H. Kruyer
Impact in
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
-
- Cystic Fibrosis Research Advances
- Sarcoma Diagnosis and Treatment
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
Papers in
-
- Neurofibromatosis and Schwannoma Cases 8
- Neuroblastoma Research and Treatments 2
-
- Cystic Fibrosis Research Advances 7
- Sarcoma Diagnosis and Treatment 6
- Tracheal and airway disorders 2
- Co-authors
- Xavier Estivill (14 shared papers)Antonia Gaona (7 shared papers)Conxi Lázaro (7 shared papers)Nicholas Lench (8 shared papers)Brandon J. Wainwright (6 shared papers)Elisabet Ars (5 shared papers)Philip Stanier (5 shared papers)Peter James Scambler (6 shared papers)
- Journals
- Prenatal Diagnosis (4 papers)Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)Genomics (2 papers)Journal of Medical Genetics (1 paper)
- Partner nations
- SpainUnited KingdomUnited States
In The Last Decade
H. Kruyer
20 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 79
- Neurology 307
- Pulmonary and Respiratory Medicine 450
- Genetics 273
- Genetics 92
- Rheumatology 121
Countries citing papers authored by H. Kruyer
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
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-authors
The 25 scholars most cited alongside H. Kruyer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 304 | |
| 2 | 1997 | 199 | |
| 3 | Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins. | 1994 | 87 |
| 4 | 1991 | 84 | |
| 5 | 1996 | 82 | |
| 6 | Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. | 1988 | 53 |
| 7 | 1998 | 44 | |
| 8 | Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism. | 1995 | 41 |
| 9 | 1985 | 40 | |
| 10 | 1994 | 21 | |
| 11 | 2006 | 18 | |
| 12 | 1995 | 17 | |
| 13 | 2004 | 15 | |
| 14 | Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11. | 1986 | 12 |
| 15 | 1999 | 12 | |
| 16 | 1990 | 11 | |
| 17 | 1994 | 11 | |
| 18 | 1994 | 4 | |
| 19 | 1999 | 2 | |
| 20 | Linkage of the Col1A2 collagen gene to cystic fibrosis | 1985 | 1 |
About H. Kruyer
H. Kruyer is a scholar working on Neurology, Pulmonary and Respiratory Medicine, Rheumatology, Genetics and Molecular Biology, having authored 21 papers that have together received 1.1k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (8 papers), Cystic Fibrosis Research Advances (7 papers), Sarcoma Diagnosis and Treatment (6 papers), Soft tissue tumor case studies (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Tracheal and airway disorders (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Neuroblastoma Research and Treatments (2 papers). The work is most often cited by research in Neurology (307 citations), Pulmonary and Respiratory Medicine (450 citations), Genetics (273 citations), Genetics (92 citations) and Rheumatology (121 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, Philip Stanier, Peter James Scambler, Eduard Serra and Robert Brady Williamson. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, The American Journal of Human Genetics, Genomics and Journal of Medical Genetics.
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.