D Fontan

1.4k total citations
43 papers, 719 citations indexed

About

D Fontan is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, D Fontan has authored 43 papers receiving a total of 719 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Neurology and 8 papers in Genetics. Recurrent topics in D Fontan's work include Muscle Physiology and Disorders (6 papers), Metabolism and Genetic Disorders (5 papers) and Epilepsy research and treatment (5 papers). D Fontan is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Metabolism and Genetic Disorders (5 papers) and Epilepsy research and treatment (5 papers). D Fontan collaborates with scholars based in France, Switzerland and Italy. D Fontan's co-authors include Jean‐Michel Pedespan, Jean‐François Chateil, Thierry Deonna, Eliane Roulet, Didier Lacombe, Muriel Brun, Delphine Denis, Olivier Brissaud, A. Vital and C Vital and has published in prestigious journals such as Annals of Neurology, Epilepsia and Acta Neuropathologica.

In The Last Decade

D Fontan

40 papers receiving 688 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D Fontan France	14	271	185	181	152	149	43	719
Kimiko Tamagawa Japan	17	392 1.4×	137 0.7×	179 1.0×	113 0.7×	163 1.1×	35	764
Aron J. Diament Brazil	14	214 0.8×	143 0.8×	127 0.7×	152 1.0×	75 0.5×	59	561
Karine Lascelles United Kingdom	16	295 1.1×	109 0.6×	137 0.8×	183 1.2×	136 0.9×	25	858
T Deonna Switzerland	14	180 0.7×	212 1.1×	174 1.0×	71 0.5×	203 1.4×	29	702
Ignacio Pascual Castroviejo Spain	11	170 0.6×	236 1.3×	182 1.0×	216 1.4×	131 0.9×	67	600
Sawa Yasumoto Japan	17	344 1.3×	569 3.1×	190 1.0×	345 2.3×	253 1.7×	44	947
Tomohiro Chiyonobu Japan	20	455 1.7×	140 0.8×	176 1.0×	217 1.4×	135 0.9×	56	966
Nina Barišić Croatia	17	396 1.5×	107 0.6×	53 0.3×	106 0.7×	261 1.8×	61	860
Ichiro Kuki Japan	13	203 0.7×	192 1.0×	106 0.6×	143 0.9×	107 0.7×	87	675
Shin Okazaki Japan	12	243 0.9×	148 0.8×	66 0.4×	160 1.1×	112 0.8×	79	620

Countries citing papers authored by D Fontan

Since Specialization

Citations

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

Fields of papers citing papers by D Fontan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Fontan

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

Fontan, D, et al.. (2002). Lupus néonatal et atteinte neurologique : une association fortuite ?. Archives de Pédiatrie. 9(5). 503–505. 7 indexed citations

Chabrol, B., Dominique Figarella‐Branger, M Coquet, et al.. (2001). X-linked myopathy with excessive autophagy: a clinicopathological study of five new families. Neuromuscular Disorders. 11(4). 376–388. 24 indexed citations

Denis, Delphine, Jean‐François Chateil, Muriel Brun, et al.. (2000). Schizencephaly: clinical and imaging features in 30 infantile cases. Brain and Development. 22(8). 475–483. 92 indexed citations

Ferreiro, Ana, B. Estournet, Danielle Château, et al.. (2000). Multi-minicore disease-searching for boundaries: Phenotype analysis of 38 cases. Annals of Neurology. 48(5). 745–757. 75 indexed citations

Sarlangue, J, et al.. (1998). Congenital Cutaneous Defects as Complications in Surviving Co-twins. Archives of Dermatology. 134(9). 1121–4. 33 indexed citations

Pedespan, Jean‐Michel, et al.. (1998). Myopathie facio-scapulohumérale et mosaïque germinale. Archives de Pédiatrie. 5(8). 880–883. 1 indexed citations

Marsac, C., Chantal Benelli, Isabelle Desguerre, et al.. (1997). Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1α deficiency. Human Genetics. 99(6). 785–792. 41 indexed citations

Coquet, M & D Fontan. (1997). X-linked vacuolated myopathy: a new family. Neuromuscular Disorders. 7(6-7). 432–432. 1 indexed citations

Pedespan, Jean‐Michel, et al.. (1996). Thromboses du sinus longitudinal supérieur chez l'enfant au cours de la première année de vie: aspects cliniques, imagerie etévolution. Archives de Pédiatrie. 3(6). 561–565. 7 indexed citations

10.

Humbertclaude, Véronique, et al.. (1996). Schizencéphalie et malformation du membre supérieur. Archives de Pédiatrie. 3(4). 357–359. 6 indexed citations

11.

Vogt, Nicolas, Dominique Récan, Bernard Malfoy, et al.. (1994). Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter. Human Genetics. 93(5). 563–7. 17 indexed citations

12.

Degoul, Françoise, Anne Vital, Monique Malgat, et al.. (1993). MERRF family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsies. Neuromuscular Disorders. 3(5-6). 593–597. 13 indexed citations

13.

Fontan, D, et al.. (1993). [Contribution of nuclear magnetic imaging in the diagnosis of Hallervorden-Spatz syndrome].. PubMed. 50(1). 35–7. 1 indexed citations

14.

Vital, Anne, C Vital, Jean‐Philippe Julien, & D Fontan. (1992). Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I. Acta Neuropathologica. 84(4). 433–6. 24 indexed citations

15.

Vital, A., C Vital, C Brechenmacher, D Fontan, & Y. Castaing. (1990). Chronic inflammatory demyelinating polyneuropathy in childhood: ultrastructural features of peripheral nerve biopsies in four cases. European Journal of Pediatrics. 149(9). 654–658. 9 indexed citations

16.

Chateil, Jean‐François, et al.. (1990). [Pelizaeus-Merzbacher disease: the diagnostic contribution of MRI].. PubMed. 47(4). 265–9. 2 indexed citations

17.

Lacombe, Didier, et al.. (1990). Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.. PubMed. 1(3-4). 273–7. 31 indexed citations

18.

Fontan, D, et al.. (1977). [Hypo-hyperparathyroidism in a boy with an 8-20 translocation in mosaicism].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 32(2). 171–9.

19.

Serville, F, et al.. (1973). [Karyotype 49, XXXXY in an infant].. PubMed. 28(1). 83–90. 1 indexed citations

20.

Martin, Carine, et al.. (1971). [A case of osteodysplasty (Melnick-Needles syndrome)].. PubMed. 28(4). 446–7. 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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