A Joannard

910 total citations
34 papers, 208 citations indexed

About

A Joannard is a scholar working on Epidemiology, Genetics and Surgery. According to data from OpenAlex, A Joannard has authored 34 papers receiving a total of 208 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Epidemiology, 6 papers in Genetics and 5 papers in Surgery. Recurrent topics in A Joannard's work include Metabolism and Genetic Disorders (4 papers), Glycogen Storage Diseases and Myoclonus (3 papers) and Genetic Syndromes and Imprinting (2 papers). A Joannard is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Glycogen Storage Diseases and Myoclonus (3 papers) and Genetic Syndromes and Imprinting (2 papers). A Joannard collaborates with scholars based in France, Tunisia and Switzerland. A Joannard's co-authors include Henri Roché, Didier Frappaz, P Tron, Jean Claude Gentet, Thierry Philip, Charles Raybaud, P Jalbert, Matthieu Carton, C Lapras and Éric Bouffet and has published in prestigious journals such as International Journal of Radiation Oncology*Biology*Physics, Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease.

In The Last Decade

A Joannard

32 papers receiving 197 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A Joannard France	9	98	48	41	28	27	34	208
Wanda A. Gordon United States	8	67 0.7×	22 0.5×	12 0.3×	16 0.6×	13 0.5×	9	309
A. M. Bardelli Italy	10	116 1.2×	11 0.2×	73 1.8×	8 0.3×	39 1.4×	23	265
N. Logghe Belgium	9	104 1.1×	14 0.3×	85 2.1×	26 0.9×	7 0.3×	14	243
Vicharn Panich Thailand	10	43 0.4×	267 5.6×	35 0.9×	19 0.7×	24 0.9×	19	391
Silvia Vannelli Italy	11	86 0.9×	12 0.3×	71 1.7×	8 0.3×	8 0.3×	29	270
Márta Czakó Hungary	11	112 1.1×	18 0.4×	141 3.4×	25 0.9×	5 0.2×	40	245
Konstantina Kosma Greece	10	130 1.3×	28 0.6×	137 3.3×	18 0.6×	6 0.2×	30	288
Manuel Méndez Spain	13	322 3.3×	98 2.0×	47 1.1×	62 2.2×	18 0.7×	46	473
Naama Orenstein Israel	10	103 1.1×	30 0.6×	123 3.0×	17 0.6×	15 0.6×	31	311
L.C. Stranc Canada	7	86 0.9×	11 0.2×	67 1.6×	17 0.6×	7 0.3×	10	230

Countries citing papers authored by A Joannard

Since Specialization

Citations

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

Fields of papers citing papers by A Joannard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Joannard

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

Slama, Abdelhamid, C. Lacroix, Violaine Planté‐Bordeneuve, et al.. (2005). Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome. Molecular Genetics and Metabolism. 84(4). 326–331. 34 indexed citations

Kahn, Philip, Lorella Minotti, Adnan Koudsié, et al.. (2003). Surgery in severe factor XIII deficiency: report of a case of epilepsy neurosurgery and review. Haemophilia. 9(1). 121–124. 8 indexed citations

Portes, V. des, Fiona Francis, Jean-Marc Pinard, et al.. (2002). So-called ‘cryptogenic’ partial seizures resulting from a subtle cortical dysgenesis due to adoublecortin gene mutation. Seizure. 11(4). 273–277. 13 indexed citations

Lucet, V., et al.. (2000). [Angelman syndrome and severe vagal hypertonia. Three pediatric case reports].. PubMed. 93(5). 559–63. 8 indexed citations

Bouffet, Éric, J Bernard, Didier Frappaz, et al.. (1992). M4 protocol for cerebellar medulloblastoma: Supratentorial radiotherapy may not be avoided. International Journal of Radiation Oncology*Biology*Physics. 24(1). 79–85. 47 indexed citations

Pin, Isabelle, et al.. (1990). [Meningo-encephalomyelitis in Lyme disease].. PubMed. 47(1). 39–41. 2 indexed citations

Gerdes, Anne‐Marie, T. Tønnesen, Nina Horn, et al.. (1990). Clinical expression of Menkes syndrome in females. Clinical Genetics. 38(6). 452–459. 23 indexed citations

François, Patrice, et al.. (1990). [Osteoarticular infections in newborn infants].. PubMed. 45(9). 611–7. 1 indexed citations

Plantaz, Dominique, et al.. (1987). [Hydranencephaly and congenital toxoplasmosis. Apropos of 4 cases].. PubMed. 42(3). 161–5. 4 indexed citations

10.

Bost, M, et al.. (1987). [Thrombocytosis and reduced levels of factor VIII in rheumatoid purpura in children].. PubMed. 41(5). 401–11. 1 indexed citations

11.

Andrini, P, et al.. (1985). [Bourneville's tuberous sclerosis of neonatal disclosure. Apropos of 2 cases].. PubMed. 40(8). 633–8. 1 indexed citations

12.

Joannard, A, et al.. (1980). [Hereditary deficiencies of the complement system].. PubMed. 35(4). 293–300. 1 indexed citations

13.

Rossignol, Annette MacKay, et al.. (1980). [Hypertension in 3 adolescents with Williams-Beuren syndrome].. PubMed. 35(3). 243–9. 1 indexed citations

14.

Joannard, A, et al.. (1978). [Spondylo-vertebral and spondylo-thoracic dysostosis. Clinical, radiological and genetic study, apropos of 7 observations].. PubMed. 33(2). 173–88. 12 indexed citations

15.

Joannard, A, et al.. (1978). Formes Myocloniques De La Chorée De Huntington. Revue d Electroencé phalographie et de Neurophysiologie Clinique. 8(1). 123–128. 2 indexed citations

16.

Sèle, B, et al.. (1977). [Ring 6-chromosome: a nonspecific clinical picture].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 20(4). 232–6. 9 indexed citations

17.

Joannard, A, et al.. (1977). [Kearns' syndrome with transitory hypocalcemia. Apropos of a case].. PubMed. 32(8). 797–806. 2 indexed citations

18.

Joannard, A, et al.. (1977). [Papilloma of the choroid plexus in children. Apropos of 2 recent cases].. PubMed. 32(1). 19–28. 1 indexed citations

19.

Joannard, A, et al.. (1974). [Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects].. PubMed. 29(8). 825–41. 3 indexed citations

20.

Joannard, A, et al.. (1971). [Dermatomyositis in children. Study of 22 cases].. PubMed. 26(5). 471–90. 1 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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