P.F. Ippel
Impact in
-
- Genetic Neurodegenerative Diseases
- Developmental Biology top 10%
- Congenital limb and hand anomalies
Papers in
-
- Genetic Neurodegenerative Diseases 7
- Genetics 6
- Genomic variations and chromosomal abnormalities 2
- Dermatoglyphics and Human Traits 1
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Egbert Bakker (4 shared papers)Marianne de Visser (5 shared papers)Edo M Hoogerwaard (3 shared papers)Arthur A.M. Wilde (3 shared papers)Nico J. Leschot (3 shared papers)Danielle F. Majoor‐Krakauer (3 shared papers)Anthonie J. van Essen (2 shared papers)Frits A. Beemer (7 shared papers)
- Journals
- Clinical Genetics (3 papers)Neuromuscular Disorders (2 papers)Journal of Neurology (2 papers)Neurology (2 papers)Human Genetics (2 papers)
- Partner nations
- NetherlandsGermanyUnited States
In The Last Decade
P.F. Ippel
32 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 39
- Cellular and Molecular Neuroscience 312
- Developmental Biology 27
- Aging 7
- Cardiology and Cardiovascular Medicine 102
- Molecular Biology 231
Countries citing papers authored by P.F. Ippel
This map shows the geographic impact of P.F. Ippel'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 P.F. Ippel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P.F. Ippel more than expected).
Fields of papers citing papers by P.F. Ippel
This network shows the impact of papers produced by P.F. Ippel. 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 P.F. Ippel. The network helps show where P.F. Ippel may publish in the future.
Co-authors
The 25 scholars most cited alongside P.F. Ippel, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 191 | |
| 2 | 1999 | 189 | |
| 3 | 1999 | 145 | |
| 4 | 2010 | 80 | |
| 5 | 2001 | 51 | |
| 6 | 2011 | 51 | |
| 7 | 1996 | 42 | |
| 8 | 2009 | 42 | |
| 9 | 1985 | 40 | |
| 10 | 2005 | 35 | |
| 11 | 2005 | 30 | |
| 12 | 1984 | 28 | |
| 13 | 1992 | 26 | |
| 14 | 2000 | 20 | |
| 15 | 2002 | 19 | |
| 16 | 1998 | 15 | |
| 17 | 1994 | 12 | |
| 18 | 2008 | 12 | |
| 19 | 1992 | 11 | |
| 20 | 1994 | 11 |
About P.F. Ippel
P.F. Ippel is a scholar working on Cellular and Molecular Neuroscience, Genetics, Pediatrics, Perinatology and Child Health, Neurology and Developmental Biology, having authored 33 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Muscle Physiology and Disorders (5 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Dermatoglyphics and Human Traits (1 paper), Congenital limb and hand anomalies (1 paper), Cytomegalovirus and herpesvirus research (1 paper) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (312 citations), Developmental Biology (27 citations), Aging (7 citations), Cardiology and Cardiovascular Medicine (102 citations) and Molecular Biology (231 citations). P.F. Ippel has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Egbert Bakker, Marianne de Visser, Edo M Hoogerwaard, Arthur A.M. Wilde, Nico J. Leschot, Danielle F. Majoor‐Krakauer, Anthonie J. van Essen, Frits A. Beemer, Poll A. van der Wouw and Richard J. Sinke. Their work appears in journals such as Clinical Genetics, Neuromuscular Disorders, Journal of Neurology, Neurology and Human 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.