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1

Association of DISC1 with autism and Asperger syndrome

Kilpinen, H, Ylisaukko-oja, T, Hennah, W, Palo, O M, Varilo, T, Vanhala, R, Nieminen-von Wendt, T, von Wendt, L, Paunio, T, Peltonen, L

Journal:

Molecular Psychiatry

Year:

2007

Language:

english

File:

PDF, 181 KB

english, 2007

2

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia

Annamari Tuulio-Henriksson, Jari Haukka, Timo Partonen, Teppo Varilo, Tiina Paunio, Jesper Ekelund, Tyrone D. Cannon, Joanne M. Meyer, Jouko Lönnqvist

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 89 KB

english, 2002

3

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

Polvi, Anne, Linturi, Henna, Varilo, Teppo, Anttonen, Anna-Kaisa, Byrne, Myles, Fokkema, Ivo F.A.C., Almusa, Henrikki, Metzidis, Anthony, Avela, Kristiina, Aula, Pertti, Kestilä, Marjo, Muilu, Juha

Journal:

Year:

2013

Language:

english

File:

PDF, 238 KB

english, 2013

4

Genome-wide scan for loci of Asperger syndrome

Ylisaukko-oja, T, Nieminen-von Wendt, T, Kempas, E, Sarenius, S, Varilo, T, Wendt, L von, Peltonen, L, Järvelä, I

Journal:

Molecular Psychiatry

Year:

2004

Language:

english

File:

PDF, 245 KB

english, 2004

5

Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland

Auranen, M, Varilo, T, Alen, R, Vanhala, R, Ayers, K, Kempas, E, Ylisaukko-oja, T, Peltonen, L, Järvelä, I

Journal:

Molecular Psychiatry

Year:

2003

Language:

english

File:

PDF, 94 KB

english, 2003

6

Affective flattening and alogia associate with the familial form of schizophrenia

Ritva Arajärvi, Teppo Varilo, Jari Haukka, Jaana Suvisaari, Jaana Suokas, Hannu Juvonen, Maria Muhonen, Kirsi Suominen, Jukka Hintikka, Marjut Schreck, Annamari Tuulio-Henriksson, Timo Partonen, Jouko

Journal:

Psychiatry Research

Year:

2006

Language:

english

File:

PDF, 199 KB

english, 2006

7

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, Tuula Kieseppä, Timo Partonen, Jouko Lönnqvist, Tiina Paunio, Leena Peltonen

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2010

Language:

english

File:

PDF, 500 KB

english, 2010

8

Assignment of the Locus for a New Lethal Neonatal Metabolic Syndrome to 2q33-37

Ilona Visapää, Vineta Fellman, Teppo Varilo, Aarno Palotie, Kari O. Raivio, Leena Peltonen

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 746 KB

english, 1998

9

Mutant CHUK and Severe Fetal Encasement Malformation

Lahtela, Jenni, Nousiainen, Heidi O., Stefanovic, Vedran, Tallila, Jonna, Viskari, Heli, Karikoski, Riitta, Gentile, Massimiliano, Saloranta, Carola, Varilo, Teppo, Salonen, Riitta, Kestilä, Marjo

Journal:

Boston Medical and Surgical Journal

Year:

2010

Language:

english

File:

PDF, 1.15 MB

english, 2010

10

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G, Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 13.03 MB

english, 2008

11

Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis

Haataja, Ritva, Karjalainen, Minna K., Luukkonen, Aino, Teramo, Kari, Puttonen, Hilkka, Ojaniemi, Marja, Varilo, Teppo, Chaudhari, Bimal P., Plunkett, Jevon, Murray, Jeffrey C., McCarroll, Steven A.,

Journal:

Year:

2011

Language:

english

File:

PDF, 827 KB

english, 2011

12

The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland

Joni A. Turunen, Juho O. Peltonen, Olli P.H. Pietiläinen, William Hennah, Anu Loukola, Tiina Paunio, Kaisa Silander, Jesper Ekelund, Teppo Varilo, Timo Partonen, Jouko Lönnqvist, Leena Peltonen

Journal:

