Kristin Ardlie

100.0k total citations · 7 hit papers
71 papers, 9.7k citations indexed

About

Kristin Ardlie is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Kristin Ardlie has authored 71 papers receiving a total of 9.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 40 papers in Molecular Biology and 9 papers in Cancer Research. Recurrent topics in Kristin Ardlie's work include Genetic Associations and Epidemiology (23 papers), Genetic Mapping and Diversity in Plants and Animals (14 papers) and Molecular Biology Techniques and Applications (7 papers). Kristin Ardlie is often cited by papers focused on Genetic Associations and Epidemiology (23 papers), Genetic Mapping and Diversity in Plants and Animals (14 papers) and Molecular Biology Techniques and Applications (7 papers). Kristin Ardlie collaborates with scholars based in United States, Sweden and Canada. Kristin Ardlie's co-authors include Mark Seielstad, Leonid Kruglyak, David Altshuler, François Aguet, Joel N. Hirschhorn, Michele Cargill, Leif Groop, Kathryn L. Lunetta, Nila Patil and Janet A. Warrington and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Kristin Ardlie

70 papers receiving 9.5k citations

Hit Papers

5 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.

Characterization of single-nucleotide polymorphisms in coding regions of human genes

1999 1.3k citations David Altshuler, Kristin Ardlie et al. Nature Genetics profile →
Patterns of linkage disequilibrium in the human genome

2002 855 citations Kristin Ardlie, Mark Seielstad et al. profile →
A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes

2007 833 citations Kristin Ardlie et al. The American Journal of Human Genetics profile →
Landscape of X chromosome inactivation across human tissues

2017 665 citations François Aguet, Tuuli Lappalainen et al. profile →
Massively parallel single-nucleus RNA-seq with DroNc-seq

2017 630 citations Naomi Habib, Inbal Avraham‐Davidi et al. Nature Methods profile →
Transcriptional and Cellular Diversity of the Human Heart

2020 332 citations Nathan R. Tucker, Mark Chaffin et al. Circulation profile →
RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues

2019 310 citations Keren Yizhak, François Aguet et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kristin Ardlie United States	37	4.4k	4.1k	1.5k	906	761	71	9.7k
Pui–Yan Kwok United States	56	5.6k 1.3×	3.0k 0.7×	1.7k 1.2×	795 0.9×	944 1.2×	237	11.9k
David A. Hinds United States	50	4.2k 1.0×	4.9k 1.2×	845 0.6×	765 0.8×	415 0.5×	95	11.3k
Pauline C. Ng United States	19	7.3k 1.7×	5.2k 1.3×	791 0.5×	1.4k 1.5×	873 1.1×	23	12.5k
David Fitzpatrick United Kingdom	65	6.9k 1.6×	5.4k 1.3×	2.6k 1.7×	894 1.0×	1.1k 1.4×	271	14.3k
Bryan Howie United States	15	2.6k 0.6×	4.5k 1.1×	925 0.6×	549 0.6×	706 0.9×	17	7.6k
Peter Nürnberg Germany	71	9.0k 2.0×	4.9k 1.2×	1.5k 1.0×	1.0k 1.1×	1.0k 1.4×	407	17.7k
Michael Krawczak Germany	64	7.7k 1.7×	7.1k 1.7×	1.7k 1.1×	813 0.9×	642 0.8×	282	16.4k
Shrikant Mane United States	41	6.5k 1.5×	2.8k 0.7×	1.3k 0.8×	1.8k 2.0×	1.2k 1.5×	100	12.5k
Kelly A. Frazer United States	55	9.5k 2.2×	5.2k 1.3×	1.2k 0.8×	1.5k 1.6×	723 1.0×	138	15.2k
Henry H. Heng United States	60	7.0k 1.6×	2.9k 0.7×	779 0.5×	1.7k 1.8×	989 1.3×	202	11.8k

Countries citing papers authored by Kristin Ardlie

Since Specialization

Citations

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

Fields of papers citing papers by Kristin Ardlie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristin Ardlie

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

All Works

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20 of 20 papers shown

Rath, Sneha, Rahul Gupta, Ellen Todres, et al.. (2024). Mitochondrial genome copy number variation across tissues in mice and humans. Proceedings of the National Academy of Sciences. 121(33). e2402291121–e2402291121. 9 indexed citations

