Madeleine Carreau

2.5k total citations
44 papers, 1.9k citations indexed

About

Madeleine Carreau is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, Madeleine Carreau has authored 44 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 9 papers in Cancer Research and 8 papers in Hematology. Recurrent topics in Madeleine Carreau's work include DNA Repair Mechanisms (28 papers), Carcinogens and Genotoxicity Assessment (7 papers) and CRISPR and Genetic Engineering (7 papers). Madeleine Carreau is often cited by papers focused on DNA Repair Mechanisms (28 papers), Carcinogens and Genotoxicity Assessment (7 papers) and CRISPR and Genetic Engineering (7 papers). Madeleine Carreau collaborates with scholars based in Canada, United States and Netherlands. Madeleine Carreau's co-authors include Manuel Buchwald, Lucine Bosnoyan-Collins, Noa Alon, Laura S. Haneline, Hans Joenje, D. Wade Clapp, Jan C. Pronk, Carola G.M. van Berkel, Fré Arwert and Olga I. Gan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Madeleine Carreau

44 papers receiving 1.8k citations

Peers

Madeleine Carreau

GENET

HEMAT

ONCOL

José F. Ruiz Spain

Carol Reifsteck United States

Enrico Cappelli Italy

Verónica Ayllón Spain

Eric M. Kallin United States

Silvia Grisendi United States

G. Levan Sweden

Lauren D. Wood United States

Teijiro Aso Japan

Irmgard Irminger‐Finger Switzerland

José F. Ruiz Spain

Madeleine Carreau

1.0k ×0.6

377 ×0.8

158 ×0.6

GENET

139 ×0.6

HEMAT

171 ×0.8

ONCOL

Citations per year, relative to Madeleine Carreau Madeleine Carreau (= 1×) peers José F. Ruiz

Countries citing papers authored by Madeleine Carreau

Since Specialization

Citations

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

Fields of papers citing papers by Madeleine Carreau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Madeleine Carreau

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

Tremblay, Cédric S., et al.. (2018). Fanconi anemia core complex-dependent HES1 mono-ubiquitination regulates its transcriptional activity. BMC Research Notes. 11(1). 138–138. 2 indexed citations

Aissa, Manel Ben, et al.. (2018). FANCC localizes with UNC5A at neurite outgrowth and promotes neuritogenesis. BMC Research Notes. 11(1). 662–662. 2 indexed citations

Elowe, Sabine, et al.. (2015). The Fanconi Anemia C Protein Binds to and Regulates Stathmin-1 Phosphorylation. PLoS ONE. 10(10). e0140612–e0140612. 5 indexed citations

Aissa, Manel Ben, et al.. (2014). The Fanconi Anemia Group C Protein Interacts with Uncoordinated 5A and Delays Apoptosis. PLoS ONE. 9(3). e92811–e92811. 9 indexed citations

Carreau, Madeleine, et al.. (2012). Fanconi Anemia Proteins and Their Interacting Partners: A Molecular Puzzle. Anemia. 2012. 1–11. 13 indexed citations

Tremblay, Cédric S., et al.. (2009). The Fanconi Anemia Core Complex Acts as a Transcriptional Co-regulator in Hairy Enhancer of Split 1 Signaling. Journal of Biological Chemistry. 284(20). 13384–13395. 17 indexed citations

Tremblay, Cédric S., Feng Huang, Caroline Huard, et al.. (2008). HES1 is a novel interactor of the Fanconi anemia core complex. Blood. 112(5). 2062–2070. 46 indexed citations

Carreau, Madeleine, et al.. (2005). The Caenorhabditis elegans FancD2 ortholog is required for survival following DNA damage. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 141(4). 453–460. 16 indexed citations

Godin, Chantal, et al.. (2003). Presenilin-1 is indirectly implicated in Notch1 cleavage. Neuroreport. 14(12). 1613–1616. 6 indexed citations

10.

Hébert, Sébastien S., et al.. (2003). Presenilin-1 interacts directly with the β-site amyloid protein precursor cleaving enzyme (BACE1). Neurobiology of Disease. 13(3). 238–245. 33 indexed citations

11.

Carreau, Madeleine, Olga I. Gan, Lili Liu, et al.. (1999). Hematopoietic compartment of Fanconi anemia group C null mice contains fewer lineage-negative CD34+ primitive hematopoietic cells and shows reduced reconstitution ability. Experimental Hematology. 27(11). 1667–1674. 50 indexed citations

12.

Carreau, Madeleine & Manuel Buchwald. (1998). Fanconi's anemia: what have we learned from the genes so far?. Molecular Medicine Today. 4(5). 201–206. 8 indexed citations

13.

Carreau, Madeleine & Manuel Buchwald. (1998). The Fanconi anemia genes. Current Opinion in Pediatrics. 10(1). 65–69. 6 indexed citations

14.

Tomkins, Darrell J., Melanie Care, Madeleine Carreau, & Manuel Buchwald. (1998). Development and characterization of immortalized fibroblastoid cell lines from an FA(C) mouse model. Mutation Research/DNA Repair. 408(1). 27–35. 3 indexed citations

15.

Winter, Johan P. de, Quinten Waisfisz, Carola G.M. van Berkel, et al.. (1998). The Fanconi anaemia group G gene FANCG is identical with XRCC9. Nature Genetics. 20(3). 281–283. 269 indexed citations

16.

Carreau, Madeleine, Éric Eveno, Xavier Quilliet, et al.. (1995). Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes. Carcinogenesis. 16(5). 1003–1009. 41 indexed citations

17.

Mezzina, M., Éric Eveno, Odile Chevallier-Lagente, et al.. (1994). Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells. Carcinogenesis. 15(8). 1493–1498. 16 indexed citations

18.

Carreau, Madeleine & D. J. Hunting. (1992). Transcription-dependent and independent DNA excision repair pathways in human cells. Mutation Research/DNA Repair. 274(1). 57–64. 38 indexed citations

19.

Laviolette, Michel, et al.. (1988). Metabolism of arachidonic acid through the 5-lipoxygenase pathway in normal human peritoneal macrophages.. The Journal of Immunology. 141(6). 2104–2109. 17 indexed citations

20.

Laviolette, Michel, et al.. (1988). Bronchoalveolar Lavage Cell Differential on Microscope Glass Cover: A Simple and Accurate Technique. American Review of Respiratory Disease. 138(2). 451–457. 65 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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