J P Harpey

644 total citations
21 papers, 442 citations indexed

About

J P Harpey is a scholar working on Molecular Biology, Epidemiology and Rheumatology. According to data from OpenAlex, J P Harpey has authored 21 papers receiving a total of 442 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Epidemiology and 4 papers in Rheumatology. Recurrent topics in J P Harpey's work include Myasthenia Gravis and Thymoma (2 papers), Muscle Physiology and Disorders (2 papers) and Metabolism and Genetic Disorders (2 papers). J P Harpey is often cited by papers focused on Myasthenia Gravis and Thymoma (2 papers), Muscle Physiology and Disorders (2 papers) and Metabolism and Genetic Disorders (2 papers). J P Harpey collaborates with scholars based in France, United Kingdom and United States. J P Harpey's co-authors include R Moulias, J M Goust, Dominique Vidaud, Michel Bahuau, Jean Michel Cayuela, Michel Vidaud, Justin S. Smith, Brigitte Assouline, Benjamin Alderete and David W. Kimmel and has published in prestigious journals such as The Lancet, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

J P Harpey

19 papers receiving 420 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J P Harpey France	9	232	98	84	58	58	21	442
Patricia N. Konrad United States	12	194 0.8×	37 0.4×	36 0.4×	21 0.4×	46 0.8×	20	610
Johji Inazawa Japan	10	308 1.3×	34 0.3×	34 0.4×	47 0.8×	67 1.2×	16	452
A. Merat Iran	14	167 0.7×	35 0.4×	57 0.7×	25 0.4×	32 0.6×	25	516
Esther Vamos Belgium	15	286 1.2×	54 0.6×	46 0.5×	22 0.4×	30 0.5×	21	533
Xiaoyan Qiu China	11	399 1.7×	61 0.6×	126 1.5×	85 1.5×	17 0.3×	26	618
Y Moromizato United States	7	371 1.6×	55 0.6×	38 0.5×	59 1.0×	8 0.1×	8	833
Shobhana Vora United States	19	504 2.2×	187 1.9×	23 0.3×	210 3.6×	190 3.3×	25	870
Stephanie Needham United Kingdom	9	370 1.6×	156 1.6×	87 1.0×	89 1.5×	8 0.1×	12	620
Hiroyuki Ishiguro Japan	15	210 0.9×	25 0.3×	61 0.7×	57 1.0×	9 0.2×	23	574
Valeria Bafunno Italy	14	233 1.0×	57 0.6×	32 0.4×	25 0.4×	140 2.4×	22	657

Countries citing papers authored by J P Harpey

Since Specialization

Citations

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

Fields of papers citing papers by J P Harpey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J P Harpey. 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 J P Harpey. The network helps show where J P Harpey may publish in the future.

Co-authorship network of co-authors of J P Harpey

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

Héron, Delphine, et al.. (2004). Early diagnosis of Maroteaux-Lamy syndrome in two patients with accelerated growth and advanced bone maturation. European Journal of Pediatrics. 163(6). 323–326. 16 indexed citations

Bahuau, Michel, Dominique Vidaud, Robert B. Jenkins, et al.. (1998). Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.. PubMed. 58(11). 2298–303. 121 indexed citations

Guicheney, Pascale, Yi He, Corinne Cruaud, et al.. (1998). PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.. Journal of Medical Genetics. 35(3). 211–217. 45 indexed citations

Bahuau, Michel, Dominique Vidaud, M Kujas, et al.. (1997). Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness.. PubMed. 40(2). 78–91. 18 indexed citations

Andresen, Brage Storstein, Peter Bross, Szabolcs Udvari, et al.. (1997). The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?. Human Molecular Genetics. 6(5). 695–707. 105 indexed citations

Harpey, J P, et al.. (1996). Nécrose aiguë des noyaux gris d'évolution favorable lors d'une encéphalite à mycoplasme. Archives de Pédiatrie. 3(11). 1107–1110. 8 indexed citations

Charpentier, C., et al.. (1995). L-carnitine: a way to decrease cellular toxicity of ifosfamide?. European Journal of Pediatrics. 154(8). 686–687. 7 indexed citations

Pierot, Laurent, et al.. (1994). Acute bilateral striatal necrosis in an infant: CT and MRI. Neuroradiology. 36(3). 245–246. 6 indexed citations

Noseda, G, et al.. (1990). [Rendu Osler disease revealed by ruptured cerebral arterial aneurysm in an infant].. PubMed. 47(10). 741–2. 13 indexed citations

10.

Eymard, B., et al.. (1989). [Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)].. PubMed. 145(10). 696–701. 11 indexed citations

11.

Marlhens, F., Jamel Chelly, J.‐C. Kaplan, et al.. (1987). Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia. Human Genetics. 77(4). 379–383. 12 indexed citations

12.

Eymard, B., Élodie Morel, J P Harpey, et al.. (1986). [Assay of anti-acetylcholine receptor antibodies in myasthenic syndromes of newborn infants].. PubMed. 15(22). 1019–22. 2 indexed citations

13.

Leeming, R.J., et al.. (1982). TETRAHYDROFOLATE AND HYDROXOCOBOLAMIN IN THE MANAGEMENT OF DIHYDROPTERIDINE REDUCTASE DEFICIENCY. Journal of Intellectual Disability Research. 26(1). 21–25. 5 indexed citations

14.

Roy, Christopher D., et al.. (1981). [Pseudohypoaldosteronism: familial forms. Eight case-reports, with a review of the literature (author's transl)].. PubMed. 28(15). 553–32. 2 indexed citations

15.

Roy, Christopher D., M Roger, L Boccon-Gibod, et al.. (1980). CLINICAL, CYTOGENETICAL, HISTOLOGICAL, IMMUNOLOGICAL AND HORMONAL STUDIES IN A CASE OF TRUE HERMAPHRODITISM. Clinical Endocrinology. 12(5). 423–434. 6 indexed citations

16.

Roger, M, Christopher D. Roy, M Fellous, et al.. (1980). [Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditism (author's transl)].. PubMed. 41(1). 73–5. 1 indexed citations

17.

Harpey, J P. (1973). DRUGS AND ???DISSEMINATED LUPUS ERYTHEMATOSUS???. Adverse Drug Reaction Bulletin. 43(1). 140–143. 5 indexed citations

18.

Harpey, J P, et al.. (1971). LUPUS-LIKE SYNDROME INDUCED BY D-PENICILLAMINE IN WILSON'S DISEASE. The Lancet. 297(7693). 292–292. 51 indexed citations

19.

Goust, J M, et al.. (1971). [Immunological approach to chronic rheumatoid polyarthritis: 1st results].. PubMed. 79(38). 1687–1687. 1 indexed citations

20.

Harpey, J P, et al.. (1971). [Lupoid syndrome due to D-penicillamine associated with Wilson's disease: clinical study of a case].. PubMed. 122(2). 255–60. 5 indexed citations

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