H. Kruyer

1.2k citations

20 papers · 930 indexed · h-index 13

Pulmonary and Respiratory Medicine top 5%
Molecular Biology
Neurology top 5%
Genetics top 10%
Rheumatology top 10%

Co-authors: Xavier Estivill Antonia Gaona Conxi Lázaro Nicholas Lench Brandon J. Wainwright Elisabet Ars Peter Scambler Eduard Serra
Topics: Neurofibromatosis and Schwannoma Cases (8 papers)Sarcoma Diagnosis and Treatment (6 papers)Cystic Fibrosis Research Advances (6 papers)
Cited by: Neurology Pulmonary and Respiratory Medicine Genetics
Journals: Nature The American Journal of Human Genetics Genomics
Partner nations: Spain United Kingdom United States

In The Last Decade

H. Kruyer

20 papers receiving 904 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	NF1mutation rather than individual genetic variability is the main determinant of theNF1-transcriptional profile of mutations affecting splicing 2006 ·Human Mutation ·Eva Pros,Sara Larriba,Eva López,Anna Ravella,Manuela Gili,H. Kruyer,Joan Valls,Eduard Serra,Conxi Lázaro	16
2	First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene 2004 ·Prenatal Diagnosis ·(unknown),H. Kruyer,Carolina de la Torre,María Teresa Calvo,Virginia Nunes	12
3	Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation 1999 ·Prenatal Diagnosis ·Elisabet Ars,H. Kruyer,Antonia Gaona,Eduard Serra,Conxi Lázaro,Xavier Estivill	2
4	Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation 1999 ·Prenatal Diagnosis ·Elisabet Ars,H. Kruyer,Antonia Gaona,Eduard Serra,Conxi Lázaro,Xavier Estivill	12
5	A Clinical Variant of Neurofibromatosis Type 1: Familial Spinal Neurofibromatosis with a Frameshift Mutation in the NF1 Gene 1998 ·The American Journal of Human Genetics ·Elisabet Ars,H. Kruyer,Antonia Gaona,Pilar Casquero,Jordi Rosell,Vı́ctor Volpini,Eduard Serra,Conxi Lázaro,Xavier Estivill	34
6	Confirmation of a Double-Hit Model for the NF1Gene in Benign Neurofibromas 1997 ·The American Journal of Human Genetics ·Eduard Serra,Susana Puig,(unknown),Antonia Gaona,H. Kruyer,Elisabet Ars,Xavier Estivill,Conxi Lázaro	173
7	Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients 1996 ·Human Genetics ·Conxi Lázaro,Antonia Gaona,Peter Ainsworth,Romano Tenconi,Dominique Vidaud,H. Kruyer,Elisabet Ars,Vı́ctor Volpini,Xavier Estivill	75
8	Two further cases of mutation R1947X in the NF1 gene: screening for a relatively common recurrent mutation 1995 ·Human Genetics ·(unknown),H. Kruyer,Antonia Gaona,Xavier Estivill	16
9	Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism. 1995 ·PubMed ·Conxi Lázaro,Antonia Gaona,Michael Lynch,H. Kruyer,Anna Ravella,Xavier Estivill	34
10	Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins. 1994 ·PubMed ·H. Kruyer,Montserrat Milà,G. Glóver,Pablo Carbonell,F Ballesta,Xavier Estivill	79
11	Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families 1994 ·Human Genetics ·(unknown),H. Kruyer,G. Glóver,(unknown),Pablo Carbonell,(unknown),V. Volpini,Jordi Rosell,(unknown),(unknown),(unknown),F Ballesta,Xavier Estivill	21
12	Carrier detection and microsatellite analysis of duchenne and becker muscular dystrophy in spanish families 1994 ·Prenatal Diagnosis ·H. Kruyer,Merce Miranda,Vı́ctor Volpini,Xavier Estivill	4
13	Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1). 1994 ·Journal of Medical Genetics ·Sergi Castellvı́-Bel,T. Matilla,(unknown),H. Kruyer,Jordi Corral,Montserrat Milà,Xavier Estivill	9
14	Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene 1991 ·Genomics ·(unknown),Philip Stanier,Carol Wicking,Stephanie Halford,H. Kruyer,Nicholas Lench,Peter Scambler,Connie Hansen,Jeffrey C. Braman,Robert Williamson,Brandon J. Wainwright	84
15	A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis 1990 ·Genomics ·Michèle Ramsay,Brandon J. Wainwright,Martin Farrall,Xavier Estivill,Helen Sutherland,(unknown),R. Davies,Stephanie Halford,(unknown),Carol Wicking,Nicholas Lench,Ingrid Bauer,Claude Férec,Peter Farndon,H. Kruyer,Philip Stanier,R. Williamson,Peter Scambler	11
16	Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. 1988 ·PubMed ·G.M. Lathrop,M Farrall,P. O’Connell,Brandon J. Wainwright,M. Leppert,Yusuke Nakamura,Nicholas Lench,H. Kruyer,Michael Dean,(unknown)	50
17	A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers 1987 ·Cytogenetic and Genome Research ·Brandon J. Wainwright,Nicholas Lench,Kay E. Davies,Peter Scambler,H. Kruyer,R. Williamson,Tore Jahnsen,M Farrall	8
18	A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands 1987 ·Nature ·Xavier Estivill,(unknown),Peter Scambler,G. Bell,(unknown),Nicholas Lench,Gillian P. Bates,H. Kruyer,(unknown),Philip Stanier,Eila Watson,Robert Williamson,Brandon J. Wainwright	278
19	Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11. 1986 ·PubMed ·M Farrall,(unknown),Gillian P. Bates,G. Bell,Joseph Martin Bell,Kevin Davies,Xavier Estivill,H. Kruyer,Hai‐Yang Law,Nicholas Lench	11
20	Linkage of the Col1A2 collagen gene to cystic fibrosis 1985 ·UCL Discovery (University College London) ·Peter Scambler,(unknown),Martin Farrall,Jimmy D. Bell,Philip Stanier,Nicholas Lench,George W. Bell,H. Kruyer,(unknown),R Williamson	1

About H. Kruyer

H. Kruyer is a scholar working on Neurology, Pulmonary and Respiratory Medicine and Rheumatology, having authored 20 papers that have together received 930 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (8 papers), Sarcoma Diagnosis and Treatment (6 papers) and Cystic Fibrosis Research Advances (6 papers). The work is most often cited by research in Neurology (270 citations), Pulmonary and Respiratory Medicine (397 citations) and Genetics (251 citations). H. Kruyer has collaborated with scholars based in Spain, United Kingdom and United States. Frequent 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. Their work appears in journals such as Nature, The American Journal of Human Genetics and Genomics.

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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