C. Picat

823 total citations
21 papers, 708 citations indexed

About

C. Picat is a scholar working on Molecular Biology, Physiology and Rheumatology. According to data from OpenAlex, C. Picat has authored 21 papers receiving a total of 708 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Physiology and 6 papers in Rheumatology. Recurrent topics in C. Picat's work include Erythrocyte Function and Pathophysiology (11 papers), Porphyrin Metabolism and Disorders (9 papers) and Folate and B Vitamins Research (6 papers). C. Picat is often cited by papers focused on Erythrocyte Function and Pathophysiology (11 papers), Porphyrin Metabolism and Disorders (9 papers) and Folate and B Vitamins Research (6 papers). C. Picat collaborates with scholars based in France, Netherlands and Finland. C. Picat's co-authors include Bernard Grandchamp, Y Nordmann, Catherine Porcher, Jean‐Charles Deybach, C. Beaumont, Paul‐Henri Roméo, M. Goossens, Felix de Rooij, J. H. P. Wilson and Vincent Mignotte and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

C. Picat

21 papers receiving 689 citations

Peers

Countries citing papers authored by C. Picat

Since Specialization

Citations

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

Fields of papers citing papers by C. Picat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Picat

This figure shows the co-authorship network connecting the top 25 collaborators of C. Picat. A scholar is included among the top collaborators of C. Picat 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 C. Picat. C. Picat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	A simplified method for determination of specific DNA or RNA copy number using quantitative PCR and an automatic DNA sequencer. 1992 ·PubMed ·Catherine Porcher, Marie‐Claire Malinge, C. Picat, Bernard Grandchamp	66
2	Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation. 1991 ·Journal of Clinical Investigation ·M Garbarz, William Tse, PG Gallagher, C. Picat, Marie‐Christine Lecomte, Francis Galibert, D Dhermy, BG Forget	30
3	PCR detection of a C/T polymorphism in exon 1 of the porphobilinogen deaminase gene (PBGD) 1991 ·Nucleic Acids Research ·C. Picat, F. Bourgeois, (unknown)	13
4	Molecular heterogeneity of acute intermittent porphyria: identification of four additional mutations resulting in the CRIM-negative subtype of the disease. 1991 ·PubMed ·Marie Hélène Delfau, C. Picat, Felix de Rooij, Gardi Voortman, Jean‐Charles Deybach, Y Nordmann, Bernard Grandchamp	42
5	Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria. 1990 ·Journal of Clinical Investigation ·Marie Hélène Delfau, C. Picat, (unknown), Karien M. Hamer, M. Bogard, J. H. P. Wilson, Jean‐Charles Deybach, Y Nordmann, Bernard Grandchamp	65
6	Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain 1990 ·Blood ·(unknown), (unknown), Carlo V. Feo, Isabelle Devaux, C. Picat, Christine Lefebvre, Francis Galibert, H Gautero, Odile Bournier, C Galand	48
7	Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminase 1989 ·European Journal of Clinical Investigation ·Bernard Grandchamp, C. Picat, Raili Kauppinen, Vincent Mignotte, Leena Peltonen, Pertti Mustajoki, Paul‐Henri Roméo, M. Goossens, Y Nordmann	59
8	A point mutation G—A in exon 12 of the porphoblllnogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria 1989 ·Nucleic Acids Research ·Bernard Grandchamp, C. Picat, Felix de Rooij, C. Beaumont, Peter J. Wilson, Jean‐Charles Deybach, Y Nordmann	106
9	Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyria 1989 ·Journal of Inherited Metabolic Disease ·C. Picat, Marie Hélène Delfau, (unknown), (unknown), B.G. Wolthers, S. K. Wadman, Y Nordmann, Bernard Grandchamp	15
10	Tissue-specific splicing mutation in acute intermittent porphyria. 1989 ·Proceedings of the National Academy of Sciences ·Bernard Grandchamp, C. Picat, Vincent Mignotte, J. H. P. Wilson, (unknown), L. A. Sandkuyl, Paul‐Henri Roméo, M. Goossens, Y Nordmann	98
11	[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant]. 1989 ·PubMed ·M Garbarz, Isabelle Devaux, Bernard Grandchamp, C. Picat, D Dhermy, (unknown), Pierre Boivin, (unknown), Bernard G. Forget	5
12	Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family 1987 ·Human Genetics ·Marie‐Christine Lecomte, D Dhermy, M Garbarz, Carlo V. Feo, H Gautero, Odile Bournier, C. Picat, (unknown), C Galand, Pierre Boivin	8
13	DNA POLYMORPHISM OF HUMAN PORPHOBILINOGEN DEAMINASE GENE IN ACUTE INTERMITTENT PORPHYRIA 1987 ·The Lancet ·David H. Llewellyn, Noor Kalsheker, Paul R. Harrison, C. Picat, Paul‐Henri Roméo, George H. Elder, (unknown), Bernard Grandchamp, Y Nordmann, M. Goossens	44
14	A liver-type mutation in a case of pronounced erythrocyte phosphofructokinase deficiency without clinical expression 1983 ·Biochimica et Biophysica Acta (BBA) - General Subjects ·Jeanne Étiemble, Jacqueline Siméon, H. Buc, C. Picat, Mathieu Boulard, Pierre Boivin	7
15	ENZYMOPATHIES INDUCED BY DRUGS AND ACUTE LEUKAEMIA 1982 ·British Journal of Haematology ·Jeanne Étiemble, C. Picat, (unknown)	1
16	Influence of free Mg2+ on the kinetics of human erythrocyte phosphofructokinase 1981 ·Biochimie ·Jeanne Étiemble, Jacqueline Siméon, C. Picat, Pierre Boivin	7
17	Inherited erythrocyte phosphofructokinase deficiency: Molecular mechanism 1980 ·Human Genetics ·Jeanne Étiemble, C. Picat, Jean Simon, C Blatrix, Pierre Boivin	7
18	Gd(-) Rennes a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France 1980 ·Human Genetics ·C. Picat, Jeanne Étiemble, Pierre Boivin, P. Y. Le Prise	3
19	Red Blood Cell Enzyme Abnormalities in Patients Treated with Chemotherapy 1979 ·British Journal of Haematology ·Jeanne Étiemble, J. F. Bernard, C. Picat, D Belpomme, Pierre Boivin	19
20	Phosphofructokinase Isozymes from Human Organs andBlood Cells 1979 ·Enzyme ·Jeanne Étiemble, Jacqueline Siméon, C. Picat, Pierre Boivin	2

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