Teppo Varilo

5.4k citations

51 papers · 2.7k indexed · h-index 29

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 38
- Genetic Associations and Epidemiology 17
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 11
- Genetics and Neurodevelopmental Disorders 10
Molecular Biology 14

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)Biological Psychiatry (2 papers)European Journal of Human Genetics (2 papers)
Partner nations: Finland United States United Kingdom

In The Last Decade

Teppo Varilo

51 papers receiving 2.5k citations

Peers

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-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.

Border = papers with Teppo Varilo Line = papers co-authored together Teppo Varilo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin The American Journal of Human Genetics ·Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen, Ilse Lappalainen, Petri Luoma, Maria Rantamäki, Gert Van Goethem, A. Löfgren, Peter Hackman, Anders Paetau, Seppo Kaakkola, Kari Majamaa, Teppo Varilo, Bjarne Udd, Helena Kääriäinen, Laurence A. Bindoff, Anu Suomalainen	2005	227
2	A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci The American Journal of Human Genetics ·Iiris Hovatta, Teppo Varilo, Jaana Suvisaari, Joseph D. Terwilliger, Vesa Ollikainen, Ritva Arajärvi, Hannu Juvonen, Marja-Liisa Kokko-Sahin, Leena Väisänen, Heikki Mannila, Jouko Lönnqvist, Leena Peltonen	1999	219
3	A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27 The American Journal of Human Genetics ·Mari Auranen, Raija Vanhala, Teppo Varilo, Kristin L. Ayers, Elli Kempas, Tero Ylisaukko‐oja, Janet S. Sinsheimer, Leena Peltonen, Irma Järvelä	2002	174
4	Association of DISC1 with autism and Asperger syndrome Molecular Psychiatry ·Helena Kilpinen, Tero Ylisaukko‐oja, William Hennah, Outi M. Palo, Teppo Varilo, Raija Vanhala, Taina Nieminen‐von Wendt, L. von Wendt, Tiina Paunio, Leena Peltonen	2007	150
5	Prevalence and Psychiatric Comorbidity of Attention-Deficit/Hyperactivity Disorder in an Adolescent Finnish Population Journal of the American Academy of Child & Adolescent Psychiatry ·Susan L. Smalley, James J. McGough, Irma Moilanen, Sandra K. Loo, Anja Taanila, Hanna Ebeling, Tuula Hurtig, Marika Kaakinen, Lorie A. Humphrey, James T. McCracken, Teppo Varilo, May Yang, Stanley F. Nelson, Leena Peltonen, Marjo‐Riitta Järvelin	2007	134
6	A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia Molecular Psychiatry ·William Hennah, Annamari Tuulio‐Henriksson, Tiina Paunio, Jesper Ekelund, Teppo Varilo, Timo Partonen, Tyrone D. Cannon, Jouko Lönnqvist, Leena Peltonen	2005	121
7	The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population The American Journal of Human Genetics ·Eveliina Jakkula, Karola Rehnström, Teppo Varilo, Olli Pietiläinen, Tiina Paunio, Nancy L. Pedersen, Ulf DeFaire, Marjo‐Riitta Järvelin, Juha Saharinen, Nelson B. Freimer, Samuli Ripatti, Shaun Purcell, Andrew Collins, Mark J. Daly, Aarno Palotie, Leena Peltonen	2008	111
8	Isolates and their potential use in complex gene mapping efforts Current Opinion in Genetics & Development ·Teppo Varilo, (unknown)	2004	93
9	The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories Human Molecular Genetics ·Teppo Varilo	2003	87
10	Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families Molecular Psychiatry ·Juho Wedenoja, Anu Loukola, Annamari Tuulio‐Henriksson, Tiina Paunio, Jesper Ekelund, Kaisa Silander, Teppo Varilo, Kauko Heikkilä, Jaana Suvisaari, Timo Partonen, Jouko Lönnqvist, Leena Peltonen	2007	83
11	Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria The Lancet ·Vineta Fellman, Juhani Rapola, Helena Pihko, Teppo Varilo, Kari O. Raivio	1998	75
12	The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population. PubMed ·Teppo Varilo, Minna Savukoski, Reijo Norio, Pirkko Santavuori, Laura‐Maria Peltonen, Irma Järvelä	1996	67
13	Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia American Journal of Medical Genetics ·Annamari Tuulio‐Henriksson, Jari Haukka, Timo Partonen, Teppo Varilo, Tiina Paunio, Jesper Ekelund, Tyrone D. Cannon, Joanne M. Meyer, Jouko Lönnqvist	2002	66
14	Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients Biological Psychiatry ·Annamari Tuulio‐Henriksson, Ritva Arajärvi, Timo Partonen, Jari Haukka, Teppo Varilo, Marjut Schreck, Tyrone D. Cannon, Jouko Lönnqvist	2003	62
15	Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency The American Journal of Human Genetics ·Mikko Kuokkanen, Jorma Kokkonen, Nabil Enattah, Tero Ylisaukko‐oja, Hanna Komu, Teppo Varilo, Leena Peltonen, Erkki Savilahti, Irma Järvelä	2006	61
16	Genome-wide scan for loci of Asperger syndrome Molecular Psychiatry ·Tero Ylisaukko‐oja, Taina Nieminen‐von Wendt, Elli Kempas, Susan Sarenius, Teppo Varilo, L. von Wendt, Leena Peltonen, Irma Järvelä	2004	60
17	Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo European Journal of Human Genetics ·Teppo Varilo, Maris Laan, Iiris Hovatta, Victor Wiebe, Joseph D. Terwilliger, Leena Peltonen	2000	55
18	Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis PLoS Genetics ·Ritva Haataja, Minna K. Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Marja Ojaniemi, Teppo Varilo, Bimal P. Chaudhari, Jevon Plunkett, Jeffrey C. Murray, Steven A. McCarroll, Leena Peltonen, Louis J. Muglia, Aarno Palotie, Mikko Hallman	2011	53
19	Regional variation in the incidence of schizophrenia in Finland: a study of birth cohorts born from 1950 to 1969 Psychological Medicine ·Jari Haukka, Jaana Suvisaari, Teppo Varilo, Jouko Lönnqvist	2001	52
20	MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features Neurology ·Mari Auranen, Raija Vanhala, M. Vosman, Minna Levander, Teppo Varilo, Marja Hietala, Raili Riikonen, Leena Peltonen, Irma Järvelä	2001	52

About Teppo Varilo

Teppo Varilo is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Psychiatry and Mental health and Cellular and Molecular Neuroscience, having authored 51 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (17 papers), Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (7 papers), Bipolar Disorder and Treatment (4 papers), Schizophrenia research and treatment (4 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 (491 citations), Cognitive Neuroscience (542 citations), Clinical Biochemistry (174 citations) and Biological Psychiatry (49 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, Biological Psychiatry 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.

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