F Poggi

852 total citations
22 papers, 635 citations indexed

About

F Poggi is a scholar working on Clinical Biochemistry, Molecular Biology and Surgery. According to data from OpenAlex, F Poggi has authored 22 papers receiving a total of 635 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Clinical Biochemistry, 13 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in F Poggi's work include Metabolism and Genetic Disorders (17 papers), Peroxisome Proliferator-Activated Receptors (6 papers) and Mitochondrial Function and Pathology (4 papers). F Poggi is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Peroxisome Proliferator-Activated Receptors (6 papers) and Mitochondrial Function and Pathology (4 papers). F Poggi collaborates with scholars based in France, Belgium and Netherlands. F Poggi's co-authors include Daniel Rabier, Jean Marie Saudubray, Jean‐Paul Bonnefont, Jean‐Marie Saudubray, Ronald J. A. Wanders, M. Brivet, Philippe Hubert, Lodewijk IJlst, A Munnich and P. Kamoun and has published in prestigious journals such as American Journal of Clinical Nutrition, Hepatology and PEDIATRICS.

In The Last Decade

F Poggi

22 papers receiving 609 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F Poggi France	14	478	403	94	87	80	22	635
Gaetano Sabetta Italy	10	402 0.8×	340 0.8×	125 1.3×	174 2.0×	78 1.0×	11	631
Udo Wendel Germany	12	229 0.5×	245 0.6×	68 0.7×	55 0.6×	233 2.9×	18	525
José Antonio Arranz Spain	13	206 0.4×	208 0.5×	38 0.4×	53 0.6×	44 0.6×	29	578
Mary Anne Preece United Kingdom	11	166 0.3×	162 0.4×	75 0.8×	39 0.4×	66 0.8×	20	377
Jean-Marie Saudubray France	14	397 0.8×	383 1.0×	133 1.4×	115 1.3×	43 0.5×	15	952
Sheldon Orloff United States	13	126 0.3×	171 0.4×	70 0.7×	145 1.7×	35 0.4×	26	561
R. C. A. Sengers Netherlands	13	101 0.2×	209 0.5×	102 1.1×	59 0.7×	64 0.8×	32	424
Tomozumi Takatani Japan	13	89 0.2×	238 0.6×	68 0.7×	60 0.7×	47 0.6×	48	525
A. Hunter Canada	7	92 0.2×	122 0.3×	78 0.8×	29 0.3×	24 0.3×	12	342
Mark M. Danney United States	7	93 0.2×	137 0.3×	96 1.0×	35 0.4×	20 0.3×	8	376

Countries citing papers authored by F Poggi

Since Specialization

Citations

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

Fields of papers citing papers by F Poggi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F Poggi

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

Lonlay-Debeney, Pascale de, Delphine Martin, F Poggi, et al.. (1998). Hypoglycémie hyperinsulinémique persistante du nouveau-né et du nourrisson. Archives de Pédiatrie. 5(12). 1347–1352. 3 indexed citations

Marsac, C., Chantal Benelli, Isabelle Desguerre, et al.. (1997). Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1α deficiency. Human Genetics. 99(6). 785–792. 41 indexed citations

Jouvet, Philippe, F Poggi, Daniel Rabier, et al.. (1997). Continuous venovenous haemodiafiltration in the acute phase of neonatal maple syrup urine disease. Journal of Inherited Metabolic Disease. 20(4). 463–472. 35 indexed citations

Geoffroy, Valérie, Chantal Benelli, F Poggi, et al.. (1996). Defect in the X-Lipoyl-Containing Component of the Pyruvate Dehydrogenase Complex in a Patient With a Neonatal Lactic Acidemia. PEDIATRICS. 97(2). 267–272. 21 indexed citations

Meer, S. B. van der, F Poggi, Marco Spada, et al.. (1996). Clinical outcome and long-term management of 17 patients with propionic acidaemia. European Journal of Pediatrics. 155(3). 205–210. 60 indexed citations

Brivet, M., Abdelhamid Slama, David S. Millington, et al.. (1996). Retrospective diagnosis of carnitine‐acylcarnitine translocase deficiency by acylcarnitine analysis in the proband Guthrie card and enzymatic studies in the parents. Journal of Inherited Metabolic Disease. 19(2). 181–184. 22 indexed citations

Roels, Frank, Marc Espeel, Hannah Mandel, et al.. (1995). Cell and tissue heterogeneity in peroxisomal patients. Ghent University Academic Bibliography (Ghent University). 11 indexed citations

Sempoux, Christine, F Poggi, Françis Brunelle, et al.. (1995). Nesidioblastosis and persistent neonatal hyperinsulinism.. PubMed. 21(6). 402–7. 18 indexed citations

Espeel, Marc, Frank Roels, M. Girós, et al.. (1995). Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.. PubMed. 67(4). 319–27. 18 indexed citations

10.

Laurent, J., Florence Lacaille, Philippe Jouvet, et al.. (1995). Liver transplantation in children with inherited metabolic disorders.. PubMed. 27(2). 1706–7. 4 indexed citations

11.

Espeel, Marc, Hanna Mandel, F Poggi, et al.. (1995). Peroxisome mosaicism in the livers of peroxisomal deficiency patients. Hepatology. 22(2). 497–504. 29 indexed citations

12.

Meırleır, Linda De, Willy Lissens, Chantal Benelli, et al.. (1994). Aberrant Splicing of Exon 6 in the Pyruvate Denydrogenase-Elα mRNA Linked to a Silent Mutation in a Large Family with Leigh's Encephalomyelopathy. Pediatric Research. 36(6). 707–712. 26 indexed citations

13.

Meer, S. B. van der, F Poggi, Marco Spada, et al.. (1994). Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemia. The Journal of Pediatrics. 125(6). 903–908. 96 indexed citations

14.

Mariotti, André, et al.. (1994). Contribution of odd-chain fatty acid oxidation to propionate production in disorders of propionate metabolism. American Journal of Clinical Nutrition. 59(6). 1332–1337. 32 indexed citations

15.

Poggi, F, et al.. (1994). [Protocol of metabolic investigations in hereditary metabolic diseases].. PubMed. 1(7). 667–73. 3 indexed citations

16.

Poggi, F, J. Laurent, Daniel Rabier, et al.. (1994). Liver transplantation: new indications in metabolic disorders?. PubMed. 26(1). 189–90. 4 indexed citations

17.

Poggi, F, Philippe Jouvet, Daniel Rabier, et al.. (1994). Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases.. PubMed. 26(1). 188–188. 13 indexed citations

18.

Espeel, Marc, F Poggi, Frank Roels, & J. M. Saudubray. (1993). Cytoplasmic catalase but correct localization of four peroxisomal enzymes in the liver of a child with several peroxisomal dysfunctions. European Journal of Cell Biology. 60. 74–74. 1 indexed citations

19.

Roels, Frank, Marc Espeel, F Poggi, et al.. (1993). Human liver pathology in peroxisomal diseases: A review including novel data. Biochimie. 75(3-4). 281–292. 39 indexed citations

20.

Wanders, Ronald J. A., Lodewijk IJlst, F Poggi, et al.. (1992). Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation. Biochemical and Biophysical Research Communications. 188(3). 1139–1145. 134 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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