Nicole Bigi

552 total citations
10 papers, 92 citations indexed

About

Nicole Bigi is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Surgery. According to data from OpenAlex, Nicole Bigi has authored 10 papers receiving a total of 92 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pediatrics, Perinatology and Child Health, 3 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Nicole Bigi's work include Prenatal Screening and Diagnostics (4 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Nicole Bigi is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Nicole Bigi collaborates with scholars based in France. Nicole Bigi's co-authors include Pierre Sarda, Patricia Blanchet, Christine Coubes, Jacques Puechberty, Geneviève Lefort, Marie‐Dominique Piercecchi‐Marti, M. Gonzalés, Caroline Rouleau, C. Fredouille and J. F. Pellissier and has published in prestigious journals such as Journal of Hepatology, Journal of Neuro-Oncology and Archives of Disease in Childhood Fetal & Neonatal.

In The Last Decade

Nicole Bigi

9 papers receiving 89 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 Bigi France 6 43 39 32 20 15 10 92
Joanna Lazier Canada 8 55 1.3× 46 1.2× 67 2.1× 12 0.6× 10 0.7× 19 126
Katharina Löhner Netherlands 4 28 0.7× 59 1.5× 87 2.7× 11 0.6× 19 1.3× 5 137
Erica Schindewolf United States 7 28 0.7× 63 1.6× 41 1.3× 40 2.0× 26 1.7× 24 121
Joseph W. Ray United States 8 22 0.5× 52 1.3× 56 1.8× 20 1.0× 16 1.1× 16 116
Evelin Mihailov Estonia 7 21 0.5× 37 0.9× 30 0.9× 9 0.5× 4 0.3× 10 114
Aurélie Coussement France 7 38 0.9× 40 1.0× 67 2.1× 9 0.5× 26 1.7× 16 141
Sara Caylor United States 4 34 0.8× 44 1.1× 109 3.4× 18 0.9× 22 1.5× 4 139
V. Ickowicz France 6 66 1.5× 42 1.1× 34 1.1× 17 0.8× 17 1.1× 9 138
Myrthe van den Born Netherlands 7 30 0.7× 29 0.7× 38 1.2× 62 3.1× 16 1.1× 12 160
Hallie Coltin Canada 7 41 1.0× 18 0.5× 13 0.4× 13 0.7× 13 0.9× 14 89

Countries citing papers authored by Nicole Bigi

Since Specialization
Citations

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

Fields of papers citing papers by Nicole Bigi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicole Bigi

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

All Works

10 of 10 papers shown
1.
Gâtinois, Vincent, Nicole Bigi, E. Mousty, et al.. (2019). Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations. Molecular Genetics & Genomic Medicine. 7(11). e00895–e00895.
2.
Laurichesse, Hélène, Nicole Bigi, Émeline Maisonneuve, et al.. (2018). The Pubic Diastasis Measurement, a Key Element for the Diagnosis, Management, and Prognosis of the Bladder Exstrophy. Fetal Diagnosis and Therapy. 45(6). 435–440. 5 indexed citations
3.
Lamouroux, Audrey, E. Mousty, O. Prodhomme, et al.. (2015). La dysgénésie thymique : marqueur de microdélétion 22q11.2 dans le bilan d’un hydramnios. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 45(4). 388–396. 7 indexed citations
4.
Bergougnoux, Anne, Isabelle Rivals, Alessandro Liquori, et al.. (2014). A balance between activating and repressive histone modifications regulatescystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo. Epigenetics. 9(7). 1007–1017. 12 indexed citations
5.
Rouleau, Caroline, Nicole Bigi, A. Couture, et al.. (2011). Prevalence and timing of pregnancy termination for brain malformations: Table 1. Archives of Disease in Childhood Fetal & Neonatal. 96(5). F360–F364. 11 indexed citations
6.
Maran-Gonzalez, Aurélie, et al.. (2010). Posterior fossa solitary fibrous tumour: report of a fetal case and review of the literature. Journal of Neuro-Oncology. 101(2). 297–300. 2 indexed citations
7.
Ramos, José, Agnès Robert, Daniel Lafitte, et al.. (2009). Identification of proteomic changes during human liver development by 2D-DIGE and mass spectrometry. Journal of Hepatology. 51(1). 114–126. 9 indexed citations
8.
Schneider, Anouck, Anne‐Marie Chaze, Nicole Bigi, et al.. (2009). Epiphyseal punctate calcifications (stippling) in complete trisomy 9. Prenatal Diagnosis. 29(11). 1085–1088. 2 indexed citations
9.
Bigi, Nicole, Christine Coubes, Jacques Puechberty, et al.. (2008). Prader‐Willi syndrome: is there a recognizable fetal phenotype?. Prenatal Diagnosis. 28(9). 796–799. 29 indexed citations
10.
Fredouille, C., Marie‐Dominique Piercecchi‐Marti, Agnès Liprandi, et al.. (2002). Linear Insertion of Atrioventricular Valves without Septal Defect: A New Anatomical Landmark for Down’s Syndrome?. Fetal Diagnosis and Therapy. 17(3). 188–192. 15 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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