Publications by authors named "Teppo Varilo"

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The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia.
Marja Hakkarainen, Ilse Kaaja, Suvi P M Douglas, Tom Vulliamy, Inderjeet Dokal, Teppo Varilo

Blood· June 2023

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The Finnish genetic heritage in 2022 - from diagnosis to translational research.
Johanna Uusimaa, Johannes Kettunen, Teppo Varilo, Irma Järvelä, Jukka Kallijärvi

Dis Model Mech· October 2022

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Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland.
Irma Järvelä, Tuomo Määttä, Anushree Acharya, Juha Leppälä, Shalini N Jhangiani, Teppo Varilo

Hum Genet· July 2021

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Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Daniel L Polla, Elisa Rahikkala, Michaela K Bode, Tuomo Määttä, Teppo Varilo

Eur J Hum Genet· April 2020

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Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Daniel L Polla, Elisa Rahikkala, Michaela K Bode, Tuomo Määttä, Teppo Varilo

Eur J Hum Genet· August 2019

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NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease.
Johanna Uusimaa, Riitta Kaarteenaho, Teija Paakkola, Hannu Tuominen, Minna K Karjalainen, Teppo Varilo

Acta Neuropathol· May 2018

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Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes.
Tiia Maria Luukkonen, Mana M Mehrjouy, Minna Pöyhönen, Anna-Kaisa Anttonen, Päivi Lahermo, Teppo Varilo

Mol Genet Genomic Med· January 2018

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A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate.
Zuzanna Misiewicz, Tero Hiekkalinna, Tiina Paunio, Teppo Varilo, Joseph D Terwilliger

Sci Rep· December 2016

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The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.
Anne Polvi, Henna Linturi, Teppo Varilo, Anna-Kaisa Anttonen, Myles Byrne

Hum Mutat· November 2013

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Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders.
Georg Stoll, Olli P H Pietiläinen, Bastian Linder, Jaana Suvisaari, Cornelia Brosi, Teppo Varilo

Nat Neurosci· September 2013

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Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?
Minna Torniainen, Juho Wedenoja, Teppo Varilo, Timo Partonen, Jaana Suokas

Psychiatry Res· July 2013

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A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm.
Tiia M Luukkonen, Minna Pöyhönen, Aarno Palotie, Pekka Ellonen, Sonja Lagström, Teppo Varilo

J Med Genet· October 2012

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Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort.
Emma S Nyman, Anu Loukola, Teppo Varilo, Anja Taanila, Tuula Hurtig

Psychiatr Genet· August 2012

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Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.
Ritva Haataja, Minna K Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Teppo Varilo

PLoS Genet· February 2011

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Mutant CHUK and severe fetal encasement malformation.
Jenni Lahtela, Heidi O Nousiainen, Vedran Stefanovic, Jonna Tallila, Heli Viskari, Teppo Varilo

N Engl J Med· October 2010

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Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia.
Juho Wedenoja, Annamari Tuulio-Henriksson, Jaana Suvisaari, Anu Loukola, Tiina Paunio, Teppo Varilo

Biol Psychiatry· May 2010

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Identification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated population.
Outi M Palo, Pia Soronen, Kaisa Silander, Teppo Varilo, Katja Tuononen

Am J Med Genet B Neuropsychiatr Genet· April 2010

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Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, Teppo Varilo, Suvi Kallio

Am J Hum Genet· February 2010

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Linkage analysis of schizophrenia controlling for population substructure.
Tiina Paunio, Ritva Arajärvi, Joseph D Terwilliger, Tero Hiekkalinna, Perttu Haimi, Teppo Varilo

Am J Med Genet B Neuropsychiatr Genet· September 2009

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Impact of the dopamine receptor gene family on temperament traits in a population-based birth cohort.
Emma S Nyman, Anu Loukola, Teppo Varilo, Jesper Ekelund, Juha Veijola

Am J Med Genet B Neuropsychiatr Genet· September 2009

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Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.
Helena Kilpinen, Tero Ylisaukko-oja, Karola Rehnström, Emilia Gaál, Joni A Turunen, Teppo Varilo

Hum Mol Genet· August 2009

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Chiara Sabatti, Susan K Service, Anna-Liisa Hartikainen, Anneli Pouta, Samuli Ripatti, Teppo Varilo

Nat Genet· January 2009

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The genome-wide patterns of variation expose significant substructure in a founder population.
Eveliina Jakkula, Karola Rehnström, Teppo Varilo, Olli P H Pietiläinen, Tiina Paunio

Am J Hum Genet· December 2008

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Prevalence and psychiatric comorbidity of attention-deficit/hyperactivity disorder in an adolescent Finnish population.
Susan L Smalley, James J McGough, Irma K Moilanen, Sandra K Loo, Anja Taanila, Teppo Varilo

J Am Acad Child Adolesc Psychiatry· December 2007

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ADHD candidate gene study in a population-based birth cohort: association with DBH and DRD2.
Emma S Nyman, Matthew N Ogdie, Anu Loukola, Teppo Varilo, Anja Taanila

J Am Acad Child Adolesc Psychiatry· December 2007

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