australia. Elizabeth T. Cirulli's co-authors include David B. Goldstein, Anna C. Need, Kevin V. Shianna, Dongliang Ge, Deborah K. Attix, Alex J. Bartholomew, Jessica M. Maia, Curtis Gumbs, Tim D. Spector and Erin L. Heinzen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Nature Communications.

In The Last Decade

Elizabeth T. Cirulli

50 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Uncovering the roles of rare variants in common disease through whole-genome sequencing

2010 777 citations Elizabeth T. Cirulli, David B. Goldstein Nature Reviews Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elizabeth T. Cirulli United States	28	1.1k	1.1k	270	265	242	50	2.8k
Brendan J. Keating United States	28	823 0.7×	909 0.8×	239 0.9×	279 1.1×	140 0.6×	102	2.8k
Audrey C. Papp United States	33	444 0.4×	1.7k 1.6×	244 0.9×	357 1.3×	387 1.6×	57	3.9k
Thomas F. Wienker Germany	32	755 0.7×	1.9k 1.8×	238 0.9×	317 1.2×	112 0.5×	79	4.1k
B.K. Thelma India	32	873 0.8×	768 0.7×	209 0.8×	371 1.4×	205 0.8×	139	2.8k
D. Holmes Morton United States	39	925 0.8×	2.5k 2.3×	562 2.1×	454 1.7×	260 1.1×	76	4.7k
Joyce Y. Tung United States	20	1.2k 1.1×	840 0.8×	344 1.3×	386 1.5×	187 0.8×	28	3.1k
Marie‐Pierre Dubé Canada	39	877 0.8×	1.7k 1.6×	479 1.8×	207 0.8×	400 1.7×	185	5.6k
Stacey B. Gabriel United States	11	1.6k 1.5×	1.7k 1.6×	121 0.4×	163 0.6×	262 1.1×	13	3.6k
Raquel Iniesta United Kingdom	13	384 0.3×	640 0.6×	253 0.9×	214 0.8×	203 0.8×	32	2.5k
Albert Tenesa United Kingdom	36	2.0k 1.8×	1.6k 1.5×	388 1.4×	473 1.8×	141 0.6×	90	5.7k

Countries citing papers authored by Elizabeth T. Cirulli

Since Specialization

Citations

This map shows the geographic impact of Elizabeth T. Cirulli'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 Elizabeth T. Cirulli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elizabeth T. Cirulli more than expected).

Fields of papers citing papers by Elizabeth T. Cirulli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth T. Cirulli. 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 Elizabeth T. Cirulli. The network helps show where Elizabeth T. Cirulli may publish in the future.

Co-authorship network of co-authors of Elizabeth T. Cirulli

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth T. Cirulli. A scholar is included among the top collaborators of Elizabeth T. Cirulli 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 Elizabeth T. Cirulli. Elizabeth T. Cirulli 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

Telis, Natalie, Douglas Stoller, Christopher Chapman, et al.. (2025). P190: Scalable system-wide CYP2C19 pharmacogenomic testing reveals excess incidence of adverse events in metabolizers receiving inappropriate prescriptions. Genetics in Medicine Open. 3. 102155–102155. 1 indexed citations

Barrett, Kelly M. Schiabor, Natalie Telis, Lisa M. McEwen, et al.. (2024). Underestimated risk of secondary complications in pathogenic and glucose-elevating GCK variant carriers with type 2 diabetes. SHILAP Revista de lepidopterología. 4(1). 239–239. 1 indexed citations

Washington, Nicole, Natalie Telis, Daniel P. Judge, et al.. (2024). Abstract 4147064: Retrospective study shows pharmacogenomic testing could reduce adverse events associated with clopidogrel use by 38%. Circulation. 150(Suppl_1). 1 indexed citations

Cirulli, Elizabeth T., Kelly M. Schiabor Barrett, Alexandre Bolze, et al.. (2024). A power-based sliding window approach to evaluate the clinical impact of rare genetic variants in the nucleotide sequence or the spatial position of the folded protein. Human Genetics and Genomics Advances. 5(3). 100284–100284. 1 indexed citations

Barrett, Kelly M. Schiabor, Elizabeth T. Cirulli, Alexandre Bolze, et al.. (2023). Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation. Genetics in Medicine. 25(4). 100012–100012. 20 indexed citations

Bolze, Alexandre, Iva Neveux, Kelly M. Schiabor Barrett, et al.. (2022). HLA-A∗03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination. Human Genetics and Genomics Advances. 3(2). 100084–100084. 29 indexed citations

Read, Robert W., Karen Schlauch, Vincent C. Lombardi, et al.. (2021). Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. Frontiers in Genetics. 12. 639418–639418. 9 indexed citations

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

Gelfman, Sahar, Sarah A. Dugger, Cristiane Araújo Martins Moreno, et al.. (2019). A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS. Genome Research. 29(5). 809–818. 14 indexed citations

10.

Fontana, Robert J., Elizabeth T. Cirulli, Jiezhun Gu, et al.. (2018). The role of HLA-A*33:01 in patients with cholestatic hepatitis attributed to terbinafine. Journal of Hepatology. 69(6). 1317–1325. 32 indexed citations

11.

Mori, Mari, Gloria Haskell, Zoheb B. Kazi, et al.. (2017). Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease. Molecular Genetics and Metabolism. 122(4). 189–197. 19 indexed citations

12.

Bartholomew, Alex J., Warren H. Meck, & Elizabeth T. Cirulli. (2015). Analysis of Genetic and Non-Genetic Factors Influencing Timing and Time Perception. PLoS ONE. 10(12). e0143873–e0143873. 39 indexed citations

13.

Bartholomew, Alex J. & Elizabeth T. Cirulli. (2014). Individual Variation in Contagious Yawning Susceptibility Is Highly Stable and Largely Unexplained by Empathy or Other Known Factors. PLoS ONE. 9(3). e91773–e91773. 49 indexed citations

14.

Zhu, Mingfu, Anna C. Need, Yujun Han, et al.. (2012). Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes. The American Journal of Human Genetics. 91(3). 408–421. 86 indexed citations

15.

Cirulli, Elizabeth T., Deborah K. Attix, Patrick J. Smith, et al.. (2011). Contribution of Pastimes and Testing Strategies to the Performance of Healthy Volunteers on Cognitive Tests. The Clinical Neuropsychologist. 25(5). 778–798. 5 indexed citations

16.

Cirulli, Elizabeth T., Erin L. Heinzen, Fred S. Dietrich, et al.. (2011). A whole-genome analysis of premature termination codons. Genomics. 98(5). 337–342. 10 indexed citations

17.

Fellay, Jacques, Nicole Frahm, Kevin V. Shianna, et al.. (2011). Host Genetic Determinants of T Cell Responses to the MRKAd5 HIV-1 gag/pol/nef Vaccine in the Step Trial. The Journal of Infectious Diseases. 203(6). 773–779. 23 indexed citations

18.

Cirulli, Elizabeth T. & David B. Goldstein. (2010). Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nature Reviews Genetics. 11(6). 415–425. 777 indexed citations breakdown →

19.

Cirulli, Elizabeth T., Dalia Kasperavičiūtė, Deborah K. Attix, et al.. (2010). Common genetic variation and performance on standardized cognitive tests. European Journal of Human Genetics. 18(7). 815–820. 74 indexed citations

20.

Cirulli, Elizabeth T. & Mohamed A. F. Noor. (2006). Localization and Characterization of X Chromosome Inversion Breakpoints Separating Drosophila mojavensis and Drosophila arizonae. Journal of Heredity. 98(2). 111–114. 6 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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