Tara Funari

801 total citations
7 papers, 457 citations indexed

About

Tara Funari is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Tara Funari has authored 7 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Sensory Systems. Recurrent topics in Tara Funari's work include Connective tissue disorders research (3 papers), Cell Adhesion Molecules Research (2 papers) and TGF-β signaling in diseases (2 papers). Tara Funari is often cited by papers focused on Connective tissue disorders research (3 papers), Cell Adhesion Molecules Research (2 papers) and TGF-β signaling in diseases (2 papers). Tara Funari collaborates with scholars based in United States, Belgium and Uruguay. Tara Funari's co-authors include Daniel H. Cohn, David L. Rimoin, Thomas Voets, Bernd Nilius, Ralph S. Lachman, Annelies Janssens, Deborah Krakow, William R. Wilcox, Vincent Funari and Carlos A. Bacino and has published in prestigious journals such as Nature Genetics, Neurology and The American Journal of Human Genetics.

In The Last Decade

Tara Funari

7 papers receiving 450 citations

Peers

Tara Funari
M. Korostishevsky Israel
Shenglian Yang China
Premanand Sundivakkam United States
Fabiana Fattori Italy
Yuki Miyasaka Japan
Isabelle Riedel Germany
Xiaorei Sai Japan
Arancha Rodrı́guez-Garcı́a Spain
Takahiko Yoshino Japan
An Vanden Bosch Belgium
M. Korostishevsky Israel
Tara Funari
Citations per year, relative to Tara Funari Tara Funari (= 1×) peers M. Korostishevsky

Countries citing papers authored by Tara Funari

Since Specialization
Citations

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

Fields of papers citing papers by Tara Funari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tara Funari

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

All Works

7 of 7 papers shown
1.
Vincent, Lisa M., et al.. (2018). 78: Multi-gene NGS panel yields high diagnostic rate of skeletal dysplasias detected by fetal ultrasound. American Journal of Obstetrics and Gynecology. 218(1). S57–S58. 1 indexed citations
2.
Pizzino, Amy, Tyler Mark Pierson, Yiran Guo, et al.. (2014). TUBB4A de novo mutations cause isolated hypomyelination. Neurology. 83(10). 898–902. 39 indexed citations
3.
Tompson, Stuart W., Eissa Faqeih, Leena Ala‐Kokko, et al.. (2012). Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2. American Journal of Medical Genetics Part A. 158A(2). 309–314. 13 indexed citations
4.
Tompson, Stuart W., Carlos A. Bacino, Nicole P. Safina, et al.. (2010). Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene. The American Journal of Human Genetics. 87(5). 708–712. 54 indexed citations
5.
Funari, Vincent, Deborah Krakow, Lisette Nevarez, et al.. (2010). BMPER Mutation in Diaphanospondylodysostosis Identified by Ancestral Autozygosity Mapping and Targeted High-Throughput Sequencing. The American Journal of Human Genetics. 87(4). 532–537. 26 indexed citations
6.
Krakow, Deborah, Joris Vriens, Natalia Camacho, et al.. (2009). Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia. The American Journal of Human Genetics. 84(3). 307–315. 148 indexed citations
7.
Rock, Matthew J., Jean Prenen, Vincent Funari, et al.. (2008). Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia. Nature Genetics. 40(8). 999–1003. 176 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

Breakdown of academic impact, for papers by M. Korostishevsky Breakdown of academic impact, for papers by Shenglian Yang Breakdown of academic impact, for papers by Premanand Sundivakkam Breakdown of academic impact, for papers by Fabiana Fattori Breakdown of academic impact, for papers by Yuki Miyasaka Breakdown of academic impact, for papers by Isabelle Riedel Breakdown of academic impact, for papers by Xiaorei Sai Breakdown of academic impact, for papers by Arancha Rodrı́guez-Garcı́a Breakdown of academic impact, for papers by Takahiko Yoshino Breakdown of academic impact, for papers by An Vanden Bosch
Rankless by CCL
2026