Ardlie, Kristin, Kent D. Taylor, Peter Durda, et al.. (2024). Transcriptome-wide association study of the plasma proteome reveals cis and trans regulatory mechanisms underlying complex traits. The American Journal of Human Genetics. 111(3). 445–455. 2 indexed citations

Hou, Lei, Xushen Xiong, Yongjin Park, et al.. (2023). Multitissue H3K27ac profiling of GTEx samples links epigenomic variation to disease. Nature Genetics. 55(10). 1665–1676. 11 indexed citations

Flynn, Elise D., Silva Kasela, Sarah Kim-Hellmuth, et al.. (2022). Transcription factor regulation of eQTL activity across individuals and tissues. PLoS Genetics. 18(1). e1009719–e1009719. 21 indexed citations

García-Pérez, Raquel, José Miguel Ramírez, Mattia Bosio, et al.. (2022). The landscape of expression and alternative splicing variation across human traits. Cell Genomics. 3(1). 100244–100244. 20 indexed citations

Lange, Leslie A., François Aguet, Kristin Ardlie, et al.. (2022). Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis. International Journal of Obesity. 47(2). 109–116. 5 indexed citations

Sofer, Tamar, Nuzulul Kurniansyah, François Aguet, et al.. (2021). Benchmarking association analyses of continuous exposures with RNA-seq in observational studies. Briefings in Bioinformatics. 22(6). 3 indexed citations

Liang, Yanyu, François Aguet, Alvaro Barbeira, Kristin Ardlie, & Hae Kyung Im. (2021). A scalable unified framework of total and allele-specific counts for cis-QTL, fine-mapping, and prediction. Nature Communications. 12(1). 1424–1424. 14 indexed citations

Graubert, Aaron, François Aguet, Arvind Ravi, Kristin Ardlie, & Gad Getz. (2021). RNA-SeQC 2: efficient RNA-seq quality control and quantification for large cohorts. Bioinformatics. 37(18). 3048–3050. 47 indexed citations

10.

Barbeira, Alvaro, Yanyu Liang, Rodrigo Bonazzola, et al.. (2020). Fine‐mapping and QTL tissue‐sharing information improves the reliability of causal gene identification. Genetic Epidemiology. 44(8). 854–867. 26 indexed citations

11.

Tucker, Nathan R., Mark Chaffin, Stephen J. Fleming, et al.. (2020). Transcriptional and Cellular Diversity of the Human Heart. Circulation. 142(5). 466–482. 332 indexed citations breakdown →

12.

He, Yuan, Surya B. Chhetri, Marios Arvanitis, et al.. (2020). sn-spMF: matrix factorization informs tissue-specific genetic regulation of gene expression. Genome biology. 21(1). 235–235. 11 indexed citations

13.

Yizhak, Keren, François Aguet, Jaegil Kim, et al.. (2019). RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. Science. 364(6444). 310 indexed citations breakdown →

14.

Gamazon, Eric R., Ayellet V. Segrè, Martijn van de Bunt, et al.. (2018). Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nature Genetics. 50(7). 956–967. 242 indexed citations

15.

Klarin, Derek, Qiuyu Zhu, Connor A. Emdin, et al.. (2017). Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease. Nature Genetics. 49(9). 1392–1397. 150 indexed citations

16.

Habib, Naomi, Inbal Avraham‐Davidi, Anindita Basu, et al.. (2017). Massively parallel single-nucleus RNA-seq with DroNc-seq. Nature Methods. 14(10). 955–958. 630 indexed citations breakdown →

17.

Oberholzer, Patrick A., Damien Kee, Piotr Dziunycz, et al.. (2011). RAS Mutations Are Associated With the Development of Cutaneous Squamous Cell Tumors in Patients Treated With RAF Inhibitors. Journal of Clinical Oncology. 30(3). 316–321. 298 indexed citations

18.

Winckler, Wendy, Michael N. Weedon, Robert Graham, et al.. (2007). Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes. Diabetes. 56(3). 685–693. 130 indexed citations

19.

Mahan, Scott, et al.. (2004). Collaborative Design for Automated DNA Storage That Allows for Rapid, Accurate, Large-Scale Studies. Assay and Drug Development Technologies. 2(6). 683–689. 9 indexed citations

20.

Ardlie, Kristin, Kathryn L. Lunetta, & Mark Seielstad. (2002). Testing for Population Subdivision and Association in Four Case-Control Studies. The American Journal of Human Genetics. 71(2). 304–311. 174 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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