Amy Shikany

436 total citations
26 papers, 255 citations indexed

About

Amy Shikany is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Surgery. According to data from OpenAlex, Amy Shikany has authored 26 papers receiving a total of 255 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Cardiology and Cardiovascular Medicine and 11 papers in Surgery. Recurrent topics in Amy Shikany's work include Aortic Disease and Treatment Approaches (8 papers), Congenital Heart Disease Studies (8 papers) and Congenital heart defects research (8 papers). Amy Shikany is often cited by papers focused on Aortic Disease and Treatment Approaches (8 papers), Congenital Heart Disease Studies (8 papers) and Congenital heart defects research (8 papers). Amy Shikany collaborates with scholars based in United States, Australia and Saudi Arabia. Amy Shikany's co-authors include Stephanie M. Ware, Robert B. Hinton, Benjamin J. Landis, Erin M. Miller, K. Nicole Weaver, Angela Lorts, Jeffrey Schubert, Jeanne James, Richard J. Czosek and Paula Goldenberg and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Genetics in Medicine.

In The Last Decade

Amy Shikany

23 papers receiving 246 citations

Peers

Amy Shikany

CCM

GENET

PRM

EPIDE

Darroch Hall United Kingdom

H. Pannu United States

Lidia Ziółkowska Poland

Meenakshi Maitra United States

K Joho Japan

Yu‐Min Sun China

Ilse Luyckx Belgium

Ruo-Gu Li China

Simone Salemink Netherlands

Fabiana Cerrato Italy

Darroch Hall United Kingdom

Amy Shikany

148 ×1.3

53 ×0.5

CCM

81 ×0.9

GENET

54 ×0.7

PRM

80 ×1.1

EPIDE

Citations per year, relative to Amy Shikany Amy Shikany (= 1×) peers Darroch Hall

Countries citing papers authored by Amy Shikany

Since Specialization

Citations

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

Fields of papers citing papers by Amy Shikany

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Shikany

This figure shows the co-authorship network connecting the top 25 collaborators of Amy Shikany. A scholar is included among the top collaborators of Amy Shikany 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 Amy Shikany. Amy Shikany 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

Yang, Zeyu, Amy Shikany, Ammar Husami, et al.. (2025). Sequencing validates deep learning models for EHR-based detection of Noonan syndrome in pediatric patients. npj Genomic Medicine. 10(1). 56–56.

Zhang, Xue, et al.. (2024). Genetic investigation and diagnosis in adults with congenital heart disease with or without structural or neurodevelopmental comorbidity: a retrospective chart review. Frontiers in Genetics. 15. 1412806–1412806.

Strong, Alanna, Michael March, Christopher J. Cardinale, et al.. (2024). Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndrome. Genetics in Medicine. 26(10). 101222–101222. 2 indexed citations

Opotowsky, Alexander R., et al.. (2024). Current approach to genetic testing and genetic evaluation referrals for adults with congenital heart disease. Frontiers in Genetics. 15. 1398887–1398887. 2 indexed citations

Anderson, Jeffrey, Adam L. Kushner, Lisa J. Martin, et al.. (2024). Cardiac genetic counseling services: Exploring downstream revenue in a pediatric medical center. Journal of Genetic Counseling. 34(2). e1984–e1984.

Weaver, K. Nicole, Jing Chen, Amy Shikany, et al.. (2022). Prevalence of Genetic Diagnoses in a Cohort With Valvar Pulmonary Stenosis. Circulation Genomic and Precision Medicine. 15(4). e003635–e003635. 7 indexed citations

Yang, Zeyu, Amy Shikany, Yizhao Ni, et al.. (2022). Using deep learning and electronic health records to detect Noonan syndrome in pediatric patients. Genetics in Medicine. 24(11). 2329–2337. 9 indexed citations

Miller, Daniel, Lisa J. Martin, Justin T. Tretter, et al.. (2021). Uptake of Screening and Recurrence of Bicuspid Aortic Valve and Thoracic Aortic Aneurysm Among At-Risk Siblings of Pediatric Probands. The Journal of Pediatrics. 239. 219–224. 3 indexed citations

Alsaied, Tarek, Amy Shikany, Laura E. Riley, et al.. (2021). Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys–Dietz Syndrome. Pediatric Cardiology. 42(5). 1157–1161. 5 indexed citations

10.

Shikany, Amy, Benjamin J. Landis, Erin M. Miller, et al.. (2020). A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy. The Journal of Pediatrics. 227. 231–238.e14. 26 indexed citations

11.

Khoury, Philip R., et al.. (2020). Investigation of de novo variation in pediatric cardiomyopathy. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 116–123. 10 indexed citations

12.

Shikany, Amy, et al.. (2020). Comparison of Evolution of Aortic Root Dilation and Ghent Criteria in Preadolescents and Adolescents with and without Marfan Syndrome. The Journal of Pediatrics. 221. 188–195.e1. 2 indexed citations

13.

Shikany, Amy, Laura Baker, Deborah L. Stabley, et al.. (2019). Medically actionable comorbidities in adults with Costello syndrome. American Journal of Medical Genetics Part A. 182(1). 130–136. 8 indexed citations

14.

Jefferies, John L., et al.. (2018). Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population. Pediatric Cardiology. 39(4). 709–717. 8 indexed citations

15.

Landis, Benjamin J., Jeffrey Schubert, Dongbing Lai, et al.. (2017). Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity. Journal of Cardiovascular Translational Research. 10(4). 423–432. 21 indexed citations

16.

Allain, Dawn C., Patricia Arscott, Gretchen MacCarrick, et al.. (2017). At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease. Journal of Genetic Counseling. 26(4). 669–688. 4 indexed citations

17.

Ritter, Alyssa, Carrie Atzinger, J. Howard James, et al.. (2017). Natural history of aortic root dilation through young adulthood in a hypermobile Ehlers–Danlos syndrome cohort. American Journal of Medical Genetics Part A. 173(6). 1467–1472. 13 indexed citations

18.

Landis, Benjamin J., Stephanie M. Ware, Jeanne James, et al.. (2015). Clinical Stratification of Pediatric Patients with Idiopathic Thoracic Aortic Aneurysm. The Journal of Pediatrics. 167(1). 131–137.e5. 9 indexed citations

19.

James, Jeanne, Paula Goldenberg, Robert B. Hinton, et al.. (2014). Aortopathy in the 7q11.23 microduplication syndrome. American Journal of Medical Genetics Part A. 167(2). 363–370. 25 indexed citations

20.

Ware, Stephanie M., Amy Shikany, Benjamin J. Landis, Jeanne James, & Robert B. Hinton. (2014). Twins With Progressive Thoracic Aortic Aneurysm, Recurrent Dissection andACTA2Mutation. PEDIATRICS. 134(4). e1218–e1223. 13 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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