Hélène Ogier

1.7k total citations
16 papers, 877 citations indexed

About

Hélène Ogier is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Hélène Ogier has authored 16 papers receiving a total of 877 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 4 papers in Physiology. Recurrent topics in Hélène Ogier's work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (3 papers) and Folate and B Vitamins Research (3 papers). Hélène Ogier is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (3 papers) and Folate and B Vitamins Research (3 papers). Hélène Ogier collaborates with scholars based in France, Canada and United Kingdom. Hélène Ogier's co-authors include Jean‐Marie Saudubray, L de Parscau, B. Chabrol, Bénédicte Héron, Louis Dallaire, Vassili Valayannopoulos, Andrée Weber, Albert Larbrisseau, Jacques Lacroix and Michel Vanasse and has published in prestigious journals such as New England Journal of Medicine, The Lancet and European Journal of Biochemistry.

In The Last Decade

Hélène Ogier

16 papers receiving 844 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hélène Ogier France	13	443	415	292	113	109	16	877
Ali Dursun Türkiye	17	434 1.0×	438 1.1×	215 0.7×	165 1.5×	88 0.8×	97	995
Ayşegül Tokatlı Türkiye	17	610 1.4×	575 1.4×	249 0.9×	184 1.6×	77 0.7×	101	1.3k
Janet A. Thomas United States	18	505 1.1×	481 1.2×	454 1.6×	240 2.1×	149 1.4×	40	1.1k
Dimitar Gavrilov United States	15	403 0.9×	437 1.1×	345 1.2×	152 1.3×	102 0.9×	35	901
Joyce A. Kobori United States	11	277 0.6×	234 0.6×	329 1.1×	178 1.6×	113 1.0×	14	686
Murray Bain United Kingdom	20	476 1.1×	353 0.9×	271 0.9×	118 1.0×	26 0.2×	35	957
Ksenija Fumić Croatia	15	498 1.1×	329 0.8×	248 0.8×	286 2.5×	80 0.7×	62	868
Zuhair Rahbeeni Saudi Arabia	18	537 1.2×	453 1.1×	152 0.5×	110 1.0×	39 0.4×	63	989
Shlomo Almashanu Israel	16	390 0.9×	271 0.7×	128 0.4×	67 0.6×	62 0.6×	45	838
Carolina Fischinger Moura de Souza Brazil	19	507 1.1×	362 0.9×	427 1.5×	279 2.5×	170 1.6×	110	1.2k

Countries citing papers authored by Hélène Ogier

Since Specialization

Citations

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

Fields of papers citing papers by Hélène Ogier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hélène Ogier

This figure shows the co-authorship network connecting the top 25 collaborators of Hélène Ogier. A scholar is included among the top collaborators of Hélène 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 Hélène Ogier. Hélène Ogier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Béghin, Laurent, Stéphanie Coopman, Manuel Schiff, et al.. (2016). Doubling diet fat on sugar ratio in children with mitochondrial OXPHOS disorders: Effects of a randomized trial on resting energy expenditure, diet induced thermogenesis and body composition. Clinical Nutrition. 35(6). 1414–1422. 2 indexed citations

Gall, Émilie Cornec-Le, Yahsou Delmas, L de Parscau, et al.. (2013). Adult-Onset Eculizumab-Resistant Hemolytic Uremic Syndrome Associated With Cobalamin C Deficiency. American Journal of Kidney Diseases. 63(1). 119–123. 58 indexed citations

Héron, Bénédicte, Vassili Valayannopoulos, Julien Baruteau, et al.. (2012). Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C. Orphanet Journal of Rare Diseases. 7(1). 36–36. 64 indexed citations

Nowak, Emmanuel, Murielle Assoun, Karine Mention, et al.. (2012). Maternal phenylketonuria: low phenylalaninemia might increase the risk of intra uterine growth retardation. Journal of Inherited Metabolic Disease. 35(6). 993–999. 34 indexed citations

Héron, Bénédicte, Yann Mikaeloff, Roseline Froissart, et al.. (2010). Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece. American Journal of Medical Genetics Part A. 155(1). 58–68. 128 indexed citations

Feillet, François, Véronique Abadie, Jacques Berthelot, et al.. (2004). Maternal phenylketonuria: the French survey. European Journal of Pediatrics. 163(9). 540–546. 15 indexed citations

Chinnery, Patrick F., Salvatore DiMauro, Sara Shanske, et al.. (2004). Risk of developing a mitochondrial DNA deletion disorder. The Lancet. 364(9434). 592–596. 144 indexed citations

Castelnau, Pierre, Mônica Zilbovicius, Maria-João Ribeiro, et al.. (2001). Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndrome. Pediatric Neurology. 25(2). 170–174. 7 indexed citations

Sfaello, Ignacio, Pierre Castelnau, Nathalie Blanc, et al.. (2000). Infantile spasms and Menkes disease. Epileptic Disorders. 2(4). 227–230. 17 indexed citations

10.

Cormier‐Daire, Valérie, Jean‐Paul Bonnefont, Pierre Rustin, et al.. (1994). Mitochondrial DNA rearrangements with onset as chronic diarrhea with villous atrophy. The Journal of Pediatrics. 124(1). 63–70. 62 indexed citations

11.

Russo, Pierre, Josée Doyon, E Sonsino, Hélène Ogier, & Jean‐Marie Saudubray. (1992). A congenital anomaly of vitamin B12 metabolism: A study of three cases. Human Pathology. 23(5). 504–512. 45 indexed citations

12.

Mitchell, Grant A., Jean Larochelle, Marie Lambert, et al.. (1990). Neurologic Crises in Hereditary Tyrosinemia. New England Journal of Medicine. 322(7). 432–437. 147 indexed citations

13.

Skopek, T R, Leslie Recio, Louis Dallaire, et al.. (1990). Molecular analyses of a Lesch-Nyhan syndrome mutation (hprt Montreal) by use of T-lymphocyte cultures. Human Genetics. 85(1). 111–6. 21 indexed citations

14.

Ogier, Hélène, Arnold Münnich, Stanislas Lyonnet, et al.. (1987). Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestine. European Journal of Biochemistry. 166(2). 365–370. 12 indexed citations

15.

Roels, Frank, Alfons Cornelis, Bwee Tien Poll‐The, et al.. (1986). Hepatic peroxisomes are deficient in infantile refsum disease: A cytochemical study of 4 cases. American Journal of Medical Genetics. 25(2). 257–271. 77 indexed citations

16.

Saudubray, Jean Marie, C. Marsac, J.M. Limal, et al.. (1981). Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: Relationship to age. The Journal of Pediatrics. 98(6). 904–908. 44 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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