H. Kruyer

1.2k total citations
20 papers, 930 citations indexed

About

H. Kruyer is a scholar working on Pulmonary and Respiratory Medicine, Neurology and Molecular Biology. According to data from OpenAlex, H. Kruyer has authored 20 papers receiving a total of 930 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pulmonary and Respiratory Medicine, 9 papers in Neurology and 7 papers in Molecular Biology. Recurrent topics in H. Kruyer's work include Neurofibromatosis and Schwannoma Cases (8 papers), Sarcoma Diagnosis and Treatment (6 papers) and Cystic Fibrosis Research Advances (6 papers). H. Kruyer is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (8 papers), Sarcoma Diagnosis and Treatment (6 papers) and Cystic Fibrosis Research Advances (6 papers). H. Kruyer collaborates with scholars based in Spain, United Kingdom and United States. H. Kruyer's co-authors include Xavier Estivill, Antonia Gaona, Conxi Lázaro, Nicholas Lench, Brandon J. Wainwright, Elisabet Ars, Peter Scambler, Eduard Serra, Philip Stanier and Robert Williamson and has published in prestigious journals such as Nature, The American Journal of Human Genetics and Genomics.

In The Last Decade

H. Kruyer

20 papers receiving 904 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. Kruyer Spain 13 397 388 270 251 112 20 930
Diane Beysen Belgium 12 129 0.3× 397 1.0× 326 1.2× 357 1.4× 121 1.1× 20 951
Günter Assum Germany 17 102 0.3× 450 1.2× 227 0.8× 215 0.9× 92 0.8× 33 819
Eeva‐Mari Jouhilahti Finland 15 67 0.2× 507 1.3× 212 0.8× 121 0.5× 89 0.8× 23 830
Yves Lacassie United States 18 49 0.1× 475 1.2× 112 0.4× 425 1.7× 39 0.3× 70 952
Andrea L. Halliday United States 8 40 0.1× 307 0.8× 173 0.6× 177 0.7× 44 0.4× 9 751
Judith Goodship United Kingdom 11 112 0.3× 729 1.9× 50 0.2× 517 2.1× 30 0.3× 13 978
Dennis May Germany 8 126 0.3× 233 0.6× 51 0.2× 58 0.2× 76 0.7× 8 650
Gurbax S. Sekhon United States 17 42 0.1× 596 1.5× 187 0.7× 522 2.1× 18 0.2× 42 1.1k
Heleena Hurskainen Finland 7 108 0.3× 337 0.9× 496 1.8× 399 1.6× 22 0.2× 10 1.0k
Chiharu Torii Japan 16 75 0.2× 313 0.8× 54 0.2× 243 1.0× 106 0.9× 42 721

Countries citing papers authored by H. Kruyer

Since Specialization
Citations

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

Fields of papers citing papers by H. Kruyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Kruyer

This figure shows the co-authorship network connecting the top 25 collaborators of H. Kruyer. A scholar is included among the top collaborators of H. Kruyer 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. Kruyer. H. Kruyer 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.
Pros, Eva, Sara Larriba, Eva López, et al.. (2006). NF1mutation rather than individual genetic variability is the main determinant of theNF1-transcriptional profile of mutations affecting splicing. Human Mutation. 27(11). 1104–1114. 16 indexed citations
2.
Kruyer, H., et al.. (2004). First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene. Prenatal Diagnosis. 24(10). 787–789. 12 indexed citations
3.
Ars, Elisabet, H. Kruyer, Antonia Gaona, et al.. (1999). Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation. Prenatal Diagnosis. 19(8). 739–742. 2 indexed citations
4.
Ars, Elisabet, H. Kruyer, Antonia Gaona, et al.. (1999). Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation. Prenatal Diagnosis. 19(8). 739–742. 12 indexed citations
5.
Ars, Elisabet, H. Kruyer, Antonia Gaona, et al.. (1998). A Clinical Variant of Neurofibromatosis Type 1: Familial Spinal Neurofibromatosis with a Frameshift Mutation in the NF1 Gene. The American Journal of Human Genetics. 62(4). 834–841. 34 indexed citations
6.
Serra, Eduard, Susana Puig, Antonia Gaona, et al.. (1997). Confirmation of a Double-Hit Model for the NF1Gene in Benign Neurofibromas. The American Journal of Human Genetics. 61(3). 512–519. 173 indexed citations
7.
Lázaro, Conxi, Antonia Gaona, Peter Ainsworth, et al.. (1996). Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients. Human Genetics. 98(6). 696–699. 75 indexed citations
8.
Kruyer, H., et al.. (1995). Two further cases of mutation R1947X in the NF1 gene: screening for a relatively common recurrent mutation. Human Genetics. 96(3). 361–3. 16 indexed citations
9.
Lázaro, Conxi, Antonia Gaona, Michael Lynch, et al.. (1995). Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism.. PubMed. 57(5). 1044–9. 34 indexed citations
10.
Kruyer, H., Montserrat Milà, G. Glóver, et al.. (1994). Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.. PubMed. 54(3). 437–42. 79 indexed citations
11.
Kruyer, H., G. Glóver, Pablo Carbonell, et al.. (1994). Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families. Human Genetics. 94(4). 395–400. 21 indexed citations
12.
Kruyer, H., Merce Miranda, Vı́ctor Volpini, & Xavier Estivill. (1994). Carrier detection and microsatellite analysis of duchenne and becker muscular dystrophy in spanish families. Prenatal Diagnosis. 14(2). 123–130. 4 indexed citations
13.
Castellvı́-Bel, Sergi, T. Matilla, H. Kruyer, et al.. (1994). Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1).. Journal of Medical Genetics. 31(8). 654–655. 9 indexed citations
14.
Stanier, Philip, Carol Wicking, Stephanie Halford, et al.. (1991). Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene. Genomics. 10(2). 301–307. 84 indexed citations
15.
Ramsay, Michèle, Brandon J. Wainwright, Martin Farrall, et al.. (1990). A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis. Genomics. 6(1). 39–47. 11 indexed citations
16.
Lathrop, G.M., M Farrall, P. O’Connell, et al.. (1988). Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene.. PubMed. 42(1). 38–44. 50 indexed citations
17.
Wainwright, Brandon J., Nicholas Lench, Kay E. Davies, et al.. (1987). A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers. Cytogenetic and Genome Research. 45(3-4). 237–239. 8 indexed citations
18.
Estivill, Xavier, Peter Scambler, G. Bell, et al.. (1987). A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands. Nature. 326(6116). 840–845. 278 indexed citations
19.
Farrall, M, Gillian P. Bates, G. Bell, et al.. (1986). Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11.. PubMed. 39(6). 713–9. 11 indexed citations
20.
Scambler, Peter, Martin Farrall, Jimmy D. Bell, et al.. (1985). Linkage of the Col1A2 collagen gene to cystic fibrosis. UCL Discovery (University College London). 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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