Cécile Ged

3.8k total citations · 1 hit paper
94 papers, 2.7k citations indexed

About

Cécile Ged is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Cécile Ged has authored 94 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 34 papers in Pediatrics, Perinatology and Child Health and 16 papers in Genetics. Recurrent topics in Cécile Ged's work include Porphyrin Metabolism and Disorders (49 papers), Neonatal Health and Biochemistry (32 papers) and Heme Oxygenase-1 and Carbon Monoxide (19 papers). Cécile Ged is often cited by papers focused on Porphyrin Metabolism and Disorders (49 papers), Neonatal Health and Biochemistry (32 papers) and Heme Oxygenase-1 and Carbon Monoxide (19 papers). Cécile Ged collaborates with scholars based in France, United States and Spain. Cécile Ged's co-authors include Hubert de Verneuil, François Moreau‐Gaudry, Alain Taı̈eb, Frédéric Mazurier, Philippe Beaune, Emmanuel Richard, Muriel Cario, Isabelle Lamrissi‐Garcia, Hamid Rezvani and Élodie Richard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Cécile Ged

92 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations

2019 310 citations Isabelle Lamrissi‐Garcia, Veronique Guyonnet‐Dupérat et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cécile Ged France	27	1.8k	593	436	347	341	94	2.7k
James O’Kelly United States	30	1.4k 0.8×	52 0.1×	179 0.4×	381 1.1×	477 1.4×	59	3.0k
Shigeki Tsuchida Japan	30	2.3k 1.3×	58 0.1×	311 0.7×	232 0.7×	631 1.9×	116	3.2k
Anders Åström Sweden	25	1.2k 0.7×	43 0.1×	466 1.1×	391 1.1×	232 0.7×	48	1.9k
Roger Drew Australia	18	1.0k 0.6×	98 0.2×	337 0.8×	320 0.9×	595 1.7×	47	2.1k
David M. Nelson United States	24	2.0k 1.1×	89 0.2×	117 0.3×	309 0.9×	466 1.4×	45	2.9k
S.L. Hsia United States	27	538 0.3×	82 0.1×	253 0.6×	167 0.5×	534 1.6×	104	2.2k
Henk van Lenthe Netherlands	28	1.5k 0.8×	181 0.3×	74 0.2×	147 0.4×	600 1.8×	73	2.3k
Frank K. Jugert Germany	18	467 0.3×	48 0.1×	152 0.3×	172 0.5×	200 0.6×	35	1.4k
Wolfgang Hagmann Germany	23	626 0.4×	119 0.2×	219 0.5×	139 0.4×	637 1.9×	49	2.1k
Patrick M. Navolanic United States	19	2.3k 1.3×	69 0.1×	67 0.2×	207 0.6×	1.0k 3.0×	23	3.5k

Countries citing papers authored by Cécile Ged

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Ged

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Ged

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

Ged, Cécile, Kévin Uguen, Isabelle Gourlaouen, et al.. (2025). Identification of New Key Players for Ferrous Iron Export in the Asymmetric Inner Gate of Human Ferroportin 1. The FASEB Journal. 39(14). e70821–e70821.

Ged, Cécile, Audrey Petit, Aïcha Salhi, et al.. (2024). Severe Perinatal Presentations of Günther’s Disease: Series of 20 Cases and Perspectives. Life. 14(1). 130–130. 1 indexed citations

Blouin, Jean‐Marc, Cécile Ged, Ganeko Bernardo‐Seisdedos, et al.. (2021). Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomy. Molecular Genetics and Metabolism Reports. 27. 100722–100722. 9 indexed citations

Morice‐Picard, Fanny, Hamid Rezvani, Frédéric Austerlitz, et al.. (2019). Xeroderma pigmentosum in South Africa: Evidence for a prevalent founder effect. British Journal of Dermatology. 181(5). 1070–1072. 9 indexed citations

Trompezinski, S., Muriel Cario, Fanny Morice‐Picard, et al.. (2018). Pigmentation abnormalities in nucleotide excision repair disorders: Evidence and hypotheses. Pigment Cell & Melanoma Research. 32(1). 25–40. 5 indexed citations

