Christine Lambert

2.3k total citations
11 papers, 411 citations indexed

About

Christine Lambert is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Christine Lambert has authored 11 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Christine Lambert's work include Genomics and Rare Diseases (4 papers), Genomics and Phylogenetic Studies (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Christine Lambert is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomics and Phylogenetic Studies (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Christine Lambert collaborates with scholars based in United States, United Kingdom and Netherlands. Christine Lambert's co-authors include Primo Baybayan, Jonas Korlach, Sarah B. Kingan, Aaron M. Wenger, Juliana Cudini, Brendan D. Galvin, Mara Lawniczak, Richard Durbin, Kevin Eng and Haynes Heaton and has published in prestigious journals such as PLoS ONE, Scientific Reports and Genetics in Medicine.

In The Last Decade

Christine Lambert

10 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christine Lambert United States 8 241 171 87 55 39 11 411
Shay Covo Israel 12 356 1.5× 78 0.5× 121 1.4× 48 0.9× 13 0.3× 28 490
Alejandro Vasquez-Rifo Canada 9 298 1.2× 49 0.3× 31 0.4× 107 1.9× 26 0.7× 11 368
Nga Thi Thuy Nguyen France 8 287 1.2× 119 0.7× 101 1.2× 34 0.6× 5 0.1× 12 451
Sarah Behrens Germany 11 205 0.9× 65 0.4× 62 0.7× 15 0.3× 81 2.1× 17 359
Douglass Turner United States 4 422 1.8× 134 0.8× 156 1.8× 43 0.8× 22 0.6× 4 555
Devika Ganesamoorthy Australia 16 390 1.6× 323 1.9× 65 0.7× 69 1.3× 7 0.2× 25 719
Wesley Brashear United States 12 169 0.7× 198 1.2× 64 0.7× 19 0.3× 7 0.2× 28 406
Eric F. Tsung United States 4 307 1.3× 111 0.6× 97 1.1× 35 0.6× 9 0.2× 4 418
Terry Brown United Kingdom 10 269 1.1× 51 0.3× 62 0.7× 17 0.3× 20 0.5× 14 361
Masahiro Kasahara Japan 10 323 1.3× 72 0.4× 137 1.6× 36 0.7× 7 0.2× 20 408

Countries citing papers authored by Christine Lambert

Since Specialization
Citations

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

Fields of papers citing papers by Christine Lambert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Lambert

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

All Works

11 of 11 papers shown
1.
Rowell, William J., et al.. (2025). Resolving the Diagnostic Odyssey in Inherited Retinal Dystrophies Through Long‐Read Genome Sequencing. American Journal of Medical Genetics Part A. 197(10). e64139–e64139.
2.
Kingan, Sarah B., Douglas A. Shoue, Lutz Froenicke, et al.. (2024). Improved high quality sand fly assemblies enabled by ultra low input long read sequencing. Scientific Data. 11(1). 918–918. 5 indexed citations
3.
Kwint, Michael, Ronny Derks, Aaron M. Wenger, et al.. (2023). Comprehensive de novo mutation discovery with HiFi long-read sequencing. Genome Medicine. 15(1). 34–34. 18 indexed citations
4.
Gobbo, Giulia, Xueqi Wang, Madeline Couse, et al.. (2023). Long‐read genome sequencing reveals a novel intronic retroelement insertion in NR5A1 associated with 46,XY differences of sexual development. American Journal of Medical Genetics Part A. 194(5). e63522–e63522. 6 indexed citations
5.
Kobayashi, Erica Sanford, Serge Batalov, Aaron M. Wenger, et al.. (2022). Approaches to long-read sequencing in a clinical setting to improve diagnostic rate. Scientific Reports. 12(1). 16945–16945. 28 indexed citations
6.
Benton, Michael G., Wallace Akerley, George F. Mayhew, et al.. (2020). Structural variation and its potential impact on genome instability: Novel discoveries in the EGFR landscape by long-read sequencing. PLoS ONE. 15(1). e0226340–e0226340. 23 indexed citations
7.
Kingan, Sarah B., Julie Urban, Christine Lambert, et al.. (2019). A high-quality genome assembly from a single, field-collected spotted lanternfly ( Lycorma delicatula ) using the PacBio Sequel II system. GigaScience. 8(10). 32 indexed citations
8.
Kingan, Sarah B., Haynes Heaton, Juliana Cudini, et al.. (2019). A High-Quality De novo Genome Assembly from a Single Mosquito Using PacBio Sequencing. Genes. 10(1). 62–62. 89 indexed citations
9.
10.
Merker, Jason D., Aaron M. Wenger, Tam P. Sneddon, et al.. (2017). Long-read genome sequencing identifies causal structural variation in a Mendelian disease. Genetics in Medicine. 20(1). 159–163. 158 indexed citations
11.
Vembar, Shruthi Sridhar, Matthew G. Seetin, Christine Lambert, et al.. (2016). Complete telomere-to-telomerede novoassembly of thePlasmodium falciparumgenome through long-read (>11 kb), single molecule, real-time sequencing. DNA Research. 23(4). 339–351. 36 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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