Schizophrenia Research

Year:

2007

Language:

english

File:

PDF, 529 KB

english, 2007

13

Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Polla, Daniel L., Rahikkala, Elisa, Bode, Michaela K., Määttä, Tuomo, Varilo, Teppo, Loman, Thyrza, Philips, Anju K., Kurki, Mitja, Palotie, Aarno, Körkkö, Jarmo, Vieira, Päivi, Avela, Kristiina, Jacq

Journal:

European Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 237 KB

english, 2019

14

Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort

Nyman, Emma S., Loukola, Anu, Varilo, Teppo, Taanila, Anja, Hurtig, Tuula, Moilanen, Irma, Loo, Sandra, McGough, James J., Järvelin, Marjo-Riitta, Smalley, Susan L., Nelson, Stanley F., Peltonen, Leen

Journal:

Psychiatric Genetics

Year:

2012

Language:

english

File:

PDF, 278 KB

english, 2012

15

MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features

Auranen, M., Vanhala, R., Vosman, M., Levander, M., Varilo, T., Hietala, M., Riikonen, R., Peltonen, L., Jarvela, I.

Journal:

Year:

2001

Language:

english

File:

PDF, 221 KB

english, 2001

16

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families

Wedenoja, J, Loukola, A, Tuulio-Henriksson, A, Paunio, T, Ekelund, J, Silander, K, Varilo, T, Suvisaari, J, Partonen, T, Heikkilä, K

Journal:

Molecular Psychiatry

Year:

2007

Language:

english

File:

PDF, 239 KB

english, 2007

17

Fine-Scale Mapping of a Novel Dementia Gene, PLOSL, by Linkage Disequilibrium

P. Pekkarinen, M. Kestilä, J. Paloneva, J. Terwilliger, T. Varilo, O. Järvi, P. Hakola, L. Peltonen

Journal:

Year:

1998

Language:

english

File:

PDF, 155 KB

english, 1998

18

Bipolar disorder susceptibility region on Xq24–q27.1 in Finnish families

Ekholm, J M, Pekkarinen, P, Pajukanta, P, Kieseppä, T, Partonen, T, Paunio, T, Varilo, T, Perola, M, Lönnqvist, J, Peltonen, L

Journal:

Molecular Psychiatry

Year:

2002

Language:

english

File:

PDF, 186 KB

english, 2002

19

A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci

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 Pel

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 907 KB

english, 1999

20

Clinical phenotype of schizophrenia in a Finnish isolate

Ritva Arajärvi, Jari Haukka, Teppo Varilo, Jaana Suokas, Hannu Juvonen, Jaana Suvisaari, Maria Muhonen, Kirsi Suominen, Annamari Tuulio-Henriksson, Marjut Schreck, Iiris Hovatta, Timo Partonen, Jouko

Journal:

Schizophrenia Research

Year:

2004

Language:

english

File:

PDF, 275 KB

english, 2004

21

NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease

Uusimaa, Johanna, Kaarteenaho, Riitta, Paakkola, Teija, Tuominen, Hannu, Karjalainen, Minna K., Nadaf, Javad, Varilo, Teppo, Uusi-Mäkelä, Meri, Suo-Palosaari, Maria, Pietilä, Ilkka, Hiltunen, Anniina

Journal:

Acta Neuropathologica

Year:

2018

Language:

english

File:

PDF, 4.98 MB

english, 2018

22

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, Anu Kemppinen, Shaun Purcell, Keijo Koivisto, Pentti Tienari, Marja-Liisa Sumelahti, Irina Elovaara, Tuula Pirttilä, Mauri

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 507 KB

english, 2010

23

Isolates and their potential use in complex gene mapping efforts

Teppo Varilo, Leena Peltonen

Journal:

Current Opinion in Genetics & Development

Year:

2004

Language:

english

File:

PDF, 261 KB

english, 2004

24

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories

Journal:

Human Molecular Genetics

Year:

2003

Language:

english

File:

PDF, 1.24 MB

english, 2003

25

Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?

