Françoise Haeseleer

3.6k total citations
49 papers, 2.9k citations indexed

About

Françoise Haeseleer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Françoise Haeseleer has authored 49 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 18 papers in Cellular and Molecular Neuroscience and 11 papers in Ophthalmology. Recurrent topics in Françoise Haeseleer's work include Retinal Development and Disorders (26 papers), Neuroscience and Neuropharmacology Research (14 papers) and Retinal Diseases and Treatments (11 papers). Françoise Haeseleer is often cited by papers focused on Retinal Development and Disorders (26 papers), Neuroscience and Neuropharmacology Research (14 papers) and Retinal Diseases and Treatments (11 papers). Françoise Haeseleer collaborates with scholars based in United States, Germany and Netherlands. Françoise Haeseleer's co-authors include Krzysztof Palczewski, Amy Lee, Izabela Sokal, Yoshikazu Imanishi, Robert N. Fariss, Wolfgang Baehr, Christophe L. M. J. Verlinde, Silke Haverkamp, Anita E. Hendrickson and Fred Rieke and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Françoise Haeseleer

49 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Françoise Haeseleer United States	29	2.5k	1.4k	474	427	216	49	2.9k
Yoshikazu Imanishi United States	30	2.9k 1.1×	1.0k 0.7×	945 2.0×	468 1.1×	198 0.9×	61	3.3k
Mark P. Gray-Keller United States	20	1.7k 0.7×	1.0k 0.7×	176 0.4×	176 0.4×	132 0.6×	24	2.4k
Jeanne M. Frederick United States	34	2.8k 1.1×	1.1k 0.8×	889 1.9×	613 1.4×	50 0.2×	68	3.5k
Rameshwar K. Sharma United States	37	2.7k 1.1×	1.4k 1.0×	317 0.7×	315 0.7×	219 1.0×	148	3.8k
W. Clay Smith United States	25	1.2k 0.5×	769 0.6×	246 0.5×	128 0.3×	43 0.2×	67	1.7k
Michael O. Hall United States	26	1.9k 0.8×	611 0.4×	863 1.8×	373 0.9×	26 0.1×	62	2.6k
Igor V. Peshenko United States	29	2.0k 0.8×	923 0.7×	801 1.7×	242 0.6×	35 0.2×	63	2.1k
Paul P. M. Schnetkamp Canada	35	2.6k 1.0×	1.5k 1.1×	99 0.2×	464 1.1×	271 1.3×	104	3.2k
Nikolai O. Artemyev United States	34	3.0k 1.2×	1.1k 0.8×	288 0.6×	383 0.9×	47 0.2×	118	3.2k
Dror Sharon Israel	34	2.9k 1.1×	627 0.4×	1.4k 2.9×	494 1.2×	404 1.9×	136	3.7k

Countries citing papers authored by Françoise Haeseleer

Since Specialization

Citations

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

Fields of papers citing papers by Françoise Haeseleer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Françoise Haeseleer

This figure shows the co-authorship network connecting the top 25 collaborators of Françoise Haeseleer. A scholar is included among the top collaborators of Françoise Haeseleer 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 Françoise Haeseleer. Françoise Haeseleer 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

Corey, Daniel, et al.. (2022). Novel engineered chimeric engulfment receptors trigger T cell effector functions against SIV-infected CD4+ T cells. Molecular Therapy — Methods & Clinical Development. 28. 1–10. 1 indexed citations

Haeseleer, Françoise, Yoshinori Fukazawa, Haesun Park, et al.. (2021). Immune inactivation of anti-simian immunodeficiency virus chimeric antigen receptor T cells in rhesus macaques. Molecular Therapy — Methods & Clinical Development. 22. 304–319. 5 indexed citations

Haeseleer, Françoise, Karsten Eichholz, Mario Roederer, et al.. (2020). Real-Time Killing Assays to Assess the Potency of a New Anti-Simian Immunodeficiency Virus Chimeric Antigen Receptor T Cell. AIDS Research and Human Retroviruses. 36(12). 998–1009. 4 indexed citations

Sinha, Raunak, Amy Lee, Fred Rieke, & Françoise Haeseleer. (2016). Lack of CaBP1/Caldendrin or CaBP2 Leads to Altered Ganglion Cell Responses. eNeuro. 3(5). ENEURO.0099–16.2016. 13 indexed citations

Yang, Tian, et al.. (2016). Expression and Localization of CaBP Ca2+ Binding Proteins in the Mouse Cochlea. PLoS ONE. 11(1). e0147495–e0147495. 24 indexed citations

Lee, Amy, Shiyi Wang, Brittany Williams, et al.. (2014). Characterization of Cav1.4 Complexes (α11.4, β2, and α2δ4) in HEK293T Cells and in the Retina. Journal of Biological Chemistry. 290(3). 1505–1521. 48 indexed citations

Sokal, Izabela & Françoise Haeseleer. (2011). Insight into the Role of Ca²⁺-Binding Protein 5 in Vesicle Exocytosis. Investigative Ophthalmology & Visual Science. 52(12). 9131–9131. 11 indexed citations

Palczewski, Krzysztof, Christophe L. M. J. Verlinde, & Françoise Haeseleer. (2007). Molecular Mechanism of Visual Transduction. Novartis Foundation symposium. 224. 191–207. 3 indexed citations

Lee, Amy, et al.. (2007). Phosphorylation of the Ca²⁺-Binding Protein CaBP4 by Protein Kinase C ζ in Photoreceptors. Journal of Neuroscience. 27(46). 12743–12754. 20 indexed citations

10.

