Christiane Baussan

1.8k total citations
27 papers, 1.2k citations indexed

About

Christiane Baussan is a scholar working on Rheumatology, Organic Chemistry and Physiology. According to data from OpenAlex, Christiane Baussan has authored 27 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Rheumatology, 10 papers in Organic Chemistry and 7 papers in Physiology. Recurrent topics in Christiane Baussan's work include Glycogen Storage Diseases and Myoclonus (15 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Lysosomal Storage Disorders Research (6 papers). Christiane Baussan is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (15 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Lysosomal Storage Disorders Research (6 papers). Christiane Baussan collaborates with scholars based in France, United Kingdom and United States. Christiane Baussan's co-authors include Emmanuel Jacquemin, Anne Davit–Spraul, Emmanuel Gonzalès, Olivier Bernard, Monique Fabrè, Bruno Stieger, Sophie Branchereau, N. Moatti, B. Hermeziu and Philippe Labrune and has published in prestigious journals such as Hepatology, PEDIATRICS and The American Journal of Human Genetics.

In The Last Decade

Christiane Baussan

25 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christiane Baussan France 14 607 516 277 250 209 27 1.2k
Gustav Paumgartner Germany 9 471 0.8× 554 1.1× 449 1.6× 36 0.1× 464 2.2× 11 1.1k
Michael Becker Germany 18 1.4k 2.3× 920 1.8× 145 0.5× 42 0.2× 88 0.4× 28 1.8k
B. Isaksson Sweden 16 457 0.8× 193 0.4× 142 0.5× 26 0.1× 156 0.7× 34 884
Jeremy French United Kingdom 20 584 1.0× 521 1.0× 480 1.7× 25 0.1× 322 1.5× 63 1.4k
S A Jenkins United Kingdom 20 438 0.7× 198 0.4× 564 2.0× 80 0.3× 543 2.6× 65 1.2k
Alessandro Gigliozzi Italy 15 418 0.7× 343 0.7× 207 0.7× 18 0.1× 268 1.3× 31 767
Stephen J. Rulyak United States 16 411 0.7× 495 1.0× 230 0.8× 33 0.1× 50 0.2× 25 993
Renato Bisonni Italy 17 309 0.5× 840 1.6× 44 0.2× 107 0.4× 103 0.5× 33 1.3k
Hiroyuki Muro Japan 16 338 0.6× 114 0.2× 123 0.4× 52 0.2× 181 0.9× 41 687
Takahiro Yoshikawa Japan 16 247 0.4× 226 0.4× 143 0.5× 71 0.3× 131 0.6× 69 716

Countries citing papers authored by Christiane Baussan

Since Specialization
Citations

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

Fields of papers citing papers by Christiane Baussan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christiane Baussan

