Harriet von Koskull
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 11
- Connective tissue disorders research 3
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- Prenatal Screening and Diagnostics 17
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research 5
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- Cell Adhesion Molecules Research 4
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- Chromosomal and Genetic Variations 5
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- Erythrocyte Function and Pathophysiology 3
- Co-authors
- Perttì AulaIsmo VirtanenPirkko ÄmmäläRiitta SalonenJean‐Louis MandelMaarit PeippoJaakko LeistiT Vartio
- Partner nations
- FinlandUnited StatesGermany
In The Last Decade
Harriet von Koskull
52 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 90
- Genetics 689
- Pediatrics, Perinatology and Child Health 272
- Cognitive Neuroscience 225
- Molecular Biology 465
- Immunology and Allergy 40
Countries citing papers authored by Harriet von Koskull
This map shows the geographic impact of Harriet von Koskull'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 Harriet von Koskull with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Harriet von Koskull more than expected).
Fields of papers citing papers by Harriet von Koskull
This network shows the impact of papers produced by Harriet von Koskull. 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 Harriet von Koskull. The network helps show where Harriet von Koskull may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Harriet von Koskull, 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 | 2009 | 2 | |
| 2 | 2008 | 28 | |
| 3 | 2003 | 276 | |
| 4 | FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 2000 | 2 |
| 5 | 1997 | 14 | |
| 6 | 1995 | 15 | |
| 7 | 1994 | 9 | |
| 8 | 1994 | 15 | |
| 9 | 1994 | 1 | |
| 10 | 1993 | 7 | |
| 11 | 1993 | 31 | |
| 12 | 1993 | 48 | |
| 13 | 1993 | 18 | |
| 14 | 1992 | 1 | |
| 15 | 1992 | 29 | |
| 16 | 1989 | 5 | |
| 17 | 1989 | 35 | |
| 18 | 1989 | 8 | |
| 19 | 1987 | 38 | |
| 20 | 1980 | 27 |
About Harriet von Koskull
Harriet von Koskull is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Immunology and Allergy, Cell Biology and Speech and Hearing, having authored 52 papers that have together received 1.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (5 papers), Chromosomal and Genetic Variations (5 papers), Cell Adhesion Molecules Research (4 papers), Erythrocyte Function and Pathophysiology (3 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Genetics (689 citations), Pediatrics, Perinatology and Child Health (272 citations), Cognitive Neuroscience (225 citations), Molecular Biology (465 citations) and Immunology and Allergy (40 citations). Harriet von Koskull has collaborated with scholars based in Finland, United States and Germany. Frequent co-authors include Perttì Aula, Ismo Virtanen, Pirkko Ämmälä, Riitta Salonen, Jean‐Louis Mandel, Maarit Peippo, Jaakko Leisti, T Vartio, Peter Steinbach and V.-P. Lehto. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Clinical Genetics, The American Journal of Human Genetics and Human Reproduction.
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.