Michel Cohen‐Solal

432 total citations
21 papers, 331 citations indexed

About

Michel Cohen‐Solal is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Michel Cohen‐Solal has authored 21 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 9 papers in Physiology. Recurrent topics in Michel Cohen‐Solal's work include Erythrocyte Function and Pathophysiology (9 papers), Hemoglobinopathies and Related Disorders (9 papers) and Neonatal Health and Biochemistry (7 papers). Michel Cohen‐Solal is often cited by papers focused on Erythrocyte Function and Pathophysiology (9 papers), Hemoglobinopathies and Related Disorders (9 papers) and Neonatal Health and Biochemistry (7 papers). Michel Cohen‐Solal collaborates with scholars based in France, United States and Denmark. Michel Cohen‐Solal's co-authors include Bernard G. Forget, Arthur S. Schneider, Constantin T. Craescu, Joëlle Thillet, Philippe Kourilsky, Jean Rosa, Frédéric Galactéros, Christian Vincent, Paul Tchen and Edward J. Benz and has published in prestigious journals such as Cell, Nucleic Acids Research and Blood.

In The Last Decade

Michel Cohen‐Solal

20 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michel Cohen‐Solal France 12 147 122 119 75 70 21 331
Yasuhiro Yamashiro Japan 9 168 1.1× 43 0.4× 187 1.6× 136 1.8× 35 0.5× 43 360
H. Lam United States 11 120 0.8× 117 1.0× 449 3.8× 254 3.4× 156 2.2× 41 622
Sebastian Koochaki United States 4 216 1.5× 107 0.9× 87 0.7× 64 0.9× 17 0.2× 5 339
Kerrie Wilson United Kingdom 8 147 1.0× 153 1.3× 29 0.2× 141 1.9× 24 0.3× 10 473
CM Cohen Pakistan 7 166 1.1× 407 3.3× 52 0.4× 70 0.9× 85 1.2× 14 495
Stuart Jaffe United States 7 252 1.7× 80 0.7× 16 0.1× 12 0.2× 14 0.2× 7 396
L-H. Gu United States 9 49 0.3× 44 0.4× 251 2.1× 193 2.6× 75 1.1× 29 313
Andrei M. Vacaru United States 8 121 0.8× 38 0.3× 28 0.2× 18 0.2× 12 0.2× 16 196
Agnieszka Styś Poland 9 134 0.9× 29 0.2× 88 0.7× 158 2.1× 24 0.3× 16 358
Yaser Heshmati Sweden 9 103 0.7× 30 0.2× 23 0.2× 38 0.5× 20 0.3× 15 201

Countries citing papers authored by Michel Cohen‐Solal

Since Specialization
Citations

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

Fields of papers citing papers by Michel Cohen‐Solal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michel Cohen‐Solal. 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 Michel Cohen‐Solal. The network helps show where Michel Cohen‐Solal may publish in the future.

