P. Divry

2.7k total citations
97 papers, 2.0k citations indexed

About

P. Divry is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, P. Divry has authored 97 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Clinical Biochemistry, 56 papers in Molecular Biology and 21 papers in Physiology. Recurrent topics in P. Divry's work include Metabolism and Genetic Disorders (70 papers), Mitochondrial Function and Pathology (23 papers) and Diet and metabolism studies (20 papers). P. Divry is often cited by papers focused on Metabolism and Genetic Disorders (70 papers), Mitochondrial Function and Pathology (23 papers) and Diet and metabolism studies (20 papers). P. Divry collaborates with scholars based in France, United States and Netherlands. P. Divry's co-authors include C. Vianey‐Liaud, Christine Vianey‐Saban, M. Mathieu, N. Gregersen, J Cotte, K. Michael Gibson, M. T. Zabot, C. Charpentier, Friedrich K. Trefz and Marie-Odile Rolland and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and Biochemical Journal.

In The Last Decade

P. Divry

93 papers receiving 1.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
P. Divry 1.3k 1.2k 337 239 197 97 2.0k
C. Charpentier 1.2k 0.9× 1.0k 0.9× 285 0.8× 254 1.1× 271 1.4× 85 2.3k
W. G. Sherwood 751 0.6× 952 0.8× 216 0.6× 112 0.5× 353 1.8× 35 1.4k
Yoshiyuki Okano 905 0.7× 1.3k 1.1× 391 1.2× 381 1.6× 303 1.5× 62 1.7k
E. Christensen 1.6k 1.2× 1.6k 1.3× 224 0.7× 257 1.1× 324 1.6× 70 2.2k
Jean‐Marc Nuoffer 934 0.7× 518 0.4× 274 0.8× 171 0.7× 167 0.8× 112 2.0k
Peter Schadewaldt 572 0.4× 663 0.6× 424 1.3× 161 0.7× 223 1.1× 70 1.4k
Elisabetta Pasquini 589 0.5× 698 0.6× 232 0.7× 346 1.4× 121 0.6× 59 1.4k
N. Gregersen 2.0k 1.5× 1.5k 1.3× 496 1.5× 233 1.0× 172 0.9× 104 3.1k
Haruo Shintaku 777 0.6× 693 0.6× 698 2.1× 374 1.6× 132 0.7× 116 2.1k
Georges Berghe 1.4k 1.1× 358 0.3× 290 0.9× 205 0.9× 112 0.6× 46 2.1k

Countries citing papers authored by P. Divry

Since Specialization
Citations

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

Fields of papers citing papers by P. Divry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Divry

This figure shows the co-authorship network connecting the top 25 collaborators of P. Divry. A scholar is included among the top collaborators of P. Divry 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 P. Divry. P. Divry 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.
Lamhonwah, Anne‐Marie, S. E. Olpin, R. J. Pollitt, et al.. (2002). NovelOCTN2mutations: No genotype–phenotype correlations: Early carnitine therapy prevents cardiomyopathy. American Journal of Medical Genetics. 111(3). 271–284. 93 indexed citations
2.
Wolf, Barry, Kevin P. Jensen, Mübeccel Demirkol, et al.. (2002). Seventeen novel mutations that cause profound biotinidase deficiency. Molecular Genetics and Metabolism. 77(1-2). 108–111. 31 indexed citations
3.
Bataillard, Marc, et al.. (2000). An Adult Form of <i>L</i>-2-Hydroxyglutaric Aciduria Revealed by Tremor. European Neurology. 43(2). 119–120. 9 indexed citations
4.
Hinson, Debra D., Skaidrite K. Krisans, Joanne Shaw, et al.. (1999). Identification of a Mutation Cluster in Mevalonate Kinase Deficiency, Including a New Mutation in a Patient of Mennonite Ancestry. The American Journal of Human Genetics. 65(2). 327–335. 35 indexed citations
5.
Cochat, Pierre, Jean‐Michel Gaulier, Paulo César Koch Nogueira, et al.. (1999). Combined liver-kidney transplantation in primary hyperoxaluria type 1. European Journal of Pediatrics. 158(S2). S075–S080. 59 indexed citations
6.
Burlina, Alessandro P., V. Ferrari, P. Divry, et al.. (1999). N-acetylaspartylglutamate in Canavan disease: an adverse effector?. European Journal of Pediatrics. 158(5). 406–409. 32 indexed citations
7.
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
8.
Rolland, M. O., et al.. (1998). Succinyl‐CoA:acetoacetate transferase deficiency. Identification of a new case; prenatal exclusion in three further pregnancies. Journal of Inherited Metabolic Disease. 21(6). 687–688. 7 indexed citations
9.
Divry, P. & H. Ogier de Baulny. (1996). Erreurs innées du métabolisme du GABA. Archives de Pédiatrie. 3. S169–S171. 3 indexed citations
10.
Vallée, Louis, Monique Fontaine, Guy Ricart, et al.. (1994). Stroke, hemiparesis and deficient mitochondrial β-oxidation. European Journal of Pediatrics. 153(8). 598–603. 20 indexed citations
11.
Guffon, Nathalie, Christine Vianey‐Saban, Marianne Till, et al.. (1993). [Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings].. PubMed. 48(5). 365–71. 1 indexed citations
12.
Costeff, Hanan, et al.. (1993). 3‐Methylglutaconic aciduria in “optic atrophy plus”. Annals of Neurology. 33(1). 103–104. 29 indexed citations
13.
Mancini, Josette, Nicole Philip, B. Chabrol, et al.. (1993). Mevalonic aciduria in 3 siblings: A new recognizable metabolic encephalopathy. Pediatric Neurology. 9(3). 243–246. 19 indexed citations
14.
15.
Stanley, Charles A., Paul M. Coates, C. Vianey‐Liaud, et al.. (1991). Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake. Annals of Neurology. 30(5). 709–716. 163 indexed citations
16.
Échenne, Bernard, P. Divry, & C. Vianey‐Liaud. (1989). Spongy Degeneration of the Neuraxis (Canavan-Van Bogaert Disease) and N-Acetylaspartic Aciduria. Neuropediatrics. 20(2). 79–81. 17 indexed citations
17.
Divry, P., C. Vianey‐Liaud, & J Cotte. (1987). Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period. Journal of Mass Spectrometry. 14(11). 663–668. 23 indexed citations
18.
Divry, P., et al.. (1979). Acidurie glutarique. Une nouvelle observation.. 36(5). 6 indexed citations
19.
Divry, P.. (1956). De la notion d'amyloïdose cérébrale dans les processus séniles.. Cellular and Molecular Life Sciences. 1 indexed citations
20.
Divry, P.. (1955). De la nature des formations argentophiles des plexus chorïdes.. 55(3). 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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