H. Ogier

2.2k total citations
55 papers, 1.4k citations indexed

About

H. Ogier is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, H. Ogier has authored 55 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Clinical Biochemistry, 31 papers in Molecular Biology and 17 papers in Physiology. Recurrent topics in H. Ogier's work include Metabolism and Genetic Disorders (38 papers), Diet and metabolism studies (14 papers) and Folate and B Vitamins Research (11 papers). H. Ogier is often cited by papers focused on Metabolism and Genetic Disorders (38 papers), Diet and metabolism studies (14 papers) and Folate and B Vitamins Research (11 papers). H. Ogier collaborates with scholars based in France, Netherlands and Belgium. H. Ogier's co-authors include C. Charpentier, Bwee Tien Poll‐The, J Scotto, Jean‐Marie Saudubray, Frank Roels, A. W. Schram, Arnold Münnich, Jean Marie Saudubray, Jean‐Paul Bonnefont and R. B. H. Schutgens and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Pediatric Research.

In The Last Decade

H. Ogier

55 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. Ogier France 21 902 892 293 207 146 55 1.4k
K. Narisawa Japan 22 734 0.8× 743 0.8× 110 0.4× 170 0.8× 121 0.8× 68 1.1k
J. M. Saudubray France 18 615 0.7× 717 0.8× 164 0.6× 93 0.4× 100 0.7× 49 1.0k
Uta Lichter‐Konecki United States 23 969 1.1× 774 0.9× 260 0.9× 388 1.9× 121 0.8× 47 1.3k
Elisabetta Pasquini Italy 23 698 0.8× 589 0.7× 232 0.8× 366 1.8× 346 2.4× 59 1.4k
Mübeccel Demirkol Türkiye 20 685 0.8× 632 0.7× 294 1.0× 202 1.0× 155 1.1× 43 1.2k
T. Ohura Japan 15 543 0.6× 495 0.6× 114 0.4× 198 1.0× 145 1.0× 33 959
Esmeralda Martins Portugal 20 495 0.5× 484 0.5× 226 0.8× 219 1.1× 132 0.9× 77 988
W.O. Renier Netherlands 16 324 0.4× 532 0.6× 143 0.5× 164 0.8× 67 0.5× 32 849
Ksenija Fumić Croatia 15 329 0.4× 498 0.6× 248 0.8× 286 1.4× 78 0.5× 62 868
Ubaldo Caruso Italy 15 338 0.4× 349 0.4× 136 0.5× 150 0.7× 108 0.7× 21 662

Countries citing papers authored by H. Ogier

Since Specialization
Citations

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

Fields of papers citing papers by H. Ogier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Ogier

This figure shows the co-authorship network connecting the top 25 collaborators of H. Ogier. A scholar is included among the top collaborators of H. Ogier 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 H. Ogier. H. Ogier 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.
Héron, Bénédicte & H. Ogier. (2010). La maladie de Niemann-Pick type C : diagnostic clinique des formes pédiatriques. Archives de Pédiatrie. 17. S45–S49. 3 indexed citations
2.
Lonlay, Pascale de, Nathalie Séta, M. Besnard, et al.. (2003). Hypotrophie et manifestations digestives des désordres congénitaux de la glycosylation. Archives de Pédiatrie. 10(7). 590–595. 8 indexed citations
3.
Debray, Dominique, et al.. (1999). Évolution favorable sous traitement par NTBC de l'insuffisance hépatique aiguë révélatrice de la tyrosinémie héréditaire de type I. Archives de Pédiatrie. 6(5). 540–544. 5 indexed citations
4.
Garel, Cathérine, et al.. (1998). Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplex. Skeletal Radiology. 27(1). 43–45. 21 indexed citations
5.
Saudubray, Jean‐Marie, F Poggi-Travert, Douglas Martin, et al.. (1996). Management and Long Term Follow-up of Organic Acidemias : Criteria for Therapeutic Decisions. 12(1). 9–18. 1 indexed citations
6.
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
7.
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
8.
Romero, Norma B., C. Marsac, Marion Paturneau-Jouas, et al.. (1993). Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency. Neuromuscular Disorders. 3(1). 31–42. 9 indexed citations
9.
Michaud, Joris, Bernard Lemieux, H. Ogier, & Marie Lambert. (1992). Nutritional vitamin B12 deficiency: Two cases detected by routine newborn urinary screening. European Journal of Pediatrics. 151(3). 218–220. 25 indexed citations
10.
Bonnefont, Jean‐Paul, Norma Spécola, Anne Vassault, et al.. (1990). The fasting test in paediatrics: Application to the diagnosis of pathological hypo- and hyperketotic states. European Journal of Pediatrics. 150(2). 80–85. 109 indexed citations
11.
Ogier, H., Anne Lombès, H.R. Scholte, et al.. (1988). de Toni-Fanconi-Debré syndrome with leigh syndrome revealing severe muscle cytochrome c oxidase deficiency. The Journal of Pediatrics. 112(5). 734–739. 38 indexed citations
12.
Roels, Frank, Marina Pauwels, J Scotto, et al.. (1988). Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: Cytochemical and morphometric data. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 413(4). 275–285. 29 indexed citations
13.
Saudubray, J. M., F.A. Rey, H. Ogier, et al.. (1987). Intellectual and school performances in early-treated classical PKU patients. European Journal of Pediatrics. 146(1). A20–A22. 31 indexed citations
14.
Poll‐The, Bwee Tien, J. M. Saudubray, H. Ogier, et al.. (1987). Infantile Refsum disease: an inherited peroxisomal disorder. European Journal of Pediatrics. 146(5). 477–483. 98 indexed citations
15.
Bonnefont, Jean‐Paul, H. Ogier, G. H. Mitchell, et al.. (1986). [Heterogeneity of carnitine palmitoyltransferase deficiencies. Deficiency of CPT I in the hepatic form and CPT II in the muscular form].. PubMed. 42 Suppl 1. 613–7. 2 indexed citations
16.
Ogier, H., et al.. (1984). [Type II oculo-cutaneous tyrosinosis].. PubMed. 111(8). 697–8. 1 indexed citations
17.
Münnich, Arnold, J. M. Saudubray, C. Charpentier, et al.. (1983). Multiple molybdoenzyme deficiencies due to an inborn error of molybdenum cofactor metabolism: Two additional cases in a new family. Journal of Inherited Metabolic Disease. 6(S2). 95–96. 12 indexed citations
18.
Coudé, F. X., et al.. (1982). Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia.. PubMed. 69(1). 115–7. 20 indexed citations
19.
Coudé, F. X., H. Ogier, C. Charpentier, et al.. (1981). Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder. Human Genetics. 59(3). 263–5. 25 indexed citations
20.
Saudubray, J. M., O Amédée-Manesme, H. Ogier, et al.. (1979). [Emergency treatment of inborn amino errors of amino acid metabolism detected in the neonatal period].. PubMed. 36(10). 969–80. 2 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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