Isabelle Gicquel

1.0k total citations
21 papers, 453 citations indexed

About

Isabelle Gicquel is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Isabelle Gicquel has authored 21 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Isabelle Gicquel's work include Hedgehog Signaling Pathway Studies (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Iron Metabolism and Disorders (4 papers). Isabelle Gicquel is often cited by papers focused on Hedgehog Signaling Pathway Studies (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Iron Metabolism and Disorders (4 papers). Isabelle Gicquel collaborates with scholars based in France, United States and Italy. Isabelle Gicquel's co-authors include Véronique David, Christèle Dubourg, Claude Bendavid, Valérie Dupé, Sylvie Odent, Lucie Rochard, Laurent Pasquier, Leslie Ratié, Sandra Mercier and Jean‐Yves Le Gall and has published in prestigious journals such as Nucleic Acids Research, Development and Human Molecular Genetics.

In The Last Decade

Isabelle Gicquel

20 papers receiving 445 citations

Peers

Isabelle Gicquel

GENET

PPCH

HEMAT

GENET

Dorothée Cailley France

Fred Petrij Netherlands

Satoshi Ishikiriyama Japan

Jaime Garcia‐Heras United States

Bela Patel United States

Kari Casas United States

Cornelia Daumer‐Haas Germany

Boyan Dimitrov Bulgaria

Andreas Hehr Germany

Hasmik Mkrtchyan Germany

Dorothée Cailley France

Isabelle Gicquel

166 ×0.5

215 ×0.9

GENET

73 ×0.8

PPCH

84 ×1.4

HEMAT

46 ×0.9

GENET

Citations per year, relative to Isabelle Gicquel Isabelle Gicquel (= 1×) peers Dorothée Cailley

Countries citing papers authored by Isabelle Gicquel

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Gicquel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Gicquel

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

Pinot, Mathieu, et al.. (2020). Clathrin adaptor AP-1 and Stratum act in parallel pathways to control Notch activation in Drosophila Sensory Organ Precursor Cells. Development. 148(1). 7 indexed citations

Gicquel, Isabelle, et al.. (2018). Stratum recruits Rab8 at Golgi exit sites to regulate the basolateral sorting of Notch and Sanpodo. Development. 145(13). 9 indexed citations

Ratié, Leslie, Frédérique Barloy-Hubler, Isabelle Gicquel, et al.. (2013). Novel genes upregulated when NOTCH signalling is disrupted during hypothalamic development. Neural Development. 8(1). 25–25. 26 indexed citations

Démurger, Florence, Laurent Pasquier, Christèle Dubourg, et al.. (2013). Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis. Molecular Syndromology. 4(6). 267–272. 11 indexed citations

Mercier, Sandra, Véronique David, Leslie Ratié, et al.. (2012). NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos. Disease Models & Mechanisms. 6(2). 537–43. 16 indexed citations

Mercier, Sandra, Christèle Dubourg, Nicolas Garcelon, et al.. (2011). New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases. Journal of Medical Genetics. 48(11). 752–760. 73 indexed citations

Dupé, Valérie, Lucie Rochard, Sandra Mercier, et al.. (2010). NOTCH, a new signaling pathway implicated in holoprosencephaly. Human Molecular Genetics. 20(6). 1122–1131. 37 indexed citations

Bendavid, Claude, Valérie Dupé, Lucie Rochard, et al.. (2010). Holoprosencephaly: An update on cytogenetic abnormalities. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 154C(1). 86–92. 33 indexed citations

Bendavid, Claude, Lucie Rochard, Jonathan Séguin, et al.. (2009). Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci. Human Mutation. 30(8). 1175–1182. 35 indexed citations

10.

Bendavid, Claude, Christèle Dubourg, Laurent Pasquier, et al.. (2007). MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly. Human Mutation. 28(12). 1189–1197. 17 indexed citations

11.

Bendavid, Claude, Laurent Pasquier, Tanguy Watrin, et al.. (2006). Phenotypic variability of a 4q34 → qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. European Journal of Medical Genetics. 50(1). 66–72. 27 indexed citations

12.

Bendavid, Claude, Christèle Dubourg, Isabelle Gicquel, et al.. (2005). Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes. Human Genetics. 119(1-2). 1–8. 44 indexed citations

13.

Meur, Nolwenn Le, Isabelle Gicquel, Martine Le Cunff, et al.. (2004). Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption. Genomics. 83(5). 772–789. 23 indexed citations

14.

Derrien, C., E. Sonnet, Isabelle Gicquel, et al.. (2001). Non-hyperfunctioning nodules from multinodular goiters: A minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsα subunit genes. Journal of Endocrinological Investigation. 24(5). 321–325. 1 indexed citations

15.

Gicquel, Isabelle, et al.. (2000). The HFE Gene Undergoes Alternate Splicing Processes. Blood Cells Molecules and Diseases. 26(2). 155–162. 13 indexed citations

16.

Chauvel, Bruno, Patricia Fergelot, Laurent Pichon, et al.. (1995). A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-A. Immunogenetics. 41(6). 380–382. 8 indexed citations

17.

Chauvel, Bruno, et al.. (1994). Localization of Seven New Genes Around the HLA-A Locus. Advances in experimental medicine and biology. 356. 319–330.

18.

Chauvel, Bruno, et al.. (1993). Localization of seven new genes around the HLA-A locus. Human Molecular Genetics. 2(1). 55–60. 38 indexed citations

19.

Chorney, Michael J., et al.. (1991). A new polymorphic porbe close to HLA-A. Nucleic Acids Research. 19(18). 5100–5100. 11 indexed citations

20.

David, Véronique, Pascale Paul, M. Simon, et al.. (1986). DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family. Human Genetics. 74(2). 113–120. 20 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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