Yuri A. Zárate

3.1k total citations · 1 hit paper
67 papers, 1.3k citations indexed

About

Yuri A. Zárate is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Yuri A. Zárate has authored 67 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 34 papers in Molecular Biology and 11 papers in Surgery. Recurrent topics in Yuri A. Zárate's work include Connective tissue disorders research (11 papers), Congenital heart defects research (10 papers) and Digestive system and related health (8 papers). Yuri A. Zárate is often cited by papers focused on Connective tissue disorders research (11 papers), Congenital heart defects research (10 papers) and Digestive system and related health (8 papers). Yuri A. Zárate collaborates with scholars based in United States, Canada and Japan. Yuri A. Zárate's co-authors include Robert J. Hopkin, Jennifer L. Fish, G. Bradley Schaefer, R. Thomas Collins, Carlos E. Prada, Katherine A. Bosanko, Julie R. Jones, Julie Kaylor, Lisa J. Martin and Aisling R. Caffrey and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PEDIATRICS.

In The Last Decade

Yuri A. Zárate

62 papers receiving 1.3k citations

Hit Papers

Fabry's disease 2008 2026 2014 2020 2008 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuri A. Zárate United States 17 503 451 427 223 192 67 1.3k
Young Bae Sohn South Korea 19 293 0.6× 402 0.9× 382 0.9× 235 1.1× 204 1.1× 93 1.1k
Sung Yoon Cho South Korea 19 260 0.5× 287 0.6× 322 0.8× 178 0.8× 177 0.9× 105 939
Esther Brusse Netherlands 24 612 1.2× 458 1.0× 143 0.3× 123 0.6× 313 1.6× 59 1.6k
Gisela Nogales‐Gadea Spain 24 740 1.5× 436 1.0× 340 0.8× 124 0.6× 816 4.3× 70 2.3k
Sarju Mehta United Kingdom 16 985 2.0× 321 0.7× 333 0.8× 271 1.2× 100 0.5× 27 1.9k
Maarten Arends Netherlands 13 783 1.6× 664 1.5× 306 0.7× 340 1.5× 224 1.2× 18 1.5k
Josep Gámez Spain 27 877 1.7× 167 0.4× 208 0.5× 90 0.4× 245 1.3× 97 2.0k
Pierre Lozeron France 20 582 1.2× 180 0.4× 139 0.3× 101 0.5× 146 0.8× 65 1.2k
Nadia Sakati Saudi Arabia 22 819 1.6× 121 0.3× 546 1.3× 123 0.6× 123 0.6× 78 1.7k
Julia Wanschitz Austria 26 741 1.5× 204 0.5× 68 0.2× 287 1.3× 182 0.9× 78 1.9k

Countries citing papers authored by Yuri A. Zárate

Since Specialization
Citations

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

Fields of papers citing papers by Yuri A. Zárate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yuri A. Zárate. 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 Yuri A. Zárate. The network helps show where Yuri A. Zárate may publish in the future.

