Michel Cohen‐Solal

432 citations

21 papers · 331 indexed · h-index 12

Molecular Biology
Physiology
Genetics top 10%
Hematology top 10%
Pediatrics, Perinatology and Child Health

Co-authors: Bernard G. Forget Arthur S. Schneider Constantin T. Craescu Jean Rosa Christian Vincent Philippe Kourilsky Joëlle Thillet Paul Tchen
Topics: Erythrocyte Function and Pathophysiology (9 papers)Hemoglobinopathies and Related Disorders (9 papers)Neonatal Health and Biochemistry (7 papers)
Cited by: Genetics Hematology Physiology
Journals: Cell Nucleic Acids Research Blood
Partner nations: France United States Denmark

In The Last Decade

Michel Cohen‐Solal

20 papers receiving 317 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Identical germ-line mutations in the triosephosphate isomerase alleles of two brothers are associated with distinct clinical phenotypes 2000 ·Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie ·(unknown),Michel Cohen‐Solal,Lynne E. Maquat,(unknown),(unknown),Susan R. Hollán	10
2	Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris). 2000 ·Blood ·(unknown),Serge Pissard,Josiane Martin,Delphine Héron,Philippe Labrune,Marie-Odile Livet,M. Mayer,Terri Gelbart,Arthur S. Schneider,Isabelle Max‐Audit,Michel Cohen‐Solal	18
3	A phosphoglycerate kinase mutant (PGK Herlev; D285V) in a Danish patient with isolated chronic hemolytic anemia: Mechanism of mutation and structure–function relationships 1998 ·Human Mutation ·(unknown),Henrik Birgens,Constantin T. Craescu,(unknown),Michel Cohen‐Solal	18
4	A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an α2 globin gene variant (Hb Conakry) 1998 ·British Journal of Haematology ·Michel Cohen‐Solal,Claude Préhu,Henri Wajcman,Claire Poyart,Josiane Bardakdjian‐Michau,J. Kister,Danièlle Promé,(unknown),Dora Bachir,Frédéric Galactéros	30
5	A phosphoglycerate kinase mutant (PGK Herlev; D285V) in a Danish patient with isolated chronic hemolytic anemia: Mechanism of mutation and structure–function relationships 1998 ·Human Mutation ·(unknown),Henrik Birgens,Constantin T. Craescu,(unknown),Michel Cohen‐Solal	2
6	The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families 1996 ·Blood Cells Molecules and Diseases ·Arthur S. Schneider,Beryl Westwood,(unknown),Michel Cohen‐Solal,R Rosa,Richard Labotka,Stefan Eber,Raoul Wolf,Ahti Lammi,Ernest Beutler	13
7	Hematologically Important Mutations: Triosephosphate Isomerase 1996 ·Blood Cells Molecules and Diseases ·Arthur S. Schneider,Michel Cohen‐Solal	15
8	Five unknown mutations in the LR pyruvate kinase gene associated with severe hereditary nonspherocytic haemolytic anaemia in France 1996 ·British Journal of Haematology ·H Rouger,(unknown),Constantin T. Craescu,Frédéric Galactéros,Michel Cohen‐Solal	23
9	Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase 1990 ·Gene ·(unknown),David M. Ojcius,Philippe Leboulch,V. Joulin,Y. Blouquit,(unknown),(unknown),R Rosa,(unknown),Michel Cohen‐Solal	24
10	Nucleotide sequence of a cDNA encoding a larval α-globin chain of the amphibianPleurodeles waltlii 1989 ·Nucleic Acids Research ·(unknown),(unknown),Michèle Meunier–Rotival,Michel Cohen‐Solal	0
11	A computer program for the design of optimal synthetic oligonucleotide probes for protein coding genes 1987 ·Computer applications in the biosciences ·Anne Danckaert,Claude Mugnier,Philippe Dessen,Michel Cohen‐Solal	6
12	Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22 1987 ·Human Genetics ·F. Barichard,V. Joulin,Isabelle Henry,(unknown),(unknown),R Rosa,Michel Cohen‐Solal,Claudine Junien	14
13	Cloning and sequencing of mRNAs coding for two adult α globin chains of the salamander Pleurodeles waltlii 1986 ·Gene ·(unknown),Paul‐Henri Roméo,Michel Cohen‐Solal,Anne‐Marie Duprat,(unknown),Jean Rosa	2
14	Reaction products formed after strong acid treatment of α-amino-δ-hydroxyvaleric acid 1985 ·Analytical Biochemistry ·L Cohen-Solal,Y. Blouquit,Michel Cohen‐Solal,Melvin J. Glimcher	6
15	Cloning and Nucleotide Sequence Analysis of Human Embryonic ζ-Globin cDNA 1982 ·DNA ·Michel Cohen‐Solal,(unknown),Jon K. deRiel,Mary Jo Murnane,Bernard G. Forget	16
16	Synthesis of 8-(2-4 dinitrophenyl 2-6 aminohexyl) amino–adenosine 5′ triphosphate: biological properties and potential uses 1982 ·Nucleic Acids Research ·Christian Vincent,Paul Tchen,Michel Cohen‐Solal,Philippe Kourilsky	33
17	Nucleotide Sequence Analysis of Coding and Noncoding Regions of Human β-Globin mRNA 1977 ·Progress in nucleic acid research and molecular biology ·Charles A. Marotta,Bernard G. Forget,Michel Cohen‐Solal,Sherman M. Weissman	9
18	Haemoglobin lyon (β17–18 (A 14–15) Lys-Val → O) 1974 ·Biochimica et Biophysica Acta (BBA) - Protein Structure ·Michel Cohen‐Solal,Y. Blouquit,(unknown),Joëlle Thillet,(unknown),(unknown),(unknown),Jean Rosa	7
19	Haemoglobin Lyon (beta17-18 (A 14-15) Lys-Val leads to O). Determination by sequenator analysis. 1974 ·PubMed ·Michel Cohen‐Solal,Y. Blouquit,(unknown),Joëlle Thillet,(unknown),(unknown),(unknown),Jean Rosa	10
20	Haemoglobin Saint Louis β28 (B10) Leucine → Glutamine A new unstable haemoglobin only present in a ferri form 1973 ·FEBS Letters ·Michel Cohen‐Solal,Maxime Seligmann,Joëlle Thillet,Jean Rosa	22

About Michel Cohen‐Solal

Michel Cohen‐Solal is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Physiology, having authored 21 papers that have together received 331 indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (9 papers), Hemoglobinopathies and Related Disorders (9 papers) and Neonatal Health and Biochemistry (7 papers). The work is most often cited by research in Genetics (119 citations), Hematology (75 citations) and Physiology (122 citations). Michel Cohen‐Solal has collaborated with scholars based in France, United States and Denmark. Frequent co-authors include Bernard G. Forget, Arthur S. Schneider, Constantin T. Craescu, Jean Rosa, Christian Vincent, Philippe Kourilsky, Joëlle Thillet, Paul Tchen, Frédéric Galactéros and Edward J. Benz. Their work appears in journals such as Cell, Nucleic Acids Research and Blood.

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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