Torniainen, Minna, Wedenoja, Juho, Varilo, Teppo, Partonen, Timo, Suokas, Jaana, Häkkinen, Laura, Lönnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari

Journal:

Psychiatry Research

Year:

2013

Language:

english

File:

PDF, 232 KB

english, 2013

26

Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria

Vineta Fellman, Juhani Rapola, Helena Pihko, Teppo Varilo, Kari O Raivio

Journal:

Year:

1998

Language:

english

File:

PDF, 75 KB

english, 1998

27

Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland

Kilpinen, H., Ylisaukko-oja, T., Rehnstrom, K., Gaal, E., Turunen, J. A., Kempas, E., von Wendt, L., Varilo, T., Peltonen, L.

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 326 KB

english, 2009

28

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, Nancy L. Pedersen, Ulf deFaire, Marjo-Riitta Järvelin, Juha Saharinen, Nelson Freimer, Samuli Ripatti, Shaun Purc

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 596 KB

english, 2008

29

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, Timo Partonen, Teppo Varilo, Jouko Lönnqvist, Leena Peltonen

Journal:

Biological Psychiatry

Year:

2010

Language:

english

File:

PDF, 485 KB

english, 2010

30

A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate

Misiewicz, Zuzanna, Hiekkalinna, Tero, Paunio, Tiina, Varilo, Teppo, Terwilliger, Joseph D., Partonen, Timo, Hovatta, Iiris

Journal:

Scientific Reports

Year:

2016

Language:

english

File:

PDF, 677 KB

english, 2016

31

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo

Varilo, Teppo, Laan, Maris, Hovatta, Iiris, Wiebe, Victor, Terwilliger, Joseph D, Peltonen, Leena

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 195 KB

english, 2000

32

Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency

Mikko Kuokkanen, Jorma Kokkonen, Nabil Sabri Enattah, Tero Ylisaukko-oja, Hanna Komu, Teppo Varilo, Leena Peltonen, Erkki Savilahti, Irma Järvelä

Journal:

The American Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 754 KB

english, 2006

33

Om ungdomsaddiktionens etiologi

Journal:

Nordic Journal of Psychiatry

Year:

1970

File:

PDF, 1004 KB

1970

34

Regional variation in the incidence of schizophrenia in Finland: a study of birth cohorts born from 1950 to 1969

HAUKKA, J., SUVISAARI, J., VARILO, T., LÖNNQVIST, J.

Journal:

Psychological Medicine

Year:

2001

Language:

english

File:

PDF, 781 KB

english, 2001

35

Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes

Luukkonen, Tiia Maria, Mehrjouy, Mana M., Pöyhönen, Minna, Anttonen, Anna-Kaisa, Lahermo, Päivi, Ellonen, Pekka, Paulin, Lars, Tommerup, Niels, Palotie, Aarno, Varilo, Teppo

Journal:

Molecular Genetics & Genomic Medicine

Year:

2017

Language:

english

File:

PDF, 2.07 MB

english, 2017

36

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.

Varilo, T, Nikali, K, Suomalainen, A, Lonnqvist, T, Peltonen, L

Journal:

Genome Research

Year:

1996

Language:

english

File:

PDF, 766 KB

english, 1996

37

Linkage analysis of schizophrenia controlling for population substructure

Tiina Paunio, Ritva Arajärvi, Joseph D. Terwilliger, Tero Hiekkalinna, Perttu Haimi, Timo Partonen, Jouko Lönnqvist, Leena Peltonen, Teppo Varilo

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2009

Language:

english

File:

PDF, 421 KB

english, 2009

38

Assignment of the Locus for Hydrolethalus Syndrome to a Highly Restricted Region on 11q23-25

Ilona Visapää, Riitta Salonen, Teppo Varilo, Paulina Paavola, Leena Peltonen

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 515 KB

english, 1999

39

A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm

Luukkonen, T. M., Poyhonen, M., Palotie, A., Ellonen, P., Lagstrom, S., Lee, J. H., Terwilliger, J. D., Salonen, R., Varilo, T.

