H Carrier

537 total citations
40 papers, 401 citations indexed

About

H Carrier is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, H Carrier has authored 40 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 7 papers in Neurology. Recurrent topics in H Carrier's work include Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (15 papers) and ATP Synthase and ATPases Research (7 papers). H Carrier is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Mitochondrial Function and Pathology (15 papers) and ATP Synthase and ATPases Research (7 papers). H Carrier collaborates with scholars based in France, Switzerland and Germany. H Carrier's co-authors include Catherine Godinot, B. Mousson, Mohamed Fouad Bouzidi, N. Kopp, Bernard Ferrier, Marielle Martin, Gabriel Baverel, B Bady, Jean-Marc Collombet and Fabien Michel and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of the American Society of Nephrology and Acta Neuropathologica.

In The Last Decade

H Carrier

37 papers receiving 381 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 Carrier France 11 234 151 75 59 43 40 401
Thomas W. Crosby United States 7 119 0.5× 82 0.5× 26 0.3× 141 2.4× 27 0.6× 10 358
Misao Yamamoto Japan 16 249 1.1× 92 0.6× 78 1.0× 22 0.4× 51 1.2× 40 694
M. A. Farnetani Italy 14 137 0.6× 48 0.3× 59 0.8× 56 0.9× 69 1.6× 24 447
E. Pennisi Italy 16 308 1.3× 83 0.5× 174 2.3× 156 2.6× 12 0.3× 41 667
L. Manneschi Italy 9 174 0.7× 64 0.4× 34 0.5× 50 0.8× 29 0.7× 16 326
Keiko Toyooka Japan 14 196 0.8× 53 0.4× 181 2.4× 307 5.2× 25 0.6× 35 580
Alexander Shtilbans United States 12 358 1.5× 189 1.3× 70 0.9× 125 2.1× 12 0.3× 16 566
Anne Roubergue France 9 125 0.5× 52 0.3× 120 1.6× 41 0.7× 25 0.6× 18 291
Kristin Barañano United States 9 228 1.0× 74 0.5× 165 2.2× 42 0.7× 35 0.8× 21 536
Suzanne D. DeBrosse United States 12 246 1.1× 182 1.2× 55 0.7× 18 0.3× 6 0.1× 17 422

Countries citing papers authored by H Carrier

Since Specialization
Citations

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

Fields of papers citing papers by H Carrier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Carrier

This figure shows the co-authorship network connecting the top 25 collaborators of H Carrier. A scholar is included among the top collaborators of H Carrier 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 Carrier. H Carrier 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.
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
2.
Carrier, H, et al.. (2000). Immunolabelling of mitochondrial superoxide dismutase and of Hsp60 in muscles harbouring a respiratory chain deficiency. Neuromuscular Disorders. 10(2). 144–149. 8 indexed citations
3.
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
4.
Bouzidi, Mohamed Fouad, Nathalie Enjolras, H Carrier, et al.. (1996). Variations of muscle mitochondrial creatine kinase activity in in mitochondrial diseases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1316(2). 61–70. 6 indexed citations
5.
Bouzidi, Mohamed Fouad, et al.. (1996). Antimycin resistance and ubiquinol cytochrome c reductase instability associated with a human cytochrome b mutation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1317(3). 199–209. 21 indexed citations
6.
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
7.
Carrier, H, et al.. (1995). Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletion. Acta Neuropathologica. 91(1). 104–111. 5 indexed citations
8.
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
9.
Mousson, B., et al.. (1992). Diagnostic d'une intolérance musculaire à l'exercice par déficit enzymatique chez l'adulte. La Revue de Médecine Interne. 13(1). 43–48.
10.
Mousson, B., et al.. (1991). Les cytopathies mitochondriales. La Revue de Médecine Interne. 12(3). 219–226. 3 indexed citations
11.
Carrier, H, et al.. (1990). Myopathic evolution of an exertional muscle pain syndrome with phosphorylase b kinase deficiency. Acta Neuropathologica. 81(1). 84–88. 10 indexed citations
12.
Meunier, Jean‐Claude, et al.. (1982). [Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case].. PubMed. 11(37). 2767–71. 3 indexed citations
13.
Morand, Pierre, et al.. (1979). Myopathie lipidique avec cardiomyopathie sévère par déficit généralisé en carnitine. Evolution favorable sous un traitement par chlorhydrate de carnitine.. Archives Des Maladies Du Coeur Et Des Vaisseaux. 72(5). 3 indexed citations
14.
Carrier, H, et al.. (1979). [Primary cardiomyopathy in children with lipid infiltration of the myocardium and skeletal muscles and demonstration of a palmityl-carnitine transferase deficiency. Apropos of 4 cases].. PubMed. 72(5). 529–35. 2 indexed citations
15.
Chazot, G, Benjamin Berger, H Carrier, et al.. (1976). [Neurological manifestations in monoclonal gammapathies. Pure neurological manifestations. Immunofluorescence study].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 132(3). 195–212. 36 indexed citations
16.
Kopp, N., et al.. (1975). Neuropathologie de la trichopoliodystrophie (maladie de Menkes). Une observation anatomo-clinique. Revue Neurologique. 131(11). 10 indexed citations
17.
Autret, A, et al.. (1975). [Physiopathological and neuropathological study of a cerebral decortication syndrome].. PubMed. 131(7). 491–504. 6 indexed citations
18.
Carrier, H, et al.. (1973). La malformation de Dandy-Walker. Etude d'un cas anatomique et conception actuelle. 18(4). 1 indexed citations
19.
Carrier, H, et al.. (1971). [Melanotic tumor of the pineal region].. PubMed. 52(201). 105–15. 1 indexed citations
20.
Trillet, M, et al.. (1971). [Symptomatic amnesic attack in glioblastoma involving the trigone].. PubMed. 124(5). 392–6. 10 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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