Karin E. M. Diderich
Impact in
- Aging top 5%
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
-
- Prenatal Screening and Diagnostics 30
- Fetal and Pediatric Neurological Disorders 11
- Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Joost Gribnau (1 shared paper)Roberta Calzolari (1 shared paper)Peter Fraser (1 shared paper)Malgorzata I. Srebniak (36 shared papers)Diane Van Opstal (31 shared papers)Jan H.J. Hoeijmakers (9 shared papers)Marieke Joosten (27 shared papers)Maarten F. C. M. Knapen (21 shared papers)
- Journals
- Prenatal Diagnosis (10 papers)Molecular Cytogenetics (5 papers)Clinical Genetics (4 papers)European Journal of Human Genetics (3 papers)Acta Obstetricia Et Gynecologica Scandinavica (2 papers)
- Partner nations
- NetherlandsUnited StatesUnited Kingdom
In The Last Decade
Karin E. M. Diderich
56 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 77
- Aging 78
- Pediatrics, Perinatology and Child Health 520
- Genetics 406
- Molecular Biology 790
- Cancer Research 137
Countries citing papers authored by Karin E. M. Diderich
This map shows the geographic impact of Karin E. M. Diderich'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 Karin E. M. Diderich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin E. M. Diderich more than expected).
Fields of papers citing papers by Karin E. M. Diderich
This network shows the impact of papers produced by Karin E. M. Diderich. 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 Karin E. M. Diderich. The network helps show where Karin E. M. Diderich may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin E. M. Diderich, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 296 | |
| 2 | 2006 | 195 | |
| 3 | 2005 | 114 | |
| 4 | 2012 | 65 | |
| 5 | 2015 | 57 | |
| 6 | 2012 | 56 | |
| 7 | 2005 | 53 | |
| 8 | 2011 | 52 | |
| 9 | 2012 | 43 | |
| 10 | 2014 | 42 | |
| 11 | 2020 | 40 | |
| 12 | 2014 | 38 | |
| 13 | 2016 | 38 | |
| 14 | 2020 | 38 | |
| 15 | 2014 | 37 | |
| 16 | 2016 | 35 | |
| 17 | 2016 | 30 | |
| 18 | 2013 | 28 | |
| 19 | 2008 | 26 | |
| 20 | 2020 | 25 |
About Karin E. M. Diderich
Karin E. M. Diderich is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Surgery and Infectious Diseases, having authored 61 papers that have together received 1.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (30 papers), Genomic variations and chromosomal abnormalities (11 papers), Fetal and Pediatric Neurological Disorders (11 papers), Genomics and Rare Diseases (7 papers), DNA Repair Mechanisms (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Parvovirus B19 Infection Studies (4 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Aging (78 citations), Pediatrics, Perinatology and Child Health (520 citations), Genetics (406 citations), Molecular Biology (790 citations) and Cancer Research (137 citations). Karin E. M. Diderich has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Joost Gribnau, Roberta Calzolari, Peter Fraser, Malgorzata I. Srebniak, Diane Van Opstal, Jan H.J. Hoeijmakers, Marieke Joosten, Maarten F. C. M. Knapen, Lutgarde Govaerts and Attie T. J. I. Go. Their work appears in journals such as Prenatal Diagnosis, Molecular Cytogenetics, Clinical Genetics, European Journal of Human Genetics and Acta Obstetricia Et Gynecologica Scandinavica.
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.