B. Mousson

805 total citations
38 papers, 606 citations indexed

About

B. Mousson is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, B. Mousson has authored 38 papers receiving a total of 606 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 29 papers in Clinical Biochemistry and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in B. Mousson's work include Metabolism and Genetic Disorders (29 papers), Mitochondrial Function and Pathology (24 papers) and ATP Synthase and ATPases Research (8 papers). B. Mousson is often cited by papers focused on Metabolism and Genetic Disorders (29 papers), Mitochondrial Function and Pathology (24 papers) and ATP Synthase and ATPases Research (8 papers). B. Mousson collaborates with scholars based in France, Switzerland and Netherlands. B. Mousson's co-authors include Grzegorz J. Stępień, Georges Stepien, H Carrier, P Baltassat, Dominique Bozon, P. Divry, Christine Vianey‐Saban, Catherine Godinot, M. Mathieu and Jean-Marc Collombet and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and Journal of Hepatology.

In The Last Decade

B. Mousson

37 papers receiving 594 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. Mousson France	14	494	406	57	51	47	38	606
Pascale Delonlay France	11	304 0.6×	255 0.6×	62 1.1×	100 2.0×	40 0.9×	13	530
J. M. van der Klei‐van Moorsel Netherlands	9	586 1.2×	254 0.6×	29 0.5×	110 2.2×	50 1.1×	10	786
Geoffrey Sherwood Canada	7	326 0.7×	165 0.4×	25 0.4×	44 0.9×	31 0.7×	11	478
A. E. M. Stroomer Netherlands	10	271 0.5×	185 0.5×	74 1.3×	61 1.2×	22 0.5×	13	445
François‐Guillaume Debray Belgium	14	305 0.6×	211 0.5×	39 0.7×	84 1.6×	23 0.5×	26	507
Mohamed A. Nada United States	11	424 0.9×	409 1.0×	60 1.1×	151 3.0×	10 0.2×	30	636
M. E. J. den Boer Netherlands	6	346 0.7×	419 1.0×	150 2.6×	152 3.0×	13 0.3×	7	564
H. Ibel Germany	13	212 0.4×	111 0.3×	27 0.5×	84 1.6×	20 0.4×	22	433
Gaetano Sabetta Italy	10	340 0.7×	402 1.0×	174 3.1×	125 2.5×	15 0.3×	11	631
Renata C. Gallagher United States	11	235 0.5×	326 0.8×	94 1.6×	78 1.5×	9 0.2×	13	493

Countries citing papers authored by B. Mousson

Since Specialization

Citations

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

Fields of papers citing papers by B. Mousson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Mousson

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

Mousson, B., Jean-Marc Collombet, H Carrier, et al.. (2009). An abnormal exercise test response revealing a respiratory chain complex III deficiency. Acta Neurologica Scandinavica. 91(6). 488–493. 6 indexed citations

Procaccio, Vincent, B. Mousson, Réjane Beugnot, et al.. (1999). Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts. Journal of Clinical Investigation. 104(1). 83–92. 33 indexed citations

Bonod‐Bidaud, Christelle, et al.. (1999). Quantification of OXPHOS Gene Transcripts during Muscle Cell Differentiation in Patients with Mitochondrial Myopathies. Experimental Cell Research. 246(1). 91–97. 10 indexed citations

Ducluzeau, Pierre‐Henri, Alain Lachaux, Raymonde Bouvier, et al.. (1999). Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosis. Journal of Hepatology. 30(1). 149–155. 55 indexed citations

Feillet, François, B. Mousson, Y Grignon, James V. Leonard, & M. Vidailhet. (1999). Necrotizing encephalopathy and macrocephaly with mitochondrial complex I deficiency. Pediatric Neurology. 20(4). 305–308. 3 indexed citations

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

Collombet, Jean-Marc, et al.. (1997). Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies. Molecular and Cellular Biochemistry. 168(1-2). 73–85. 8 indexed citations

Nicolino, Marc, Maguelone G. Forest, Catherine Godinot, et al.. (1997). Identification of a Large-Scale Mitochondrial Deoxyribonucleic Acid Deletion in Endocrinopathies and Deafness: Report of Two Unrelated Cases with Diabetes Mellitus and Adrenal Insufficiency, Respectively¹. The Journal of Clinical Endocrinology & Metabolism. 82(9). 3063–3067. 27 indexed citations

Bozon, Dominique, et al.. (1996). A novel gly290asp mitochondrial cytochromebmutation linked to a complex III deficiency in progressive exercise intolerance. Molecular and Cellular Probes. 10(5). 389–391. 78 indexed citations

10.

Fischer, Andréas, et al.. (1996). Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cells. Journal of the Neurological Sciences. 136(1-2). 178–181. 11 indexed citations

11.

Collombet, Jean-Marc, et al.. (1996). Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathies. Molecular and General Genetics MGG. 253(1-2). 182–188. 8 indexed citations

12.

Stępień, Grzegorz J., et al.. (1995). Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia. Molecular and Cellular Probes. 9(3). 207–214. 11 indexed citations

13.

Donckerwolcke, R. A., M. Durán, Jan Smeıtınk, et al.. (1994). Rate-Dependent Distal Renal Tubular Acidosis and Carnitine Palmitoyltransferase I Deficiency. Pediatric Research. 36(5). 582–587. 29 indexed citations

14.

Bouzidi, Mohamed Fouad, Hermann Schägger, Jean-Marc Collombet, et al.. (1993). Decreased expression o ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intolerance. Neuromuscular Disorders. 3(5-6). 599–604. 23 indexed citations

15.

Bohbot, A., et al.. (1993). Failure to obtain hybridomas between human macrophages and human tumoral U-937 cells is probably due to parental macrophages. In Vitro Cellular & Developmental Biology - Animal. 29(5). 362–370. 1 indexed citations

16.

Tranchant, Christine, et al.. (1993). Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion. Neuromuscular Disorders. 3(5-6). 561–566. 32 indexed citations

17.

Vianey‐Saban, Christine, B. Mousson, C. Bertrand, et al.. (1993). Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia. European Journal of Pediatrics. 152(4). 334–338. 35 indexed citations

18.

Mousson, B., et al.. (1991). Les cytopathies mitochondriales. La Revue de Médecine Interne. 12(3). 219–226. 3 indexed citations

19.

Sann, L, et al.. (1988). Prevention of neonatal hypoglycaemia by oral lipid supplementation in low birth weight infants. European Journal of Pediatrics. 147(2). 158–161. 12 indexed citations

20.

Bouvier, Michel, et al.. (1979). [Phosphoribosylpyrophosphate synthetase anomalies in 2 cases of gout beginning at an early age].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 46(7-9). 457–65. 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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