Flavia M. Facio

1.9k total citations · 1 hit paper
25 papers, 1.0k citations indexed

About

Flavia M. Facio is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Flavia M. Facio has authored 25 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Cancer Research. Recurrent topics in Flavia M. Facio's work include Genomics and Rare Diseases (15 papers), BRCA gene mutations in cancer (12 papers) and Cancer Genomics and Diagnostics (6 papers). Flavia M. Facio is often cited by papers focused on Genomics and Rare Diseases (15 papers), BRCA gene mutations in cancer (12 papers) and Cancer Genomics and Diagnostics (6 papers). Flavia M. Facio collaborates with scholars based in United States, Japan and Australia. Flavia M. Facio's co-authors include Leslie G. Biesecker, Barbara B. Biesecker, Haley Eidem, Campbell K. Brasington, Kelly E. Ormond, Pamela Flodman, Patricia Devers, Amy Cronister, James C. Mullikin and David Ng and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Atherosclerosis.

In The Last Decade

Flavia M. Facio

22 papers receiving 992 citations

Hit Papers

align trajectories sort by overperformance

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.

Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing

2023 78 citations Elaine Chen, Flavia M. Facio et al. JAMA Network Open profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Flavia M. Facio	650	285	260	166	149	25	1.0k
Guido M. W. R. de Wert	621 1.0×	318 1.1×	500 1.9×	140 0.8×	198 1.3×	20	1.2k
Ridgely Fisk Green	417 0.6×	161 0.6×	195 0.8×	77 0.5×	99 0.7×	23	865
Peter Könings	462 0.7×	193 0.7×	387 1.5×	142 0.9×	449 3.0×	33	1.3k
Karine Sénécal	556 0.9×	323 1.1×	262 1.0×	109 0.7×	111 0.7×	33	873
Carolyn Durham	679 1.0×	126 0.4×	174 0.7×	96 0.6×	124 0.8×	15	867
Katherine A. Schneider	817 1.3×	168 0.6×	362 1.4×	167 1.0×	329 2.2×	58	1.6k
Catherine Wicklund	451 0.7×	202 0.7×	288 1.1×	64 0.4×	59 0.4×	41	763
Irmgard Nippert	381 0.6×	128 0.4×	158 0.6×	41 0.2×	74 0.5×	44	592
Rachel Nusbaum	785 1.2×	170 0.6×	239 0.9×	175 1.1×	155 1.0×	28	1.0k
Marsha Michie	170 0.3×	231 0.8×	329 1.3×	35 0.2×	89 0.6×	44	663

Countries citing papers authored by Flavia M. Facio

Since Specialization

Citations

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

Fields of papers citing papers by Flavia M. Facio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Flavia M. Facio. 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 Flavia M. Facio. The network helps show where Flavia M. Facio may publish in the future.

Co-authorship network of co-authors of Flavia M. Facio

This figure shows the co-authorship network connecting the top 25 collaborators of Flavia M. Facio. A scholar is included among the top collaborators of Flavia M. Facio 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 Flavia M. Facio. Flavia M. Facio 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

Hatchell, Kathryn E., Emily M. Russell, Trevor Williams, et al.. (2025). Experience using conventional compared to ancestry-based population descriptors in clinical genomics laboratories. The American Journal of Human Genetics. 112(3). 481–491. 2 indexed citations

Manders, Toby, Christopher Tan, Yuya Kobayashi, et al.. (2025). Harnessing genotype and phenotype data for population-scale variant classification using large language models and bayesian inference. Human Genetics. 144(6). 605–614.

Kobayashi, Yuya, Elaine Chen, Flavia M. Facio, et al.. (2024). Clinical Variant Reclassification in Hereditary Disease Genetic Testing. JAMA Network Open. 7(11). e2444526–e2444526. 5 indexed citations

Johnson, Britt, Yuya Kobayashi, Elaine Chen, et al.. (2024). O31: The landscape of variant reclassification: Learnings from over 2 million classified variants in over 3.6 million individuals. SHILAP Revista de lepidopterología. 2. 101472–101472.

Aradhya, Swaroop, Flavia M. Facio, Toby Manders, et al.. (2023). Applications of artificial intelligence in clinical laboratory genomics. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(3). e32057–e32057. 28 indexed citations

Lehky, Tanya, Camilo Toro, Tianxia Wu, et al.. (2021). Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies. Muscle & Nerve. 63(4). 516–524. 4 indexed citations

Sapp, Julie C., Flavia M. Facio, Diane Cooper, et al.. (2021). A systematic literature review of disclosure practices and reported outcomes for medically actionable genomic secondary findings. Genetics in Medicine. 23(12). 2260–2269. 12 indexed citations

Feero, W, Flavia M. Facio, Emily Glogowski, et al.. (2014). Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General’s My Family Health Portrait. Genetics in Medicine. 17(9). 753–756. 7 indexed citations

Jamal, Leila, Julie C. Sapp, Katie L. Lewis, et al.. (2013). Research participants’ attitudes towards the confidentiality of genomic sequence information. European Journal of Human Genetics. 22(8). 964–968. 37 indexed citations

10.

Hercher, Laura, et al.. (2013). Stem Cell Research and Therapy: The Position of the National Society of Genetic Counselors. Journal of Genetic Counseling. 22(4). 407–410. 5 indexed citations

11.

Facio, Flavia M., et al.. (2012). Effects of informed consent for individual genome sequencing on relevant knowledge. Clinical Genetics. 82(5). 408–415. 90 indexed citations

12.

Johnston, Jennifer J., Wendy S. Rubinstein, Flavia M. Facio, et al.. (2012). Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes. The American Journal of Human Genetics. 91(1). 97–108. 155 indexed citations

13.

Facio, Flavia M., Haley Eidem, Stephanie Brooks, et al.. (2012). Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study. European Journal of Human Genetics. 21(3). 261–265. 139 indexed citations

14.

Facio, Flavia M., et al.. (2012). Genomic Inheritances: Disclosing Individual Research Results From Whole-Exome Sequencing to Deceased Participants’ Relatives. The American Journal of Bioethics. 12(10). 1–8. 40 indexed citations

15.

Facio, Flavia M., et al.. (2012). Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research. BMC Medical Genomics. 5(1). 15 indexed citations

16.

Facio, Flavia M., et al.. (2011). Motivators for participation in a whole-genome sequencing study: implications for translational genomics research. European Journal of Human Genetics. 19(12). 1213–1217. 113 indexed citations

17.

Facio, Flavia M., et al.. (2010). Validation of My Family Health Portrait for six common heritable conditions. Genetics in Medicine. 12(6). 370–375. 65 indexed citations

18.

Kang, Ju‐Gyeong, Ho Joong Sung, Sarah I. Jawed, et al.. (2010). FOS expression in blood as a LDL-independent marker of statin treatment. Atherosclerosis. 212(2). 567–570. 6 indexed citations

19.

Onel, Kenan, Flavia M. Facio, Noah D. Kauff, et al.. (2005). The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds. Familial Cancer. 4(2). 177–181. 19 indexed citations

20.

Onel, Kenan, et al.. (2004). The genetics of familial lymphomas. Current Oncology Reports. 6(5). 380–387. 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.

Explore authors with similar magnitude of impact