H Plauchu

1.7k total citations
29 papers, 632 citations indexed

About

H Plauchu is a scholar working on Genetics, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, H Plauchu has authored 29 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in H Plauchu's work include Vascular Anomalies and Treatments (6 papers), Genetic factors in colorectal cancer (3 papers) and RNA modifications and cancer (3 papers). H Plauchu is often cited by papers focused on Vascular Anomalies and Treatments (6 papers), Genetic factors in colorectal cancer (3 papers) and RNA modifications and cancer (3 papers). H Plauchu collaborates with scholars based in France, Italy and Germany. H Plauchu's co-authors include Elisabetta Buscarini, Gaëtan Lesca, Cesare Danesino, Carla Olivieri, Fabio Pagella, M. Le Merrer, Maurizio Grosso, L Reduzzi, Giacomo Pongiglione and Pasquale Blotta and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Journal of Thoracic and Cardiovascular Surgery.

In The Last Decade

H Plauchu

27 papers receiving 614 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H Plauchu France 11 307 230 151 122 108 29 632
Gennaro Mariano Lenato Italy 13 436 1.4× 364 1.6× 180 1.2× 36 0.3× 85 0.8× 27 704
Fatima S Govani United Kingdom 8 393 1.3× 331 1.4× 133 0.9× 26 0.2× 38 0.4× 9 648
Susan Schelley United States 13 385 1.3× 337 1.5× 263 1.7× 25 0.2× 258 2.4× 17 1.0k
Lora K. Hedges United States 18 97 0.3× 680 3.0× 88 0.6× 67 0.5× 128 1.2× 26 1.0k
Toshihito Fujii Japan 16 97 0.3× 139 0.6× 114 0.8× 106 0.9× 185 1.7× 54 913
Jeffrey A. Ucran United States 8 118 0.4× 82 0.4× 47 0.3× 103 0.8× 44 0.4× 10 696
Lucía Recio-Poveda Spain 12 189 0.6× 150 0.7× 102 0.7× 24 0.2× 9 0.1× 24 388
Yoshihisa Fukushima Japan 15 40 0.1× 98 0.4× 150 1.0× 37 0.3× 92 0.9× 80 733
Virginia Albiñana Spain 13 265 0.9× 218 0.9× 138 0.9× 14 0.1× 15 0.1× 30 471
Valentina Zernetkina United States 11 388 1.3× 79 0.3× 229 1.5× 88 0.7× 33 0.3× 20 740

Countries citing papers authored by H Plauchu

Since Specialization
Citations

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

Fields of papers citing papers by H Plauchu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Plauchu

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

All Works

20 of 20 papers shown
1.
Plauchu, H, Julie De Backer, Anne De Paepe, et al.. (2009). 3.3 EFFECT OF CELIPROLOL ON PREVENTION OF CARDIOVASCULAR EVENTS IN VASCULAR EHLERS-DANLOS SYNDROME. Artery Research. 3(4). 153–153. 1 indexed citations
2.
Olivieri, Carla, Fabio Pagella, L Semino, et al.. (2006). Echocardiographic screening discloses increased values of pulmonary artery systolic pressure in 9 of 68 unselected patients affected with hereditary hemorrhagic telangiectasia. Genetics in Medicine. 8(3). 183–190. 39 indexed citations
3.
Buscarini, Elisabetta, H Plauchu, Robert I. White, et al.. (2006). Liver involvement in hereditary hemorrhagic telangiectasia: consensus recommendations. Liver International. 26(9). 1040–1046. 101 indexed citations
4.
Sève, P., Olivier Dubreuil, Fadi Farhat, et al.. (2005). Acute mitral regurgitation caused by papillary muscle rupture in the immediate postpartum period revealing Ehlers-Danlos syndrome type IV. Journal of Thoracic and Cardiovascular Surgery. 129(3). 680–681. 10 indexed citations
5.
Buscarini, Elisabetta, Cesare Danesino, Carla Olivieri, et al.. (2004). Doppler Ultrasonographic Grading of Hepatic Vascular Malformations in Hereditary Hemorrhagic Telangiectasia - Results of Extensive Screening. Ultraschall in der Medizin - European Journal of Ultrasound. 25(5). 348–355. 73 indexed citations
6.
Buscarini, Elisabetta, Cesare Danesino, H Plauchu, et al.. (2004). High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia. Ultrasound in Medicine & Biology. 30(9). 1089–1097. 74 indexed citations
7.
Morlé, Laurette, Muriel Bozon, Laurent Duret, et al.. (2004). Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome 15q12–q15 and refinement to a 4.4 Mb region. European Journal of Human Genetics. 12(7). 574–578. 6 indexed citations
8.
Faivre, Laurence, M. Le Merrer, Stanislas Lyonnet, et al.. (2002). Clinical and genetic heterogeneity of Seckel syndrome. American Journal of Medical Genetics. 112(4). 379–383. 43 indexed citations
9.
Martin‐Denavit, Tanguy, et al.. (2001). Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?. Clinical Genetics. 60(2). 125–131. 5 indexed citations
10.
Morlé, Laurette, Muriel Bozon, Jean‐Christophe Zech, et al.. (2000). A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15. The American Journal of Human Genetics. 67(6). 1592–1597. 35 indexed citations
11.
Dumortier, Jérôme, et al.. (2000). [Hepatic vascular malformations in Rendu-Osler disease].. PubMed. 24(1). 89–93. 7 indexed citations
12.
Mornet, Étienne, A. Taillandier, Fiona Kaper, et al.. (1998). Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia. European Journal of Human Genetics. 6(4). 308–314. 97 indexed citations
13.
Legeai‐Mallet, Laurence, Patricia Margaritte‐Jeannin, M. Le Merrer, et al.. (1997). An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses. Human Genetics. 99(3). 298–302. 29 indexed citations
14.
Plauchu, H, et al.. (1984). [Acro-coxo-mesomelic dwarfism: a new variety of autosomal recessive dwarfism].. PubMed. 27(2). 83–7. 1 indexed citations
15.
Bouvier, R, et al.. (1981). [Familial infradiaphragmatic total anomalous pulmonary venous return].. PubMed. 36(6). 463–8. 3 indexed citations
16.
Plauchu, H, et al.. (1981). [Gonadic dysgenesis and dicentric chromosome Y. A report of two cases, one of which had a gonadoblastoma (author's transl)].. PubMed. 10(8). 839–44. 2 indexed citations
17.
Plauchu, H, et al.. (1978). [Hereditary bisalbuminemia. Study of a new familial case in France (author's transl)].. PubMed. 36(1). 11–7. 1 indexed citations
18.
Claustrat, Bruno, et al.. (1976). [Proceedings: Frequency of antigonadotropins antibodies in central hypogonadisms (author's transl)].. PubMed. 36(6). 337–8. 5 indexed citations
19.
Chambon, Aurélie, et al.. (1975). [Triploidy in the child. II. Evaluation of data on genotype and pathogenesis].. PubMed. 30(4). 371–89. 1 indexed citations
20.
Plauchu, H, et al.. (1975). [Lipo-atrophic diabetes].. PubMed. 30(8). 837–49. 2 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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