Nicole Créau

1.1k total citations
25 papers, 801 citations indexed

About

Nicole Créau is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Nicole Créau has authored 25 papers receiving a total of 801 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 12 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Nicole Créau's work include Down syndrome and intellectual disability research (12 papers), Congenital heart defects research (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Nicole Créau is often cited by papers focused on Down syndrome and intellectual disability research (12 papers), Congenital heart defects research (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Nicole Créau collaborates with scholars based in France, United States and Switzerland. Nicole Créau's co-authors include Jean Maurice Delabar, Jean‐Maurice Delabar, Marie‐Claude Potier, Yann Hérault, Isabelle Rivals, Luce Dauphinot, M Prieur, Emilie Ait‐Yahya, Henri Bléhaut and L. Personnaz and has published in prestigious journals such as PLoS ONE, The Journal of Comparative Neurology and Scientific Reports.

In The Last Decade

Nicole Créau

24 papers receiving 777 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicole Créau France 16 397 370 335 66 61 25 801
Andrew C. Warren United States 14 397 1.0× 217 0.6× 472 1.4× 223 3.4× 39 0.6× 22 963
James Nguyen United States 7 151 0.4× 207 0.6× 205 0.6× 28 0.4× 114 1.9× 15 496
Xingyu Zhou China 17 243 0.6× 159 0.4× 78 0.2× 73 1.1× 19 0.3× 44 614
Renata Pellegrino Brazil 14 191 0.5× 57 0.2× 195 0.6× 52 0.8× 124 2.0× 38 650
Tatiana Fila Italy 9 209 0.5× 265 0.7× 187 0.6× 47 0.7× 27 0.4× 9 482
Marcella Ma United Kingdom 15 505 1.3× 84 0.2× 200 0.6× 72 1.1× 9 0.1× 22 895
Guida Landouré Mali 13 304 0.8× 68 0.2× 153 0.5× 23 0.3× 21 0.3× 54 715
Debra Rimmington United Kingdom 15 453 1.1× 43 0.1× 214 0.6× 47 0.7× 31 0.5× 18 1.0k
Nora E. Renthal United States 9 251 0.6× 174 0.5× 74 0.2× 63 1.0× 18 0.3× 16 876
S D Detera-Wadleigh United States 12 289 0.7× 38 0.1× 250 0.7× 27 0.4× 21 0.3× 19 777

Countries citing papers authored by Nicole Créau

Since Specialization
Citations

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

Fields of papers citing papers by Nicole Créau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicole Créau

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

All Works

20 of 20 papers shown
1.
Souchet, Benoît, Arnaud Duchon, Yuchen Gu, et al.. (2019). Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models. Scientific Reports. 9(1). 3914–3914. 38 indexed citations
2.
Créau, Nicole, et al.. (2016). Specific age-related molecular alterations in the cerebellum of Down syndrome mouse models. Brain Research. 1646. 342–353. 10 indexed citations
3.
Souchet, Benoît, Fayçal Guedj, Arnaud Duchon, et al.. (2015). Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models. Frontiers in Behavioral Neuroscience. 9. 267–267. 56 indexed citations
4.
Souchet, Benoît, Fayçal Guedj, Ignasi Sahún, et al.. (2014). Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage. Neurobiology of Disease. 69. 65–75. 91 indexed citations
5.
Mouton‐Liger, François, Ignasi Sahún, Thibault Collin, et al.. (2013). Developmental molecular and functional cerebellar alterations induced by PCP4/PEP19 overexpression: Implications for Down syndrome. Neurobiology of Disease. 63. 92–106. 16 indexed citations
6.
Rivals, Isabelle, Emilie Ait‐Yahya, Luce Dauphinot, et al.. (2012). Molecular Signatures of Cardiac Defects in Down Syndrome Lymphoblastoid Cell Lines Suggest Altered Ciliome and Hedgehog Pathways. PLoS ONE. 7(8). e41616–e41616. 22 indexed citations
7.
Ait‐Yahya, Emilie, Julie Aubert, Luce Dauphinot, et al.. (2007). Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes. The American Journal of Human Genetics. 81(3). 475–491. 210 indexed citations
8.
Delabar, Jean Maurice, et al.. (2006). Developmental Defects in Trisomy 21 and Mouse Models. 1. 121–140. 2 indexed citations
9.
Thomas, Sophie, et al.. (2003). PCP4 is highly expressed in ectoderm and particularly in neuroectoderm derivatives during mouse embryogenesis. Gene Expression Patterns. 3(1). 93–97. 13 indexed citations
10.
Thomas, Sophie, et al.. (2003). Chromosome 21 KIR channels in brain development. Journal of neural transmission. Supplementum. 105–115. 7 indexed citations
11.
Gosset, Philippe, et al.. (2000). Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15). Mechanisms of Development. 95(1-2). 313–316. 20 indexed citations
12.
Gosset, Philippe, Ghania Ait‐Ghezala, P.-M. Sinet, & Nicole Créau. (1999). Isolation and analysis of chromosome 21 genes potentially involved in Down Syndrome. PubMed. 57. 197–209. 5 indexed citations
13.
Gosset, Philippe, Catherine Vayssettes, Tiziana Vitali, et al.. (1998). Construction of a 2.5-Mb Integrated Physical and Gene Map of Distal 21q22.3. Genomics. 49(1). 1–13. 16 indexed citations
14.
Potier, Marie‐Claude, et al.. (1998). Conservation of pericentromeric duplications of a 200-kb part of the human 21q22.1 region in primates. Cytogenetic and Genome Research. 83(3-4). 262–265. 13 indexed citations
15.
Dahmane, Nadia, Ghania Ait‐Ghezala, Philippe Gosset, et al.. (1998). Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome. Genomics. 48(1). 12–23. 36 indexed citations
16.
Benelli, Chantal, Ghania Ait‐Ghezala, Mohamed Amessou, et al.. (1997). Mutations in PDX1, the Human Lipoyl-Containing Component X of the Pyruvate Dehydrogenase–Complex Gene on Chromosome 11p1, in Congenital Lactic Acidosis. The American Journal of Human Genetics. 61(6). 1318–1326. 39 indexed citations
17.
Gosset, Philippe, Ghania Ait‐Ghezala, Bernhard Korn, et al.. (1997). A New Inward Rectifier Potassium Channel Gene (KCNJ15) Localized on Chromosome 21 in the Down Syndrome Chromosome Region 1 (DCR1). Genomics. 44(2). 237–241. 46 indexed citations
18.
Gosset, Philippe, Didier Theophile, Christine Van Broeckhoven, et al.. (1995). A High-resolution map of 1.6 Mb in the Down syndrome region: a new map between D21S55 and ETS2. Mammalian Genome. 6(2). 127–130. 12 indexed citations
19.
Delabar, Jean Maurice, Nicole Créau, Otto Ritter, et al.. (1993). Report of the fourth international workshop on human chromosome 21. Genomics. 18(3). 735–745. 30 indexed citations
20.
Pillot, Jean‐Paul, et al.. (1974). An immunochemical study of an immunofluorescent serum factor present in normal subjects and active against T. pallidum.. 125(4). 1 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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