Denise L. Lind

7.2k total citations
7 papers, 335 citations indexed

About

Denise L. Lind is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Denise L. Lind has authored 7 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Oncology. Recurrent topics in Denise L. Lind's work include Genetic Associations and Epidemiology (2 papers), Moyamoya disease diagnosis and treatment (1 paper) and Nutrition, Genetics, and Disease (1 paper). Denise L. Lind is often cited by papers focused on Genetic Associations and Epidemiology (2 papers), Moyamoya disease diagnosis and treatment (1 paper) and Nutrition, Genetics, and Disease (1 paper). Denise L. Lind collaborates with scholars based in United States, Canada and Denmark. Denise L. Lind's co-authors include Pui–Yan Kwok, PC Vincent, Angie Phong, Steven R. Cummings, Tamara B. Harris, Nicholas J. Schork, Esteban G. Burchard, Elad Ziv, Caroline M. Nievergelt and Bruce M. Psaty and has published in prestigious journals such as Blood, Stroke and The American Journal of Human Genetics.

In The Last Decade

Denise L. Lind

7 papers receiving 320 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Denise L. Lind United States 6 107 92 69 57 50 7 335
Concetta Coronella Italy 13 121 1.1× 74 0.8× 8 0.1× 31 0.5× 51 1.0× 14 657
G. Wendell Richmond United States 9 37 0.3× 53 0.6× 29 0.4× 88 1.5× 13 0.3× 18 325
B. Petrák Czechia 8 66 0.6× 53 0.6× 12 0.2× 44 0.8× 12 0.2× 19 212
Vincent Damotte United States 8 34 0.3× 88 1.0× 17 0.2× 66 1.2× 40 0.8× 12 369
Ken Saida Japan 10 92 0.9× 18 0.2× 27 0.4× 114 2.0× 17 0.3× 37 275
Armando Flor United States 6 27 0.3× 91 1.0× 15 0.2× 48 0.8× 36 0.7× 8 315
Eva Krasulová Czechia 5 16 0.1× 71 0.8× 50 0.7× 69 1.2× 54 1.1× 12 314
P. Berlier France 10 51 0.5× 25 0.3× 25 0.4× 84 1.5× 22 0.4× 23 387
Nathan R. McGee United States 11 55 0.5× 194 2.1× 7 0.1× 51 0.9× 64 1.3× 18 297
Dan Whittam United Kingdom 4 19 0.2× 265 2.9× 25 0.4× 34 0.6× 86 1.7× 5 399

Countries citing papers authored by Denise L. Lind

Since Specialization
Citations

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

Fields of papers citing papers by Denise L. Lind

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Denise L. Lind. 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 Denise L. Lind. The network helps show where Denise L. Lind may publish in the future.

Co-authorship network of co-authors of Denise L. Lind

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

All Works

7 of 7 papers shown
1.
Lind, Denise L., Janean L. Fidel, John Gay, & Katrina L. Mealey. (2013). Evaluation of vincristine-associated myelosuppression in Border Collies. American Journal of Veterinary Research. 74(2). 257–261. 4 indexed citations
2.
Reiner, Alexander P., Elad Ziv, Denise L. Lind, et al.. (2005). Population Structure, Admixture, and Aging-Related Phenotypes in African American Adults: The Cardiovascular Health Study. The American Journal of Human Genetics. 76(3). 463–477. 120 indexed citations
3.
Pawlikowska, Ludmila, Achal S. Achrol, Charles E. McCulloch, et al.. (2004). Polymorphisms in Genes Involved in Inflammatory and Angiogenic Pathways and the Risk of Hemorrhagic Presentation of Brain Arteriovenous Malformations. Stroke. 35(10). 2294–2300. 104 indexed citations
4.
Taillon‐Miller, Patricia, Scott F. Saccone, Nancy L. Saccone, et al.. (2004). Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens. Genomics. 84(6). 899–912. 16 indexed citations
5.
Maksymowych, Walter P., et al.. (1997). Polymorphism of the LMP2 gene and disease phenotype in ankylosing spondylitis: No association with disease severity. Clinical Rheumatology. 16(5). 461–465. 16 indexed citations
6.
Tranebjærg, Lisbeth, et al.. (1994). Prevalence of fra(X) in the county of Funen in Denmark is lower than expected. American Journal of Medical Genetics. 51(4). 423–427. 8 indexed citations
7.
Vincent, PC, et al.. (1977). Marrow culture studies in adult acute leukemia at presentation and during remission. Blood. 49(6). 903–912. 67 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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