Muriel Giansily

487 total citations
7 papers, 385 citations indexed

About

Muriel Giansily is a scholar working on Genetics, Hematology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Muriel Giansily has authored 7 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 5 papers in Hematology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Muriel Giansily's work include Hemoglobinopathies and Related Disorders (3 papers), Iron Metabolism and Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Muriel Giansily is often cited by papers focused on Hemoglobinopathies and Related Disorders (3 papers), Iron Metabolism and Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Muriel Giansily collaborates with scholars based in France, Netherlands and Italy. Muriel Giansily's co-authors include Jean‐François Schved, Suzette Beguı́n, Elena Santagostino, Flora Peyvandi, H.C. Hemker, Raed Al Dieri, Pier Mannuccio Mannucci, Mireille Claustres, Marie Desgeorges and Jacques Demaille and has published in prestigious journals such as Blood, Human Molecular Genetics and British Journal of Haematology.

In The Last Decade

Muriel Giansily

7 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Muriel Giansily France	7	255	101	98	80	47	7	385
B. Ravid Israel	8	247 1.0×	43 0.4×	119 1.2×	29 0.4×	56 1.2×	8	334
James Uprichard United Kingdom	8	235 0.9×	27 0.3×	114 1.2×	45 0.6×	30 0.6×	16	355
Hubert Galinat France	11	112 0.4×	34 0.3×	107 1.1×	61 0.8×	66 1.4×	34	277
F. A. Scaraggi Italy	11	424 1.7×	21 0.2×	110 1.1×	40 0.5×	41 0.9×	17	505
Elisabetta Cosi Italy	10	163 0.6×	21 0.2×	110 1.1×	26 0.3×	24 0.5×	37	272
Christine Trzeciak France	5	287 1.1×	27 0.3×	74 0.8×	59 0.7×	39 0.8×	7	326
Sam Ackroyd United Kingdom	4	176 0.7×	57 0.6×	105 1.1×	12 0.1×	14 0.3×	5	233
Marianne Sigaud France	10	331 1.3×	14 0.1×	114 1.2×	52 0.7×	84 1.8×	26	424
D. RAPSON Canada	8	501 2.0×	26 0.3×	86 0.9×	26 0.3×	92 2.0×	13	582
Mario Lapecorella Italy	9	179 0.7×	31 0.3×	63 0.6×	23 0.3×	14 0.3×	17	265

Countries citing papers authored by Muriel Giansily

Since Specialization

Citations

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

Fields of papers citing papers by Muriel Giansily

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muriel Giansily

This figure shows the co-authorship network connecting the top 25 collaborators of Muriel Giansily. A scholar is included among the top collaborators of Muriel Giansily 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 Muriel Giansily. Muriel Giansily 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:

7 of 7 papers shown

1.

Fawzy, Manal S., Dina El‐Metwally, Muriel Giansily, et al.. (2007). Rapid Detection of β-Thalassemia Alleles in Egypt Using Naturally or Amplified Created Restriction Sites and Direct Sequencing: A Step in Disease Control. Hemoglobin. 31(1). 49–62. 30 indexed citations

2.

Dieri, Raed Al, Flora Peyvandi, Elena Santagostino, et al.. (2002). The Thrombogram in Rare Inherited Coagulation Disorders: Its Relation to Clinical Bleeding. Thrombosis and Haemostasis. 88(10). 576–582. 228 indexed citations

3.

Giansily, Muriel, et al.. (2001). Denaturing gradient gel electrophoresis screening for mutations in the hereditary hyperferritinaemia cataract syndrome. British Journal of Haematology. 112(1). 51–54. 16 indexed citations

4.

Giansily, Muriel, et al.. (1999). Haplotype Analysis of the HFE Gene: Implications for the Origins of Hemochromatosis Related Mutations. Blood Cells Molecules and Diseases. 25(3). 166–169. 15 indexed citations

5.

Giansily, Muriel, et al.. (1998). An Even Easier Method for One-Step Detection of Both FV Leiden and FII G20210A Transition. Blood. 92(9). 3478–3479. 10 indexed citations

6.

Giansily, Muriel, et al.. (1998). An Even Easier Method for One-Step Detection of Both FV Leiden and FII G20210A Transition. Blood. 92(9). 3478–3479. 6 indexed citations

7.

Claustres, Mireille, et al.. (1993). Analysis of the 27 exons and flanking regions of the cystic fibrosis gene: 40 different mutations account for 91.2% of the mutant alleles in Southern France. Human Molecular Genetics. 2(8). 1209–1213. 80 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