Ingrid Marino

1.6k total citations · 1 hit paper
3 papers, 1.0k citations indexed

About

Ingrid Marino is a scholar working on Pathology and Forensic Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Ingrid Marino has authored 3 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Pathology and Forensic Medicine, 2 papers in Genetics and 1 paper in Molecular Biology. Recurrent topics in Ingrid Marino's work include Genomics and Rare Diseases (2 papers), Genetic factors in colorectal cancer (1 paper) and BRCA gene mutations in cancer (1 paper). Ingrid Marino is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetic factors in colorectal cancer (1 paper) and BRCA gene mutations in cancer (1 paper). Ingrid Marino collaborates with scholars based in United States. Ingrid Marino's co-authors include Christopher Arnell, Kelsey Moyes, Richard Wenstrup, Kirstin M. Roundy, Aaron Theisen, Jennifer Saam, Mark S. Walker, Roger Luo and Susan Manley and has published in prestigious journals such as Oncology, Personalized Medicine and Journal of Comparative Effectiveness Research.

In The Last Decade

Ingrid Marino

3 papers receiving 1.0k citations

Hit Papers

Patients Tested at a Laboratory for Hereditary Cancer Syn... 2015 2026 2018 2022 2015 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories
    2015 1.0k citations Jennifer Saam, Christopher Arnell et al. Oncology profile →

Peers

Ingrid Marino
Christopher Arnell United States
Prathap Bandipalliam United States
H. T. Lynch United States
Verena Steinke Germany
E Gabrielson United States
E Capozzi Italy
Premysl Slezak Sweden
Sheryl L. Parker United States
Mirjam Tariverdian Germany
Mark A. Glaire United Kingdom
Christopher Arnell United States
Ingrid Marino
Citations per year, relative to Ingrid Marino Ingrid Marino (= 1×) peers Christopher Arnell

Countries citing papers authored by Ingrid Marino

Since Specialization
Citations

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

Fields of papers citing papers by Ingrid Marino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Marino

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

All Works

3 of 3 papers shown
1.
Walker, Mark S., et al.. (2018). Pretreatment costs of care and time to initial treatment for patients with cancer of unknown primary. Journal of Comparative Effectiveness Research. 7(6). 523–533. 3 indexed citations
2.
Marino, Ingrid, et al.. (2017). Optimization of Quality Assurance to Increase Clinical Utility and Cost Effectiveness of Hereditary Cancer Testing. Personalized Medicine. 14(3). 213–220. 3 indexed citations
3.
Saam, Jennifer, Christopher Arnell, Aaron Theisen, et al.. (2015). Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories. Oncology. 89(5). 288–293. 1029 indexed citations breakdown →

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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2026