Teppo Varilo
Impact in
- Genetics top 1%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Psychiatry and Mental health top 2%
- Schizophrenia research and treatment
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 16
- Genetic Associations and Epidemiology 16
- Genomics and Rare Diseases 11
- Genetics and Neurodevelopmental Disorders 9
- Digestive system and related health 3
- Co-authors
- Leena Peltonen (18 shared papers)Jouko Lönnqvist (15 shared papers)Irma Järvelä (11 shared papers)Tiina Paunio (13 shared papers)Tero Ylisaukko‐oja (6 shared papers)Timo Partonen (14 shared papers)Jaana Suvisaari (7 shared papers)Annamari Tuulio‐Henriksson (8 shared papers)
- Journals
- The American Journal of Human Genetics (8 papers)Molecular Psychiatry (6 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (3 papers)Psychiatry Research (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- FinlandUnited StatesUnited Kingdom
In The Last Decade
Teppo Varilo
51 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 112
- Genetics 1.3k
- Psychiatry and Mental health 478
- Cognitive Neuroscience 535
- Clinical Biochemistry 170
- Biological Psychiatry 45
Countries citing papers authored by Teppo Varilo
This map shows the geographic impact of Teppo Varilo'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 Teppo Varilo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Teppo Varilo more than expected).
Fields of papers citing papers by Teppo Varilo
This network shows the impact of papers produced by Teppo Varilo. 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 Teppo Varilo. The network helps show where Teppo Varilo may publish in the future.
Co-authors
The 25 scholars most cited alongside Teppo Varilo, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 254 | |
| 2 | 1999 | 230 | |
| 3 | 2002 | 194 | |
| 4 | 2007 | 160 | |
| 5 | 2007 | 145 | |
| 6 | 2005 | 132 | |
| 7 | 2008 | 112 | |
| 8 | 2004 | 96 | |
| 9 | 2003 | 89 | |
| 10 | 2007 | 88 | |
| 11 | 1998 | 86 | |
| 12 | 2002 | 72 | |
| 13 | 2006 | 71 | |
| 14 | The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population. | 1996 | 70 |
| 15 | 2003 | 68 | |
| 16 | 2004 | 65 | |
| 17 | 1998 | 60 | |
| 18 | 2002 | 59 | |
| 19 | 2001 | 57 | |
| 20 | 2011 | 56 |
About Teppo Varilo
Teppo Varilo is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Cognitive Neuroscience and Cellular and Molecular Neuroscience, having authored 51 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Genetic Associations and Epidemiology (16 papers), Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers), Schizophrenia research and treatment (4 papers), Digestive system and related health (3 papers) and Attention Deficit Hyperactivity Disorder (3 papers). The work is most often cited by research in Genetics (1.3k citations), Psychiatry and Mental health (478 citations), Cognitive Neuroscience (535 citations), Clinical Biochemistry (170 citations) and Biological Psychiatry (45 citations). Teppo Varilo has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Leena Peltonen, Jouko Lönnqvist, Irma Järvelä, Tiina Paunio, Tero Ylisaukko‐oja, Timo Partonen, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Raija Vanhala and William Hennah. Their work appears in journals such as The American Journal of Human Genetics, Molecular Psychiatry, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Psychiatry Research and European Journal of 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.