Guus Hamers
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
- Genetic and rare skin diseases. 1
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- Prenatal Screening and Diagnostics 7
- Co-authors
- J.J.M. Engelen (8 shared papers)Joep Geraedts (5 shared papers)C. T. R. M. Schrander‐Stumpel (4 shared papers)E Haan (1 shared paper)M.J. Wagner (1 shared paper)Moshe Frydman (1 shared paper)Julia Parrish (1 shared paper)Patrick J. Willems (1 shared paper)
- Journals
- Clinical Genetics (2 papers)Prenatal Diagnosis (2 papers)Human Genetics (2 papers)Molecular Cytogenetics (1 paper)Leukemia (1 paper)
- Partner nations
- NetherlandsBelgiumGermany
In The Last Decade
Guus Hamers
18 papers receiving 382 citations
Peers
Comparison fields: 5 of 44
- Genetics 245
- Developmental Biology 11
- Pediatrics, Perinatology and Child Health 75
- Genetics 29
- Oral Surgery 19
Countries citing papers authored by Guus Hamers
This map shows the geographic impact of Guus Hamers'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 Guus Hamers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Guus Hamers more than expected).
Fields of papers citing papers by Guus Hamers
This network shows the impact of papers produced by Guus Hamers. 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 Guus Hamers. The network helps show where Guus Hamers may publish in the future.
Co-authors
The 25 scholars most cited alongside Guus Hamers, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 95 | |
| 2 | 1994 | 79 | |
| 3 | 1998 | 41 | |
| 4 | 1999 | 21 | |
| 5 | 1990 | 20 | |
| 6 | 1991 | 19 | |
| 7 | 1988 | 19 | |
| 8 | 2004 | 19 | |
| 9 | 2011 | 14 | |
| 10 | 1998 | 13 | |
| 11 | 1989 | 12 | |
| 12 | 2003 | 11 | |
| 13 | 1996 | 9 | |
| 14 | 2005 | 7 | |
| 15 | Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child. | 2003 | 6 |
| 16 | 1994 | 4 | |
| 17 | 22q11 deletion: the Maastricht experience focussing on some unusual presentations | 1999 | 2 |
| 18 | 1999 | 2 | |
| 19 | 1998 | 0 |
About Guus Hamers
Guus Hamers is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Molecular Biology and Surgery, having authored 19 papers that have together received 393 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (7 papers), Chromosomal and Genetic Variations (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genomics and Chromatin Dynamics (2 papers), Dermatological and COVID-19 studies (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Genetics (245 citations), Developmental Biology (11 citations), Pediatrics, Perinatology and Child Health (75 citations), Genetics (29 citations) and Oral Surgery (19 citations). Guus Hamers has collaborated with scholars based in Netherlands, Belgium and Germany. Frequent co-authors include J.J.M. Engelen, Joep Geraedts, C. T. R. M. Schrander‐Stumpel, E Haan, M.J. Wagner, Moshe Frydman, Julia Parrish, Patrick J. Willems, H.-J. Lüdecke and Bernhard Horsthemke. Their work appears in journals such as Clinical Genetics, Prenatal Diagnosis, Human Genetics, Molecular Cytogenetics and Leukemia.
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.