Brigitte Nédelec

2.4k total citations
15 papers, 459 citations indexed

About

Brigitte Nédelec is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Brigitte Nédelec has authored 15 papers receiving a total of 459 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Ophthalmology and 4 papers in Genetics. Recurrent topics in Brigitte Nédelec's work include Inflammasome and immune disorders (3 papers), Glaucoma and retinal disorders (3 papers) and Retinal Development and Disorders (3 papers). Brigitte Nédelec is often cited by papers focused on Inflammasome and immune disorders (3 papers), Glaucoma and retinal disorders (3 papers) and Retinal Development and Disorders (3 papers). Brigitte Nédelec collaborates with scholars based in France, United States and Italy. Brigitte Nédelec's co-authors include Marc Delpech, Sophie Valleix, Gilles Grateau, Tamara Sarkisian, Cécile Cazeneuve, Catherine Dodé, Philippe Reinert, Michel Goossens, Christophe Pécheux and M Dervichian and has published in prestigious journals such as Blood, The American Journal of Human Genetics and European Journal of Biochemistry.

In The Last Decade

Brigitte Nédelec

15 papers receiving 447 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brigitte Nédelec France	10	345	144	83	64	61	15	459
Fathiya Al-Murshedi Oman	10	221 0.6×	266 1.8×	99 1.2×	52 0.8×	29 0.5×	20	534
David F. Carney United States	10	183 0.5×	349 2.4×	17 0.2×	40 0.6×	33 0.5×	13	530
Virginia Miraldi Utz United States	12	194 0.6×	20 0.1×	66 0.8×	81 1.3×	28 0.5×	33	405
Emily I. Schindler United States	9	179 0.5×	58 0.4×	26 0.3×	46 0.7×	21 0.3×	12	311
Sara Ekvall Sweden	11	238 0.7×	78 0.5×	54 0.7×	7 0.1×	16 0.3×	14	313
Jeannette Ossewaarde‐van Norel Netherlands	13	110 0.3×	16 0.1×	155 1.9×	40 0.6×	13 0.2×	32	476
Carsten Faber Denmark	15	115 0.3×	241 1.7×	15 0.2×	175 2.7×	19 0.3×	44	627
Anja Williams United Kingdom	7	85 0.2×	292 2.0×	30 0.4×	80 1.3×	48 0.8×	13	454
Hadia Hijazi Saudi Arabia	11	333 1.0×	20 0.1×	226 2.7×	59 0.9×	38 0.6×	15	579
Emmanuel Barreau France	13	205 0.6×	17 0.1×	53 0.6×	135 2.1×	9 0.1×	47	573

Countries citing papers authored by Brigitte Nédelec

Since Specialization

Citations

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

Fields of papers citing papers by Brigitte Nédelec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brigitte Nédelec

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

All Works

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15 of 15 papers shown

Nédelec, Brigitte, et al.. (2021). Congenital Microcoria: Clinical Features and Molecular Genetics. Genes. 12(5). 624–624. 7 indexed citations

Nédelec, Brigitte, et al.. (2019). Genetic architecture of retinoic-acid signaling-associated ocular developmental defects. Human Genetics. 138(8-9). 937–955. 11 indexed citations

Fares‐Taie, Lucas, Brigitte Nédelec, S. Gerber, et al.. (2018). Is the modification of the 13q32.1 regulatory landscape the cause of congenital microcoria?. Acta Ophthalmologica. 96(S261). 39–39. 1 indexed citations

Garnier, Cyrille, Fatma Briki, Brigitte Nédelec, et al.. (2017). VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variants. Blood. 130(25). 2799–2807. 13 indexed citations

Rothschild, Pierre-Raphaël, et al.. (2015). Spectral-Domain Optical Coherence Tomography in Wagner Syndrome: Characterization of Vitreoretinal Interface and Foveal Changes. American Journal of Ophthalmology. 160(5). 1065–1072.e1. 7 indexed citations

Rothschild, Pierre-Raphaël, et al.. (2013). A family with Wagner syndrome with uveitis and a new versican mutation.. PubMed. 19. 2040–9. 17 indexed citations

Brézin, Antoine P., et al.. (2011). A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features.. PubMed. 17. 1669–78. 21 indexed citations

Zanni, Ginevra, Enrico Bertini, Cecelia Bellcross, et al.. (2008). X‐linked congenital ataxia: A new locus maps to Xq25‐q27.1. American Journal of Medical Genetics Part A. 146A(5). 593–600. 9 indexed citations

Valleix, Sophie, Florence Niel, Brigitte Nédelec, et al.. (2006). Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans. The American Journal of Human Genetics. 79(2). 358–364. 74 indexed citations

10.

Valleix, Sophie, Brigitte Nédelec, Florence Rigaudière, et al.. (2005). H244R VSX1 Is Associated with Selective Cone ON Bipolar Cell Dysfunction and Macular Degeneration in a PPCD Family. Investigative Ophthalmology & Visual Science. 47(1). 48–48. 32 indexed citations

11.

Antoine, B, et al.. (2004). Upregulation of rat P23 (a member of the YjgF protein family) by fasting, glucose diet and fatty acid feeding. Cellular and Molecular Life Sciences. 61(22). 2886–2892. 7 indexed citations

12.

Nédelec, Brigitte, et al.. (2001). INTERLEUKIN 1 GENE CLUSTER POLYMORPHISMS IN MULTIPLEX FAMILIES WITH SPONDYLARTHROPATHIES. Cytokine. 13(2). 98–103. 28 indexed citations

13.

Cazeneuve, Cécile, Tamara Sarkisian, Christophe Pécheux, et al.. (1999). MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications. The American Journal of Human Genetics. 65(1). 88–97. 203 indexed citations

14.

Dupont, Madeleine, Nizar Smaoui, Brigitte Nédelec, et al.. (1997). Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees.. Journal of Medical Genetics. 34(5). 375–381. 3 indexed citations

15.

Cuisset, Laurence, et al.. (1993). Characterization, purification and cDNA cloning of a rat perchloric‐acid‐soluble 23‐kDa protein present only in liver and kidney. European Journal of Biochemistry. 212(3). 665–673. 26 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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