Rena Vanzo

1.1k total citations
25 papers, 504 citations indexed

About

Rena Vanzo is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rena Vanzo has authored 25 papers receiving a total of 504 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rena Vanzo's work include Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Rena Vanzo is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Rena Vanzo collaborates with scholars based in United States, Australia and Italy. Rena Vanzo's co-authors include Megan Martin, Nicola Longo, Marzia Pasquali, Sarah T. South, Orly Ardon, E. Robert Wassman, Charles H. Hensel, Catherine J. Auger, Aparna Prasad and Karen S. Ho and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Rena Vanzo

25 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rena Vanzo United States 14 302 186 94 82 74 25 504
Tiziana Pisano Italy 17 448 1.5× 420 2.3× 81 0.9× 248 3.0× 91 1.2× 49 1.1k
Kathryn B. Garber United States 11 466 1.5× 392 2.1× 70 0.7× 54 0.7× 182 2.5× 19 700
Bernardo Dalla Bernardina Italy 16 573 1.9× 486 2.6× 75 0.8× 135 1.6× 208 2.8× 31 972
Aziz Mazarib Israel 9 312 1.0× 335 1.8× 40 0.4× 81 1.0× 50 0.7× 10 807
Amy Lawson‐Yuen United States 6 223 0.7× 154 0.8× 31 0.3× 23 0.3× 172 2.3× 7 363
Jennifer R. Davies United Kingdom 13 113 0.4× 556 3.0× 142 1.5× 22 0.3× 31 0.4× 20 768
Fatema Serajee United States 12 186 0.6× 177 1.0× 12 0.1× 26 0.3× 188 2.5× 19 459
Kirstine Ravn Denmark 19 541 1.8× 606 3.3× 184 2.0× 45 0.5× 267 3.6× 37 971
Nan Pang China 10 268 0.9× 219 1.2× 13 0.1× 38 0.5× 151 2.0× 21 519
Sarah C. Borrie Belgium 9 98 0.3× 207 1.1× 24 0.3× 13 0.2× 74 1.0× 13 378

Countries citing papers authored by Rena Vanzo

Since Specialization
Citations

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

Fields of papers citing papers by Rena Vanzo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rena Vanzo

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

All Works

20 of 20 papers shown
1.
Davis, Kyle, Colleen G. Bilancia, Megan Martin, et al.. (2022). NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system. Scientific Reports. 12(1). 5427–5427. 1 indexed citations
2.
Vanzo, Rena, Aparna Prasad, Charles H. Hensel, et al.. (2020). The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism. Journal of Personalized Medicine. 11(1). 21–21. 3 indexed citations
3.
Cogan, Joy D., Lynette Rives, Amy K. Robertson, et al.. (2020). Limitations of exome sequencing in detecting rare and undiagnosed diseases. American Journal of Medical Genetics Part A. 182(6). 1400–1406. 53 indexed citations
4.
Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2019). Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing. Scientific Reports. 9(1). 15315–15315. 8 indexed citations
5.
Vanzo, Rena, Karen S. Ho, Aparna Prasad, et al.. (2018). Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders. European Journal of Medical Genetics. 62(1). 15–20. 13 indexed citations
6.
Prasad, Aparna, Rena Vanzo, Patricia Mowery‐Rushton, et al.. (2018). Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis. BMC Medical Genetics. 19(1). 46–46. 19 indexed citations
7.
Hensel, Charles H., Rena Vanzo, Megan Martin, et al.. (2017). Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions. PLoS Currents. 9. 7 indexed citations
8.
Vivian, Jay L., R. Tanner Hagelstrom, Waheeda A. Hossain, et al.. (2017). A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome. Molecular Syndromology. 8(4). 211–218. 15 indexed citations
9.
Ho, Karen S., E. Robert Wassman, Charles H. Hensel, et al.. (2016). Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders. International Journal of Molecular Sciences. 17(12). 2070–2070. 50 indexed citations
10.
Ho, Karen S., Sarah T. South, Charles H. Hensel, et al.. (2016). Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome. Journal of Medical Genetics. 53(4). 256–263. 29 indexed citations
11.
Peabody, John, Megan Martin, Lisa DeMaria, et al.. (2016). Clinical Utility of a Comprehensive, Whole Genome CMA Testing Platform in Pediatrics: A Prospective Randomized Controlled Trial of Simulated Patients in Physician Practices. PLoS ONE. 11(12). e0169064–e0169064. 5 indexed citations
12.
Rothwell, Erin, et al.. (2015). Initial Investigation of Comfort Levels, Motivations, and Attitudes of Volunteers During Therapeutic Recreation Programs. Therapeutic Recreation Journal. 49(3). 3 indexed citations
13.
Martin, Megan, et al.. (2015). Mosaic deletion of 20pter due to rescue by somatic recombination. American Journal of Medical Genetics Part A. 170(1). 243–248. 19 indexed citations
14.
Martin, Megan, et al.. (2015). Variants of unknown significance on chromosomal microarray analysis: parental perspectives. Journal of Community Genetics. 6(4). 343–349. 28 indexed citations
15.
Vanzo, Rena, Megan Martin, Erin E. Baldwin, et al.. (2014). Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients. Journal of Genetic Counseling. 23(6). 922–927. 13 indexed citations
16.
Vanzo, Rena, et al.. (2013). Familial KANK1 deletion that does not follow expected imprinting pattern. European Journal of Medical Genetics. 56(5). 256–259. 19 indexed citations
17.
Stevenson, David A., Rena Vanzo, Kristy Damjanovich, et al.. (2012). Mosaicism in Stickler syndrome. European Journal of Medical Genetics. 55(6-7). 418–422. 10 indexed citations
18.
Viau, Krista, Sharon L. Ernst, Rena Vanzo, et al.. (2012). Glutaric acidemia Type 1: Outcomes before and after expanded newborn screening. Molecular Genetics and Metabolism. 106(4). 430–438. 52 indexed citations
19.
Longo, Nicola, et al.. (2011). Disorders of creatine transport and metabolism. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 157(1). 72–78. 83 indexed citations
20.
Gammie, Stephen C., Anthony P. Auger, Heather M. Jessen, et al.. (2006). Altered gene expression in mice selected for high maternal aggression. Genes Brain & Behavior. 6(5). 432–443. 30 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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