Journal:

Journal of Medical Genetics

Year:

2012

Language:

english

File:

PDF, 552 KB

english, 2012

40

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, Matti Joukamaa, Anja Taanila, Anneli Pouta, Jouko Miettunen, Nelson Freimer, Marjo-Riitta Järvelin, Leena Peltonen

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2009

Language:

english

File:

PDF, 180 KB

english, 2009

41

ADHD Candidate Gene Study in a Population-Based Birth Cohort: Association with DBH and DRD2

NYMAN, EMMA S., OGDIE, MATTHEW N., LOUKOLA, ANU, VARILO, TEPPO, TAANILA, ANJA, HURTIG, TUULA, MOILANEN, IRMA K., LOO, SANDRA K., McGOUGH, JAMES J., JÄRVELIN, MARJO-RIITTA, SMALLEY, SUSAN L., NELSON, S

Journal:

Journal of the American Academy of Child & Adolescent Psychiatry

Year:

2007

Language:

english

File:

PDF, 167 KB

english, 2007

42

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia

Hennah, W, Tuulio-Henriksson, A, Paunio, T, Ekelund, J, Varilo, T, Partonen, T, Cannon, T D, Lönnqvist, J, Peltonen, L

Journal:

Molecular Psychiatry

Year:

2005

Language:

english

File:

PDF, 132 KB

english, 2005

43

A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27

Mari Auranen, Raija Vanhala, Teppo Varilo, Kristin Ayers, Elli Kempas, Tero Ylisaukko-oja, Janet S. Sinsheimer, Leena Peltonen, Irma Järvelä

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 2.09 MB

english, 2002

44

Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries

H. Mannila, M. Koivisto, M. Perola, T. Varilo, W. Hennah, J. Ekelund, M. Lukk, L. Peltonen, E. Ukkonen

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 1.31 MB

english, 2003

45

Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients

Annamari Tuulio-Henriksson, Ritva Arajärvi, Timo Partonen, Jari Haukka, Teppo Varilo, Marjut Schreck, Tyrone Cannon, Jouko Lönnqvist

Journal:

Biological Psychiatry

Year:

2003

Language:

english

File:

PDF, 57 KB

english, 2003

46

Prevalence and Psychiatric Comorbidity of Attention-Deficit/Hyperactivity Disorder in an Adolescent Finnish Population

SMALLEY, SUSAN L., McGOUGH, JAMES J., MOILANEN, IRMA K., LOO, SANDRA K., TAANILA, ANJA, EBELING, HANNA, HURTIG, TUULA, KAAKINEN, MARIKA, HUMPHREY, LORIE A., McCRACKEN, JAMES T., VARILO, TEPPO, YANG, M

Journal:

Journal of the American Academy of Child & Adolescent Psychiatry

Year:

2007

Language:

english

File:

PDF, 325 KB

english, 2007

47

Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Polla, Daniel L., Rahikkala, Elisa, Bode, Michaela K., Määttä, Tuomo, Varilo, Teppo, Loman, Thyrza, Philips, Anju K., Kurki, Mitja, Palotie, Aarno, Körkkö, Jarmo, Vieira, Päivi, Avela, Kristiina, Jacq

Journal:

European Journal of Human Genetics

Year:

2019

File:

PDF, 237 KB

2019

48

Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene

Irma Järvelä, Nabil Sabri Enattah, Jorma Kokkonen, Teppo Varilo, Erkki Savilahti, Leena Peltonen

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 1.31 MB

english, 1998

49

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia

Hennah, William, Varilo, Teppo, Paunio, Tiina, Peltonen, Leena

Journal:

Annals of Medicine

Year:

2004

Language:

english

File:

PDF, 366 KB

english, 2004

50

Identification of C12orf4 as a gene for autosomal recessive intellectual disability

Philips, A.K., Pinelli, M., de Bie, C.I., Mustonen, A., Määttä, T., Arts, H.H., Wu, K., Roepman, R., Moilanen, J.S., Raza, S., Varilo, T., Scala, G., Cocozza, S., Gilissen, C., van Gassen, K.L.I., Jär

Journal:

Clinical Genetics

Year:

2016

Language:

english

File:

PDF, 1.23 MB

english, 2016

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