Co-authorship network of co-authors of Yuri A. Zárate

This figure shows the co-authorship network connecting the top 25 collaborators of Yuri A. Zárate. A scholar is included among the top collaborators of Yuri A. Zárate 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 Yuri A. Zárate. Yuri A. Zárate 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.
Zárate, Yuri A., Andrew White, Margaret Au, et al.. (2025). ACTC1 Variants Result in Isolated and Syndromic Cardiac Phenotypes. Clinical Genetics. 108(6). 713–719.
2.
Zárate, Yuri A., et al.. (2024). Abnormalities in pharyngeal arch‐derived structures in SATB2‐associated syndrome. Clinical Genetics. 106(2). 209–213. 2 indexed citations
3.
Zárate, Yuri A., Katherine A. Bosanko, Nihit Kumar, et al.. (2023). Quantitative Phenotype Morbidity Description of SATB2-Associated Syndrome. Human Mutation. 2023. 1–9.
4.
Zárate, Yuri A., et al.. (2021). Genetic and phenotypic heterogeneity in KIAA0753‐related ciliopathies. American Journal of Medical Genetics Part A. 188(1). 104–115. 5 indexed citations
5.
Weaver, K. Nicole, Marguerite M. Caré, Yuri A. Zárate, et al.. (2021). Craniosynostosis is a feature of Costello syndrome. American Journal of Medical Genetics Part A. 188(4). 1280–1286. 3 indexed citations
7.
Zárate, Yuri A., et al.. (2020). Aortic Geometry in Patients with Duplication 7q11.23 Compared to Healthy Controls. Pediatric Cardiology. 41(6). 1199–1205.
8.
Caffrey, Aisling R., et al.. (2019). Speech, language, and feeding phenotypes of SATB2 ‐associated syndrome. Clinical Genetics. 96(6). 485–492. 10 indexed citations
9.
Schwager, Evelyn E., et al.. (2019). Satb2 regulates proliferation and nuclear integrity of pre-osteoblasts. Bone. 127. 488–498. 18 indexed citations
10.
Hardin, Joshua S., Yuri A. Zárate, Bert Callewaert, & David Warner. (2017). Corneal Findings in Arterial Tortuosity Syndrome. Investigative Ophthalmology & Visual Science. 58(8). 5661–5661. 1 indexed citations
11.
Zárate, Yuri A. & Jennifer L. Fish. (2016). SATB2‐associated syndrome: Mechanisms, phenotype, and practical recommendations. American Journal of Medical Genetics Part A. 173(2). 327–337. 72 indexed citations
12.
Zárate, Yuri A., Hazel Perry, Tawfeg Ben‐Omran, et al.. (2015). Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing. American Journal of Medical Genetics Part A. 167(5). 1026–1032. 37 indexed citations
13.
Zárate, Yuri A., et al.. (2015). STAR syndrome is part of the differential diagnosis of females with anorectal malformations. American Journal of Medical Genetics Part A. 167(8). 1940–1943. 12 indexed citations
14.
Zárate, Yuri A., Katherine A. Bosanko, Elizabeth Bhoj, et al.. (2015). Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses. American Journal of Medical Genetics Part A. 167(9). 2168–2175. 4 indexed citations
15.
Collins, R. Thomas, et al.. (2014). Severe neonatal presentation of Kleefstra syndrome in a patient with hypoplastic left heart syndrome and 9q34.3 microdeletion. Birth Defects Research Part A Clinical and Molecular Teratology. 100(12). 985–990. 13 indexed citations
16.
Zárate, Yuri A., Huadong Zhan, & Julie R. Jones. (2012). Infrequent Manifestations of Kabuki Syndrome in a Patient with Novel <b><i>MLL2</i></b> Mutation. Molecular Syndromology. 3(4). 180–184. 19 indexed citations
17.
Prada, Carlos E., et al.. (2011). Lethal presentation of neurofibromatosis and Noonan syndrome. American Journal of Medical Genetics Part A. 155(6). 1360–1366. 16 indexed citations
18.
Zárate, Yuri A., Alka Dwivedi, Frank Bartel, Ken Corning, & Barbara R. DuPont. (2010). 47, XY, +der(Y),t(X;Y)(p21.1;p11.2): A unique case of XY sex reversal. American Journal of Medical Genetics Part A. 155(2). 386–391. 4 indexed citations
19.
Zárate, Yuri A., Larry T. Patterson, Hong Yin, & Robert J. Hopkin. (2009). A case of minimal change disease in a Fabry patient. Pediatric Nephrology. 25(3). 553–556. 12 indexed citations
20.
Zárate, Yuri A., Larry W. Markham, Linda Cripe, et al.. (2007). Novel Fibrillin 1 Mutation in a Case of Neonatal Marfan Syndrome: The Increasing Importance of Early Recognition. Congenital Heart Disease. 2(5). 342–346. 16 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

Rankless by CCL
2026