Danielle Frappier

1.1k total citations
11 papers, 806 citations indexed

About

Danielle Frappier is a scholar working on Molecular Biology, Nephrology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Danielle Frappier has authored 11 papers receiving a total of 806 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 2 papers in Nephrology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Danielle Frappier's work include RNA Research and Splicing (3 papers), RNA modifications and cancer (2 papers) and Viral Infections and Immunology Research (2 papers). Danielle Frappier is often cited by papers focused on RNA Research and Splicing (3 papers), RNA modifications and cancer (2 papers) and Viral Infections and Immunology Research (2 papers). Danielle Frappier collaborates with scholars based in Canada, United States and Israel. Danielle Frappier's co-authors include Takuya Fujiwara, Kenneth Morgan, Nicole M. Roslin, Martin Tieder, Harriet S. Tenenhouse, Thomas O. Carpenter, Celia M.T. Greenwood, Mark A. Miller, Erwin Schurr and Lucy J. Boothroyd and has published in prestigious journals such as Nucleic Acids Research, Journal of Virology and Journal of the American Society of Nephrology.

In The Last Decade

Danielle Frappier

11 papers receiving 787 citations

Peers

Danielle Frappier
Ina S. Klasen Netherlands
Beiyun C. Liu United States
Paul Risley United Kingdom
M W Hilgartner United States
S P Sisson United States
Danielle Frappier
Citations per year, relative to Danielle Frappier Danielle Frappier (= 1×) peers Muneo Inaba

Countries citing papers authored by Danielle Frappier

Since Specialization
Citations

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

Fields of papers citing papers by Danielle Frappier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle Frappier

This figure shows the co-authorship network connecting the top 25 collaborators of Danielle Frappier. A scholar is included among the top collaborators of Danielle Frappier 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 Danielle Frappier. Danielle Frappier 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.
Bergwitz, Clemens, Nicole M. Roslin, Martin Tieder, et al.. (2006). SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis. The American Journal of Human Genetics. 78(2). 179–192. 324 indexed citations
2.
Croteau, Sylvie, David Roquis, Danielle Frappier, et al.. (2005). Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors. Mammalian Genome. 16(2). 127–135. 19 indexed citations
3.
Frosk, Patrick, Cheryl R. Greenberg, Ryan E. Lamont, et al.. (2004). The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations. Human Mutation. 25(1). 38–44. 53 indexed citations
4.
Lamont, Ryan E., J. Concepción Loredo‐Osti, Nicole M. Roslin, et al.. (2004). A locus for Bowen–Conradi syndrome maps to chromosome region 12p13.3. American Journal of Medical Genetics Part A. 132A(2). 136–143. 10 indexed citations
5.
Manning, Andrew, Parviz Ghadirian, Danielle Frappier, et al.. (2001). Haplotype Analysis of <i>BRCA2</i> 8765delAG Mutation Carriers in French Canadian and Yemenite Jewish Hereditary Breast Cancer Families. Human Heredity. 52(2). 116–120. 20 indexed citations
6.
Jones, A, Danielle Frappier, M. JOYCE CRUMLEY, et al.. (2001). Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Not Caused by Mutations in the Na/Pi Cotransporter NPT2 Gene. Journal of the American Society of Nephrology. 12(3). 507–514. 50 indexed citations
7.
Greenwood, Celia M.T., Takuya Fujiwara, Lucy J. Boothroyd, et al.. (2000). Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1, in a Large Aboriginal Canadian Family. The American Journal of Human Genetics. 67(2). 405–416. 164 indexed citations
8.
Liu, Jie, Takuya Fujiwara, Fabio Orlando Neira Sánchez, et al.. (1995). Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene.. PubMed. 56(4). 845–53. 145 indexed citations
9.
Chabot, Benoı̂t, et al.. (1992). Differential ASF/SF2 activity in extracts from normal WI38 and transformed WI38VA13 cells. Nucleic Acids Research. 20(19). 5197–5204. 12 indexed citations
10.
Frappier, Danielle, et al.. (1991). Proteolysis of splicing factors during rat and monkey cell fractionation. Nucleic Acids Research. 19(16). 4509–4514. 6 indexed citations
11.
Frappier, Danielle, Daniel Gendron, Danielle Bourgaux-Ramoisy, & Pierre Bourgaux. (1990). Alternative homologous and nonhomologous products arising from intramolecular recombination. Journal of Virology. 64(10). 5058–5065. 3 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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