Candace Guiducci

42.0k total citations · 1 hit paper
13 papers, 2.4k citations indexed

About

Candace Guiducci is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Candace Guiducci has authored 13 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 3 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in Candace Guiducci's work include Genetic Associations and Epidemiology (10 papers), Lipoproteins and Cardiovascular Health (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). Candace Guiducci is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Lipoproteins and Cardiovascular Health (3 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). Candace Guiducci collaborates with scholars based in United States, Sweden and Australia. Candace Guiducci's co-authors include Marju Orho‐Melander, Olle Melander, Sekar Kathiresan, Noël P. Burtt, David Altshuler, Joel N. Hirschhorn, Leif Groop, Dragi Anevski, Christopher Newton‐Cheh and Göran Berglund and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Nature Genetics.

In The Last Decade

Candace Guiducci

13 papers receiving 2.4k citations

Hit Papers

align trajectories

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.

2009 500 citations David J. Hunter, Leena Peltonen et al. Edinburgh Research Explorer (University of Edinburgh) profile →

Peers

Candace Guiducci

GENET

MB

SURGE

CCM

EPIDE

Chris Van Geet Belgium

Anubha Mahajan United Kingdom

Bermseok Oh South Korea

Mary R. Loeken United States

Samuel Canizales‐Quinteros Mexico

Ralph Burkhardt Germany

Lars Ulrik Gerdes Denmark

Belén Beltrán Spain

Samuel T. Keating Australia

Chris Van Geet Belgium

Candace Guiducci

444 ×0.4

GENET

926 ×1.1

MB

272 ×0.7

SURGE

291 ×0.7

CCM

266 ×0.8

EPIDE

Citations per year, relative to Candace Guiducci Candace Guiducci (= 1×) peers Chris Van Geet

Countries citing papers authored by Candace Guiducci

Since Specialization

Citations

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

Fields of papers citing papers by Candace Guiducci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Candace Guiducci

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

All Works

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13 of 13 papers shown

1.

Ford, Christopher B., Jason Funt, Darren Abbey, et al.. (2015). The evolution of drug resistance in clinical isolates of Candida albicans. eLife. 4. e00662–e00662. 245 indexed citations

2.

Billings, Liana K., Kathleen A. Jablonski, Andrew M. Taylor, et al.. (2014). The Influence of Rare Genetic Variation in SLC30A8 on Diabetes Incidence and β-Cell Function. The Journal of Clinical Endocrinology & Metabolism. 99(5). E926–E930. 20 indexed citations

3.

Grant, Richard W., Kelsey OʼBrien, Jessica L. Waxler, et al.. (2012). Personalized Genetic Risk Counseling to Motivate Diabetes Prevention. Diabetes Care. 36(1). 13–19. 109 indexed citations

4.

Chiang, Charleston W. K., Zofia K. Z. Gajdos, Joshua M. Korn, et al.. (2011). The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA. Human Genetics. 130(5). 607–621. 2 indexed citations

5.

Shea, Jessica, Vineeta Agarwala, Anthony Philippakis, et al.. (2011). Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction. Nature Genetics. 43(8). 801–805. 65 indexed citations

6.

Ripatti, Samuli, Emmi Tikkanen, Marju Orho‐Melander, et al.. (2010). A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses. The Lancet. 376(9750). 1393–1400. 386 indexed citations

7.

Chiang, Charleston W. K., Zofia K. Z. Gajdos, Joshua M. Korn, et al.. (2010). Rapid Assessment of Genetic Ancestry in Populations of Unknown Origin by Genome-Wide Genotyping of Pooled Samples. PLoS Genetics. 6(3). e1000866–e1000866. 40 indexed citations

8.

Calvo, Sarah E., Elena J. Tucker, Alison G. Compton, et al.. (2010). High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nature Genetics. 42(10). 851–858. 279 indexed citations

9.

Keebler, Mary, Rahul C. Deo, Aarti Surti, et al.. (2010). Fine-Mapping in African Americans of 8 Recently Discovered Genetic Loci for Plasma Lipids. Circulation Cardiovascular Genetics. 3(4). 358–364. 22 indexed citations

10.

Keebler, Mary, Christopher Sanders, Aarti Surti, et al.. (2009). Association of Blood Lipids With Common DNA Sequence Variants at 19 Genetic Loci in the Multiethnic United States National Health and Nutrition Examination Survey III. Circulation Cardiovascular Genetics. 2(3). 238–243. 45 indexed citations

11.

Hunter, David J., Leena Peltonen, Candace Guiducci, et al.. (2009). . Edinburgh Research Explorer (University of Edinburgh). 500 indexed citations breakdown →

12.

Kathiresan, Sekar, Olle Melander, Dragi Anevski, et al.. (2008). Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events. New England Journal of Medicine. 358(12). 1240–1249. 494 indexed citations

13.

Kathiresan, Sekar, Alisa K. Manning, Serkalem Demissie, et al.. (2007). A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. BMC Medical Genetics. 8(S1). S17–S17. 226 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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