C Largillière

789 total citations
30 papers, 608 citations indexed

About

C Largillière is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C Largillière has authored 30 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Clinical Biochemistry, 17 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C Largillière's work include Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (9 papers) and Peroxisome Proliferator-Activated Receptors (6 papers). C Largillière is often cited by papers focused on Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (9 papers) and Peroxisome Proliferator-Activated Receptors (6 papers). C Largillière collaborates with scholars based in France, Netherlands and United Kingdom. C Largillière's co-authors include Serge B. Melançon, J. P. Farriaux, Christine Vianey‐Saban, C. Bertrand, Jean‐Louis Dhondt, Monique Mathieu, Pierre Degand, A Checoury, D Houssin and D Alagille and has published in prestigious journals such as The Lancet, Analytical Biochemistry and Clinical Chemistry.

In The Last Decade

C Largillière

27 papers receiving 581 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C Largillière France 13 398 341 117 79 60 30 608
Milena Sochor United Kingdom 15 149 0.4× 322 0.9× 163 1.4× 99 1.3× 63 1.1× 50 722
Tomoyuki Katsuzaki Japan 10 409 1.0× 129 0.4× 135 1.2× 12 0.2× 32 0.5× 13 611
R. Reitano Italy 14 559 1.4× 202 0.6× 200 1.7× 12 0.2× 24 0.4× 17 834
M Luciak Poland 14 129 0.3× 89 0.3× 141 1.2× 21 0.3× 39 0.7× 48 562
Genoveva Durán-Reyes Mexico 11 45 0.1× 157 0.5× 102 0.9× 48 0.6× 20 0.3× 17 461
Z. Zaman Belgium 13 43 0.1× 239 0.7× 116 1.0× 107 1.4× 21 0.3× 22 588
Norman J. Hochella United States 10 94 0.2× 190 0.6× 189 1.6× 29 0.4× 26 0.4× 12 498
Nadia Bortolotti Italy 11 103 0.3× 144 0.4× 185 1.6× 11 0.1× 18 0.3× 17 706
A. Montfoort Netherlands 11 64 0.2× 252 0.7× 81 0.7× 24 0.3× 144 2.4× 18 515
Inger Holmberg Sweden 19 42 0.1× 152 0.4× 168 1.4× 80 1.0× 16 0.3× 27 808

Countries citing papers authored by C Largillière

Since Specialization
Citations

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

Fields of papers citing papers by C Largillière

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Largillière

This figure shows the co-authorship network connecting the top 25 collaborators of C Largillière. A scholar is included among the top collaborators of C Largillière 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 C Largillière. C Largillière 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.
Fontaine, Monique, Gilbert Briand, C Largillière, et al.. (1998). Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiency. Clinica Chimica Acta. 273(2). 161–170. 20 indexed citations
2.
Dobbelaere, D., et al.. (1998). Neurological outcome of a patient with Gaucher disease type III treated by enzymatic replacement therapy. Journal of Inherited Metabolic Disease. 21(1). 74–76. 9 indexed citations
3.
Dhondt, Jean‐Louis, C Largillière, L. Moreno, & J. P. Farriaux. (1995). Physical growth in patients with phenylketonuria. Journal of Inherited Metabolic Disease. 18(2). 135–137. 30 indexed citations
4.
Largillière, C. (1995). Psychiatric manifestations in girl with ornithine transcarbamylase deficiency. The Lancet. 345(8957). 1113–1113. 9 indexed citations
5.
Manouvrier, Sylvie, Agnès Rötig, Arnold Münnich, et al.. (1995). Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.. Journal of Medical Genetics. 32(8). 654–656. 59 indexed citations
6.
Bertrand, C., et al.. (1993). Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1180(3). 327–329. 98 indexed citations
7.
Brink, H.J. ten, et al.. (1993). Diagnosis of peroxisomal disorders by analysis of phytanic and pristanic acids in stored blood spots collected at neonatal screening. Clinical Chemistry. 39(9). 1904–1906. 10 indexed citations
8.
Feldmann, D, Jean‐Michel Rozet, Anna Pelet, et al.. (1992). Site specific screening for point mutations in ornithine transcarbamylase deficiency.. PubMed. 29(7). 471–5. 9 indexed citations
9.
Largillière, C, et al.. (1991). d‐Glyceric acidaemia: clinical report and biochemical studies in a patient. Journal of Inherited Metabolic Disease. 14(2). 263–264. 5 indexed citations
10.
Turck, Dominique, et al.. (1990). [Auriculotemporal syndrome in an infant. A case report].. PubMed. 47(8). 615–615.
11.
Gottrand, Frédèric, et al.. (1990). [The bronze baby syndrome Apropos of 3 cases].. PubMed. 37(10). 669–71. 1 indexed citations
12.
Largillière, C, D Houssin, Frédèric Gottrand, et al.. (1989). Liver transplantation for ornithine transcarbamylase deficiency in a girl. The Journal of Pediatrics. 115(3). 415–417. 54 indexed citations
13.
Destée, A., et al.. (1989). [Mitochondrial myopathy. Encephalopathy with lactic acidosis and cerebral infarction].. PubMed. 145(1). 37–48. 11 indexed citations
14.
Porchet, Nicole, et al.. (1989). Biochemical contribution to diagnosis and study of a new case of D-glyceric acidemia/aciduria.. Clinical Chemistry. 35(10). 2148–2151. 24 indexed citations
15.
Largillière, C & Serge B. Melançon. (1988). Free malondialdehyde determination in human plasma by high-performance liquid chromatography. Analytical Biochemistry. 170(1). 123–126. 100 indexed citations
16.
Manouvrier‐Hanu, Sylvie, et al.. (1988). [The GAPO syndrome (growth retardation, alopecia, pseudo-anodontia, optic atrophy). A new case report].. PubMed. 36(4). 373–8. 1 indexed citations
17.
Manouvrier‐Hanu, Sylvie, et al.. (1987). The GAPO syndrome. American Journal of Medical Genetics. 26(3). 683–688. 16 indexed citations
18.
Largillière, C, Jean‐Louis Dhondt, & J. P. Farriaux. (1986). Hepatic phenylalanine hydroxylase and dietary tolerance in hyperphenylalaninaemic patients. Journal of Inherited Metabolic Disease. 9(S2). 209–211. 3 indexed citations
19.
Largillière, C, et al.. (1983). [An attempt at classification of the hyperphenylalaninemias. Apropos of 62 patients].. PubMed. 40 Suppl 1. 243–5. 2 indexed citations
20.
Dhondt, Jean‐Louis, et al.. (1981). Diagnosis of variants of hyperphenylalaninemia by determination of pterins in urine. Clinica Chimica Acta. 110(2-3). 205–214. 37 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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