This figure shows the co-authorship network connecting the top 25 collaborators of Christiane Baussan. A scholar is included among the top collaborators of Christiane Baussan 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 Christiane Baussan. Christiane Baussan 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.
Azzouz, Hatem, François Petit, Mariem Ben Khelifa, et al.. (2013). Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III. Molecular Biology Reports. 40(7). 4197–4202. 7 indexed citations
2.
Billot, S., Dominique Hervé, Hasan O. Akman, et al.. (2012). Acute but transient neurological deterioration revealing adult polyglucosan body disease. Journal of the Neurological Sciences. 324(1-2). 179–182. 12 indexed citations
3.
Davit–Spraul, Anne, Monique Piraud, Dries Dobbelaere, et al.. (2011). Liver glycogen storage diseases due to phosphorylase system deficiencies: Diagnosis thanks to non invasive blood enzymatic and molecular studies. Molecular Genetics and Metabolism. 104(1-2). 137–143. 42 indexed citations
4.
Valayannopoulos, Vassili, Fanny Bajolle, Jean‐Baptiste Arnoux, et al.. (2011). Successful Treatment of Severe Cardiomyopathy in Glycogen Storage Disease Type III With D,L-3-Hydroxybutyrate, Ketogenic and High-Protein Diet. Pediatric Research. 70(6). 638–641. 85 indexed citations
5.
6.
Davit–Spraul, Anne, Emmanuel Gonzalès, Christiane Baussan, & Emmanuel Jacquemin. (2010). The Spectrum of Liver Diseases Related toABCB4Gene Mutations: Pathophysiology and Clinical Aspects. Seminars in Liver Disease. 30(2). 134–146. 163 indexed citations
7.
Hermeziu, B., Djamila Messous, Monique Fabrè, et al.. (2009). Evaluation of FibroTest–ActiTest in children with chronic hepatitis C virus infection. Gastroentérologie Clinique et Biologique. 34(1). 16–22. 18 indexed citations
8.
Davit–Spraul, Anne, Emmanuel Gonzalès, Christiane Baussan, & Emmanuel Jacquemin. (2009). Progressive familial intrahepatic cholestasis. Orphanet Journal of Rare Diseases. 4(1). 314 indexed citations
9.
Davit–Spraul, Anne, Cathérine Costa, Mokhtar Zater, et al.. (2008). Hereditary fructose intolerance: Frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France—Identification of eight new mutations. Molecular Genetics and Metabolism. 94(4). 443–447. 18 indexed citations
10.
Laforêt, Pascal, Pascale Richard, Mina Ait Saïd, et al.. (2006). A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis. Neuromuscular Disorders. 16(3). 178–182. 41 indexed citations
11.
Baussan, Christiane, Danièle Cresteil, Emmanuel Gonzalès, et al.. (2004). Genetic cholestatic liver diseases: the example of progressive familial intrahepatic cholestasis and related disorders.. PubMed. 67(2). 179–83. 13 indexed citations
12.
Gonzalès, Emmanuel, Danièle Cresteil, Christiane Baussan, et al.. (2004). P0188 SRD5B1 (AKR1D1) GENE ANALYSIS IN DELTA4???3-OXOSTEROID 5BETA-REDUCTASE DEFICIENCY: EVIDENCE FOR PRIMARY GENETIC DEFECT. Journal of Pediatric Gastroenterology and Nutrition. 39(Supplement 1). S129–S130. 20 indexed citations
13.
Saudubray, Jean‐Marie, Pascale de Lonlay, Guy Touati, et al.. (2000). Genetic hypoglycaemia in infancy and childhood: Pathophysiology and diagnosis. Journal of Inherited Metabolic Disease. 23(3). 197–214. 10 indexed citations
14.
Hendrickx, Jan, Philip Lee, James Keating, et al.. (1999). Complete Genomic Structure and Mutational Spectrum of PHKA2 in Patients with X-Linked Liver Glycogenosis Type I and II. The American Journal of Human Genetics. 64(6). 1541–1549. 41 indexed citations
15.
Costa, Cathérine, Jean Marc Costa, Jean‐François Deleuze, et al.. (1998). Simple, Rapid Nonradioactive Method to Detect the Three Most Prevalent Hereditary Fructose Intolerance Mutations. Clinical Chemistry. 44(5). 1041–1043. 9 indexed citations
16.
Baussan, Christiane, Jacqueline Chalas, Annie Abella, et al.. (1996). Blood lipids and rheological modifications in glycogen storage disease. Clinical Biochemistry. 29(1). 73–78. 10 indexed citations
17.
Thérond, Patrice, et al.. (1996). Alterations in erythrocyte membrane fluidity and fatty acid composition in glycogen storage disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1315(1). 61–65. 13 indexed citations
18.
Labrune, Philippe, Jacqueline Chalas, Christiane Baussan, & M Odièvre. (1993). Tolerance to prolonged fasting in two children with type I glycogen storage disease. Journal of Inherited Metabolic Disease. 16(6). 1044–1045. 1 indexed citations
19.
Hendrickx, Jan, Paul Coucke, Paul Bossuyt, et al.. (1993). X-linked liver glycogenosis: localization and isolation of a candidate gene. Human Molecular Genetics. 2(5). 583–589. 15 indexed citations
20.
Maire, Irène, Christiane Baussan, N. Moatti, Monique Mathieu, & Alain Lemonnier. (1991). Biochemical diagnosis of hepatic glycogen storage diseases: 20 years French experience. Clinical Biochemistry. 24(2). 169–178. 41 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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