Lea K. Davis

18.0k total citations
105 papers, 2.1k citations indexed

About

Lea K. Davis is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Cognitive Neuroscience. According to data from OpenAlex, Lea K. Davis has authored 105 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 17 papers in Public Health, Environmental and Occupational Health and 16 papers in Cognitive Neuroscience. Recurrent topics in Lea K. Davis's work include Genetic Associations and Epidemiology (32 papers), Autism Spectrum Disorder Research (13 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Lea K. Davis is often cited by papers focused on Genetic Associations and Epidemiology (32 papers), Autism Spectrum Disorder Research (13 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Lea K. Davis collaborates with scholars based in United States, United Kingdom and Canada. Lea K. Davis's co-authors include Barbara E. Stranger, Ekaterina Khramtsova, Val C. Sheffield, Thomas H. Wassink, Sandra Sanchez‐Roige, Edwin H. Cook, Abraham A. Palmer, Nancy J. Cox, Kacie J. Meyer and Danielle S. Rudd and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Lea K. Davis

96 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lea K. Davis United States	26	811	603	277	213	202	105	2.1k
Joyce Y. Tung United States	20	1.2k 1.5×	840 1.4×	187 0.7×	110 0.5×	113 0.6×	28	3.1k
Marlies de Lange United Kingdom	18	676 0.8×	437 0.7×	230 0.8×	104 0.5×	144 0.7×	21	2.5k
Hannah Jones United Kingdom	23	586 0.7×	207 0.3×	230 0.8×	528 2.5×	410 2.0×	68	2.2k
Narelle K. Hansell Australia	30	689 0.8×	411 0.7×	755 2.7×	203 1.0×	183 0.9×	78	2.5k
Shing Wan Choi United Kingdom	15	1.3k 1.6×	644 1.1×	213 0.8×	327 1.5×	260 1.3×	24	2.6k
Tim Becker Germany	32	1.1k 1.4×	1.3k 2.2×	318 1.1×	411 1.9×	141 0.7×	122	3.6k
Kyoko Watanabe Netherlands	16	1.9k 2.4×	1.3k 2.2×	323 1.2×	333 1.6×	258 1.3×	34	3.9k
Alexandre Bureau Canada	21	500 0.6×	714 1.2×	98 0.4×	243 1.1×	487 2.4×	79	2.1k
Hiroaki Tomita Japan	30	712 0.9×	1.8k 2.9×	282 1.0×	473 2.2×	487 2.4×	178	4.1k
Izumi Kawachi Japan	18	770 0.9×	754 1.3×	125 0.5×	237 1.1×	75 0.4×	81	5.3k

Countries citing papers authored by Lea K. Davis

Since Specialization

Citations

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

Fields of papers citing papers by Lea K. Davis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lea K. Davis. 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 Lea K. Davis. The network helps show where Lea K. Davis may publish in the future.

Co-authorship network of co-authors of Lea K. Davis

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Thorpe, Hayley H. A., Pierre Fontanillas, Mariela Jennings, et al.. (2025). Genome-wide association studies of lifetime and frequency of cannabis use in 131,895 individuals. Molecular Psychiatry. 31(2). 1061–1073.

Galimberti, Marco, Daniel F. Levey, Joseph D. Deak, et al.. (2025). A contextual genomic perspective on physical activity and its relationship to health, well being and illness. Nature Genetics. 57(8). 1860–1871.

Wade, Alisha N., Lindsay Guare, Péter Straub, et al.. (2025). Strength of Genetic Associations with Thyrotropin Values Differs Between Populations with Similarity to African and European Reference Populations. Thyroid. 35(2). 131–142.

Singh, Kritika, Hyunjoon Lee, Julia Sealock, et al.. (2024). Genes associated with depression and coronary artery disease are enriched for cardiomyopathy and inflammatory phenotypes. Nature Mental Health. 2(5). 574–582. 2 indexed citations

Walsh, Colin G., Yirui Hu, Yi-han Sheu, et al.. (2024). Development and multi-site external validation of a generalizable risk prediction model for bipolar disorder. Translational Psychiatry. 14(1). 58–58. 4 indexed citations

Wilson, Jo Ellen, Julia Sealock, Péter Straub, et al.. (2023). Exploring genetic risk for catatonia in a genome wide association study and polygenic risk score analysis. Schizophrenia Research. 263. 178–190. 3 indexed citations

Khramtsova, Ekaterina, Stacey J. Winham, Lea K. Davis, Barbara E. Stranger, & Melissa A. Wilson. (2023). Toward a deeper understanding of gene-by-sex interaction models. Cell Genomics. 3(5). 100324–100324.

Moscati, Arden, Annika Faucon, Sara Larsson Lönn, et al.. (2023). Life is pain: Fibromyalgia as a nexus of multiple liability distributions. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 192(7-8). 171–182. 1 indexed citations

Khramtsova, Ekaterina, Melissa A. Wilson, Joanna Martin, et al.. (2023). Quality control and analytic best practices for testing genetic models of sex differences in large populations. Cell. 186(10). 2044–2061. 18 indexed citations

10.

Hammack‐Aviran, Catherine M., et al.. (2022). LGBTQ+ Perspectives on Conducting Genomic Research on Sexual Orientation and Gender Identity. Behavior Genetics. 52(4-5). 246–267. 13 indexed citations

11.

Jennings, Mariela, Hyunjoon Lee, Daniel Rocha, et al.. (2022). Identifying High-Risk Comorbidities Associated with Opioid Use Patterns Using Electronic Health Record Prescription Data. PubMed. 8(1-2). 47–56. 9 indexed citations

12.

Actkins, Ky’Era V., Kritika Singh, Donald Hucks, et al.. (2020). Characterizing the Clinical and Genetic Spectrum of Polycystic Ovary Syndrome in Electronic Health Records. The Journal of Clinical Endocrinology & Metabolism. 106(1). 153–167. 16 indexed citations

13.

Tilot, Amanda K., Ekaterina Khramtsova, Dan Liang, et al.. (2020). The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cerebral Cortex. 31(4). 1873–1887. 14 indexed citations

14.

Li, Yu, Hanxin Zhang, Ishanu Chattopadhyay, et al.. (2019). Estimating heritability and genetic correlations from large health datasets in the absence of genetic data. Nature Communications. 10(1). 5508–5508. 20 indexed citations

15.

Zheutlin, Amanda B., Jessica Dennis, Richard Karlsson Linnér, et al.. (2019). Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems. American Journal of Psychiatry. 176(10). 846–855. 129 indexed citations

16.

Khramtsova, Ekaterina, et al.. (2018). Sex differences in the genetic architecture of obsessive–compulsive disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(6). 351–364. 31 indexed citations

17.

Khramtsova, Ekaterina, Lea K. Davis, & Barbara E. Stranger. (2018). The role of sex in the genomics of human complex traits. Nature Reviews Genetics. 20(3). 173–190. 179 indexed citations

18.

Morselli, Lisa L., Eric R. Gamazon, Esra Tasali, et al.. (2017). Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study. Diabetes. 67(1). 155–164. 3 indexed citations

19.

Fingert, John H., Alan L. Robin, Jennifer Stone, et al.. (2011). Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Human Molecular Genetics. 20(12). 2482–2494. 159 indexed citations

20.

Urraca, Nora, Lea K. Davis, Edwin H. Cook, N. Carolyn Schanen, & Lawrence T. Reiter. (2010). A Single-Tube Quantitative High-Resolution Melting Curve Method for Parent-of-Origin Determination of 15q Duplications. Genetic Testing and Molecular Biomarkers. 14(4). 571–576. 8 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.

Explore authors with similar magnitude of impact