Haverkamp, Silke, Françoise Haeseleer, & Anita E. Hendrickson. (2003). A comparison of immunocytochemical markers to identify bipolar cell types in human and monkey retina. Visual Neuroscience. 20(6). 589–600. 117 indexed citations

11.

Yang, Jun, Sean McBride, Noga Vardi, et al.. (2002). Identification of a family of calcium sensors as protein ligands of inositol trisphosphate receptor Ca ²⁺ release channels. Proceedings of the National Academy of Sciences. 99(11). 7711–7716. 168 indexed citations

12.

Haeseleer, Françoise, Yoshikazu Imanishi, Izabela Sokal, Sławomir Filipek, & Krzysztof Palczewski. (2002). Calcium-Binding Proteins: Intracellular Sensors from the Calmodulin Superfamily. Biochemical and Biophysical Research Communications. 290(2). 615–623. 133 indexed citations

13.

Haeseleer, Françoise & Krzysztof Palczewski. (2002). Calmodulin And Ca2+-Binding Proteins (CaBPs): Variations on a Theme. Advances in experimental medicine and biology. 514. 303–317. 30 indexed citations

14.

Haeseleer, Françoise, Yoshikazu Imanishi, C.A.G.G. Driessen, et al.. (2002). Dual-substrate Specificity Short Chain Retinol Dehydrogenases from the Vertebrate Retina. Journal of Biological Chemistry. 277(47). 45537–45546. 168 indexed citations

15.

Haeseleer, Françoise, Izabela Sokal, Christophe L. M. J. Verlinde, et al.. (2000). Five Members of a Novel Ca2+-binding Protein (CABP) Subfamily with Similarity to Calmodulin. Journal of Biological Chemistry. 275(2). 1247–1260. 216 indexed citations

16.

Cideciyan, Artur V., Françoise Haeseleer, Robert N. Fariss, et al.. (2000). Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man. Visual Neuroscience. 17(5). 667–678. 93 indexed citations

17.

Sokal, Izabela, Ning Li, Christophe L. M. J. Verlinde, et al.. (2000). Ca2+-binding proteins in the retina: from discovery to etiology of human disease11The nucleotide sequences reported in this manuscript have been submitted to the GenBank™/EMBL databank with the following accession numbers: short form of human CaBP1, AF169148; long form of human CaBP1, AF169149; short form of bovine CaBP1, AF169150; long form of bovine CaBP1, AF169151; short form of mouse CaBP1, AF169153; long form of mouse CaBP1, AF1691152; human CaBP2, AF169154; bovine CaBP2, AF169155; short form of mouse CaBP2, AF169156; long form of mouse CaBP2, AF169157; human CaBP3, AF169158; human CaBP5, AF169159; bovine CaBP5, AF169160; mouse CaBP5, AF169161; human CaBP2 genomic sequence, AF170811; exons 1, 2-3-4, 5, 6 of human CaBP5 genomic sequence, AF170812, AF170813, AF170814, AF170815, respectively, and exons 1-2, 3-4, 5, 6 of human CaBP3 genomic sequence, AF170816, AF170817, AF170818, AF170815, respectively, and published recently [F. Haeseleer et al. (2000) J. Biol. Chem. 275, 1247–1260].. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1498(2-3). 233–251. 38 indexed citations

18.

Haeseleer, Françoise, Jing Huang, Lukasz Lebioda, John C. Saari, & Krzysztof Palczewski. (1998). Molecular Characterization of a Novel Short-chain Dehydrogenase/Reductase That Reduces All-trans-retinal. Journal of Biological Chemistry. 273(34). 21790–21799. 151 indexed citations

19.

Haeseleer, Françoise, et al.. (1992). Molecular cloning and sequencing of the attachment site and integrase gene of the temperate mycobacteriophage FRAT1. Nucleic Acids Research. 20(6). 1420–1420. 8 indexed citations

20.

Timm, Juliano, Catherine Tricot, Marc Massaer, et al.. (1992). Molecular cloning, characterization and purification of ornithine carbamoyltransferase from Mycobacterium bovis BCG. Molecular and General Genetics MGG. 234(3). 475–480. 11 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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