Lea K. Davis

3.6k total citations
5 papers, 143 citations indexed

About

Lea K. Davis is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Lea K. Davis has authored 5 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Lea K. Davis's work include Genomic variations and chromosomal abnormalities (3 papers), Autism Spectrum Disorder Research (3 papers) and Congenital heart defects research (3 papers). Lea K. Davis is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Autism Spectrum Disorder Research (3 papers) and Congenital heart defects research (3 papers). Lea K. Davis collaborates with scholars based in United States and Poland. Lea K. Davis's co-authors include Eric R. Gamazon, Nancy J. Cox, James S. Sutcliffe, Edwin H. Cook, Patrícia B. S. Celestino-Soper, Tomasz Gambin, Susanne Thomson, Matthew W. State, Arthur L. Beaudet and Stephan Sanders and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Human Mutation.

In The Last Decade

Lea K. Davis

5 papers receiving 142 citations

Peers

Lea K. Davis

GENET

MB

CN

CMN

CB

Patrícia B. S. Celestino-Soper United States

Laura L. Klitten Denmark

Sohnee Ahmed Canada

Lisa Robertson United Kingdom

Gail Reiner United States

Vinay Puri United Kingdom

Qingping Zhang China

Olve Moldestad Norway

Victoria M. James United Kingdom

Kameryn M. Butler United States

Patrícia B. S. Celestino-Soper United States

Lea K. Davis

76 ×0.9

GENET

97 ×1.4

MB

35 ×0.8

CN

26 ×1.2

CMN

12 ×1.0

CB

Citations per year, relative to Lea K. Davis Lea K. Davis (= 1×) peers Patrícia B. S. Celestino-Soper

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:

5 of 5 papers shown

1.

Wassink, Thomas H., Heather C. Hazlett, Lea K. Davis, Allan L. Reiss, & Joseph Piven. (2014). Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome. Journal of Neurodevelopmental Disorders. 6(1). 6–6. 13 indexed citations

2.

Gamazon, Eric R., Nancy J. Cox, & Lea K. Davis. (2014). Structural Architecture of SNP Effects on Complex Traits. The American Journal of Human Genetics. 95(5). 477–489. 18 indexed citations

3.

Davis, Lea K., Eric R. Gamazon, Emily Kistner‐Griffin, et al.. (2012). Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci. Molecular Autism. 3(1). 3–3. 26 indexed citations

4.

Celestino-Soper, Patrícia B. S., Chad A. Shaw, Stephan Sanders, et al.. (2011). Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Human Molecular Genetics. 20(22). 4360–4370. 85 indexed citations

5.

Davis, Lea K.. (2011). In Search of Genomic Stability: Characterizing Copy Number Stable Regions. Human Mutation. 32(8). 1 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