Teppo Varilo

5.4k total citations
51 papers, 2.7k citations indexed

About

Teppo Varilo is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Teppo Varilo has authored 51 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 14 papers in Molecular Biology and 9 papers in Cognitive Neuroscience. Recurrent topics in Teppo Varilo's work include Genetic Associations and Epidemiology (17 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genomics and Rare Diseases (11 papers). Teppo Varilo is often cited by papers focused on Genetic Associations and Epidemiology (17 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genomics and Rare Diseases (11 papers). Teppo Varilo collaborates with scholars based in Finland, United States and United Kingdom. Teppo Varilo's 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 and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Neurology.

In The Last Decade

Teppo Varilo

51 papers receiving 2.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Teppo Varilo Finland 29 1.3k 1.0k 542 491 265 51 2.7k
Petter Strømme Norway 28 1.1k 0.9× 1.2k 1.2× 311 0.6× 243 0.5× 296 1.1× 76 2.7k
Ann E. Pulver United States 32 1.1k 0.8× 991 1.0× 515 1.0× 985 2.0× 284 1.1× 54 2.9k
Roberto Sacco Italy 28 931 0.7× 759 0.7× 1.3k 2.3× 567 1.2× 173 0.7× 67 2.3k
Jonathan L. Haines United States 35 1.7k 1.3× 1.6k 1.6× 1.1k 2.0× 318 0.6× 469 1.8× 66 4.2k
Michael S. Hildebrand Australia 36 854 0.7× 1.6k 1.6× 628 1.2× 333 0.7× 246 0.9× 167 4.0k
Miki Bundo Japan 29 1.3k 1.0× 2.3k 2.3× 266 0.5× 639 1.3× 471 1.8× 70 3.6k
Tim Becker Germany 32 1.1k 0.8× 1.3k 1.3× 318 0.6× 411 0.8× 558 2.1× 122 3.6k
Bruria Ben‐Zeev Israel 33 994 0.8× 1.3k 1.3× 530 1.0× 892 1.8× 737 2.8× 105 3.4k
Isabelle Gourfinkel‐An France 21 883 0.7× 955 0.9× 447 0.8× 1.1k 2.2× 905 3.4× 45 2.3k
Chihiro Kakiuchi Japan 26 684 0.5× 990 1.0× 151 0.3× 499 1.0× 265 1.0× 51 2.1k

Countries citing papers authored by Teppo Varilo

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Teppo Varilo

This figure shows the co-authorship network connecting the top 25 collaborators of Teppo Varilo. A scholar is included among the top collaborators of Teppo Varilo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Teppo Varilo. Teppo Varilo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Polla, D.L., Elisa Rahikkala, Michaela K. Bode, et al.. (2019). Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population. European Journal of Human Genetics. 27(8). 1235–1243. 7 indexed citations
2.
Torniainen, Minna, Juho Wedenoja, Teppo Varilo, et al.. (2012). Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?. Psychiatry Research. 208(2). 111–117. 1 indexed citations
3.
Nyman, Emma, Anu Loukola, Teppo Varilo, et al.. (2012). Sex-specific influence of DRD 2 on ADHD-type temperament in a large population-based birth cohort. Psychiatric Genetics. 22(4). 197–201. 1 indexed citations
4.
Haataja, Ritva, Minna K. Karjalainen, Kari Teramo, et al.. (2011). Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis. PLoS Genetics. 7(2). e1001293–e1001293. 53 indexed citations
5.
Lahtela, Jenni, Heidi O. Nousiainen, Vedran Stefanović, et al.. (2010). MutantCHUKand Severe Fetal Encasement Malformation. New England Journal of Medicine. 363(17). 1631–1637. 41 indexed citations
6.
Wedenoja, Juho, Annamari Tuulio‐Henriksson, Jaana Suvisaari, et al.. (2009). Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia. Biological Psychiatry. 67(10). 983–991. 51 indexed citations
7.
Nyman, Emma, Anu Loukola, Teppo Varilo, et al.. (2008). Impact of the dopamine receptor gene family on temperament traits in a population‐based birth cohort. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(6). 854–865. 15 indexed citations
8.
Paunio, Tiina, Ritva Arajärvi, Joseph D. Terwilliger, et al.. (2008). Linkage analysis of schizophrenia controlling for population substructure. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(6). 827–835. 12 indexed citations
9.
Nyman, Emma, Matthew N. Ogdie, Anu Loukola, et al.. (2007). ADHD Candidate Gene Study in a Population-Based Birth Cohort: Association with DBH and DRD2. Journal of the American Academy of Child & Adolescent Psychiatry. 46(12). 1614–1621. 48 indexed citations
10.
Wedenoja, Juho, Anu Loukola, Annamari Tuulio‐Henriksson, et al.. (2007). Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families. Molecular Psychiatry. 13(7). 673–684. 83 indexed citations
11.
Forsman, Eva, Susanna Lemmelä, Teppo Varilo, et al.. (2003). The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study.. PubMed. 9. 217–22. 32 indexed citations
12.
Auranen, Mari, Teppo Varilo, Reija Alén, et al.. (2003). Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland. Molecular Psychiatry. 8(10). 879–884. 29 indexed citations
13.
Tuulio‐Henriksson, Annamari, Ritva Arajärvi, Timo Partonen, et al.. (2003). Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients. Biological Psychiatry. 54(6). 623–628. 62 indexed citations
14.
Hovatta, Iiris, Teppo Varilo, Jaana Suvisaari, et al.. (1999). A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci. The American Journal of Human Genetics. 65(4). 1114–1124. 219 indexed citations
15.
Visapää, Ilona, Riitta Salonen, Teppo Varilo, Paulina Paavola, & Leena Peltonen. (1999). Assignment of the Locus for Hydrolethalus Syndrome to a Highly Restricted Region on 11q23-25. The American Journal of Human Genetics. 65(4). 1086–1095. 21 indexed citations
16.
Järvelä, Irma, Nabil Enattah, Jorma Kokkonen, et al.. (1998). Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene. The American Journal of Human Genetics. 63(4). 1078–1085. 50 indexed citations
17.
Pekkarinen, P., Marjo Kestilä, Juha Paloneva, et al.. (1998). Fine-Scale Mapping of a Novel Dementia Gene, PLOSL, by Linkage Disequilibrium. Genomics. 54(2). 307–315. 19 indexed citations
18.
Visapää, Ilona, Vineta Fellman, Teppo Varilo, et al.. (1998). Assignment of the Locus for a New Lethal Neonatal Metabolic Syndrome to 2q33-37. The American Journal of Human Genetics. 63(5). 1396–1403. 17 indexed citations
19.
Fellman, Vineta, Juhani Rapola, Helena Pihko, Teppo Varilo, & Kari O. Raivio. (1998). Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria. The Lancet. 351(9101). 490–493. 75 indexed citations
20.
Varilo, Teppo, Kaisu Nikali, Anu Suomalainen, Tuula Lönnqvist, & Leena Peltonen. (1996). Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.. Genome Research. 6(9). 870–875. 19 indexed citations

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.

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