Kelsey Grinde

1.0k total citations
13 papers, 193 citations indexed

About

Kelsey Grinde is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Kelsey Grinde has authored 13 papers receiving a total of 193 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Kelsey Grinde's work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and phenotypic traits in livestock (4 papers). Kelsey Grinde is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and phenotypic traits in livestock (4 papers). Kelsey Grinde collaborates with scholars based in United States, Sweden and Hong Kong. Kelsey Grinde's co-authors include Timothy A. Thornton, Alexander P. Reiner, Sharon R. Browning, Tamar Sofer, Aladdin H. Shadyab, Simin Liu, Kei Hang Katie Chan, Qibin Qi, Cathy C. Laurie and Stephanie M. Gogarten and has published in prestigious journals such as The American Journal of Human Genetics, PLoS Genetics and Journal of Thrombosis and Haemostasis.

In The Last Decade

Kelsey Grinde

13 papers receiving 192 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kelsey Grinde United States 7 115 49 26 12 10 13 193
İhsan Turan Türkiye 10 110 1.0× 98 2.0× 21 0.8× 9 0.8× 7 0.7× 34 242
Peikuan Cong China 8 62 0.5× 75 1.5× 15 0.6× 26 2.2× 5 0.5× 12 168
Casey T. Finnicum United States 7 49 0.4× 50 1.0× 9 0.3× 32 2.7× 13 1.3× 13 147
Margaux L.A. Hujoel United States 10 139 1.2× 81 1.7× 21 0.8× 4 0.3× 8 0.8× 18 247
Sini Kerminen Finland 4 141 1.2× 39 0.8× 17 0.7× 8 0.7× 9 0.9× 7 185
Ravindranath Duggirala United States 4 90 0.8× 37 0.8× 27 1.0× 10 0.8× 9 0.9× 5 181
Luis Socha Australia 7 53 0.5× 62 1.3× 17 0.7× 14 1.2× 12 1.2× 12 238
Pagé C. Goddard United States 5 160 1.4× 142 2.9× 10 0.4× 35 2.9× 10 1.0× 11 255
Angad Johar Australia 9 91 0.8× 83 1.7× 24 0.9× 46 3.8× 25 2.5× 14 245
Vered Madar United States 5 88 0.8× 123 2.5× 14 0.5× 9 0.8× 17 1.7× 8 271

Countries citing papers authored by Kelsey Grinde

Since Specialization
Citations

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

Fields of papers citing papers by Kelsey Grinde

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelsey Grinde

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

All Works

13 of 13 papers shown
1.
Grinde, Kelsey, Brian L. Browning, Alex P. Reiner, Timothy A. Thornton, & Sharon R. Browning. (2024). Adjusting for principal components can induce collider bias in genome-wide association studies. PLoS Genetics. 20(12). e1011242–e1011242. 4 indexed citations
2.
Horimoto, Andréa R. V. R., Elizabeth Blue, Kelsey Grinde, et al.. (2023). Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations. Human Genetics and Genomics Advances. 4(3). 100207–100207. 8 indexed citations
3.
Mills, Lauren J., Andrew R. Raduski, Erin L. Marcotte, et al.. (2022). Genetic ancestry, differential gene expression, and survival in pediatric B‐cell acute lymphoblastic leukemia. Cancer Medicine. 12(4). 4761–4772. 3 indexed citations
4.
5.
Raffield, Laura M., Ake T. Lu, Mindy D Szeto, et al.. (2020). Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome‐wide analysis in African Americans. Journal of Thrombosis and Haemostasis. 18(6). 1335–1347. 14 indexed citations
6.
Grinde, Kelsey, Lisa Brown, Alexander P. Reiner, Timothy A. Thornton, & Sharon R. Browning. (2019). Genome-wide Significance Thresholds for Admixture Mapping Studies. The American Journal of Human Genetics. 104(3). 454–465. 25 indexed citations
7.
Sofer, Tamar, Xiuwen Zheng, Stephanie M. Gogarten, et al.. (2019). A fully adjusted two‐stage procedure for rank‐normalization in genetic association studies. Genetic Epidemiology. 43(3). 263–275. 23 indexed citations
8.
Grinde, Kelsey, Qibin Qi, Timothy A. Thornton, et al.. (2018). Generalizing polygenic risk scores from Europeans to Hispanics/Latinos. Genetic Epidemiology. 43(1). 50–62. 54 indexed citations
9.
Grinde, Kelsey, et al.. (2017). Illustrating, Quantifying, and Correcting for Bias in Post-hoc Analysis of Gene-Based Rare Variant Tests of Association. Frontiers in Genetics. 8. 4 indexed citations
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12.
Browning, Sharon R., Kelsey Grinde, Anna Plantinga, et al.. (2016). Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL). G3 Genes Genomes Genetics. 6(6). 1525–1534. 38 indexed citations
13.
Arbet, Jaron, et al.. (2015). A general approach for combining diverse rare variant association tests provides improved robustness across a wider range of genetic architectures. European Journal of Human Genetics. 24(5). 767–773. 10 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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