Renae Judy

4.2k total citations
21 papers, 378 citations indexed

About

Renae Judy is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, Renae Judy has authored 21 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Cardiology and Cardiovascular Medicine and 5 papers in Molecular Biology. Recurrent topics in Renae Judy's work include Genetic Associations and Epidemiology (8 papers), BRCA gene mutations in cancer (4 papers) and Genomics and Rare Diseases (3 papers). Renae Judy is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), BRCA gene mutations in cancer (4 papers) and Genomics and Rare Diseases (3 papers). Renae Judy collaborates with scholars based in United States, United Kingdom and Sweden. Renae Judy's co-authors include Scott M. Damrauer, Daniel J. Rader, Michael G. Levin, Marylyn D. Ritchie, Yuki Bradford, Shefali S. Verma, Benjamin F. Voight, Rachel L. Kember, Katherine L. Nathanson and Matthew C. Hyman and has published in prestigious journals such as Journal of the American College of Cardiology, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Renae Judy

19 papers receiving 375 citations

Peers

Renae Judy
Pınar Ata Türkiye
Renae Judy
Citations per year, relative to Renae Judy Renae Judy (= 1×) peers Pınar Ata

Countries citing papers authored by Renae Judy

Since Specialization
Citations

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

Fields of papers citing papers by Renae Judy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renae Judy

This figure shows the co-authorship network connecting the top 25 collaborators of Renae Judy. A scholar is included among the top collaborators of Renae Judy 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 Renae Judy. Renae Judy 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.
Judy, Renae, et al.. (2025). Detecting Bicuspid Aortic Valve From Echocardiographic Reports Using Natural Language Processing. JACC Advances. 5(1). 102463–102463.
2.
Cho, So Mi Jemma, Michael G. Levin, Renae Judy, et al.. (2025). AHA PREVENT Equations and Cardiovascular Disease Risk in Diverse Health Care Populations. Journal of the American College of Cardiology. 86(3). 181–192. 7 indexed citations
3.
Judy, Renae, Jeffrey Duda, James C. Gee, et al.. (2025). Predicting Thoracic Aortic Dissection in a Diverse Biobank Using a Polygenic Risk Score. JACC Advances. 4(5). 101743–101743. 2 indexed citations
4.
Paranjpe, Ishan, Renae Judy, Shuai Yuan, et al.. (2024). Abstract 3117: Cannabis Use Disorder And The Risk Of Atherosclerotic Cardiovascular Diseases. Arteriosclerosis Thrombosis and Vascular Biology. 44(Suppl_1).
5.
Neylan, Christopher J., Renae Judy, Venexia Walker, et al.. (2024). Genome-Wide Association Study Identifies Genes for Hair Growth and Patterning are Associated With Pilonidal Disease. Diseases of the Colon & Rectum. 67(9). 1149–1157. 1 indexed citations
6.
Kember, Rachel L., Shefali S. Verma, Anurag Verma, et al.. (2024). Polygenic risk scores for cardiometabolic traits demonstrate importance of ancestry for predictive precision medicine. 748–765. 1 indexed citations
7.
Huang, Brian, et al.. (2023). Relationships between body fat distribution and metabolic syndrome traits and outcomes: A mendelian randomization study. PLoS ONE. 18(10). e0293017–e0293017. 9 indexed citations
8.
Kember, Rachel L., Shefali S. Verma, Anurag Verma, et al.. (2023). Polygenic risk scores for cardiometabolic traits demonstrate importance of ancestry for predictive precision medicine. PubMed. 29. 611–626. 2 indexed citations
9.
Yu, Mengyao, Catherine Tcheandjieu, Adrien Georges, et al.. (2022). Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. JCI Insight. 7(3). 6 indexed citations
10.
Park, Joseph, Matthew T. MacLean, Anastasia Lucas, et al.. (2022). Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Cell Reports Medicine. 3(12). 100855–100855. 8 indexed citations
11.
Verma, Anurag, Scott M. Damrauer, Nawar Naseer, et al.. (2022). The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population. Journal of Personalized Medicine. 12(12). 1974–1974. 43 indexed citations
12.
Wang, Louise, Shefali S. Verma, Anh N. Le, et al.. (2021). Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank. Genetics in Medicine. 24(3). 601–609. 11 indexed citations
13.
Lee, Daniel J., Ryan Hausler, Anh N. Le, et al.. (2021). Association of Inherited Mutations in DNA Repair Genes with Localized Prostate Cancer. European Urology. 81(6). 559–567. 21 indexed citations
14.
Park, Joseph, Michael G. Levin, Renae Judy, et al.. (2021). A genome-first approach to rare variants in hypertrophic cardiomyopathy genes MYBPC3 and MYH7 in a medical biobank. Human Molecular Genetics. 31(5). 827–837. 13 indexed citations
15.
Kember, Rachel L., Michael G. Levin, Diana L. Cousminer, et al.. (2020). Genetically Determined Birthweight Associates With Atrial Fibrillation. Circulation Genomic and Precision Medicine. 13(3). e002553–e002553. 11 indexed citations
16.
Levin, Michael G., Renae Judy, Dipender Gill, et al.. (2020). Genetics of height and risk of atrial fibrillation: A Mendelian randomization study. PLoS Medicine. 17(10). e1003288–e1003288. 102 indexed citations
17.
Park, Joseph, Michael G. Levin, Christopher M. Haggerty, et al.. (2019). A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes. Genetics in Medicine. 22(1). 102–111. 37 indexed citations
18.
Levin, Michael G., Rachel L. Kember, Renae Judy, et al.. (2018). Genomic Risk Stratification Predicts All-Cause Mortality After Cardiac Catheterization. Circulation Genomic and Precision Medicine. 11(11). e002352–e002352. 17 indexed citations
19.
Reiss, Kim A., Shun Yu, Renae Judy, et al.. (2018). Retrospective Survival Analysis of Patients With Advanced Pancreatic Ductal Adenocarcinoma and Germline BRCA or PALB2 Mutations. JCO Precision Oncology. 2(2). 1–9. 43 indexed citations
20.
Goldberg, David S., Wei‐Ting Hwang, Renae Judy, et al.. (2017). Sustained Posttransplantation Diabetes Is Associated With Long-Term Major Cardiovascular Events Following Liver Transplantation. American Journal of Transplantation. 18(1). 207–215. 41 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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