Carla Márquez‐Luna

2.9k total citations · 1 hit paper
14 papers, 680 citations indexed

About

Carla Márquez‐Luna is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Carla Márquez‐Luna has authored 14 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Carla Márquez‐Luna's work include Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). Carla Márquez‐Luna is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). Carla Márquez‐Luna collaborates with scholars based in United States, France and Mexico. Carla Márquez‐Luna's co-authors include Alkes L. Price, Po‐Ru Loh, Scott M. Damrauer, Sridharan Raghavan, Pradeep Natarajan, Cristen J. Willer, Euan A. Ashley, Jack W. O’Sullivan, Christopher J. O’Donnell and Jasmine A. Luzum and has published in prestigious journals such as The Lancet, Circulation and Nature Communications.

In The Last Decade

Carla Márquez‐Luna

14 papers receiving 670 citations

Hit Papers

Polygenic Risk Scores for... 2022 2026 2023 2024 2022 50 100 150 200

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carla Márquez‐Luna United States 10 350 167 132 69 69 14 680
Lisa A. Bastarache United States 9 461 1.3× 309 1.9× 79 0.6× 92 1.3× 120 1.7× 11 954
Robert Goodloe United States 15 240 0.7× 182 1.1× 46 0.3× 48 0.7× 32 0.5× 41 684
Akl C. Fahed United States 15 374 1.1× 177 1.1× 181 1.4× 204 3.0× 111 1.6× 43 935
Åsa K. Hedman Sweden 13 265 0.8× 555 3.3× 125 0.9× 67 1.0× 68 1.0× 19 891
Ajay Yesupriya United States 18 197 0.6× 135 0.8× 69 0.5× 69 1.0× 75 1.1× 29 705
Toomas Haller Estonia 9 253 0.7× 280 1.7× 41 0.3× 47 0.7× 93 1.3× 21 712
Teresa Kruisselbrink United States 11 214 0.6× 252 1.5× 366 2.8× 71 1.0× 66 1.0× 23 744
Johanne Marie Justesen Denmark 14 240 0.7× 162 1.0× 83 0.6× 68 1.0× 84 1.2× 20 531
Pietari Ripatti Finland 8 255 0.7× 112 0.7× 117 0.9× 92 1.3× 109 1.6× 14 514
Helen R. Warren United Kingdom 15 254 0.7× 226 1.4× 279 2.1× 59 0.9× 45 0.7× 40 806

Countries citing papers authored by Carla Márquez‐Luna

Since Specialization
Citations

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

Fields of papers citing papers by Carla Márquez‐Luna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carla Márquez‐Luna. 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 Carla Márquez‐Luna. The network helps show where Carla Márquez‐Luna may publish in the future.

Co-authorship network of co-authors of Carla Márquez‐Luna

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

All Works

14 of 14 papers shown
1.
Duffy, Áine, Ben Omega Petrazzini, David Stein, et al.. (2024). Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications. Nature Genetics. 56(1). 51–59. 11 indexed citations
2.
Petrazzini, Ben Omega, Iain S. Forrest, Ghislain Rocheleau, et al.. (2024). Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease. Nature Genetics. 56(7). 1412–1419. 9 indexed citations
3.
Park, Joshua K., Ben Omega Petrazzini, Áine Duffy, et al.. (2024). Muesli Intake May Protect Against Coronary Artery Disease. JACC Advances. 3(4). 100888–100888. 1 indexed citations
4.
Park, Joshua K., Iain S. Forrest, Áine Duffy, et al.. (2023). Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits. eLife. 12. 4 indexed citations
5.
Márquez‐Luna, Carla, et al.. (2022). Online Education in Times of COVID: Adapting and Deploying a Data Science Program in Mexico. SHILAP Revista de lepidopterología. 1 indexed citations
6.
Petrazzini, Ben Omega, Kumardeep Chaudhary, Carla Márquez‐Luna, et al.. (2022). Coronary Risk Estimation Based on Clinical Data in Electronic Health Records. Journal of the American College of Cardiology. 79(12). 1155–1166. 22 indexed citations
7.
O’Sullivan, Jack W., Sridharan Raghavan, Carla Márquez‐Luna, et al.. (2022). Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association. Circulation. 146(8). e93–e118. 207 indexed citations breakdown →
8.
Forrest, Iain S., Ben Omega Petrazzini, Áine Duffy, et al.. (2022). Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts. The Lancet. 401(10372). 215–225. 94 indexed citations
9.
10.
Forrest, Iain S., Kumardeep Chaudhary, Ishan Paranjpe, et al.. (2021). Genome-wide polygenic risk score for retinopathy of type 2 diabetes. Human Molecular Genetics. 30(10). 952–960. 15 indexed citations
11.
Kim, Samuel S., Kushal K. Dey, Omer Weissbrod, et al.. (2020). Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease. Nature Communications. 11(1). 9 indexed citations
12.
Weissbrod, Omer, Farhad Hormozdiari, Christian Benner, et al.. (2020). Functionally informed fine-mapping and polygenic localization of complex trait heritability. Nature Genetics. 52(12). 1355–1363. 140 indexed citations
13.
Márquez‐Luna, Carla, Po‐Ru Loh, & Alkes L. Price. (2017). Multiethnic polygenic risk scores improve risk prediction in diverse populations. Genetic Epidemiology. 41(8). 811–823. 152 indexed citations
14.
García‐Velázquez, Lizbeth, Samuel Canizales‐Quinteros, Sandra Romero‐Hidalgo, et al.. (2013). Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families. Neurogenetics. 15(1). 13–17. 11 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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