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, Australia and Netherlands. Flavia M. Facio's co-authors include Leslie G. Biesecker, Barbara B. Biesecker, Haley Eidem, Kelly E. Ormond, Pamela Flodman, Patricia Devers, Amy Cronister, Campbell K. Brasington, David Ng and Wendy S. Rubinstein 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

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 →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Experience using conventional compared to ancestry-based population descriptors in clinical genomics laboratories 2025 ·The American Journal of Human Genetics ·Kathryn E. Hatchell, (unknown), Emily M. Russell, Trevor Williams, Rachel E. Ellsworth, Flavia M. Facio, (unknown), Edward D. Esplin, Alice B. Popejoy, Robert L. Nussbaum, Swaroop Aradhya	2
2	Harnessing genotype and phenotype data for population-scale variant classification using large language models and bayesian inference 2025 ·Human Genetics ·Toby Manders, Christopher Tan, Yuya Kobayashi, (unknown), Carlos L. Araya, Alexandre Colavin, Flavia M. Facio, (unknown), Jason Reuter, Laure Frésard, Samskruthi Reddy Padigepati, David Stafford, Robert L. Nussbaum, Keith Nykamp	0
3	Clinical Variant Reclassification in Hereditary Disease Genetic Testing 2024 ·JAMA Network Open ·Yuya Kobayashi, Elaine Chen, Flavia M. Facio, (unknown), (unknown), Dan Swartzlander, Britt Johnson, Swaroop Aradhya	5
4	O31: The landscape of variant reclassification: Learnings from over 2 million classified variants in over 3.6 million individuals 2024 ·SHILAP Revista de lepidopterología ·Britt Johnson, Yuya Kobayashi, Elaine Chen, Dan Swartzlander, Flavia M. Facio, Swaroop Aradhya	0
5	Applications of artificial intelligence in clinical laboratory genomics 2023 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Swaroop Aradhya, Flavia M. Facio, (unknown), Toby Manders, Alexandre Colavin, Yuya Kobayashi, Keith Nykamp, Britt Johnson, Robert L. Nussbaum	28
6	Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies 2021 ·Muscle & Nerve ·Tanya Lehky, (unknown), Camilo Toro, Tianxia Wu, Carol Van Ryzin, Andrea Gropman, Flavia M. Facio, Bryn D. Webb, Ethylin Wang Jabs, (unknown), Elizabeth C. Engle, Francis S. Collins, Irini Manoli	4
7	A systematic literature review of disclosure practices and reported outcomes for medically actionable genomic secondary findings 2021 ·Genetics in Medicine ·Julie C. Sapp, Flavia M. Facio, Diane Cooper, Katie L. Lewis, (unknown), Philip J. van der Wees, Leslie G. Biesecker	12
8	Preliminary validation of a consumer-oriented colorectal cancer risk assessment tool compatible with the US Surgeon General’s My Family Health Portrait 2014 ·Genetics in Medicine ·W Feero, Flavia M. Facio, Emily Glogowski, Heather L. Hampel, Jill E. Stopfer, Haley Eidem, Amy Pizzino, David K. Barton, Leslie G. Biesecker	7
9	Research participants’ attitudes towards the confidentiality of genomic sequence information 2013 ·European Journal of Human Genetics ·Leila Jamal, Julie C. Sapp, Katie L. Lewis, Tatiane Yanes, Flavia M. Facio, Leslie G. Biesecker, Barbara B. Biesecker	37
10	Stem Cell Research and Therapy: The Position of the National Society of Genetic Counselors 2013 ·Journal of Genetic Counseling ·(unknown), Laura Hercher, Flavia M. Facio, (unknown), Susan Hahn, Julie C. Sapp, Heather Zierhut	5
11	Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes 2012 ·The American Journal of Human Genetics ·Jennifer J. Johnston, Wendy S. Rubinstein, Flavia M. Facio, David Ng, Larry N. Singh, Jamie K. Teer, James C. Mullikin, Leslie G. Biesecker	155
12	Effects of informed consent for individual genome sequencing on relevant knowledge 2012 ·Clinical Genetics ·(unknown), Flavia M. Facio, (unknown), Stephen R. Brooks, Haley Eidem, Annē Linn, Barbara B. Biesecker, (unknown)	90
13	Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study 2012 ·European Journal of Human Genetics ·Flavia M. Facio, Haley Eidem, (unknown), Stephanie Brooks, (unknown), Kimberly A. Kaphingst, Leslie G. Biesecker, Barbara B. Biesecker	139
14	Genomic Inheritances: Disclosing Individual Research Results From Whole-Exome Sequencing to Deceased Participants’ Relatives 2012 ·The American Journal of Bioethics ·(unknown), Flavia M. Facio, Haley Eidem, Sara Chandros Hull, Leslie G. Biesecker, Benjamin E. Berkman	40
15	Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research 2012 ·BMC Medical Genomics ·Flavia M. Facio, Julie C. Sapp, (unknown), Leslie G. Biesecker	15
16	Motivators for participation in a whole-genome sequencing study: implications for translational genomics research 2011 ·European Journal of Human Genetics ·Flavia M. Facio, Stephanie Brooks, (unknown), Susannah Green, Leslie G. Biesecker, Barbara B. Biesecker	113
17	Validation of My Family Health Portrait for six common heritable conditions 2010 ·Genetics in Medicine ·Flavia M. Facio, W Feero, (unknown), Neal L. Oden, Kandamurugu Manickam, Leslie G. Biesecker	65
18	FOS expression in blood as a LDL-independent marker of statin treatment 2010 ·Atherosclerosis ·Ju‐Gyeong Kang, Ho Joong Sung, Sarah I. Jawed, (unknown), (unknown), Salman Sher, Flavia M. Facio, Leslie G. Biesecker, Arshed A. Quyyumi, Vandana Sachdev, Paul M. Hwang	6
19	The TP53 mutational spectrum and frequency of CHEK21100delC in Li–Fraumeni-like kindreds 2005 ·Familial Cancer* ·(unknown), Kenan Onel, Flavia M. Facio, (unknown), (unknown), Noah D. Kauff, Helen J. Huang, Mark E. Robson, Nathan A. Ellis, Kenneth Offit	19
20	The genetics of familial lymphomas 2004 ·Current Oncology Reports ·(unknown), Kenan Onel, Flavia M. Facio, Kenneth Offit	7

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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