Blouin, Jean‐Marc, Ganeko Bernardo‐Seisdedos, Cécile Ged, et al.. (2017). Missense UROS mutations causing congenital erythropoietic porphyria reduce UROS homeostasis that can be rescued by proteasome inhibition. Human Molecular Genetics. 26(8). 1565–1576. 19 indexed citations

Jouanolle, Anne‐Marie, et al.. (2012). Recommandations pour la (bonne) pratique du diagnostic moléculaire de l'hémochromatose liée au gène HFE. Synthesed'une enquete realisee aupres du reseau national des laboratoires pratiquant le disgnostic de maladies rares du metabolisme du fer.. Annales de biologie clinique. 70(3). 2 indexed citations

Richard, Élodie, Magalie Lalanne, Isabelle Lamrissi‐Garcia, et al.. (2010). Modeling of congenital erythropoietic porphyria by RNA interference: a new tool for preclinical gene therapy evaluation. The Journal of Gene Medicine. 12(8). 637–646. 6 indexed citations

Soufir, Nadem, Cécile Ged, Agnès Bourillon, et al.. (2010). A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa. Journal of Investigative Dermatology. 130(6). 1537–1542. 69 indexed citations

10.

Rezvani, Hamid, Walid Mahfouf, Nsrein Ali, et al.. (2009). Hypoxia-inducible factor-1α regulates the expression of nucleotide excision repair proteins in keratinocytes. Nucleic Acids Research. 38(3). 797–809. 51 indexed citations

11.

Richard, Élodie, François Moreau‐Gaudry, Magalie Lalanne, et al.. (2008). Effective Gene Therapy of Mice with Congenital Erythropoietic Porphyria Is Facilitated by a Survival Advantage of Corrected Erythroid Cells. The American Journal of Human Genetics. 82(1). 113–124. 37 indexed citations

12.

Rezvani, Hamid, Frédéric Mazurier, Muriel Cario, et al.. (2006). Protective Effects of Catalase Overexpression on UVB-induced Apoptosis in Normal Human Keratinocytes. Journal of Biological Chemistry. 281(26). 17999–18007. 101 indexed citations

13.

Ged, Cécile, Manuel Méndez, Magalie Lalanne, et al.. (2005). A knock-in mouse model of congenital erythropoietic porphyria. Genomics. 87(1). 84–92. 21 indexed citations

14.

Ged, Cécile, et al.. (2000). Retroviral Coexpression of IFN-α and IFN-γ Genes and Inhibitory Effects in Chronic Myeloid Leukemia Cells. Journal of Interferon & Cytokine Research. 20(6). 577–587. 2 indexed citations

15.

Mazurier, Frédéric, François Moreau‐Gaudry, Véronique Maguer‐Satta, et al.. (1998). Rapid analysis and efficient selection of human transduced primitive hematopoietic cells using the humanized S65T green fluorescent protein. Gene Therapy. 5(4). 556–562. 15 indexed citations

16.

Bensidhoum, Morad, Noboru Takamura, Hiroyuki Namba, et al.. (1996). A novel point mutation in congenital erythropoietic porphyria in two members of Japanese family. Human Genetics. 97(5). 557–560. 8 indexed citations

17.

Thomas, Caroline, Cécile Ged, Y Nordmann, et al.. (1996). Correction of congenital erythropoietic porphyria by bone marrow transplantation. The Journal of Pediatrics. 129(3). 453–456. 44 indexed citations

18.

Ged, Cécile, et al.. (1995). Identification of Two NewMutations in CongenitalErythropoietic Porphyria. European Journal of Human Genetics. 3(2). 102–107. 19 indexed citations

19.

Bensidhoum, Morad, Cécile Ged, Christophe Poirier, Jean‐Louis Guénet, & Hubert de Verneuil. (1994). The cDNA sequence of mouse uroporphyrinogen III synthase and assignment to mouse Chromosome 7. Mammalian Genome. 5(11). 728–730. 7 indexed citations

20.

Ged, Cécile & Philippe Beaune. (1992). Partial sequence and polymerase chain reaction-mediated analysis of expression of the human CYP2C18 gene. Pharmacogenetics. 2(3). 109–115. 5 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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