Co-authorship network of co-authors of Michel Cohen‐Solal

This figure shows the co-authorship network connecting the top 25 collaborators of Michel Cohen‐Solal. A scholar is included among the top collaborators of Michel Cohen‐Solal 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 Michel Cohen‐Solal. Michel Cohen‐Solal 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.
2.
Cohen‐Solal, Michel, et al.. (2000). Identical germ-line mutations in the triosephosphate isomerase alleles of two brothers are associated with distinct clinical phenotypes. Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie. 323(3). 245–250. 10 indexed citations
3.
Cohen‐Solal, Michel, Claude Préhu, Henri Wajcman, et al.. (1998). A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an α2 globin gene variant (Hb Conakry). British Journal of Haematology. 103(4). 950–956. 30 indexed citations
4.
5.
Rouger, H, et al.. (1996). Five unknown mutations in the LR pyruvate kinase gene associated with severe hereditary nonspherocytic haemolytic anaemia in France. British Journal of Haematology. 92(4). 825–830. 23 indexed citations
6.
Schneider, Arthur S., Beryl Westwood, Michel Cohen‐Solal, et al.. (1996). The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families. Blood Cells Molecules and Diseases. 22(2). 115–125. 13 indexed citations
7.
Schneider, Arthur S. & Michel Cohen‐Solal. (1996). Hematologically Important Mutations: Triosephosphate Isomerase. Blood Cells Molecules and Diseases. 22(1). 82–84. 15 indexed citations
8.
Ojcius, David M., Philippe Leboulch, V. Joulin, et al.. (1990). Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase. Gene. 91(2). 225–232. 24 indexed citations
9.
Meunier–Rotival, Michèle, et al.. (1989). Nucleotide sequence of a cDNA encoding a larval α-globin chain of the amphibianPleurodeles waltlii. Nucleic Acids Research. 17(7). 2850–2850.
10.
Danckaert, Anne, Claude Mugnier, Philippe Dessen, & Michel Cohen‐Solal. (1987). A computer program for the design of optimal synthetic oligonucleotide probes for protein coding genes. Computer applications in the biosciences. 3(4). 303–307. 6 indexed citations
11.
Barichard, F., V. Joulin, Isabelle Henry, et al.. (1987). Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22. Human Genetics. 77(3). 283–285. 14 indexed citations
12.
Roméo, Paul‐Henri, et al.. (1986). Cloning and sequencing of mRNAs coding for two adult α globin chains of the salamander Pleurodeles waltlii. Gene. 42(2). 159–168. 2 indexed citations
13.
Cohen-Solal, L, Y. Blouquit, Michel Cohen‐Solal, & Melvin J. Glimcher. (1985). Reaction products formed after strong acid treatment of α-amino-δ-hydroxyvaleric acid. Analytical Biochemistry. 151(1). 82–87. 6 indexed citations
14.
Cohen‐Solal, Michel, et al.. (1982). Cloning and Nucleotide Sequence Analysis of Human Embryonic ζ-Globin cDNA. DNA. 1(4). 355–363. 16 indexed citations
15.
Vincent, Christian, Paul Tchen, Michel Cohen‐Solal, & Philippe Kourilsky. (1982). Synthesis of 8-(2-4 dinitrophenyl 2-6 aminohexyl) amino–adenosine 5′ triphosphate: biological properties and potential uses. Nucleic Acids Research. 10(21). 6787–6796. 33 indexed citations
16.
Benz, Edward J., Bernard G. Forget, Diane G. Hillman, et al.. (1978). Variability in the amount of β-globin mRNA in β0 thalassemia. Cell. 14(2). 299–312. 53 indexed citations
17.
Marotta, Charles A., Bernard G. Forget, Michel Cohen‐Solal, & Sherman M. Weissman. (1977). Nucleotide Sequence Analysis of Coding and Noncoding Regions of Human β-Globin mRNA. Progress in nucleic acid research and molecular biology. 19. 165–175. 9 indexed citations
18.
Cohen‐Solal, Michel, et al.. (1974). Haemoglobin lyon (β17–18 (A 14–15) Lys-Val → O). Biochimica et Biophysica Acta (BBA) - Protein Structure. 351(2). 306–316. 7 indexed citations
19.
Cohen‐Solal, Michel, et al.. (1974). Haemoglobin Lyon (beta17-18 (A 14-15) Lys-Val leads to O). Determination by sequenator analysis.. PubMed. 351(2). 306–16. 10 indexed citations
20.
Cohen‐Solal, Michel, Maxime Seligmann, Joëlle Thillet, & Jean Rosa. (1973). Haemoglobin Saint Louis β28 (B10) Leucine → Glutamine A new unstable haemoglobin only present in a ferri form. FEBS Letters. 33(1). 37–41. 22 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Yasuhiro Yamashiro Breakdown of academic impact, for papers by H. Lam Breakdown of academic impact, for papers by Sebastian Koochaki Breakdown of academic impact, for papers by Kerrie Wilson Breakdown of academic impact, for papers by CM Cohen Breakdown of academic impact, for papers by Stuart Jaffe Breakdown of academic impact, for papers by L-H. Gu Breakdown of academic impact, for papers by Andrei M. Vacaru Breakdown of academic impact, for papers by Agnieszka Styś Breakdown of academic impact, for papers by Yaser Heshmati
Rankless by CCL
2026